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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

机译:一线西妥昔单抗联合化疗对KRAS野生型转移性结直肠癌患者的生活质量,安全性和有效性的观察性研究:ObservEr研究

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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.
机译:摘要西妥昔单抗在化疗中加入转移性结直肠癌(mCRC)时可提高疗效。西妥昔单抗对皮肤反应的有效管理可改善生活质量(QoL),并提高临床试验的治疗依从性。实际设置中没有可用数据。这项观察性,多中心,前瞻性研究评估了mCRC一线治疗的QoL,皮肤反应的发生率以及化疗加西妥昔单抗的治疗。主要终点是通过皮肤病生活质量指数(DLQI)和EORTC QLQ-C30测量的QoL。次要终点是皮肤和严重不良事件的发生率,总体中位和无进展生存期,肿瘤反应和切除率。 2011年5月至2012年11月,在意大利的28个中心招募了228名KRASwt mCRC患者,其中225名可评估,中位年龄65岁。治疗期间QoL不变,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%,没有4/5级事件。皮肤反应与生存相关(P = 0.016),其发生率受化疗方案(奥沙利铂对伊立替康的影响率[IRR] 1.72,P <0.0001)和性别(男性对女性)的影响。 (IRR 1.38,P = 0.0008)。首次基线后评估的依从性为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或反应管理时,西妥昔单抗加化学疗法不会在常规临床环境中影响生活质量。在这种情况下,我们观察到在对照临床试验中报告的总生存期(OS)与皮肤反应之间存在相同的相关性。

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