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新诊断局部晚期宫颈癌患者接受西妥昔单抗新辅助治疗后行西妥昔单抗联合放化疗的探索性研究。

An Exploratory Study of Neoadjuvant Cetuximab Followed by Cetuximab and Chemoradiotherapy in Women With Newly Diagnosed Locally Advanced Cervical Cancer.

机构信息

UVA Cancer Center.

Departments of Medicine.

出版信息

Am J Clin Oncol. 2022 Jul 1;45(7):286-293. doi: 10.1097/COC.0000000000000926. Epub 2022 Jun 7.

Abstract

OBJECTIVES

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).

PATIENTS AND METHODS

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

目的

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)。

患者和方法

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。

结果

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%。

结论

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。

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