医学
宫颈癌
根治性子宫切除术
放化疗
化疗
肿瘤科
阶段(地层学)
根治性手术
放射治疗
外科
内科学
癌症
生物
古生物学
作者
Hua Tu,He Huang,Yan‐Qiong Ouyang,Qing Liu,Bingna Xian,Kun Song,Gang Chen,Yuanming Shen,Jihong Liu
出处
期刊:International Journal of Gynecological Cancer
[BMJ]
日期:2020-06-09
卷期号:31 (1): 129-133
被引量:8
标识
DOI:10.1136/ijgc-2020-001357
摘要
Concurrent chemoradiotherapy is the first-line treatment for FIGO stage IIB cervical cancer. Neoadjuvant chemotherapy followed by radical surgery may provide another treatment option.To compare the therapeutic outcomes of neoadjuvant chemotherapy followed by surgery with cisplatin-based concurrent chemoradiotherapy for stage IIB cervical cancer.We hypothesize that the therapeutic effect of neoadjuvant chemotherapy combined with surgery and risk-adapted adjuvant treatment will be superior to that of concurrent chemoradiotherapy in stage IIB cervical cancer.Patients with stage IIB cervical cancer will be randomized 1:1 to neoadjuvant chemotherapy followed by surgery (Arm A) or concurrent chemoradiotherapy (Arm B). In arm A, patients will receive three cycles of paclitaxel and cisplatin followed by a type C radical hysterectomy and pelvic ±paraaortic lymphadenectomy. Patients showing progression after neoadjuvant chemotherapy will be referred to concurrent chemoradiotherapy. Adjuvant therapy will be recommended according to the presence of pathological risks. In Arm B, all patients will receive definitive concurrent chemoradiotherapy, including external beam pelvic radiotherapy combined with concurrent weekly cisplatin followed by brachytherapy.Patients between 18 and 60 years with histologically confirmed, untreated stage IIB cervical squamous carcinoma, adenocarcinoma, or adeno-squamous carcinoma.The primary endpoint is 2-year disease-free survival.An estimated sample size of 240 is required to fulfill the study objectives.As of February 2020, 115 eligible patients from four institutions have been enrolled. Enrollment is expected to be completed by December 2022.ClinicalTrials. gov identifier: NCT02595554.
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