TY - JOUR
T1 - Prognostic factors of lenvatinib plus pembrolizumab therapy for advanced or recurrent endometrial cancer
T2 - analysis of a multicenter cohort study in Japan
AU - Nagase, Yoshikazu
AU - Nakagawa, Satoshi
AU - Kobayashi, Mariya
AU - Kurahashi, Hiroki
AU - Ogimoto, Hiromi
AU - Tanaka, Ayaka
AU - Tsujie, Tomoko
AU - Shiomi, Mayu
AU - Otake, Akiko
AU - Masuhara, Kanji
AU - Yoshikawa, Kenichi
AU - Yotsumoto, Fusanori
AU - Kurita, Tomoko
AU - Yoshino, Kiyoshi
AU - Yoshioka, Emi
AU - Egawa-Takata, Tomomi
AU - Kudaka, Wataru
AU - Sekine, Masayuki
AU - Unno, Hikari
AU - Takemura, Masahiko
AU - Aso, Saki
AU - Kai, Kentaro
AU - Kobayashi, Eiji
AU - Yokoi, Takeshi
AU - Akada, Masashi
AU - Kakubari, Reisa
AU - Hisa, Tsuyoshi
AU - Matsuzaki, Shinya
AU - Ueda, Yutaka
N1 - Publisher Copyright:
© The Author(s) 2025.
PY - 2025/11
Y1 - 2025/11
N2 - Background: Lenvatinib plus pembrolizumab (LP) therapy has emerged as an effective treatment for patients with advanced or recurrent endometrial cancer. However, limited data are available regarding its outcomes in real-world settings. This study aimed to identify prognostic factors associated with the efficacy of LP therapy. Methods: This multicenter observational study was conducted across 15 institutions in Japan and examined patients with endometrial cancer, including uterine carcinosarcoma, who experienced disease progression after receiving at least one platinum-based chemotherapy, including adjuvant treatment, and subsequently received LP therapy. The prognostic factors for progression-free survival were assessed using a multivariate Cox proportional hazards model. Results: A total of 105 patients met the inclusion criteria. Improved progression-free survival was independently associated with performance status of 0 (adjusted hazard ratio [aHR] 0.42, 95% confidence interval [CI] 0.23–0.75), platinum-free interval (PFI) of ≥ 6 months (aHR 0.46, 95% CI 0.28–0.78), histology of grade 1–2 endometrioid carcinoma (aHR 0.52, 95% CI 0.30–0.91), and relative dose intensity during the initial 8 weeks (8w-RDI) of lenvatinib of ≥ 50% (aHR 0.53, 95% CI 0.31–0.91). Patients with PFI of ≥ 6 months also demonstrated improved overall survival (HR 0.44, 95% CI 0.25–0.76) and objective response rate (44.0% versus 20.0%, P = 0.011) compared with those with PFI of < 6 months. Additionally, 8w-RDI of lenvatinib ≥ 50% was associated with improved overall survival (HR 0.53, 95% CI 0.30–0.92) compared to those with < 50%. Conclusions: This study identified several novel prognostic factors for LP therapy. Among them, PFI may inform treatment selection for recurrent endometrial cancer following chemotherapy. Clinical trial registration: University Hospital Medical Information Network Clinical Trials Registry (UMIN-CTR) 000049997.
AB - Background: Lenvatinib plus pembrolizumab (LP) therapy has emerged as an effective treatment for patients with advanced or recurrent endometrial cancer. However, limited data are available regarding its outcomes in real-world settings. This study aimed to identify prognostic factors associated with the efficacy of LP therapy. Methods: This multicenter observational study was conducted across 15 institutions in Japan and examined patients with endometrial cancer, including uterine carcinosarcoma, who experienced disease progression after receiving at least one platinum-based chemotherapy, including adjuvant treatment, and subsequently received LP therapy. The prognostic factors for progression-free survival were assessed using a multivariate Cox proportional hazards model. Results: A total of 105 patients met the inclusion criteria. Improved progression-free survival was independently associated with performance status of 0 (adjusted hazard ratio [aHR] 0.42, 95% confidence interval [CI] 0.23–0.75), platinum-free interval (PFI) of ≥ 6 months (aHR 0.46, 95% CI 0.28–0.78), histology of grade 1–2 endometrioid carcinoma (aHR 0.52, 95% CI 0.30–0.91), and relative dose intensity during the initial 8 weeks (8w-RDI) of lenvatinib of ≥ 50% (aHR 0.53, 95% CI 0.31–0.91). Patients with PFI of ≥ 6 months also demonstrated improved overall survival (HR 0.44, 95% CI 0.25–0.76) and objective response rate (44.0% versus 20.0%, P = 0.011) compared with those with PFI of < 6 months. Additionally, 8w-RDI of lenvatinib ≥ 50% was associated with improved overall survival (HR 0.53, 95% CI 0.30–0.92) compared to those with < 50%. Conclusions: This study identified several novel prognostic factors for LP therapy. Among them, PFI may inform treatment selection for recurrent endometrial cancer following chemotherapy. Clinical trial registration: University Hospital Medical Information Network Clinical Trials Registry (UMIN-CTR) 000049997.
KW - Endometrial cancer
KW - Lenvatinib
KW - Pembrolizumab
KW - Platinum-free interval
KW - Prognostic factors
UR - https://www.scopus.com/pages/publications/105015557387
UR - https://www.scopus.com/pages/publications/105015557387#tab=citedBy
U2 - 10.1007/s10147-025-02842-x
DO - 10.1007/s10147-025-02842-x
M3 - Article
C2 - 40914783
AN - SCOPUS:105015557387
SN - 1341-9625
VL - 30
SP - 2342
EP - 2351
JO - International Journal of Clinical Oncology
JF - International Journal of Clinical Oncology
IS - 11
ER -