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Impact of Cachexia and First-Line Systemic Therapy for Previously Untreated Advanced Non-Small Cell Lung Cancer: NEJ050A.
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.
Afiliação
  • Miura K; Department of Respiratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan.
  • Shukuya T; Department of Respiratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan.
  • Furuya N; Department of Internal Medicine, Division of Respiratory Medicine, St Marianna University School of Medicine, Kawasaki, Japan.
  • Morita R; Department of Respiratory Medicine, Akita Kousei Medical Center, Akita, Japan.
  • Kisohara A; Department of Respiratory Medicine, Kasukabe Medical Center, Saitama, Japan.
  • Mouri A; Department of Respiratory Medicine, Comprehensive Cancer Center, Saitama Medical University International Medical Center, Hidaka, Japan.
  • Watanabe S; Department of Respiratory Medicine and Infectious Diseases, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
  • Tanaka H; Department of Respiratory Medicine, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
  • Hirata A; Department of Respiratory Medicine, Kyorin University School of Medicine, Tokyo, Japan.
  • Hakozaki T; Department of Thoracic Oncology and Respiratory Medicine, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital, Tokyo, Japan.
  • Hamai K; Department of Respiratory Medicine, Hiroshima Prefectural Hospital, Hiroshima, Japan.
  • Matsumoto N; Department of Respiratory Disease, Hiroshima red Cross Hospital & Atomic-Bomb Survivors Hospital, Hiroshima, Japan.
  • Watanabe K; Department of Respiratory Medicine, Miyagi Cancer Center, Miyagi, Japan.
  • Ashinuma H; Division of Respiratory Medicine, Chiba Cancer Center, Chiba, Japan.
  • Miyauchi E; Department of Respiratory Medicine, Tohoku University Hospital, Sendai, Japan.
  • Sugano K; Division of Respiratory Medicine, Juntendo Tokyo Koto Geriatric Medical Center, Tokyo, Japan.
  • Hosokawa S; Department of Respiratory Medicine, Japanese red Cross Okayama Hospital, Okayama, Japan.
  • Amano K; Department of Supportive and Palliative Care, Osaka International Cancer Institute, Osaka, Japan.
  • Morita S; Department of Biomedical Statistics and Bioinformatics, Kyoto University Graduate School of Medicine, Kyoto, Japan.
  • Kobayashi K; Department of Respiratory Medicine, Comprehensive Cancer Center, Saitama Medical University International Medical Center, Hidaka, Japan.
  • Maemonodo M; Department of Medicine, Division of Pulmonary Medicine, Jichi Medical University, Tochigi, Japan.
  • Takahashi K; Department of Respiratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Article em En | MEDLINE | ID: mdl-39351653
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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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article