Catholic University Fondazione Policlinico Universitario-IRCCS, Rome, Italy.
Regeneron Pharmaceuticals, Inc., Tarrytown, New York, USA.
Cancer Med. 2024 Jul;13(14):e7360. doi: 10.1002/cam4.7360.
A phase 2 cemiplimab study (NCT03132636) demonstrated a 24.1% objective response rate in patients diagnosed with metastatic basal cell carcinoma (mBCC) who were not candidates for continued hedgehog inhibitor (HHI) therapy due to intolerance to previous HHI therapy, disease progression while receiving HHI therapy, or having not better than stable disease on HHI therapy after 9 months. Here, health-related quality of life (QoL) for this patient population is reported.
Adult patients with mBCC were treated with intravenous cemiplimab at a dose of 350 mg every 3 weeks for 5 treatment cycles of 9 weeks/cycle then 4 treatment cycles of 12 weeks/cycle. Patients completed the European Organisation for Research and Treatment of Cancer Quality of Life-Core 30 (QLQ-C30) and Skindex-16 questionnaires at baseline and Day 1 of each cycle. Across Cycles 2 to 9, the overall change from baseline was analyzed using a mixed model with repeated measures. Responder analyses determined clinically meaningful improvement or deterioration (changes ≥10 points) or maintenance across all scales.
Patients reported low symptom burden and moderate-to-high functioning at baseline. Maintenance for QLQ-C30 global health status (GHS)/QoL and across all functioning and symptom scales was indicated by overall mean changes from baseline. Clinically meaningful improvement or maintenance was reported at Cycle 2 for GHS/QoL (77%), functioning scales (77% to 86%), and symptom scales (70% to 93%), with similar proportions of improvement or maintenance at Cycles 6 and 9, excluding fatigue. On the Skindex-16, clinically meaningful improvement or maintenance was reported across the emotional, symptom, and functional subscales, in 76%-88% of patients at Cycle 2, which were generally maintained at Cycles 6 and 9. Overall mean changes from baseline showed maintenance across these subscales.
The majority of patients treated with cemiplimab reported improvement or maintenance in GHS/QoL and functioning while maintaining a low symptom burden.
一项 cemiplimab 的 2 期研究(NCT03132636)表明,由于不耐受先前的 HH 抑制剂(HHI)治疗、在接受 HHI 治疗期间疾病进展或在 HHI 治疗后 9 个月时疾病无改善或稳定而不是继续接受 HH 抑制剂治疗的转移性基底细胞癌(mBCC)患者,客观缓解率为 24.1%。在此,报告了该患者人群的健康相关生活质量(QoL)。
患有 mBCC 的成年患者接受静脉注射 cemiplimab,剂量为 350mg,每 3 周一次,共 5 个 9 周周期的治疗周期,然后进行 4 个 12 周周期的治疗周期。患者在基线和每个周期的第 1 天完成欧洲癌症研究与治疗组织生活质量核心 30 项问卷(QLQ-C30)和 Skindex-16 问卷。在第 2 至 9 周期,使用重复测量混合模型分析从基线开始的总体变化。应答者分析确定了所有量表的临床意义上的改善或恶化(变化≥10 分)或维持。
患者在基线时报告了低症状负担和中高度功能状态。QLQ-C30 全球健康状况(GHS)/生活质量以及所有功能和症状量表的总体平均变化表明维持。在第 2 周期,GHS/QoL(77%)、功能量表(77%至 86%)和症状量表(70%至 93%)报告了临床意义上的改善或维持,在第 6 和第 9 周期,除了疲劳外,同样有类似比例的改善或维持。在 Skindex-16 上,在情绪、症状和功能子量表上,76%-88%的患者在第 2 周期报告了临床意义上的改善或维持,这些改善在第 6 和第 9 周期通常维持。从基线开始的总体平均变化表明这些子量表的维持。
接受 cemiplimab 治疗的大多数患者报告 GHS/QoL 和功能得到改善或维持,同时保持低症状负担。