Memorial Sloan Kettering Cancer Center, Weill Cornell Medical College, 300 East 66th Street, 12th Floor, New York, NY, 10065, USA.
Mapi (An ICON plc Company), Munich, Germany.
Cancer Immunol Immunother. 2019 Apr;68(4):609-618. doi: 10.1007/s00262-018-02295-4. Epub 2019 Feb 5.
Response rates are primary endpoints in many oncology trials; however, correlation with overall survival (OS) is not uniform across cancer types, treatments, or lines of therapy. This study explored the association between objective response (OR) and OS in patients with chemotherapy-refractory metastatic Merkel cell carcinoma who received avelumab (anti-PD-L1).
Eighty-eight patients enrolled in JAVELIN Merkel 200 (part A; NCT02155647) received i.v. avelumab 10 mg/kg every 2 weeks until confirmed progression, unacceptable toxicity, or withdrawal. Using conditional landmark analyses, we compared OS in patients with and without confirmed OR (RECIST v1.1). We applied a Cox model that included OR as a time-varying covariate and adjusted for age, visceral disease, and number of previous therapies.
Twenty-nine patients had confirmed OR; 20 by study week 7 and 7 more between study weeks 7 and 13. Survival probabilities 18 months after treatment initiation were 90% [95% confidence interval (CI) 65.6-97.4] in patients with OR at week 7 and 26.2% (95% CI 15.7-37.8) in patients without OR but who were alive at week 7. Median OS was not reached in patients with OR and was 8.8 months (95% CI 6.4-12.9) in patients without. Similar results were observed for the week 13 landmark. The adjusted Cox model showed OR was associated with a 95% risk reduction of death [hazard ratio 0.052 (95% CI 0.018-0.152)] compared with a nonresponse.
Patients with OR by 7 or 13 weeks had significantly longer OS than patients without, confirming that early OR is an endpoint of major importance.
缓解率是许多肿瘤学试验的主要终点;然而,在不同癌症类型、治疗方法或治疗线中,与总生存期(OS)的相关性并不一致。本研究探讨了接受avelumab(抗 PD-L1)治疗的化疗耐药转移性 Merkel 细胞癌患者的客观缓解(OR)与 OS 之间的相关性。
88 名患者入组 JAVELIN Merkel 200 研究(A 部分;NCT02155647),接受静脉注射avelumab 10 mg/kg,每 2 周一次,直至确认疾病进展、不可接受的毒性或退出。使用条件性里程碑分析,我们比较了有和无确认 OR(RECIST v1.1)患者的 OS。我们应用了包含 OR 作为时变协变量的 Cox 模型,并调整了年龄、内脏疾病和先前治疗次数。
29 名患者有确认的 OR;20 名患者在研究第 7 周时确认,7 名患者在研究第 7 周到第 13 周之间确认。治疗开始后 18 个月的生存概率在第 7 周时具有 OR 的患者中为 90%(95%CI:65.6-97.4),在第 7 周时无 OR 但存活的患者中为 26.2%(95%CI:15.7-37.8)。有 OR 的患者中位 OS 未达到,无 OR 的患者为 8.8 个月(95%CI:6.4-12.9)。第 13 周的里程碑也观察到了类似的结果。调整后的 Cox 模型显示,与无反应相比,OR 与死亡风险降低 95%相关[风险比 0.052(95%CI:0.018-0.152)]。
在第 7 或 13 周有 OR 的患者 OS 显著长于无 OR 的患者,这证实了早期 OR 是一个非常重要的终点。