Impact of Cachexia and First-Line Systemic Therapy for Previously Untreated Advanced Non-Small Cell Lung Cancer: NEJ050A.

IF 8.9 1区 医学 Journal of Cachexia, Sarcopenia and Muscle Pub Date : 2024-10-01 DOI:10.1002/jcsm.13606
Keita Miura, Takehito Shukuya, Naoki Furuya, Ryo Morita, Akira Kisohara, Atsuto Mouri, Satoshi Watanabe, Hisashi Tanaka, Aya Hirata, Taiki Hakozaki, Kosuke Hamai, Naoko Matsumoto, Kana Watanabe, Hironori Ashinuma, Eisaku Miyauchi, Koji Sugano, Shinobu Hosokawa, Koji Amano, Satoshi Morita, Kunihiko Kobayashi, Makoto Maemonodo, Kazuhisa Takahashi
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Abstract

Background: Cancer cachexia complicates advanced non-small cell lung cancer (NSCLC); however, it remains unclear how often cachexia occurs and how it affects the course of chemotherapy in patients receiving first-line systemic therapy.

Methods: We conducted a multicentre, prospective observational study and enrolled previously untreated NSCLC patients with Eastern Cooperative Oncology Group Performance Status (ECOG PS) of 0-2 and cachexia between September 2020 and September 2021. The primary outcome measure was the trends in the Functional Assessment of Anorexia/Cachexia Treatment and Anorexia/Cachexia Subscale [FAACT (A/CS)] scores by cohort. Secondary outcome measures included the incidence of cachexia before the initiation of first-line systemic therapy, quality of life (QOL) measures, body weight (BW) changes, and efficacy and safety of first-line systemic therapy.

Results: A total of 887 consecutive patients with previously untreated advanced NSCLC and ECOG PS of 0-2 who were initiated on first-line systemic therapy were evaluated. A total of 281 patients (31.7%) experienced BW loss consistent with the criteria of cachexia, and 186 were evaluated for QOL, BW and outcome measurements. Overall, 180/186 patients received first-line systemic therapy. Cohort 1 (targeted therapy), cohort 2 [cytotoxic chemotherapy (CTx) ± immune checkpoint inhibitors (ICIs)] and cohort 3 (ICIs) included 42, 98 and 40 patients, respectively. There were significant variations in QOL trends by cohort, with chemotherapy-associated emesis affecting early appetite-related QOL. The change in the FAACT (A/CS) score at 1 week from baseline was worse in cohort 2 (the least square mean change ± standard error: -3.0 ± 0.9) than in cohorts 1 (1.6 ± 1.2, p = 0.003) and 3 (1.8 ± 1.0, p = 0.002); meanwhile, the change at 6 weeks was worse in cohort 1 (-1.5 ± 1.2) than in cohorts 2 (3.6 ± 0.9, p = 0.001) and 3 (3.5 ± 1.1, p = 0.004). BW reduction was observed in all cohorts within 6 weeks of therapy initiation. The targeted therapy cohort demonstrated superior progression-free survival (PFS) and overall survival (OS) to CTx ± ICIs cohort or ICIs cohort (median PFS was 9.7 months, 6.3 months, 3.1 months, in cohort 1, 2, 3, respectively (cohort 1 vs. cohort 2: HR, 0.58, p = 0.018; cohort 1 vs. cohort 3: HR, 0.41, p = 0.001); median OS was not reached, 15.8 months, 9.9 months, respectively (cohort 1 vs. cohort 2: HR, 0.52, p = 0.033; cohort 1 vs. cohort 3: HR, 0.37, p = 0.003).

Conclusions: Approximately 1/3 patients with previously untreated advanced NSCLC have cachexia. Appetite-related QOL trends vary based on the type of first-line systemic therapy in cachectic NSCLC patients, and the PFS and OS of these patients seemed to be shorter.

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既往未接受过治疗的晚期非小细胞肺癌患者乏力和一线系统疗法的影响:NEJ050A.
背景:癌症恶病质是晚期非小细胞肺癌(NSCLC)的并发症之一:癌症恶病质是晚期非小细胞肺癌(NSCLC)的并发症;然而,目前仍不清楚恶病质发生的频率以及恶病质如何影响接受一线系统治疗患者的化疗疗程:我们开展了一项多中心、前瞻性观察研究,并在 2020 年 9 月至 2021 年 9 月期间招募了既往未接受过治疗、东部合作肿瘤学组表现状态(ECOG PS)为 0-2 且有恶病质的 NSCLC 患者。主要结局指标是各组群厌食/恶病质治疗功能评估和厌食/恶病质分量表[FAACT (A/CS)]得分的变化趋势。次要结局指标包括一线系统疗法开始前的恶病质发生率、生活质量(QOL)指标、体重(BW)变化以及一线系统疗法的疗效和安全性:共对 887 例既往未接受过治疗、ECOG PS 为 0-2 且开始接受一线系统治疗的晚期 NSCLC 患者进行了评估。共有 281 名患者(31.7%)出现了符合恶病质标准的体重减轻,186 名患者接受了 QOL、体重和结果测量评估。总体而言,180/186 名患者接受了一线系统治疗。队列1(靶向治疗)、队列2[细胞毒性化疗(CTx)±免疫检查点抑制剂(ICIs)]和队列3(ICIs)分别包括42、98和40名患者。各组群的 QOL 趋势存在明显差异,化疗相关的呕吐影响了早期食欲相关的 QOL。与基线相比,组群2中1周时的FAACT(A/CS)评分变化(最小平方均值变化±标准误差:-3.0 ± 0.9)比组群1(1.6 ± 1.2,P = 0.003) 和 3 (1.8 ± 1.0, p = 0.002);同时,6 周时的变化情况,队列 1 (-1.5 ± 1.2) 比队列 2 (3.6 ± 0.9, p = 0.001) 和队列 3 (3.5 ± 1.1, p = 0.004) 更差。在开始治疗的 6 周内,所有队列均观察到 BW 下降。靶向治疗队列的无进展生存期(PFS)和总生存期(OS)优于 CTx ± ICIs 队列或 ICIs 队列(队列 1、2、3 的中位 PFS 分别为 9.7 个月、6.3 个月、3.1 个月(队列 1 vs. 队列 2:HR,0.001))。队列1 vs. 队列2:HR,0.58,p = 0.018;队列1 vs. 队列3:HR,0.41,p = 0.001);未达到中位OS,分别为15.8个月和9.9个月(队列1 vs. 队列2:HR,0.52,p = 0.033;队列1 vs. 队列3:HR,0.37,p = 0.003):结论:约1/3既往未经治疗的晚期NSCLC患者有恶病质。结论:约有1/3的既往未接受过治疗的晚期NSCLC患者存在恶病质,根据恶病质NSCLC患者一线系统治疗的类型不同,食欲相关的QOL趋势也不同,而且这些患者的PFS和OS似乎更短。
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来源期刊
Journal of Cachexia, Sarcopenia and Muscle
Journal of Cachexia, Sarcopenia and Muscle Medicine-Orthopedics and Sports Medicine
自引率
12.40%
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期刊介绍: The Journal of Cachexia, Sarcopenia, and Muscle is a prestigious, peer-reviewed international publication committed to disseminating research and clinical insights pertaining to cachexia, sarcopenia, body composition, and the physiological and pathophysiological alterations occurring throughout the lifespan and in various illnesses across the spectrum of life sciences. This journal serves as a valuable resource for physicians, biochemists, biologists, dieticians, pharmacologists, and students alike.
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