Systemic therapy for metastatic renal cell carcinoma in the first-line setting: a systematic review and network meta-analysis

被引:47
作者
Mori, Keiichiro [1 ,2 ]
Mostafaei, Hadi [1 ,3 ]
Miura, Noriyoshi [1 ,4 ]
Karakiewicz, Pierre, I [5 ]
Luzzago, Stefano [5 ,6 ]
Schmidinger, Manuela [7 ,8 ]
Bruchbacher, Andreas [1 ,7 ,8 ]
Pradere, Benjamin [1 ,9 ,17 ]
Egawa, Shin [2 ]
Shariat, Shahrokh F. [1 ,10 ,11 ,12 ,13 ,14 ,15 ,16 ]
机构
[1] Med Univ Vienna, Dept Urol, Wahringer Gurtel 18-20, A-1090 Vienna, Austria
[2] Jikei Univ, Dept Urol, Sch Med, Tokyo, Japan
[3] Tabriz Univ Med Sci, Res Ctr Evidence Based Med, Tabriz, Iran
[4] Ehime Univ, Grad Sch Med, Dept Urol, Matsuyama, Ehime, Japan
[5] Univ Montreal Hlth Ctr, Canc Prognost & Hlth Outcomes Unit, Montreal, PQ, Canada
[6] IRCCS, Dept Urol, European Inst Oncol, Milan, Italy
[7] Med Univ Vienna, Clin Div Oncol, Dept Med 1, Vienna, Austria
[8] Med Univ Vienna, Comprehens Canc Ctr, Vienna, Austria
[9] Univ Hosp Tours, Dept Urol, Tours, France
[10] Univ Jordan, Dept Special Surg, Div Urol, Amman, Jordan
[11] Weill Cornell Med Coll, Dept Urol, New York, NY 10065 USA
[12] Univ Texas Southwestern, Dept Urol, Dallas, TX 75390 USA
[13] Karl Landsteiner Inst Urol & Androl, Vienna, Austria
[14] Charles Univ Prague, Fac Med 2, Dept Urol, Prague, Czech Republic
[15] IM Sechenov First Moscow State Med Univ, Inst Urol & Reprod Hlth, Moscow, Russia
[16] European Assoc Urol Res Fdn, Arnhem, Netherlands
[17] Univ Francois Rabelais Tours, PRES Ctr Val Loire, Tours, France
关键词
Renal cell carcinoma; Network meta-analysis; First-line; Immune-checkpoint inhibitors; OPEN-LABEL; SUNITINIB; PEMBROLIZUMAB; AXITINIB; CANCER;
D O I
10.1007/s00262-020-02684-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Management of metastatic renal cell cancer (mRCC) has undergone a paradigm shift with immune-checkpoint inhibitors (ICI) in the first-line setting. However, direct comparative data are inadequate to inform treatment decisions. Therefore, we aimed to assess first-line therapy for mRCC and indirectly compare the efficacy and safety of currently available treatments. Materials and methods Multiple databases were searched for articles published before June 2020. Studies that compared overall and/or progression-free survival (OS/PFS) and/or adverse events (AEs) in mRCC patients were considered eligible. Results Six studies matched our eligibility criteria. For OS, pembrolizumab plus axitinib [hazard ratio (HR) 0.85, 95% credible interval (CrI) 0.73-0.98] and nivolumab plus ipilimumab (HR 0.86, 95% CrI 0.75-0.99) were significantly more effective than sunitinib, and pembrolizumab plus axitinib was probably the best option based on analysis of the treatment ranking. For PFS, pembrolizumab plus axitinib (HR 0.86, 95% CrI 0.76-0.97) and avelumab plus axitinib (HR 0.85, 95% CrI 0.74-0.98) were statistically superior to sunitinib, and avelumab plus axitinib was likely to be the preferred option based on analysis of the treatment ranking, closely followed by pembrolizumab plus axitinib. Nivolumab plus ipilimumab had significantly lower rates of serious AEs than sunitinib. Conclusion Pembrolizumab plus axitinib seemed to be the most efficacious first-line agents, while nivolumab plus ipilimumab had the most favorable efficacy-tolerability equilibrium. These findings may facilitate individualized treatment strategies and inform future direct comparative trials in an expanding treatment options without direct comparison between approved drugs.
引用
收藏
页码:265 / 273
页数:9
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