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Efficacy of immune-checkpoint inhibitors combined with cytotoxic chemotherapy in advanced or recurrent endometrial cancer: A systematic review and meta-analysis.
Kim, Ji Hyun; Han, Kyung Hee; Park, Eun Young; Kim, Eun Taeg; Kim, Eun Jeong; Tan, David S P; Lee, Jung-Yun; Park, Sang-Yoon; Fotopoulou, Christina; Lim, Myong Cheol.
  • Kim JH; Center for Gynecologic Cancer, National Cancer Center, Goyang, Republic of Korea.
  • Han KH; Department of Obstetrics and Gynecology, CHA Ilsan Medical Center, CHA University, Goyang, South Korea.
  • Park EY; Biostatistics Collaboration Team, Research Core Center, National Cancer Center, Goyang, Republic of Korea.
  • Kim ET; Department of Obstetrics and Gynecology, Kosin University College of Medicine, Pusan, Republic of Korea.
  • Kim EJ; Department of Obstetrics and Gynecology, Seoul National University College of Medicine, Seoul, Republic of Korea.
  • Tan DSP; Department of Medicine, Centre for Cancer Research, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
  • Lee JY; Department of Obstetrics and Gynecology, Yonsei University College of Medicine, Seoul, Republic of Korea.
  • Park SY; Center for Gynecologic Cancer, National Cancer Center, Goyang, Republic of Korea.
  • Fotopoulou C; Department of Surgery and Cancer, Faculty of Medicine, Imperial College London, UK.
  • Lim MC; Center for Gynecologic Cancer, National Cancer Center, Goyang, Republic of Korea; Cancer Control and Policy, National Cancer Center Graduate School of Cancer Science and Policy, National Cancer Center, Goyang, Republic of Korea; Rare&Paediatric Cancer Branch and Immuno-oncology Branch, Division
Gynecol Oncol ; 187: 85-91, 2024 08.
Article en En | MEDLINE | ID: mdl-38735144
ABSTRACT

BACKGROUND:

The combination of immune checkpoint inhibitors (ICIs) and platinum-based chemotherapy has emerged as a highly promising primary option for advanced or recurrent endometrial cancer (EC). The study aimed to evaluate treatment efficacy of ICIs with cytotoxic chemotherapy in EC.

METHODS:

We conducted a comprehensive review of randomized controlled trials up to November 11, 2023, focusing on immunotherapy combined with chemotherapy versus chemotherapy alone for EC. The primary endpoint was the pooled hazard ratio (HR), which was further analyzed across subgroups based on mismatch repair (MMR) status, race, histology, and programmed death-ligand 1 (PD-L1) status. The protocol was registered in PROSPERO (CRD42023475669).

FINDINGS:

Four trials with 2335 patients were analyzed. ICIs with chemotherapy significantly prolonged progression-free survival (PFS) (HR, 0.70; 95% CI, 0.62-0.79) and overall survival (OS) (HR, 0.75; 95% CI, 0.63-0.89) compared to chemotherapy alone. Stratification by MMR status showed substantial benefits for dMMR (PFS; HR, 0.33; 95% CI, 0.26-0.43; OS; HR, 0.37; 95% CI, 0.22-0.91) over pMMR cohorts in both PFS and OS. In the subgroup analysis, there was significant PFS advantage in Caucasian (HR, 0.63; 95% CI, 0.54-0.72) over non-Caucasian, in endometrioid histology (HR, 0.66; 95% CI, 0.56-0.78) over non-endometrioid, and in PD-L1 positive (HR, 0.39; 95% CI, 0.19-0.81) over PD-L1 negative population.

INTERPRETATION:

ICIs combined with platinum-based chemotherapy significantly prolonged PFS and OS in patients with advanced or recurrent EC. Patients with dMMR status, Caucasians, endometrioid histology, and positive PD-L1 status showed significant PFS benefits, emphasizing the need for personalized treatment approaches to improve outcomes.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Neoplasias Endometriales / Inhibidores de Puntos de Control Inmunológico / Recurrencia Local de Neoplasia Límite: Female / Humans Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Neoplasias Endometriales / Inhibidores de Puntos de Control Inmunológico / Recurrencia Local de Neoplasia Límite: Female / Humans Idioma: En Año: 2024 Tipo del documento: Article