Lorlatinib for previously treated ALK-positive advanced non-small-cell lung cancer

3.1 The patient expert explained that there was a significant unmet need for patients with anaplastic lymphoma kinase (ALK)-positive non-small-cell lung cancer (NSCLC), even though 4 ALK tyrosine kinase inhibitor (TKI) treatments are available. The committee noted that neither crizotinib nor ceritinib are preferred for untreated disease since the availability of alectinib. Brigatinib has been approved for previously treated disease only after crizotinib. If alectinib's treatment effect wanes the only current option is chemotherapy. ALK TKI treatments are a significant improvement over chemotherapy. People can live relatively normally and do not need to go to hospital for treatment. They do not have distressing symptoms associated with chemotherapy such as hair loss. The patient expert explained that lorlatinib may be better tolerated than other ALK TKIs, appearing to cause less fatigue and fewer sun sensitivity and gastrointestinal problems. The clinical experts confirmed that there was a high unmet need for patients with ALK-positive NSCLC, because there is no cure for metastatic disease. Also, more than 50% of patients with ALK-positive NSCLC develop brain metastases, associated with high morbidity and mortality. Lorlatinib's ability to reach the brain means that patients whose brain tumours respond to treatment may have improved quality of life, allowing them to return to their usual activities. First and second-generation ALK TKIs (alectinib, ceritinib, crizotinib and brigatinib) are associated with the development of drug resistant mutations, leading to disease progression. Brain metastases and drug resistant mutations limit the duration of disease control and benefit from current ALK TKIs. For patients to survive for longer, and to avoid the devastating consequences of brain metastases, effective treatment that can penetrate the brain and overcome ALK-resistance mutations is needed. The committee noted that lorlatinib would be another line of ALK TKI treatment before a patient has chemotherapy or chemoimmunotherapy. The committee agreed that there was an unmet clinical need in ALK-positive NSCLC and that a third-generation ALK TKI, such as lorlatinib, would significantly benefit patients.

3.2 Current treatment options after ALK TKIs are standard care PDC, ABCP or best supportive care. The clinical experts explained that there was weak evidence for PDC-based regimens for this patient population, with a relative lack of efficacy in patients with brain metastases. The clinical experts explained that ABCP also has poor brain penetration and was not available to patients in the NHS in England with symptomatically active brain or leptomeningeal (central nervous system) metastases, which are common in ALK-positive NSCLC. In the absence of a third-generation ALK TKI such as lorlatinib, ABCP is expected to be used more in people without symptomatically active central nervous system metastases. The committee agreed that the evidence for the efficacy of current treatments after ALK TKIs was weak in ALK-positive NSCLC and it was unclear how much benefit they had in people with brain metastases.

3.3 The main clinical evidence for lorlatinib came from study 1001, a single-arm, open-label, multicentre phase 1 to 2 trial, done in 13 countries but not in the UK. This study investigated the effect of lorlatinib in adults with metastatic (stage 4) ALK-positive NSCLC. It comprised 7 cohorts with 5 (EXP‑2, EXP‑3A, EXP‑3B, EXP‑4, EXP‑5) representing populations having a mix of ALK TKIs and chemotherapy regimens. The company presented evidence for the combined cohort EXP‑3B:5 of 139 patients. This was the pooled cohort of patients from cohorts EXP‑3B, EXP‑4 and EXP‑5 whose treatment history most closely resembled that of the patient population covered by the marketing authorisation. Cohort EXP‑3B was made up of 28 patients who had had first-line treatment with alectinib or ceritinib, with or without prior chemotherapy. The clinical experts explained that most patients would have alectinib as first-line treatment in the NHS, meaning that this cohort was the closest match to the NHS population. Cohort EXP‑4 was made up of 65 patients who had previous treatment with 2 ALK TKIs, with or without prior chemotherapy. Cohort EXP‑5 consisted of 46 patients who had previous treatment with 3 or more ALK TKIs, with or without prior chemotherapy. The primary outcome of study 1001 was objective response rate. Secondary outcomes included overall survival and progression‑free survival. The results showed an objective response rate of 40.3% (95% confidence interval [CI] 32.1 to 48.9) with lorlatinib. The results also showed a progression-free survival of 6.9 months (95% CI 5.4 to 8.2) and a median overall survival of 20.4 months (95% CI 16.1 to not reached).

3.4 The company did an unanchored matching-adjusted indirect comparison (MAIC; as recommended in the NICE Decision Support Unit's technical support document 18), to compare the single-arm trial data for lorlatinib with trial data for PDC. The company chose 4 variables for matching:

3.5 The clinical effectiveness data for the PDC arm of the economic model were from the ALUR and ASCEND‑5 trials (for progression-free survival) and the PROFILE 1001 and PROFILE 1005 trials (for overall survival). The ERG emphasised its concerns about the quality and suitability of the trial data. This was because most patients in these studies had previously had PDC and crizotinib (closely matching the treatment history of cohort EXP‑2:3A from study 1001). Also, the patients in the chemotherapy arms of these trials had singlet chemotherapy (pemetrexed or docetaxel) rather than PDC. The committee agreed with the ERG and clinical experts that the company's assumption of equivalent clinical efficacy between doublet and singlet chemotherapy was not supported by clinical evidence, and that doublet chemotherapy was expected to be somewhat more effective than singlet chemotherapy. The committee noted that adjusting the hazard ratio by 20% to 0.8 to account for the difference in clinical efficacy between PDC and singlet chemotherapy was agreed to be appropriate at the technical engagement stage. It concluded that the treatment history differences between the trial populations used for PDC efficacy in the model and those of cohort EXP‑3B:5 from study 1001 meant that the clinical effectiveness evidence for the PDC arm of the model was uncertain.

3.6 The IMpower150 trial (comparing ABCP with bevacizumab plus carboplatin plus paclitaxel in people with chemotherapy-naive non-squamous NSCLC) was used to create an unanchored, unadjusted comparison of ABCP with lorlatinib. A mixed subgroup including patients with epidermal growth factor receptor (EGFR)-positive and ALK-positive NSCLC was the only evidence available on using ABCP in ALK-positive NSCLC. The company applied a population adjustment to reflect that most of the relevant subgroup from IMpower150 had EGFR-positive NSCLC (n=30) rather than ALK-positive disease (n=11). The company claimed that the prognosis for ALK-positive NSCLC was poorer than for EGFR-positive disease, so a failure to adjust would bias the results against lorlatinib. The committee heard that there was a lack of robust evidence to support the company's claim. To do the adjustment, the company used data from the IMPRESS study (comparing continued treatment with gefitinib plus chemotherapy with placebo plus chemotherapy after first-line gefitinib in people with EGFR-positive NSCLC). The company compared response to chemotherapy in patients with EGFR-positive disease (using the IMPRESS data) with response to chemotherapy in patients with ALK-positive NSCLC (using data from ALUR and ASCEND-5 for progression-free survival and from PROFILE 1001 and PROFILE 1005 for overall survival). This provided hazard ratios, which were then applied to the fitted log-logistic and exponential curves for the mixed cohort with EGFR-positive and ALK-positive disease to derive curves for a cohort with only ALK-positive disease. The ERG stated that there was not enough evidence to provide validity for the extent of this adjustment, which shifts both the progression-free survival and overall survival in favour of lorlatinib. With the 20% hazard ratio adjustment made to the PDC arm data after the technical engagement stage (see section 3.5), the ERG explained that the overall survival curve for ABCP was now almost identical to the curve for PDC in the model, and this lacked clinical plausibility. The company and experts agreed that ABCP would be expected to be more effective than PDC, especially in patients without brain metastases. To correct this, the ERG suggested reducing the company's log hazard ratio adjustment to the ABCP curve for overall survival by 25% to improve clinical plausibility relative to the overall survival curve for PDC. The exact hazard ratios were considered academic in confidence by the company and cannot be reported here. The committee agreed with the ERG that the company's log hazard ratio adjustment of the ABCP curve was uncertain and that the ERG's 25% reduction to this adjustment seemed more clinically plausible for ABCP overall survival relative to PDC overall survival in the model.

3.7 To derive long-term overall survival for lorlatinib, parametric curves were fitted to the lorlatinib overall survival data taken from the EXP‑3B:5 cohort from study 1001. The exponential curve had the best statistical fit, but the generalised gamma curve was selected as a compromise between the exponential curve and the log‑normal curve preferred by the company's clinical experts based on the 10-year survival predictions. The exact overall survival values were considered academic in confidence by the company and cannot be reported here. The clinical expert consulted by the ERG considered that 10% projected survival at 10 years would be too optimistic and 2% would be more plausible. The clinical experts at the meeting confirmed that predicting 10‑year survival in small populations with a very high incidence of brain metastases was highly uncertain because of a lack of reliable evidence. The committee heard that, in the absence of biomarkers for disease progression, brain metastases were the most reliable predictor of survival in patients with advanced ALK-positive NSCLC, and these patients would be expected to survive only for a few months. The committee noted that 66.9% of the pooled cohort EXP‑3B:5 from study 1001 and 80.4% of cohort EXP‑5 (3 or more prior ALK TKI therapies with or without any number of prior chemotherapy regimens) had brain metastases at baseline. The clinical experts at the meeting agreed that 10% projected survival at 10 years for this population was too high, and that lower values would be more plausible. The committee noted that the incremental cost-effectiveness ratio (ICER) was sensitive to the choice of curve and that using the exponential curve substantially increased the base-case ICER for lorlatinib compared with PDC. It concluded that although the generalised gamma curve had been agreed at the technical engagement stage, projecting 10-year survival in this population remained highly uncertain and it would take this uncertainty into account in its decision making.

3.8 The company did a systematic literature review to identify relevant studies with published utility values for ALK‑positive NSCLC. The study by Labbé et al. (2017) was the largest published source of NSCLC ALK-positive EQ-5D questionnaire utility values, and the company selected the value of 0.65 from the study for the progressed disease state in both arms. The ERG was concerned that this value was likely to represent the health state shortly after progression rather than the whole progressed period and was therefore too high. The committee recalled that the ERG preferred the values from Chouaid et al. (2013) for progressed disease after second-line treatment (0.59) and after third or fourth lines of treatment (0.46). The clinical experts said that the best evidence for quality of life in this population was the QUARTZ study (Mulvenna et al. 2016), which looked at the quality of life of patients after treatment for brain metastases that were unsuitable for resection or stereotactic radiotherapy. The average utility for patients ranged from 0.5 to less than 0.4. But the population in QUARTZ was considerably less well than the population in study 1001 and had higher levels of comorbidity. So they felt that the value of 0.46 was too low for progressed disease in this appraisal because some people will continue to have lorlatinib treatment after progression. The committee asked the clinical experts which of the 3 options were most clinically plausible:

3.9 The committee's preferred assumptions for decision making for PDC were:

3.10 Because lorlatinib and the comparators have commercial arrangements, the exact ICERs are confidential and cannot be reported here. The committee noted that its preferred assumptions produced a range of deterministic ICERs for lorlatinib compared with PDC and ABCP which were less than £50,000 per quality-adjusted life year (QALY) gained.

3.11 The committee considered the advice about life-extending treatments for people with a short life expectancy in NICE's guide to the methods of technology appraisal. For PDC, average life expectancy was well below 2 years in the company's base case and remained under 2 years across the scenarios assessed. Despite the limitations in the comparative evidence base, it was plausible that lorlatinib treatment would result in a survival gain of more than 3 months compared with PDC. Although there was some uncertainty around the average life expectancy with ABCP treatment because of the population adjustment applied by the company to the fitted curve, this was also expected to be less than 2 years. Also, life expectancy with ABCP remained under 2 years when the log hazard ratio for the population adjustment of overall survival was reduced by 25%, as agreed by the committee. The survival gains for lorlatinib compared with ABCP were more than 3 months across all scenarios assessed. The committee concluded that lorlatinib met the criteria to be considered a life-extending, end-of-life treatment when compared with both PDC and ABCP.

3.12 The company considered lorlatinib to be innovative, highlighting that it was a third-generation ALK TKI that penetrates the central nervous system and is retained in the intracranial space. So it potentially addresses the unmet need for additional treatment options for patients who develop brain metastases. It was specifically designed to inhibit resistant ALK mutations, including the ALKG1202R mutation that increases significantly after treatment with second-generation ALK TKIs. The clinical experts agreed that lorlatinib was an effective third-generation ALK TKI with good brain penetration and that people would welcome additional treatment options. The committee concluded that it had not been presented with any additional evidence of benefits that were not captured in the measurement of the QALYs and the resulting cost-effectiveness estimates.

3.14 The committee acknowledged the need for treatment options for people with previously treated ALK-positive advanced NSCLC. Because the range of plausible ICERs was less than £50,000 per QALY gained, the committee concluded that lorlatinib can be considered cost effective. Therefore, it can be recommended for routine commissioning as an option for previously treated ALK-positive advanced NSCLC.