Miura Keita, Shukuya Takehito, Furuya Naoki, Morita Ryo, Kisohara Akira, Mouri Atsuto, Watanabe Satoshi, Tanaka Hisashi, Hirata Aya, Hakozaki Taiki, Hamai Kosuke, Matsumoto Naoko, Watanabe Kana, Ashinuma Hironori, Miyauchi Eisaku, Sugano Koji, Hosokawa Shinobu, Amano Koji, Morita Satoshi, Kobayashi Kunihiko, Maemonodo Makoto, Takahashi Kazuhisa
Department of Respiratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Department of Internal Medicine, Division of Respiratory Medicine, St Marianna University School of Medicine, Kawasaki, Japan.
J Cachexia Sarcopenia Muscle. 2024 Dec;15(6):2618-2628. doi: 10.1002/jcsm.13606. Epub 2024 Oct 1.
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.
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.
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).
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.
癌症恶病质使晚期非小细胞肺癌(NSCLC)病情复杂化;然而,目前仍不清楚恶病质的发生频率以及它如何影响接受一线全身治疗患者的化疗进程。
我们开展了一项多中心前瞻性观察性研究,纳入了2020年9月至2021年9月期间先前未接受过治疗、东部肿瘤协作组体能状态(ECOG PS)为0 - 2且患有恶病质的NSCLC患者。主要结局指标是各队列中厌食/恶病质治疗功能评估量表(FAACT)的厌食/恶病质子量表[FAACT (A/CS)]评分趋势。次要结局指标包括一线全身治疗开始前恶病质的发生率、生活质量(QOL)指标、体重(BW)变化以及一线全身治疗的疗效和安全性。
总共评估了887例先前未接受过治疗、ECOG PS为0 - 2且开始接受一线全身治疗的晚期NSCLC连续患者。共有281例患者(31.7%)出现符合恶病质标准的体重减轻,其中186例患者接受了QOL、BW和结局指标的评估。总体而言,180/186例患者接受了一线全身治疗。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(ICI)]和队列3(ICI)分别包括42例、98例和40例患者。各队列的QOL趋势存在显著差异,化疗相关呕吐影响早期与食欲相关的QOL。与基线相比,队列2在1周时FAACT (A/CS)评分的变化更差(最小二乘均值变化±标准误:-3.0±0.9),优于队列1(1.6±1.2,p = 0.003)和队列3(1.8±1.0,p = 0.002);同时,队列1在6周时的变化(-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。在治疗开始后的6周内,所有队列均观察到体重减轻。靶向治疗队列的无进展生存期(PFS)和总生存期(OS)优于CTx±ICI队列或ICI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与队列2:HR,0.58,p = 0.018;队列1与队列3:HR,0.41,p = 0.001);队列1未达到中位OS,队列2为15.8个月,队列3为9.9个月(队列1与队列2:HR,0.52,p = 0.033;队列1与队列3:HR,0.37,p = 0.003)。
约1/3先前未接受过治疗的晚期NSCLC患者患有恶病质。恶病质NSCLC患者中,与食欲相关的QOL趋势因一线全身治疗类型而异,且这些患者的PFS和OS似乎更短。