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Real-world outcomes of nivolumab plus ipilimumab and pembrolizumab with platinum-based chemotherapy in advanced non-small cell lung cancer: a multicenter retrospective comparative study.
Matsumoto, Kinnosuke; Shiroyama, Takayuki; Tamiya, Motohiro; Minami, Toshiyuki; Kinehara, Yuhei; Tamiya, Akihiro; Suga, Yasuhiko; Kuge, Tomoki; Mori, Masahide; Suzuki, Hidekazu; Tobita, Satoshi; Ueno, Kiyonobu; Namba, Yoshinobu; Tetsumoto, Satoshi; Niki, Toshie; Morimura, Osamu; Osa, Akio; Nishino, Kazumi; Nagatomo, Izumi; Takeda, Yoshito; Kijima, Takashi; Kumanogoh, Atsushi.
Afiliación
  • Matsumoto K; Department of Respiratory Medicine and Clinical Immunology, Graduate School of Medicine, Osaka University, 2- 2 Yamadaoka, Suita City, 565-0871, Osaka, Japan.
  • Shiroyama T; Department of Respiratory Medicine and Clinical Immunology, Graduate School of Medicine, Osaka University, 2- 2 Yamadaoka, Suita City, 565-0871, Osaka, Japan. takayuki.s12@hotmail.co.jp.
  • Tamiya M; Department of Respiratory Medicine, Osaka International Cancer Institute, Osaka, Japan.
  • Minami T; Department of Respiratory Medicine and Hematology, Hyogo Medical University, Hyogo, Japan.
  • Kinehara Y; Department of Respiratory Medicine and Clinical Immunology, Nippon Life Hospital, Osaka, Japan.
  • Tamiya A; Department of Internal Medicine, National Hospital Organization Kinki-Chuo Chest Medical Center, Osaka, Japan.
  • Suga Y; Department of Respiratory Medicine, Osaka Police Hospital, Osaka, Japan.
  • Kuge T; Department of Respiratory Medicine and Clinical Immunology, Graduate School of Medicine, Osaka University, 2- 2 Yamadaoka, Suita City, 565-0871, Osaka, Japan.
  • Mori M; Department of Thoracic Oncology, National Hospital Organization Osaka Toneyama Medical Center, Osaka, Japan.
  • Suzuki H; Department of Thoracic Oncology, National Hospital Organization Osaka Toneyama Medical Center, Osaka, Japan.
  • Tobita S; Department of Thoracic Oncology, Osaka Habikino Medical Center, Osaka, Japan.
  • Ueno K; Department of Respiratory Medicine, Osaka General Medical Center, Osaka, Japan.
  • Namba Y; Department of Respiratory Medicine, Osaka General Medical Center, Osaka, Japan.
  • Tetsumoto S; Department of Respiratory Medicine, Takarazuka City Hospital, Hyogo, Japan.
  • Niki T; Department of Respiratory Medicine and Clinical Immunology, Suita Municipal Hospital, Osaka, Japan.
  • Morimura O; Department of Respiratory Medicine, Nishinomiya Municipal Central Hospital, Hyogo, Japan.
  • Osa A; Department of Respiratory Medicine, Toyonaka Municipal Hospital, Osaka, Japan.
  • Nishino K; Department of Respiratory Medicine, Kinki Central Hospital, Hyogo, Japan.
  • Nagatomo I; Department of Respiratory Medicine, Osaka International Cancer Institute, Osaka, Japan.
  • Takeda Y; Department of Respiratory Medicine and Clinical Immunology, Graduate School of Medicine, Osaka University, 2- 2 Yamadaoka, Suita City, 565-0871, Osaka, Japan.
  • Kijima T; Department of Respiratory Medicine and Clinical Immunology, Graduate School of Medicine, Osaka University, 2- 2 Yamadaoka, Suita City, 565-0871, Osaka, Japan.
  • Kumanogoh A; Department of Respiratory Medicine and Hematology, Hyogo Medical University, Hyogo, Japan.
Cancer Immunol Immunother ; 73(1): 4, 2024 Jan 04.
Article en En | MEDLINE | ID: mdl-38175294
ABSTRACT

INTRODUCTION:

Nivolumab plus ipilimumab with chemotherapy (NICT) and pembrolizumab with chemotherapy (PCT) are commonly used in patients with advanced non-small cell lung cancer (NSCLC). Compared with immune checkpoint inhibitor (ICI) monotherapy, ICI combination therapy can increase immune-related toxicity instead of prolonging survival. This study aimed to compare the efficacy and safety of NICT and PCT to decide on the favorable treatment.

METHODS:

We conducted a multi-center retrospective cohort study on patients who underwent NICT or PCT between December 2018 and May 2022. Propensity score matching (PSM) was performed with the variables age, sex, smoking status, performance status, stage, histology, and programmed cell death ligand-1 (PD-L1). The Kaplan-Meier method was used to compare survival for the matched patients.

RESULTS:

Six hundred consecutive patients were included. After PSM, 81 and 162 patients were enrolled in the NICT and PCT groups, respectively. The baseline characteristics were well-balanced. The median progression-free survival was equivalent (11.6 vs. 7.4 months; P = 0.582); however, the median overall survival (OS) was significantly longer in the NICT group than in the PCT group (26.0 vs. 16.8 months; P = 0.005). Furthermore, OS was better in PD-L1-negative patients who underwent NICT than in those who underwent PCT (26.0 vs. 16.8 months; P = 0.045). Safety profiles did not differ significantly in terms of severe adverse event and treatment-related death rates (P = 0.560, and 0.722, respectively).

CONCLUSIONS:

Real-world data suggests that NICT could be a favorable treatment option compared with PCT for patients with advanced NSCLC. Further follow-up is needed to determine the long-term prognostic benefit.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Carcinoma de Pulmón de Células no Pequeñas / Neoplasias Pulmonares Tipo de estudio: Observational_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Cancer Immunol Immunother Asunto de la revista: ALERGIA E IMUNOLOGIA / NEOPLASIAS / TERAPEUTICA Año: 2024 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Carcinoma de Pulmón de Células no Pequeñas / Neoplasias Pulmonares Tipo de estudio: Observational_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Cancer Immunol Immunother Asunto de la revista: ALERGIA E IMUNOLOGIA / NEOPLASIAS / TERAPEUTICA Año: 2024 Tipo del documento: Article País de afiliación: Japón
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