Survival outcomes and safety of nimotuzumab combined with radiotherapy ± chemotherapy for locally advanced cervical cancer.

IF 4.1 2区 医学 Q1 OBSTETRICS & GYNECOLOGY
Jiwei Li, Manbo Cai, Changjun Xie, Sijuan Ding, Tao Wu, Wen Zou, Jingjing Wang
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引用次数: 0

Abstract

Objective: Chemoradiotherapy is currently the main treatment for locally advanced cervical cancer. Nevertheless, the survival profile of locally advanced cervical cancer patients remains unsatisfactory because of metastasis and recurrence. We aimed to assess the survival outcomes and safety of radiotherapy ± chemotherapy combined with nimotuzumab (a human monoclonal antibody against epidermal growth factor receptor that has anti-tumor activities) for patients with locally advanced cervical cancer.

Methods: Patients with stage IIB to IVA (International Federation of Gynecology and Obstetrics 2018) pathological and diagnosed locally advanced cervical cancer from January 2021 to December 2022 were collected in this retrospective, multi-center, and single-arm study. All patients received platinum-based radiotherapy ± chemotherapy with nimotuzumab (200 mg once a week for 6 weeks). Primary end point was overall survival. Secondary end points were progression-free survival and safety. The adverse events were recorded. Statistical analysis was performed using Statistics Analysis System software (v 9.4).

Results: A total of 60 patients were collected with a median follow-up of 17.4 months (95% CI 14.8 to 19.2). The median age was 58 years (range; 35-90). A total of 16 patients (26.7%) had stage II, 38 patients (63.3%) had stage Ⅲ, and 6 patients (10%) had stage Ⅳ. The median overall survival was not reached, and the median progression-free survival was 20.4 months (95% CI 16.3 to not evaluable). Radiotherapy ± chemotherapy with nimotuzumab achieved 90.7% 1- and 2-year overall survival. Moreover, 1-year progression-free survival was 82.1%, and the 2-year progression-free survival was 47.7%. The most common treatment-related grade 3 to 4 adverse events included neutropenia (15%), anemia (21.7%), and thrombocytopenia (5%). No drug-related severe adverse events or deaths occurred.

Conclusions: The addition of nimotuzumab to radiotherapy ± chemotherapy was associated with favorable oncologic outcomes for patients with locally advanced cervical cancer, and the toxicity was tolerable and manageable.

尼莫单抗联合放疗±化疗治疗局部晚期宫颈癌的生存结局和安全性。
目的:放化疗是目前局部晚期宫颈癌的主要治疗方法。然而,局部晚期宫颈癌患者的生存状况仍然令人不满意,因为转移和复发。我们的目的是评估放疗±化疗联合尼莫妥珠单抗(一种抗表皮生长因子受体的人单克隆抗体,具有抗肿瘤活性)治疗局部晚期宫颈癌患者的生存结局和安全性。方法:在这项回顾性、多中心、单臂研究中,收集2021年1月至2022年12月期间病理和诊断为IIB至IVA期(国际妇产科联合会2018)的局部晚期宫颈癌患者。所有患者均接受以铂为基础的尼莫单抗放疗±化疗(200mg,每周1次,共6周)。主要终点为总生存期。次要终点是无进展生存期和安全性。记录不良事件。采用Statistics analysis System软件(v9.4)进行统计分析。结果:共收集了60例患者,中位随访时间为17.4个月(95% CI 14.8 ~ 19.2)。中位年龄为58岁(范围;35 - 90)。II期16例(26.7%),Ⅲ期38例(63.3%),Ⅳ期6例(10%)。中位总生存期未达到,中位无进展生存期为20.4个月(95% CI 16.3至不可评估)。尼莫单抗放疗±化疗的1年和2年总生存率为90.7%。1年无进展生存率为82.1%,2年无进展生存率为47.7%。最常见的治疗相关3 - 4级不良事件包括中性粒细胞减少症(15%)、贫血(21.7%)和血小板减少症(5%)。未发生与药物相关的严重不良事件或死亡。结论:局部晚期宫颈癌患者在放疗±化疗的基础上加用尼莫单抗可获得良好的肿瘤预后,且毒性可耐受、可控。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.60
自引率
10.40%
发文量
280
审稿时长
3-6 weeks
期刊介绍: The International Journal of Gynecological Cancer, the official journal of the International Gynecologic Cancer Society and the European Society of Gynaecological Oncology, is the primary educational and informational publication for topics relevant to detection, prevention, diagnosis, and treatment of gynecologic malignancies. IJGC emphasizes a multidisciplinary approach, and includes original research, reviews, and video articles. The audience consists of gynecologists, medical oncologists, radiation oncologists, radiologists, pathologists, and research scientists with a special interest in gynecological oncology.
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