Schadendorf Dirk, Dummer Reinhard, Hauschild Axel, Robert Caroline, Hamid Omid, Daud Adil, van den Eertwegh Alfons, Cranmer Lee, O'Day Steven, Puzanov Igor, Schachter Jacob, Blank Christian, Salama April, Loquai Carmen, Mehnert Janice M, Hille Darcy, Ebbinghaus Scot, Kang S Peter, Zhou Wei, Ribas Antoni
University Hospital Essen, Hufelandstrasse 55, D-45147 Essen, Germany.
Department of Dermatology, University Hospital Zurich, Gloriastrasse 31, 8091 Zurich, Switzerland.
Eur J Cancer. 2016 Nov;67:46-54. doi: 10.1016/j.ejca.2016.07.018. Epub 2016 Sep 2.
In KEYNOTE-002, pembrolizumab significantly prolonged progression-free survival and was associated with a better safety profile compared with chemotherapy in patients with advanced melanoma that progressed after ipilimumab. We present health-related quality of life (HRQoL) outcomes from KEYNOTE-002.
Patients were randomly assigned 1:1:1 to pembrolizumab 2 or 10 mg/kg every 3 weeks (Q3W) or investigator-choice chemotherapy. HRQoL was assessed using the European Organisation for Research and Treatment of Cancer Quality-of-Life Questionnaire-Core 30 instrument. A constrained longitudinal data analysis model was implemented to assess between-arm differences in HRQoL scores. The study is registered with ClinicalTrials.gov, number NCT01704287.
Of the 540 patients enrolled, 520 were included in the HRQoL analysis. Baseline global health status (GHS) was similar across treatment arms. Compliance rates at week 12 were 76.6% (n = 108), 82.3% (n = 121), and 86.4% (n = 133) for the control, pembrolizumab 2 mg/kg Q3W, and pembrolizumab 10 mg/kg Q3W arms, respectively. From baseline to week 12, GHS/HRQoL scores were maintained to a higher degree in the pembrolizumab arms compared with the chemotherapy arm (decrease of -2.6 for each pembrolizumab arm versus -9.1 for chemotherapy; P = 0.01 for each pembrolizumab arm versus chemotherapy). Fewer patients treated with pembrolizumab experienced deterioration in GHS at week 12 (31.8% for pembrolizumab 2 mg/kg, 26.6% for 10 mg/kg, and 38.3% for chemotherapy), with similar trends observed for the individual functioning and symptoms scales.
HRQoL was better maintained with pembrolizumab than with chemotherapy in KEYNOTE-002, supporting the use of pembrolizumab in patients with ipilimumab-refractory melanoma.
在KEYNOTE-002研究中,与化疗相比,帕博利珠单抗显著延长了无进展生存期,且安全性更好,该研究针对的是接受伊匹木单抗治疗后病情进展的晚期黑色素瘤患者。我们展示了KEYNOTE-002研究中与健康相关的生活质量(HRQoL)结果。
患者按1:1:1随机分配,分别接受每3周一次的2或10mg/kg帕博利珠单抗治疗,或由研究者选择的化疗方案。使用欧洲癌症研究与治疗组织生活质量核心问卷30(European Organisation for Research and Treatment of Cancer Quality-of-Life Questionnaire-Core 30)工具评估HRQoL。采用受限纵向数据分析模型评估各治疗组间HRQoL评分的差异。该研究已在ClinicalTrials.gov注册,注册号为NCT01704287。
在纳入的540例患者中,520例纳入HRQoL分析。各治疗组的基线总体健康状况(GHS)相似。对照组、每3周一次2mg/kg帕博利珠单抗组以及每3周一次10mg/kg帕博利珠单抗组在第12周时的依从率分别为76.6%(n = 108);82.3%(n = 121);86.4%(n = 133)。从基线到第12周,与化疗组相比,帕博利珠单抗组的GHS/HRQoL评分在更高程度上得以维持(帕博利珠单抗各治疗组下降2.6分,化疗组下降9.1分;帕博利珠单抗各治疗组与化疗组相比,P = 0.01)。在第12周时,接受帕博利珠单抗治疗的患者中,GHS恶化的患者较少(2mg/kg帕博利珠单抗组为31.8%,10mg/kg组为26.6%,化疗组为38.3%),在个体功能和症状量表上也观察到类似趋势。
在KEYNOTE-002研究中,帕博利珠单抗比化疗能更好地维持HRQoL,支持在伊匹木单抗难治性黑色素瘤患者中使用帕博利珠单抗。