Dizman Nazli, Austin Matthew, Considine Bryden, Jessel Shlomit, Schoenfeld David, Merl Man Yee, Hurwitz Michael, Sznol Mario, Kluger Harriet
Department of Internal Medicine, Yale School of Medicine, Yale New Haven Hospital, New Haven, CT.
Department of Medical Oncology, Yale School of Medicine, Smilow Cancer Center, New Haven, CT.
Clin Genitourin Cancer. 2023 Apr;21(2):221-229. doi: 10.1016/j.clgc.2023.01.002. Epub 2023 Jan 12.
Combination immune checkpoint inhibitors (ICI) and vascular endothelial growth factor receptor tyrosine kinase inhibitors (VEGF-R-TKI), including pembrolizumab/axitinib, are approved for first-line treatment of metastatic renal cell carcinoma (mRCC). Pembrolizumab/axitinib is associated with superior progression free survival (PFS), objective response rate (ORR), and overall survival over sunitinib. However, to date, the activity and safety of pembrolizumab/axitinib in later lines of therapy has not been reported.
Clinical data of consecutive patients receiving pembrolizumab/axitinib in the second-line or beyond for mRCC at Yale-New Haven Hospital were retrospectively collected. Best objective response was assessed using RECIST 1.1 criteria. Kaplan-Meier function was used to analyze survival.
Thirty-eight patients were included. Median age was 64, 92.1% had clear cell mRCC, 18.4% had sarcomatoid dedifferentiation; 94.7% had prior ICI and 39.5% had prior VEGF-R-TKI. Pembrolizumab/axitinib was administered as second-line therapy in 21 (55.5%) patients, third-line in 5 (13.2%) and beyond in 12 (30.2%). Adverse events (AEs) occurred in 86.8% of patients. Grade 3-4 AEs attributed to pembrolizumab and axitinib were seen in 18.4% and 6.4% of patients, respectively. No grade 5 AEs occurred. At a median follow up of 17.1 months, median PFS was 9.7 months (95% CI, 4.1-15.3). Amongst 36 response evaluable patients, the ORR was 25.0% (all partial) and disease control rate (including stable disease for at least 6 months) was 66.6%. The most frequent treatment sequence was first-line nivolumab/ipilimumab followed by second-line pembrolizumab/axitinib (n = 17, 44.7%); among this cohort, median PFS with pembrolizumab/axitinib was 11.1 (95% CI, 8.4-13.7) months, with an ORR of 31.4%.
Combination pembrolizumab/axitinib among previously treated mRCC patients has activity, with AE rates comparable to those reported in the first line. Prospective studies evaluating ICI-VEGF-R-TKI combinations beyond first-line are warranted to identify the most beneficial treatment sequencing in mRCC.
联合免疫检查点抑制剂(ICI)和血管内皮生长因子受体酪氨酸激酶抑制剂(VEGF-R-TKI),包括帕博利珠单抗/阿昔替尼,已被批准用于转移性肾细胞癌(mRCC)的一线治疗。与舒尼替尼相比,帕博利珠单抗/阿昔替尼具有更好的无进展生存期(PFS)、客观缓解率(ORR)和总生存期。然而,迄今为止,帕博利珠单抗/阿昔替尼在后续治疗线中的活性和安全性尚未见报道。
回顾性收集在耶鲁-纽黑文医院接受帕博利珠单抗/阿昔替尼二线及以上治疗的mRCC连续患者的临床资料。使用RECIST 1.1标准评估最佳客观缓解。采用Kaplan-Meier函数分析生存期。
纳入38例患者。中位年龄为64岁,92.1%为透明细胞mRCC,18.4%有肉瘤样去分化;94.7%曾接受ICI治疗,39.5%曾接受VEGF-R-TKI治疗。21例(55.5%)患者将帕博利珠单抗/阿昔替尼作为二线治疗,5例(13.2%)作为三线治疗,12例(30.2%)作为更后线治疗。86.8%的患者发生了不良事件(AE)。分别有18.4%和6.4%的患者出现归因于帕博利珠单抗和阿昔替尼的3-4级AE。未发生5级AE。中位随访17.1个月时,中位PFS为9.7个月(95%CI,4.1-15.3)。在36例可评估缓解的患者中,ORR为25.0%(均为部分缓解),疾病控制率(包括疾病稳定至少6个月)为66.6%。最常见的治疗顺序是一线纳武利尤单抗/伊匹木单抗,然后二线帕博利珠单抗/阿昔替尼(n = 17,44.7%);在该队列中,帕博利珠单抗/阿昔替尼的中位PFS为11.1(95%CI,8.4-13.7)个月,ORR为31.4%。
在先前接受过治疗的mRCC患者中,联合使用帕博利珠单抗/阿昔替尼具有活性,AE发生率与一线治疗报道的相当。有必要进行前瞻性研究,评估一线以上的ICI-VEGF-R-TKI联合方案,以确定mRCC中最有益的治疗顺序。