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Showing 240 products

Date | Title

Acalabrutinib and venetoclax with or without obinutuzumab for untreated chronic lymphocytic leukaemia ID6232
Status:
In development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Acalabrutinib for treating chronic lymphocytic leukaemia (TA689)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
21 April 2021
Acalabrutinib for treating relapsed or refractory mantle cell lymphoma [ID6389]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Acalabrutinib with bendamustine and rituximab for untreated mantle cell lymphoma [ID6155]
Status:
In development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Acalabrutinib with venetoclax and obinutuzumab for untreated chronic lymphocytic leukaemia [ID6156]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Alpha-1 antitrypsin for treating high-risk acute graft-versus-host disease after a haematopoietic stem cell transplant in people 12 years and over [TSID12036]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Anitocabtagene autoleucel for treating relapsed or refractory multiple myeloma after 3 or more treatment lines [ID6549]
Status:
Topic selection
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Arsenic trioxide for treating acute promyelocytic leukaemia (TA526)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
13 June 2018
Asciminib for treating chronic myeloid leukaemia after 2 or more tyrosine kinase inhibitors (TA813)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
3 August 2022
Avapritinib for treating advanced systemic mastocytosis (TA1012)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
6 November 2024
Axatilimab for treating active chronic graft-versus-host disease after 2 or more systemic treatments in people 2 years and over [ID6570]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Axicabtagene ciloleucel for treating diffuse large B-cell lymphoma and primary mediastinal large B-cell lymphoma after 2 or more systemic therapies (TA872)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
28 February 2023
Axicabtagene ciloleucel for treating relapsed or refractory diffuse large B-cell lymphoma after first-line chemoimmunotherapy (TA895)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
7 June 2023
Axicabtagene ciloleucel for treating relapsed or refractory follicular lymphoma (TA894)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
7 June 2023
Azacitidine for the treatment of myelodysplastic syndromes, chronic myelomonocytic leukaemia and acute myeloid leukaemia (TA218)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
23 March 2011
Azacitidine for treating acute myeloid leukaemia with more than 30% bone marrow blasts (TA399)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
27 July 2016
Belantamab mafodotin for treating relapsed or refractory multiple myeloma after 2 therapies [ID5108]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Belantamab mafodotin for treating relapsed or refractory multiple myeloma after 4 or more therapies [ID2701]
Status:
In development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Belantamab mafodotin with bortezomib and dexamethasone for treating relapsed or refractory multiple myeloma after 1 or more treatments [ID6212]
Status:
In development | In consultation
Programme:
Technology appraisal guidance
Consultation end date:
3 July 2025
Expected publication date:
TBC
Belantamab mafodotin with pomalidomide and dexamethasone for treating relapsed or refractory multiple myeloma after 1 or more treatments ID6211
Status:
In development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Belumosudil for treating chronic graft-versus-host disease after 2 or more systemic treatments in people 12 years and over (TA949)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
7 February 2024
Bendamustine for the first-line treatment of chronic lymphocytic leukaemia (TA216)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
23 February 2011
Bendamustine for the treatment of indolent (low grade) non-Hodgkin's lymphoma that is refractory to rituximab (terminated appraisal) (TA206)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
27 October 2010
Blinatumomab for previously treated Philadelphia-chromosome-negative acute lymphoblastic leukaemia (TA450)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
28 June 2017
Blinatumomab for previously treated Philadelphia-chromosome-positive acute lymphoblastic leukaemia (terminated appraisal) (TA686)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
31 March 2021
Blinatumomab for treating acute lymphoblastic leukaemia in remission with minimal residual disease activity (TA589)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
24 July 2019
Blinatumomab with chemotherapy for consolidation treatment of Philadelphia-chromosome-negative CD19-positive B-precursor acute lymphoblastic leukaemia with no measurable residual disease [TSID11991]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Blinatumomab with chemotherapy for consolidation treatment of Philadelphia-chromosome-negative CD19-positive minimal residual disease-negative B-cell precursor acute lymphoblastic leukaemia (TA1049)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
26 March 2025
Bortezomib and thalidomide for the first‑line treatment of multiple myeloma (TA228)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
27 July 2011
Bortezomib for induction therapy in multiple myeloma before high-dose chemotherapy and autologous stem cell transplantation (TA311)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
23 April 2014
Bortezomib for previously untreated mantle cell lymphoma (TA370)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
16 December 2015
Bortezomib for treating multiple myeloma after second or subsequent relapse (terminated appraisal) (TA453)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
5 July 2017
Bortezomib monotherapy for relapsed multiple myeloma (TA129)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
23 October 2007
Bosutinib for previously treated chronic myeloid leukaemia (TA401)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
24 August 2016
Bosutinib for untreated chronic myeloid leukaemia (terminated appraisal) (TA576)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
17 April 2019
Brentuximab vedotin for treating CD30-positive cutaneous T-cell lymphoma (TA577)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
24 April 2019
Brentuximab vedotin for treating CD30-positive Hodgkin lymphoma (TA524)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
13 June 2018
Brentuximab vedotin for treating relapsed or refractory systemic anaplastic large cell lymphoma (TA478)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
4 October 2017
Brentuximab vedotin in combination for untreated stage 3 or 4 CD30-positive Hodgkin lymphoma (TA1059)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
7 May 2025
Brentuximab vedotin in combination for untreated systemic anaplastic large cell lymphoma (TA641)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
12 August 2020
Brentuximab vedotin with etoposide, cyclophosphamide, doxorubicin, dacarbazine and dexamethasone for untreated advanced classical Hodgkin lymphoma [ID6437]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Brexucabtagene autoleucel for treating relapsed or refractory B-cell acute lymphoblastic leukaemia in people 26 years and over (TA893)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
7 June 2023
Brexucabtagene autoleucel for treating relapsed or refractory mantle cell lymphoma (TA677)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
24 February 2021
Brexucabtagene autoleucel for treating relapsed or refractory mantle cell lymphoma after 2 or more systemic treatments (review of TA677) [ID6325]
Status:
In development
Programme:
Technology appraisal guidance
Expected publication date:
5 November 2025
Carfilzomib for previously treated multiple myeloma (TA657)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
18 November 2020
Carfilzomib in combination for untreated multiple myeloma when an autologous stem cell transplant is suitable [TSID12176]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Carfilzomib with daratumumab and dexamethasone for treating relapsed or refractory multiple myeloma (terminated appraisal) (TA841)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
22 November 2022
Carfilzomib with dexamethasone and lenalidomide for previously treated multiple myeloma (TA695)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
28 April 2021
Chlormethine gel for treating mycosis fungoides-type cutaneous T-cell lymphoma (TA720)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
18 August 2021
Ciltacabtagene autoleucel for treating relapsed and lenalidomide-refractory multiple myeloma after 1 to 3 therapies [ID4012]
Status:
In development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Ciltacabtagene autoleucel for treating relapsed or refractory multiple myeloma (terminated appraisal) (TA889)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
17 May 2023
clonoSEQ for minimal residual disease assessment in multiple myeloma, acute lymphoblastic leukaemia and chronic lymphocytic leukaemia (MIB278)
Product type:
Advice
Programme:
Medtech innovation briefing
Published:
30 November 2021
Daratumumab for treating high-risk smouldering multiple myeloma [ID6214]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Daratumumab in combination for untreated multiple myeloma when a stem cell transplant is suitable (TA763)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
2 February 2022
Daratumumab monotherapy for treating relapsed and refractory multiple myeloma (TA783)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
13 April 2022
Daratumumab with bortezomib and dexamethasone for previously treated multiple myeloma (TA897)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
6 June 2023
Daratumumab with bortezomib, lenalidomide and dexamethasone for untreated multiple myeloma when an autologous stem cell transplant is suitable ID6249
Status:
In development
Programme:
Technology appraisal guidance
Expected publication date:
4 March 2026
Daratumumab with bortezomib, lenalidomide and dexamethasone for untreated multiple myeloma when a stem cell transplant is unsuitable [ID3843]
Status:
In development
Programme:
Technology appraisal guidance
Expected publication date:
25 February 2026
Daratumumab with bortezomib, melphalan and prednisone for untreated multiple myeloma (terminated appraisal) (TA771)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
9 February 2022
Daratumumab with lenalidomide and dexamethasone for treating relapsed or refractory multiple myeloma (terminated appraisal) (TA454)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
5 July 2017
Daratumumab with lenalidomide and dexamethasone for untreated multiple myeloma (terminated appraisal) (TA634)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
30 June 2020
Daratumumab with lenalidomide and dexamethasone for untreated multiple myeloma when a stem cell transplant is unsuitable (TA917)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
25 October 2023
Daratumumab with pomalidomide and dexamethasone for treating relapsed or refractory multiple myeloma (terminated appraisal) (TA726)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
22 September 2021
Dasatinib for treating Philadelphia-chromosome-positive acute lymphoblastic leukaemia in children and adults ID1297
Product type:
Guidance
Programme:
Technology appraisal guidance
Expected publication date:
28 July 2021
Dasatinib for treating Philadelphia-chromosome-positive acute lymphoblastic leukaemia (terminated appraisal) (TA714)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
14 July 2021
Dasatinib, nilotinib and high-dose imatinib for treating imatinib-resistant or intolerant chronic myeloid leukaemia (TA425)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
21 December 2016
Dasatinib, nilotinib and imatinib for untreated chronic myeloid leukaemia (TA426)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
21 December 2016
Decitabine–cedazuridine for untreated acute myeloid leukaemia when intensive chemotherapy is unsuitable (terminated appraisal) (TA932)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
23 November 2023
Decitabine-cedazuridine (Inqovi) + Venetoclax for Acute myeloid leukaemia (AML) [ID12200]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Decitabine for the treatment of acute myeloid leukaemia (terminated appraisal) (TA270)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
12 December 2012
Decitabine for untreated acute myeloid leukaemia (terminated appraisal) (TA548)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
5 December 2018
Denosumab biosimilar for Giant cell-rich tumours of bone or Skeletal events in bone malignancies ID12150
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Denosumab for preventing skeletal-related events in multiple myeloma (terminated appraisal) (TA549)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
5 December 2018
Dorocubicel for treating haematological cancer when a suitable donor is unavailable for an allogeneic haematopoietic stem cell transplant [ID6521]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Duvelisib for treating relapsed follicular lymphoma after 2 or more systemic therapies (terminated appraisal) (TA717)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
21 July 2021
Duvelisib for treating relapsed or refractory chronic lymphocytic leukaemia after 2 or more treatments (terminated appraisal) (TA811)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
27 July 2022
Duvelisib for treating relapsed or refractory peripheral T-cell lymphoma [ID5076]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Elotuzumab for previously treated multiple myeloma (terminated appraisal) (TA434)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
22 March 2017
Elranatamab for treating relapsed and refractory multiple myeloma after 3 or more treatments (TA1023)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
11 December 2024
Elranatamab for treating relapsed or refractory multiple myeloma after 2 treatments [ID6464]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Elranatamab for treating relapsed or refractory multiple myeloma after treatments including anti-CD38 antibody and lenalidomide therapy [ID6591]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Epcoritamab for treating relapsed or refractory diffuse large B-cell lymphoma after 2 or more systemic treatments (TA954)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
6 March 2024
Epcoritamab for treating relapsed or refractory diffuse large B-cell lymphoma after first-line systemic treatment [ID6463]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Epcoritamab for treating relapsed or refractory follicular lymphoma after 2 or more systemic treatments [ID6338]
Status:
In development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Epcoritamab with rituximab and lenalidomide for treating relapsed or refractory follicular lymphoma after 1 or more systemic treatments [ID12197]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Favezelimab–pembrolizumab for treating relapsed or refractory classical Hodgkin lymphoma after anti-PD-L1 treatment [ID6393]
Status:
In development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Fedratinib for treating disease-related splenomegaly or symptoms in myelofibrosis (TA1018)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
20 November 2024
Fludarabine monotherapy for the first-line treatment of chronic lymphocytic leukaemia (TA119)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
28 February 2007
Freelite assays for diagnosing multiple myeloma and related conditions (terminated assessment) (DG47)
Product type:
Guidance
Programme:
Diagnostics guidance
Published:
30 March 2022
Gemtuzumab ozogamicin for untreated acute myeloid leukaemia (TA545)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
14 November 2018
Gilteritinib for treating relapsed or refractory acute myeloid leukaemia (TA642)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
12 August 2020
Glasdegib with chemotherapy for untreated acute myeloid leukaemia (terminated appraisal) (TA646)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
2 September 2020
Glofitamab for treating relapsed or refractory diffuse large B-cell lymphoma after 2 or more systemic treatments (TA927)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
17 October 2023
Glofitamab with gemcitabine and oxaliplatin for treating relapsed or refractory diffuse B-cell lymphoma [ID6202]
Status:
In development
Programme:
Technology appraisal guidance
Expected publication date:
17 September 2025
Guidance on the use of fludarabine for B-cell chronic lymphocytic leukaemia (TA29)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
26 September 2001
Guidance on the use of imatinib for chronic myeloid leukaemia (TA70)
Product type:
Guidance
Programme:
Technology appraisal guidance
Last updated:
21 January 2016
Published:
22 October 2003
Haematological cancers (QS150)
Product type:
Quality standard
Published:
1 June 2017
Haematological cancers: improving outcomes (NG47)
Product type:
Guidance
Programme:
NICE guideline
Published:
25 May 2016
High intensity focused ultrasound ablation for pain caused by bone metastases
Status:
Topic selection
Programme:
Interventional procedures guidance
Expected publication date:
TBC
Histamine dihydrochloride with interleukin-2 for maintenance treatment of acute myeloid leukaemia ID1627
Status:
In development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Human acellular vessel (Humacyl; HAV) For use as an arterial venous access for patients with end stage renal disease (ESRD) requiring haemodialysis [ID3747]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Human normal immunoglobulin for preventing infection in chronic lymphocytic leukaemia [TSID12043]
Status:
Topic selection
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Human normal immunoglobulin for preventing infection in chronic lymphocytic leukaemia [TSID12043]
Status:
Topic selection
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Ibrutinib for previously treated chronic lymphocytic leukaemia and untreated chronic lymphocytic leukaemia with 17p deletion or TP53 mutation (TA429)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
25 January 2017
Ibrutinib for treating relapsed or refractory follicular lymphoma [1251]
Status:
In development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Ibrutinib for treating relapsed or refractory mantle cell lymphoma (TA502)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
31 January 2018
Ibrutinib for treating Waldenstrom’s macroglobulinaemia (TA795)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
8 June 2022
Ibrutinib for untreated chronic lymphocytic leukaemia without a 17p deletion or TP53 mutation (terminated appraisal) (TA452)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
5 July 2017
Ibrutinib with bendamustine and rituximab for treating relapsed or refractory chronic lymphocytic leukaemia after systemic therapy (terminated appraisal) (TA437)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
22 March 2017
Ibrutinib with obinutuzumab for untreated chronic lymphocytic leukaemia and small lymphocytic lymphoma (terminated appraisal) (TA702)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
26 May 2021
Ibrutinib with rituximab for treating Waldenstrom’s macroglobulinaemia (terminated appraisal) (TA608)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
30 October 2019
Ibrutinib with rituximab for untreated chronic lymphocytic leukaemia (terminated appraisal) (TA703)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
26 May 2021
Ibrutinib with venetoclax for untreated chronic lymphocytic leukaemia (TA891)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
31 May 2023
Idecabtagene vicleucel for treating relapsed and refractory multiple myeloma after 3 or more treatments (terminated appraisal) (TA936)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
30 November 2023
Idecabtagene vicleucel for treating relapsed or refractory multiple myeloma after 2 to 4 therapies [ID6491]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Idelalisib for treating chronic lymphocytic leukaemia (TA359)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
28 October 2015
Idelalisib for treating refractory follicular lymphoma (TA604)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
2 October 2019
Idelalisib with ofatumumab for treating chronic lymphocytic leukaemia (terminated appraisal) (TA469)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
23 August 2017
Imetelstat for treating intermediate-2 or high-risk relapsed or refractory myelofibrosis after a JAK inhibitor [TSID8376]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Imetelstat for treating relapsed or refractory transfusion-dependent myelodysplastic syndromes [ID3922]
Status:
In development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Inolimomab (Leukotac) for acute Graft versus host disease (aGvHD) after Allo-HSCT [ID3923]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Inotuzumab ozogamicin for treating relapsed or refractory B-cell acute lymphoblastic leukaemia (TA541)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
19 September 2018
Iodine (131I)–apamistamab for treating relapsed or refractory acute myeloid leukaemia before an allogeneic haematopoietic stem cell transplant [ID6355]
Status:
In development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Isatuximab in combination as induction therapy for untreated multiple myeloma when an autologous stem cell transplant is suitable [TSID11949]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Isatuximab in combination for untreated multiple myeloma when a stem cell transplant is unsuitable ID3981
Status:
In development | In consultation
Programme:
Technology appraisal guidance
Consultation end date:
19 June 2025
Expected publication date:
5 September 2025
Isatuximab with carfilzomib and dexamethasone for treating relapsed or refractory multiple myeloma (terminated appraisal) (TA727)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
22 September 2021
Isatuximab with pomalidomide and dexamethasone for treating relapsed and refractory multiple myeloma (TA658)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
18 November 2020
Isatuximab with pomalidomide and dexamethasone for treating relapsed and refractory multiple myeloma [Review of TA658] [ID4067]
Status:
In development
Programme:
Technology appraisal guidance
Expected publication date:
15 October 2025
Ivosidenib with azacitidine for untreated acute myeloid leukaemia with an IDH1 R132 mutation (TA979)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
5 June 2024
Ixazomib citrate for maintenance treatment of untreated multiple myeloma after autologous stem cell transplant [ID1517]
Status:
In development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Ixazomib citrate for maintenance treatment of untreated multiple myeloma in people who cannot have autologous stem cell transplant [ID2706]
Status:
In development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Ixazomib with lenalidomide and dexamethasone for treating relapsed or refractory multiple myeloma (TA870)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
22 February 2023
Lenalidomide for relapsed or refractory mantle cell lymphoma (terminated appraisal) (TA774)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
9 March 2022
Lenalidomide for the treatment of multiple myeloma in people who have received at least 2 prior therapies (TA171)
Product type:
Guidance
Programme:
Technology appraisal guidance
Last updated:
26 June 2019
Published:
18 June 2009
Lenalidomide for treating myelodysplastic syndromes associated with an isolated deletion 5q cytogenetic abnormality (TA322)
Product type:
Guidance
Programme:
Technology appraisal guidance
Last updated:
26 June 2019
Published:
24 September 2014
Lenalidomide maintenance treatment after an autologous stem cell transplant for newly diagnosed multiple myeloma (TA680)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
3 March 2021
Lenalidomide plus dexamethasone for multiple myeloma after 1 treatment with bortezomib (TA586)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
26 June 2019
Lenalidomide plus dexamethasone for previously untreated multiple myeloma (TA587)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
26 June 2019
Lenalidomide with bortezomib and dexamethasone for untreated multiple myeloma (terminated appraisal) (TA603)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
25 September 2019
Lenalidomide with rituximab for previously treated follicular lymphoma (TA627)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
7 April 2020
Liposomal cytarabine–daunorubicin for treating relapsed or refractory acute myeloid leukaemia in people aged 1 to 21 years [ID4017]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Liposomal cytarabine–daunorubicin for untreated acute myeloid leukaemia (TA552)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
19 December 2018
Lisocabtagene maraleucel for treating relapsed or refractory aggressive B-cell non-Hodgkin lymphoma after 1 systemic treatment [ID3869]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Lisocabtagene maraleucel for treating relapsed or refractory aggressive B-cell non-Hodgkin lymphoma (terminated appraisal) (TA987)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
10 July 2024
Lisocabtagene maraleucel for treating relapsed or refractory chronic lymphocytic leukaemia or small lymphocytic lymphoma [ID6174]
Status:
In development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Lisocabtagene maraleucel for treating relapsed or refractory large B-cell lymphoma after first-line chemoimmunotherapy when a stem cell transplant is suitable (TA1048)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
26 March 2025
Lisocabtagene maraleucel for treating relapsed or refractory low-grade B-cell follicular lymphoma after 1 or more treatments [ID6564]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Loncastuximab tesirine for treating relapsed or refractory diffuse large B-cell lymphoma and high-grade B-cell lymphoma after 2 or more systemic treatments (TA947)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
31 January 2024
Melphalan flufenamide with dexamethasone for treating relapsed or refractory multiple myeloma (terminated appraisal) (TA968)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
25 April 2024
Melphalan for haematological diseases before allogeneic haematopoietic stem cell transplant (terminated appraisal) (TA822)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
14 September 2022
Mezigdomide with dexamethasone and carfilzomib for treating relapsed or refractory multiple myeloma after at least 1 line of treatment [ID6513]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Midostaurin for treating advanced systemic mastocytosis (TA728)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
22 September 2021
Midostaurin for untreated acute myeloid leukaemia (TA523)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
13 June 2018
Mifamurtide for the treatment of osteosarcoma (TA235)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
26 October 2011
MMprofiler for prognostic risk classification in multiple myeloma (MIB270)
Product type:
Advice
Programme:
Medtech innovation briefing
Published:
10 August 2021
MMprofiler for prognostic risk classification in multiple myeloma (MT623) (MIB270)
Status:
Topic selection
Programme:
Diagnostics guidance
Expected publication date:
TBC
Mogamulizumab for previously treated mycosis fungoides and Sézary syndrome (TA754)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
15 December 2021
Momelotinib for treating myelofibrosis-related splenomegaly or symptoms (TA957)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
20 March 2024
Mosunetuzumab for treating relapsed or refractory follicular lymphoma (TA892)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
31 May 2023
Mosunetuzumab for treating relapsed or refractory follicular lymphoma [TSID 12081]
Status:
Topic selection
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Myeloma: diagnosis and management (NG35)
Product type:
Guidance
Programme:
NICE guideline
Last updated:
25 October 2018
Published:
10 February 2016
Navitoclax with ruxolitinib for treating myelofibrosis when stem cell transplant is unsuitable [ID5096]
Status:
In development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Nivolumab for treating relapsed or refractory classical Hodgkin lymphoma (TA462)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
26 July 2017
Non-Hodgkin’s lymphoma: diagnosis and management (NG52)
Product type:
Guidance
Programme:
NICE guideline
Published:
20 July 2016
Non-Hodgkin's lymphoma: rituximab subcutaneous injection (ESNM46)
Product type:
Advice
Programme:
Evidence summary
Published:
9 September 2014
Obecabtagene autoleucel for treating relapsed or refractory B-cell acute lymphoblastic leukaemia [ID6347]
Status:
In development | In consultation
Programme:
Technology appraisal guidance
Consultation end date:
4 July 2025
Expected publication date:
15 October 2025
Obinutuzumab for untreated advanced follicular lymphoma (TA513)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
21 March 2018
Obinutuzumab in combination with chlorambucil for untreated chronic lymphocytic leukaemia (TA343)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
2 June 2015
Obinutuzumab with bendamustine for treating follicular lymphoma after rituximab (TA629)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
13 May 2020
Oral azacitidine for maintenance treatment of acute myeloid leukaemia after induction therapy (TA827)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
5 October 2022
Panobinostat for treating multiple myeloma after at least 2 previous treatments (TA380)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
27 January 2016
Pegaspargase for treating acute lymphoblastic leukaemia (TA408)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
28 September 2016
Pembrolizumab for treating relapsed or refractory classical Hodgkin lymphoma (TA540)
Product type:
Guidance
Programme:
Technology appraisal guidance
Last updated:
1 May 2024
Published:
3 September 2018
Pembrolizumab for treating relapsed or refractory classical Hodgkin lymphoma after stem cell transplant or at least 2 previous therapies (TA772)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
23 February 2022
Pembrolizumab for treating relapsed or refractory classical Hodgkin lymphoma in people 3 years and over (TA967)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
1 May 2024
Pirtobrutinib for treating chronic lymphocytic leukaemia or small lymphocytic lymphoma after 1 or more BTK inhibitors [ID6269]
Status:
In development
Programme:
Technology appraisal guidance
Expected publication date:
29 January 2026
Pirtobrutinib for treating relapsed or refractory mantle cell lymphoma [ID3975]
Status:
In development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Pirtobrutinib for treating relapsed or refractory mantle cell lymphoma untreated with a BTK inhibitor [ID6493]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Pirtobrutinib for untreated chronic lymphocytic leukaemia or small lymphocytic lymphoma [ID6397]
Status:
In development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Pirtobrutinib with venetoclax and rituximab for previously treated chronic lymphocytic leukaemia or small lymphocytic lymphoma [TSID12182]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Pixantrone monotherapy for treating multiply relapsed or refractory aggressive non-Hodgkin's B‑cell lymphoma (TA306)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
26 February 2014
Polatuzumab vedotin in combination for untreated diffuse large B-cell lymphoma (TA874)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
1 March 2023
Polatuzumab vedotin with rituximab and bendamustine for treating relapsed or refractory diffuse large B-cell lymphoma (TA649)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
23 September 2020
Pomalidomide for multiple myeloma previously treated with lenalidomide and bortezomib (TA427)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
11 January 2017
Pomalidomide with bortezomib and dexamethasone for treating relapsed or refractory multiple myeloma (terminated appraisal) (TA602)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
25 September 2019
Ponatinib for treating chronic myeloid leukaemia and acute lymphoblastic leukaemia (TA451)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
28 June 2017
Quizartinib for induction, consolidation and maintenance treatment of newly diagnosed FLT3-ITD-positive acute myeloid leukaemia (TA1013)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
23 October 2024
REGN5458 for treating relapsed or refractory multiple myeloma [TSID10443]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Resminostat for maintenance treatment of advanced mycosis fungoides or Sézary syndrome [ID6478]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Rituximab for the first-line maintenance treatment of follicular non-Hodgkin's lymphoma (TA226)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
22 June 2011
Rituximab for the first-line treatment of chronic lymphocytic leukaemia (TA174)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
22 July 2009
Rituximab for the first-line treatment of stage III-IV follicular lymphoma (TA243)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
25 January 2012
Rituximab for the treatment of relapsed or refractory chronic lymphocytic leukaemia (TA193)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
28 July 2010
Rituximab for the treatment of relapsed or refractory stage III or IV follicular non-Hodgkin's lymphoma (TA137)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
27 February 2008
Rivogenlecleucel for treating haematological cancers in children and young people undergoing haploidentical haematopoietic stem cell transplant [ID1601]
Status:
In development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Ruxolitinib for treating acute graft-versus-host disease after allogeneic stem cell transplant in people 28 days to 17 years [ID6410]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Ruxolitinib for treating acute graft versus host disease that responds inadequately to corticosteroids in people 12 years and over (TA1054)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
15 April 2025
Ruxolitinib for treating chronic graft versus host disease refractory to corticosteroids (terminated appraisal) (TA840)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
16 November 2022
Ruxolitinib for treating disease-related splenomegaly or symptoms in adults with myelofibrosis (TA386)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
23 March 2016
Ruxolitinib for treating moderate to severe chronic graft-versus-host disease after an allogeneic stem cell transplant in people 28 days to 17 years [ID6427]
Status:
In development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Ruxolitinib for treating polycythaemia vera (TA921)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
18 October 2023
Selinexor with bortezomib and dexamethasone for previously treated multiple myeloma (TA974)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
15 May 2024
Selinexor with dexamethasone for treating relapsed or refractory multiple myeloma after 4 or more treatments (TA970)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
8 May 2024
Subcutaneous isatuximab with pomalidomide and dexamethasone for treating relapsed or refractory multiple myeloma after 1 or more treatments [TSID11969]
Status:
Topic selection
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Subcutaneous mosunetuzumab for treating relapsed or refractory follicular lymphoma after 2 or more treatments TSID 12081
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Suspected cancer (QS124)
Product type:
Quality standard
Last updated:
5 December 2017
Published:
30 June 2016
Suspected cancer: recognition and referral (NG12)
Product type:
Guidance
Programme:
NICE guideline
Last updated:
1 May 2025
Published:
23 June 2015
Suspected Cancer: recognition and referral
Status:
In development
Programme:
NICE guideline
Expected publication date:
13 March 2026
Tafasitamab with lenalidomide and R-CHOP for untreated high-intermediate-risk or high-risk diffuse large B-cell lymphoma [ID6568]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Tafasitamab with lenalidomide and rituximab for treating relapsed or refractory follicular or marginal zone lymphoma after 1 or more anti-CD20 treatments [ID6413]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Tafasitamab with lenalidomide for treating relapsed or refractory diffuse large B-cell lymphoma (TA883)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
3 May 2023
Tagraxofusp for treating blastic plasmacytoid dendritic cell neoplasm (terminated appraisal) (TA782)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
30 March 2022
Talacotuzumab for untreated acute myeloid leukaemia [ID1262]
Status:
In development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Talquetamab for treating relapsed or refractory multiple myeloma after 3 treatments [ID5082]
Status:
In development
Programme:
Technology appraisal guidance
Expected publication date:
15 October 2025
Teclistamab for treating relapsed and refractory multiple myeloma after 3 or more treatments (TA1015)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
13 November 2024
Teclistamab with daratumumab for treating relapsed or refractory multiple myeloma after 1 or more therapies [ID6201]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Temsirolimus for the treatment of relapsed or refractory mantle cell lymphoma (terminated appraisal) (TA207)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
27 October 2010
The Arrow OnControl powered bone marrow biopsy system for bone marrow aspiration and biopsy (MIB19)
Product type:
Advice
Programme:
Medtech innovation briefing
Published:
12 February 2015
Tisagenlecleucel for treating follicular lymphoma after 2 or more therapies (terminated appraisal) (TA842)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
22 November 2022
Tisagenlecleucel for treating relapsed or refractory B-cell acute lymphoblastic leukaemia in people 25 years and under (TA975)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
15 May 2024
Tisagenlecleucel for treating relapsed or refractory diffuse large B-cell lymphoma after 2 or more systemic therapies (terminated appraisal) (TA933)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
29 November 2023
Treosulfan with fludarabine for malignant disease before allogeneic stem cell transplant (TA640)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
5 August 2020
Venetoclax for treating chronic lymphocytic leukaemia (TA796)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
15 June 2022
Venetoclax with azacitidine for treating acute myeloid leukaemia before and after an allogeneic stem cell transplant [ID6468]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Venetoclax with azacitidine for untreated acute myeloid leukaemia when intensive chemotherapy is unsuitable (TA765)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
2 February 2022
Venetoclax with azacitidine for untreated high-risk myelodysplastic syndromes [ID6314]
Status:
In development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Venetoclax with ibrutinib for treating relapsed mantle cell lymphoma [ID3879]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Venetoclax with low dose cytarabine for untreated acute myeloid leukaemia when intensive chemotherapy is unsuitable (TA787)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
27 April 2022
Venetoclax with obinutuzumab for untreated chronic lymphocytic leukaemia (TA663)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
9 December 2020
Venetoclax with obinutuzumab for untreated chronic lymphocytic leukaemia when there is no 17p deletion or TP53 mutation and FCR (fludarabine, cyclophosphamide, rituximab) or BR (bendamustine, rituximab) are suitable (MA partial review of TA663) [ID6291]
Status:
In development
Programme:
Technology appraisal guidance
Expected publication date:
11 March 2026
Venetoclax with rituximab for previously treated chronic lymphocytic leukaemia (TA561)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
27 February 2019
Zamtocabtagene autoleucel for treating relapsed or refractory diffuse large B-cell lymphoma after 2 or more therapies [TSID10765]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Zamtocabtagene autoleucel for treating relapsed or refractory diffuse large B-cell lymphoma when high-dose chemotherapy and autologous stem cell transplant are unsuitable [TSID10477]
Status:
Awaiting development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Zanubrutinib for Chronic lymphocytic leukaemia (CLL) or Follicular lymphoma or Marginal zone lymphoma (MZL) or Waldenstrom's macroglobulinaemia [ID12199]
Status:
Topic selection
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Zanubrutinib for treating chronic lymphocytic leukaemia (TA931)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
22 November 2023
Zanubrutinib for treating marginal zone lymphoma after anti-CD20-based treatment (TA1001)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
4 September 2024
Zanubrutinib for treating relapsed or refractory mantle cell lymphoma after 1 or more treatments [ID6392]
Status:
In development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Zanubrutinib for treating Waldenstrom’s macroglobulinaemia (TA833)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
19 October 2022
Zanubrutinib for untreated chronic lymphocytic leukaemia [ID5079]
Status:
In development
Programme:
Technology appraisal guidance
Expected publication date:
TBC
Zanubrutinib with obinutuzumab for treating relapsed or refractory B-cell follicular lymphoma after 2 or more treatments (terminated appraisal) (TA978)
Product type:
Guidance
Programme:
Technology appraisal guidance
Published:
29 May 2024