TY - JOUR
T1 - Updated systematic review and network meta-analysis of first-line treatments for metastatic renal cell carcinoma with extended follow-up data
AU - Yanagisawa, Takafumi
AU - Mori, Keiichiro
AU - Matsukawa, Akihiro
AU - Kawada, Tatsushi
AU - Katayama, Satoshi
AU - Bekku, Kensuke
AU - Laukhtina, Ekaterina
AU - Rajwa, Pawel
AU - Quhal, Fahad
AU - Pradere, Benjamin
AU - Fukuokaya, Wataru
AU - Iwatani, Kosuke
AU - Murakami, Masaya
AU - Bensalah, Karim
AU - Grünwald, Viktor
AU - Schmidinger, Manuela
AU - Shariat, Shahrokh F.
AU - Kimura, Takahiro
N1 - Publisher Copyright:
© 2024, The Author(s).
PY - 2024/2
Y1 - 2024/2
N2 - Immune checkpoint inhibitor (ICI)-based combination therapies are the recommended first-line treatment for metastatic renal cell carcinoma (mRCC). However, no head-to-head phase-3 randomized controlled trials (RCTs) have compared the efficacy of different ICI-based combination therapies. Here, we compared the efficacy of various first-line ICI-based combination therapies in patients with mRCC using updated survival data from phase-3 RCTs. Three databases were searched in June 2023 for RCTs that analyzed oncologic outcomes in mRCC patients treated with ICI-based combination therapies as first-line treatment. A network meta-analysis compared outcomes including overall survival (OS), progression-free survival (PFS), objective response rate (ORR), and complete response (CR) rate. Subgroup analyses were based on the International mRCC Database Consortium risk classification. The treatment ranking analysis of the entire cohort showed that nivolumab + cabozantinib (81%) had the highest likelihood of improving OS, followed by nivolumab + ipilimumab (75%); pembrolizumab + lenvatinib had the highest likelihood of improving PFS (99%), ORR (97%), and CR (86%). These results remained valid even when the analysis was limited to patients with intermediate/poor risk, except that nivolumab + ipilimumab had the highest likelihood of achieving CR (100%). Further, OS benefits of ICI doublets were not inferior to those of ICI + tyrosine kinase inhibitor combinations. Recommendation of combination therapies with ICIs and/or tyrosine kinase inhibitors based on survival benefits and patient pretreatment risk classification will help advance personalized medicine for mRCC.
AB - Immune checkpoint inhibitor (ICI)-based combination therapies are the recommended first-line treatment for metastatic renal cell carcinoma (mRCC). However, no head-to-head phase-3 randomized controlled trials (RCTs) have compared the efficacy of different ICI-based combination therapies. Here, we compared the efficacy of various first-line ICI-based combination therapies in patients with mRCC using updated survival data from phase-3 RCTs. Three databases were searched in June 2023 for RCTs that analyzed oncologic outcomes in mRCC patients treated with ICI-based combination therapies as first-line treatment. A network meta-analysis compared outcomes including overall survival (OS), progression-free survival (PFS), objective response rate (ORR), and complete response (CR) rate. Subgroup analyses were based on the International mRCC Database Consortium risk classification. The treatment ranking analysis of the entire cohort showed that nivolumab + cabozantinib (81%) had the highest likelihood of improving OS, followed by nivolumab + ipilimumab (75%); pembrolizumab + lenvatinib had the highest likelihood of improving PFS (99%), ORR (97%), and CR (86%). These results remained valid even when the analysis was limited to patients with intermediate/poor risk, except that nivolumab + ipilimumab had the highest likelihood of achieving CR (100%). Further, OS benefits of ICI doublets were not inferior to those of ICI + tyrosine kinase inhibitor combinations. Recommendation of combination therapies with ICIs and/or tyrosine kinase inhibitors based on survival benefits and patient pretreatment risk classification will help advance personalized medicine for mRCC.
KW - Immune checkpoint inhibitors
KW - Metastasis
KW - Network meta-analysis
KW - Renal cell carcinoma
UR - http://www.scopus.com/inward/record.url?scp=85183630380&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85183630380&partnerID=8YFLogxK
U2 - 10.1007/s00262-023-03621-1
DO - 10.1007/s00262-023-03621-1
M3 - Review article
C2 - 38289361
AN - SCOPUS:85183630380
SN - 0340-7004
VL - 73
JO - Cancer Immunology, Immunotherapy
JF - Cancer Immunology, Immunotherapy
IS - 2
M1 - 38
ER -