UVA Cancer Center.
Departments of Medicine.
Am J Clin Oncol. 2022 Jul 1;45(7):286-293. doi: 10.1097/COC.0000000000000926. Epub 2022 Jun 7.
This study explored the feasibility of cetuximab with chemoradiation in women with cervical carcinoma and evaluated fluorine-18 fluorodeoxyglucose-positron emission tomography/computed tomography (18F-FDG-PET/CT) to assess early response to cetuximab (NCT00292955).
Eligible patients with International Federation of Gynecology and Obstetrics (FIGO) stage IB-IVB invasive carcinoma of the uterine cervix were treated on 1 of 3 dose levels (DL). DL1 consisted of neoadjuvant cetuximab, then concurrent radiotherapy with cetuximab 250 mg/m2/cisplatin 40 mg/m2, followed by weekly cetuximab. DL2 consisted of radiotherapy with cetuximab 200 mg/m2 and cisplatin 30 mg/m2. DL3 consisted of radiotherapy with cetuximab 250 mg/m2 and cisplatin 30 mg/m2. Patients underwent 18F-FDG-PET/CT before treatment, after neoadjuvant cetuximab, and at the end of treatment.
Of the 21 patients enrolled, 9, 3, and 9 were treated in DL1, DL2, and DL3, respectively. DL1 required dose reductions due to gastrointestinal toxicities. DL2 and 3 were tolerated with 1 dose-limiting toxicity (grade 4 renal failure) at DL3. Following 3 weekly treatments of neoadjuvant cetuximab in DL1, 7 patients had maximum standardized uptake value changes on 18F-FDG-PET/CT consistent with response to cetuximab. Of the 12 patients with locally advanced disease, eleven evaluable patients had no evidence of disease on 18F-FDG-PET/CT at treatment end. Five-year progression-free survival and overall survival rates for all patients were 57.5% and 58.5%, respectively.
Cetuximab with cisplatin 30 mg/m2 and radiotherapy was tolerated. 18F-FDG-PET/CT demonstrated early evidence of response to neoadjuvant cetuximab. With advances in precision oncology and the recent approval of pembrolizumab in metastatic cervical cancer, dual-target inhibition with an epidermal growth factor receptor inhibitor may be a promising treatment in the future.
本研究旨在探索西妥昔单抗联合放化疗治疗宫颈癌患者的可行性,并评估氟-18 氟代脱氧葡萄糖正电子发射断层扫描/计算机断层扫描(18F-FDG-PET/CT)评估西妥昔单抗早期疗效(NCT00292955)。
符合国际妇产科联合会(FIGO)分期 IB-IVB 期子宫颈浸润性癌的合格患者接受了 3 个剂量水平(DL)中的 1 个。DL1 组包括新辅助西妥昔单抗,然后联合西妥昔单抗 250mg/m2+顺铂 40mg/m2 同步放化疗,随后每周给予西妥昔单抗。DL2 组接受西妥昔单抗 200mg/m2+顺铂 30mg/m2 放疗。DL3 组接受西妥昔单抗 250mg/m2+顺铂 30mg/m2 放疗。患者在治疗前、新辅助西妥昔单抗治疗后和治疗结束时进行 18F-FDG-PET/CT 检查。
21 例患者中,9 例、3 例和 9 例分别在 DL1、DL2 和 DL3 中接受治疗。DL1 因胃肠道毒性而需要减少剂量。DL2 和 DL3 组各有 1 例剂量限制毒性(4 级肾衰竭)。在 DL1 中接受 3 个周期每周新辅助西妥昔单抗治疗后,7 例患者 18F-FDG-PET/CT 最大标准化摄取值变化与西妥昔单抗疗效一致。12 例局部晚期疾病患者中,11 例可评估患者治疗结束时 18F-FDG-PET/CT 无疾病证据。所有患者的 5 年无进展生存率和总生存率分别为 57.5%和 58.5%。
西妥昔单抗联合顺铂 30mg/m2 和放疗可耐受。18F-FDG-PET/CT 显示新辅助西妥昔单抗早期疗效。随着精准肿瘤学的发展以及最近 pembrolizumab 在转移性宫颈癌中的批准,表皮生长因子受体抑制剂的双重抑制可能是未来有前途的治疗方法。