Projecting long-term clinical outcomes with larotrectinib compared with immune checkpoint inhibitors in metastatic nonsmall cell lung cancer and differentiated thyroid cancer.

IF 2.3 4区 医学 Q2 HEALTH CARE SCIENCES & SERVICES Journal of managed care & specialty pharmacy Pub Date : 2024-06-01 DOI:10.18553/jmcp.2024.30.6.581
Kangho Suh, Ashley Kang, Gilbert Ko, Todd Williamson, Nick Liao, Sean D Sullivan
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Abstract

Background: Larotrectinib is approved for patients with advanced NTRK gene fusion-positive solid tumors. Prior studies demonstrated promising results with larotrectinib compared with other systemic therapy. However, comparisons to checkpoint inhibitors, such as nivolumab or pembrolizumab, have not been done.

Objective: To estimate and compare expected life-years (LYs) and quality-adjusted LYs (QALYs) for patients with nonsmall cell lung cancer (NSCLC) eligible for larotrectinib vs patients with unknown NTRK gene fusion status on nivolumab or pembrolizumab. We also assessed patients with metastatic differentiated thyroid cancer (DTC), as pembrolizumab may be considered in certain circumstances.

Methods: We developed partitioned survival models to project long-term comparative effectiveness of larotrectinib vs nivolumab or pembrolizumab. Larotrectinib survival data were derived from an updated July 2021 analysis of 21 adult patients (≥18 years of age) with metastatic NTRK gene fusion-positive NSCLC and 21 with DTC. Survival inputs for nivolumab and pembrolizumab were obtained from published articles. Progression-free and overall survival were estimated using survival distributions (Exponential, Weibull, Log-logistic, and Log-normal). Exponential fits were chosen based on goodness-of-fit and clinical plausibility.

Results: In NSCLC, larotrectinib resulted in gains of 5.87 and 5.91 LYs compared to nivolumab and pembrolizumab, respectively, which translated to gains of 3.53 and 3.56 QALYs. In DTC, larotrectinib resulted in a gain of 5.23 LYs and 4.24 QALYs compared to pembrolizumab.

Conclusions: In metastatic NSCLC and DTC, larotrectinib may produce substantial life expectancy and QALY gains compared to immune checkpoint inhibitors. Additional data with longer follow-up will further inform this comparison.

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预测拉罗替尼与免疫检查点抑制剂在转移性非小细胞肺癌和分化型甲状腺癌中的长期临床疗效。
背景拉罗替尼被批准用于晚期NTRK基因融合阳性实体瘤患者。先前的研究表明,与其他系统疗法相比,拉罗替尼的治疗效果很好。然而,尚未将其与检查点抑制剂(如 nivolumab 或 pembrolizumab)进行比较:目的:估算并比较符合拉罗替尼治疗条件的非小细胞肺癌(NSCLC)患者与NTRK基因融合状态未知的尼夫单抗或pembrolizumab患者的预期生存年(LYs)和质量调整生存年(QALYs)。我们还评估了转移性分化型甲状腺癌(DTC)患者,因为在某些情况下可以考虑使用pembrolizumab:我们建立了分区生存模型,以预测拉罗替尼与 nivolumab 或 pembrolizumab 的长期比较效果。拉罗替尼的生存期数据来自2021年7月对21例转移性NTRK基因融合阳性NSCLC成人患者(≥18岁)和21例DTC患者的最新分析。nivolumab和pembrolizumab的生存期数据来自已发表的文章。使用生存分布(指数分布、Weibull 分布、Logistic 分布和 Log-normal 分布)估算无进展生存期和总生存期。根据拟合优度和临床合理性选择指数拟合:在 NSCLC 中,与 nivolumab 和 pembrolizumab 相比,larotrectinib 分别带来了 5.87 和 5.91 LYs 的收益,即 3.53 和 3.56 QALYs 的收益。在DTC中,与pembrolizumab相比,larotrectinib的收益分别为5.23 LYs和4.24 QALYs:在转移性 NSCLC 和 DTC 中,与免疫检查点抑制剂相比,larotrectinib 可带来可观的预期寿命和 QALYs 收益。随访时间更长的其他数据将为这一比较提供更多信息。
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来源期刊
Journal of managed care & specialty pharmacy
Journal of managed care & specialty pharmacy Health Professions-Pharmacy
CiteScore
3.50
自引率
4.80%
发文量
131
期刊介绍: JMCP welcomes research studies conducted outside of the United States that are relevant to our readership. Our audience is primarily concerned with designing policies of formulary coverage, health benefit design, and pharmaceutical programs that are based on evidence from large populations of people. Studies of pharmacist interventions conducted outside the United States that have already been extensively studied within the United States and studies of small sample sizes in non-managed care environments outside of the United States (e.g., hospitals or community pharmacies) are generally of low interest to our readership. However, studies of health outcomes and costs assessed in large populations that provide evidence for formulary coverage, health benefit design, and pharmaceutical programs are of high interest to JMCP’s readership.
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