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KRAS基因野生型转移性结直肠癌患者一线西妥昔单抗联合化疗的生活质量、安全性及有效性的观察性研究:ObservEr研究

Observational study on quality of life, safety, and effectiveness of first-line cetuximab plus chemotherapy in KRAS wild-type metastatic colorectal cancer patients: the ObservEr Study.

作者信息

Pinto Carmine, Di Fabio Francesca, Rosati Gerardo, Lolli Ivan R, Ruggeri Enzo M, Ciuffreda Libero, Ferrari Daris, Lo Re Giovanni, Rosti Giovanni, Tralongo Paolo, Ferrara Raimondo, Alabiso Oscar, Chiara Silvana, Ianniello Giovanni P, Frassoldati Antonio, Bilancia Domenico, Campanella Giovanna A, Signorelli Carlo, Racca Patrizia, Benincasa Elena, Stroppolo Maria Elena, Di Costanzo Francesco

机构信息

Medical Oncology, Santa Maria Nuova IRCCS Hospital, Reggio Emilia, Italy.

Medical Oncology, S. Orsola-Malpighi Policlinic Hospital, Bologna, Italy.

出版信息

Cancer Med. 2016 Nov;5(11):3272-3281. doi: 10.1002/cam4.888. Epub 2016 Oct 17.

Abstract

Cetuximab improves efficacy when added to chemotherapy for metastatic colorectal cancer (mCRC). Effective management of skin reactions from cetuximab improves quality of life (QoL), and treatment compliance in clinical trials. No data are available from real-world settings. The ObservEr observational, multicenter, prospective study evaluated QoL, the incidence of skin reactions, and management of chemotherapy plus cetuximab in first-line for mCRC. The primary endpoint was QoL measured with the Dermatology Life Quality Index (DLQI) and EORTC QLQ-C30. Secondary endpoints were the incidence of skin and serious adverse events, median overall and progression-free survival, tumor response, and resection rates. Between May 2011 and November 2012, 228 patients with KRASwt mCRC were enrolled at 28 Italian centers, 225 evaluable, median age 65 years. QoL did not change during treatment and was not affected by the choice of prophylactic or reactive skin management. The incidence of cetuximab-specific grade ≥3 skin reactions was 14%, with no grade 4/5 events. Skin reactions correlated with survival (P = 0.016), and their incidence was influenced by chemotherapy regimen (oxaliplatin vs. irinotecan-Incidence rate ratio [IRR] 1.72, P < 0.0001) and gender (male vs. female-IRR 1.38, P = 0.0008). Compliance at first postbaseline evaluation was 97.75%. Median overall survival was 23.6 months, median progression-free survival 8.3 months. Cetuximab plus chemotherapy did not compromise QoL in the routine clinical setting when patients receive close monitoring plus prophylactic or reactive management of skin reactions. We observed the same correlation between overall survival (OS) and skin reactions reported in controlled clinical trials, also in this setting.

摘要

西妥昔单抗与化疗联合用于转移性结直肠癌(mCRC)时可提高疗效。有效管理西妥昔单抗引起的皮肤反应可改善生活质量(QoL),并提高临床试验中的治疗依从性。现实环境中尚无相关数据。观察(ObservEr)观察性、多中心、前瞻性研究评估了mCRC一线治疗中化疗联合西妥昔单抗时的QoL、皮肤反应发生率及管理情况。主要终点是用皮肤病生活质量指数(DLQI)和欧洲癌症研究与治疗组织生活质量核心问卷(QLQ-C30)测量的QoL。次要终点是皮肤和严重不良事件的发生率、中位总生存期和无进展生存期、肿瘤反应及切除率。2011年5月至2012年11月,28个意大利中心纳入了228例KRAS野生型mCRC患者,225例可评估,中位年龄65岁。治疗期间QoL未改变,且不受预防性或反应性皮肤管理选择的影响。西妥昔单抗特异性≥3级皮肤反应的发生率为14%,无4/5级事件。皮肤反应与生存期相关(P = 0.016),其发生率受化疗方案(奥沙利铂与伊立替康——发生率比值[IRR] 1.72,P < 0.0001)和性别(男性与女性——IRR 1.38,P = 0.0008)影响。基线后首次评估时的依从率为97.75%。中位总生存期为23.6个月,中位无进展生存期为8.3个月。当患者接受密切监测以及皮肤反应的预防性或反应性管理时,在常规临床环境中西妥昔单抗联合化疗不会损害QoL。在这种情况下,我们也观察到了总生存期(OS)与皮肤反应之间与对照临床试验中报告的相同相关性。

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