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Patient-Reported Outcomes From Patients Receiving Immunotherapy or Chemoimmunotherapy for Metastatic Non-Small-Cell Lung Cancer in Clinical Practice.临床实践中接受免疫治疗或化疗免疫治疗的转移性非小细胞肺癌患者的报告结果。
Clin Lung Cancer. 2020 May;21(3):255-263.e4. doi: 10.1016/j.cllc.2019.11.015. Epub 2019 Nov 29.
3
Thresholds for clinical importance were established to improve interpretation of the EORTC QLQ-C30 in clinical practice and research.临床重要性的阈值是为了提高在临床实践和研究中对 EORTC QLQ-C30 的解释而建立的。
J Clin Epidemiol. 2020 Feb;118:1-8. doi: 10.1016/j.jclinepi.2019.10.003. Epub 2019 Oct 19.
4
Discovery Stories of RET Fusions in Lung Cancer: A Mini-Review.肺癌中RET融合的发现故事:一篇综述短文
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The humanistic burden of advanced non-small cell lung cancer (NSCLC) in Europe: a real-world survey linking patient clinical factors to patient and caregiver burden.欧洲晚期非小细胞肺癌(NSCLC)的人文负担:一项将患者临床因素与患者和照护者负担联系起来的真实世界调查。
Qual Life Res. 2019 Jul;28(7):1849-1861. doi: 10.1007/s11136-019-02152-6. Epub 2019 Mar 2.
6
Symptomatic toxicities experienced during anticancer treatment: agreement between patient and physician reporting in three randomized trials.抗癌治疗期间出现的有症状毒性:三项随机试验中患者报告和医生报告的一致性。
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RET fusions define a unique molecular and clinicopathologic subtype of non-small-cell lung cancer.RET 融合定义了一种独特的非小细胞肺癌的分子和临床病理亚型。
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LIBRETTO-001 试验中 RET 融合阳性非小细胞肺癌患者中 Selpercatinib 的患者报告结局。

Patient-Reported Outcomes with Selpercatinib Among Patients with RET Fusion-Positive Non-Small Cell Lung Cancer in the Phase I/II LIBRETTO-001 Trial.

机构信息

Royal Marsden Hospital and The Institute of Cancer Research, London, UK.

National Cancer Centre Singapore, Singapore.

出版信息

Oncologist. 2022 Feb 3;27(1):22-29. doi: 10.1002/onco.13976.

DOI:10.1002/onco.13976
PMID:34523767
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9714603/
Abstract

BACKGROUND

LIBRETTO-001 is an ongoing, global, open-label, phase I/II study of selpercatinib in patients with advanced or metastatic solid tumors. We report interim patient-reported outcomes in patients with RET fusion-positive non-small cell lung cancer (NSCLC).

PATIENTS AND METHODS

Patients completed the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (QLQ-C30) version 3.0 at baseline (cycle 1, day 1), approximately every other 28-day cycle until cycle 13, and every 12 weeks thereafter. Data were evaluated through cycle 13 as few patients had reached later time points. A change of ≥10 points from baseline in domain scores was considered clinically meaningful.

RESULTS

Among 253 selpercatinib-treated patients, 239 were categorized into subgroups by prior therapy: treatment-naïve (n = 39), one prior line of therapy (n = 64), or two or more prior lines of therapy (n = 136). The QLQ-C30 was completed by >85% of patients at each time point. Most patients overall and in each subgroup maintained or improved in all health-related quality of life (HRQoL) domains during treatment. The percentage of patients who experienced clinically meaningful improvements ranged from 61.1% to 66.7% for global health status, 33.3% to 61.1% for dyspnea, and 46.2% to 63.0% for pain. The 61.1% of patients with improved dyspnea had two or more prior lines of therapy; median time to first improvement was 3.4 months. At the first postbaseline evaluation (cycle 3), 45.9% of all patients reported a ≥10-point reduction in pain.

CONCLUSION

In this interim analysis, the majority of patients with RET fusion-positive NSCLC remained stable or improved on all QLQ-C30 subscales at each study visit, demonstrating favorable HRQoL as measured by the QLQ-C30 during treatment with selpercatinib.

摘要

背景

LIBRETTO-001 是一项正在进行的、全球性的、开放标签的、I/II 期研究,评估 Selpercatinib 在晚期或转移性实体瘤患者中的疗效。我们报告了 RET 融合阳性非小细胞肺癌(NSCLC)患者的患者报告结局的中期结果。

患者和方法

患者在基线(第 1 周期,第 1 天)、大约每 28 天周期(直到第 13 周期)和之后每 12 周时使用欧洲癌症研究和治疗组织生存质量问卷(QLQ-C30)3.0 版进行评估。数据评估至第 13 周期,因为很少有患者达到更晚的时间点。域评分较基线变化≥10 分被认为具有临床意义。

结果

在 253 例接受 Selpercatinib 治疗的患者中,根据既往治疗情况将 239 例分为亚组:初治(n=39)、一线治疗(n=64)或二线及以上治疗(n=136)。大多数患者在每个时间点均完成了 QLQ-C30 问卷。在治疗期间,大多数患者(所有亚组)维持或改善了所有健康相关生存质量(HRQoL)域的评分。在所有亚组中,经历临床意义上的改善的患者比例为:总体健康状况 61.1%至 66.7%、呼吸困难 33.3%至 61.1%、疼痛 46.2%至 63.0%。呼吸困难改善的患者中 61.1%有二线及以上治疗;首次改善的中位时间为 3.4 个月。在首次基线后评估(第 3 周期),所有患者中有 45.9%报告疼痛减轻≥10 分。

结论

在这项中期分析中,大多数 RET 融合阳性 NSCLC 患者在每次研究访视时,所有 QLQ-C30 子量表的评分均保持稳定或改善,表明在 Selpercatinib 治疗期间,QLQ-C30 测量的 HRQoL 良好。