Medical Oncology, Faculty of Medicine, Akdeniz University, Dumlupınar Bulvarı, Kampus, 07070, Antalya, Turkey.
Medical Oncology, Okmeydanı Research and Training Hospital, Istanbul, Turkey.
Cancer Chemother Pharmacol. 2021 Nov;88(5):805-812. doi: 10.1007/s00280-021-04328-9. Epub 2021 Jul 26.
In this study, we looked for whether treatment-induced rash predicts treatment efficacy in patients with recurrent/metastatic HNSCC treated with Cetuximab and chemotherapy.
Patients who were treated with platinum-based chemotherapy and cetuximab for the first line treatment of recurrent/metastatic HNSCC were recruited. Presence of rash, hypomagnesemia, hypopotassemia, anemia, neutropenia, thrombocytopenia during treatment and treatment response, date of progression, date of last visit and death were recorded.
A total of 138 patients' data were available for analysis. Any grade of rash was detected in 57 (44.5%) of the patients. The incidence of rash was significantly higher in patients with objective response than in patients with disease progression (%56.8 vs %14.3, p < 0.001). Progression free survival was 7.06 months (4.98-9.15) in patients treated with cetuximab and chemotherapy as first line treatment. In the multivariate analysis; rash was significantly correlated with longer PFS (HR 2.136; 95% CI 1.067-4.278; p = 0.032). Progression free survival was 9.65 months in patients who experienced rash, and 6.02 months in patients without rash, (p = 0.019, log-rank test). Overall survival was 11.24 months (9.65-12.82). In multivariate analysis, the survival of patients with rash was significantly longer than patients without rash (HR 1.954; 95% CI 1.162-3.285; p = 0.012). Overall survival was 15.08 months in patients who experienced rash, and 8.61 months in patients without rash (p = 0.05, log-rank test).
Cetuximab-induced rash is associated with better ORR and longer PFS and OS in patients with recurrent/metastatic HNSCC treated with Cetuximab and platinum-based chemotherapy.
本研究旨在探讨接受西妥昔单抗联合化疗治疗复发性/转移性头颈部鳞状细胞癌(HNSCC)患者的治疗诱导皮疹是否与治疗疗效相关。
招募了接受铂类化疗和西妥昔单抗一线治疗复发性/转移性 HNSCC 的患者。记录治疗期间皮疹、低镁血症、低钾血症、贫血、中性粒细胞减少症、血小板减少症以及治疗反应、疾病进展日期、末次就诊日期和死亡日期。
共分析了 138 例患者的数据。57 例(44.5%)患者出现任何级别皮疹。客观缓解患者的皮疹发生率明显高于疾病进展患者(56.8% vs 14.3%,p<0.001)。接受西妥昔单抗联合化疗作为一线治疗的患者无进展生存期为 7.06 个月(4.98-9.15)。多变量分析显示;皮疹与更长的 PFS 显著相关(HR 2.136;95%CI 1.067-4.278;p=0.032)。出现皮疹的患者无进展生存期为 9.65 个月,无皮疹的患者为 6.02 个月(p=0.019,log-rank 检验)。总生存期为 11.24 个月(9.65-12.82)。多变量分析显示,皮疹患者的生存时间明显长于无皮疹患者(HR 1.954;95%CI 1.162-3.285;p=0.012)。出现皮疹的患者总生存期为 15.08 个月,无皮疹的患者为 8.61 个月(p=0.05,log-rank 检验)。
在接受西妥昔单抗联合铂类化疗治疗的复发性/转移性 HNSCC 患者中,西妥昔单抗诱导的皮疹与更好的客观缓解率以及更长的 PFS 和 OS 相关。