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Real world treatment sequences and outcomes for metastatic renal cell carcinoma.
Lai, Gu-Shun; Li, Jian-Ri; Wang, Shian-Shiang; Chen, Chuan-Shu; Yang, Chun-Kuang; Lin, Chia-Yen; Hung, Sheng-Chun; Chiu, Kun-Yuan; Yang, Shun-Fa.
  • Lai GS; Institute of Medicine, Chung Shan Medical University, Taichung, Taiwan.
  • Li JR; Division of Urology, Department of Surgery, Taichung Veterans General Hospital, Taichung, Taiwan.
  • Wang SS; Institute of Medicine, Chung Shan Medical University, Taichung, Taiwan.
  • Chen CS; Division of Urology, Department of Surgery, Taichung Veterans General Hospital, Taichung, Taiwan.
  • Yang CK; Department of Medicine and Nursing, Hungkuang University, Taichung, Taiwan.
  • Lin CY; Institute of Medicine, Chung Shan Medical University, Taichung, Taiwan.
  • Hung SC; Division of Urology, Department of Surgery, Taichung Veterans General Hospital, Taichung, Taiwan.
  • Chiu KY; Department of Applied Chemistry, National Chi Nan University, Nantou, Taiwan.
  • Yang SF; Institute of Medicine, Chung Shan Medical University, Taichung, Taiwan.
PLoS One ; 18(11): e0294039, 2023.
Article en En | MEDLINE | ID: mdl-37992086
ABSTRACT

OBJECTIVES:

The treatment landscape for metastatic renal cell carcinoma changed a lot in the last few years. This study aimed to assess the treatment sequences and outcomes for metastatic renal cell carcinoma in a real-world setting. MATERIALS AND

METHODS:

We enrolled patients with metastatic renal cell carcinomawho received first-line systemic treatment with tyrosin kinase inhibitors monotherapy, ipilimumab plus nivolumab, or pembrolizumab plus axitinibbetween January2009 and May 2023 on the database of TriNetX network. Overall survival, time on treatment and time to next treatment were evaluated using Kaplan-Meiermethod.

RESULTS:

Totally, 4183 received tyrosine kinase inhibitor monotherapy, 1555 received ipilimumab plus nivolumab, and 559 received axitinib plus pembrolizumab. Median time on treatment was 2.5 months for the tyrosine kinase inhibitor monotherapy cohort, 5.4 months for the ipilimumab plus nivolumab cohort, and 8.3 months for the pembrolizumab plus axitinib cohort. Median time to next treatment was 16.6 months for both the tyrosine kinase inhibitor monotherapy and ipilimumab plus nivolumab cohorts, and 22.1 months for the pembrolizumab plus axitinib cohort. Median overall survival was 42.2 months for the tyrosine kinase inhibitor monotherapy cohort, 39.7monthsfor the ipilimumab plus nivolumab cohort, and not reached for the pembrolizumab plus axitinib cohort. In comparison with the tyrosine kinase inhibitor monotherapy cohort, patients in the pembrolizumab plus axitinib cohort showed survival benefit (log-rank p = 0.0168) in overall survival, but not the case in the ipilimumab plus nivolumab cohort.

CONCLUSION:

There was a trend toward using first-line immuno-oncology based therapy for patients with metastatic renal cell carcinoma in a real-world practice. Axitinib plus pembrolizumuab cohort had survival benefits over tyrosine kinase inhibitor and ipilimumab plus nivolumab cohorts, while patients in the ipilimumab plus nivolumab cohort had more distant metastases and comorbidities.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Carcinoma de Células Renales / Neoplasias Renales Límite: Humans Idioma: En Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Carcinoma de Células Renales / Neoplasias Renales Límite: Humans Idioma: En Año: 2023 Tipo del documento: Article