O'Shea Julianne, Link Emma, Khaw Pearly, Chang David, Tran Krystel, Lim Andrew, Lin Ming Yin
Peter MacCallum Cancer Centre, Department of Radiation Oncology, Melbourne, VIC, Australia.
University of Melbourne, Sir Peter MacCallum Department of Oncology, Melbourne, VIC, Australia.
Int J Gynecol Cancer. 2025 Jul;35(7):101916. doi: 10.1016/j.ijgc.2025.101916. Epub 2025 May 3.
This study aimed to evaluate the outcomes of patients with node-positive vulvar carcinoma treated with radiotherapy, with or without chemotherapy, administered with curative intent, focusing on patterns of first failure, locoregional control, and overall survival.
Patients were eligible if they had a histologic diagnosis of node-positive vulvar cancer and were referred for curative-intent radiotherapy, with or without chemotherapy, either as the primary treatment or in the adjuvant setting following definitive surgery between January 2000 and December 2019 at our institution. Eligible patients were selected from the prospective database of the gynecology oncology unit, where clinical, histopathologic, treatment, and follow-up data were systematically collected for analysis.
Out of 256 patients with vulvar cancer, 88 (34.4%) patients met the inclusion criteria. The median age was 65 years (range; 33-90). Sixty-two patients underwent surgery and adjuvant radiotherapy, of whom 57 (92%) received concomitant chemotherapy. Twenty-four patients received definitive chemoradiotherapy and 2 received definitive radiotherapy alone. The median total dose to the primary site was 54 Gy in the definitive setting and 45 Gy in the adjuvant setting. The median dose was 54 Gy (range; 45-60) to gross inguinal nodes (n = 48) and 54 Gy (range; 34-64) to gross primary disease (n = 26). The median follow-up was 5.3 years (range; 0.1-21.8). Five-year overall survival was 62% in the adjuvant group and 50% in the definitive group. Of 88 patients, 46 (52%) relapsed; 16 of 46 (35%) had failure at the primary site alone. Disease control at the primary site and nodes was 64% (95% CI; 48%-75%) in the adjuvant group and 49% (26%-68%) in the definitive group at 5 years.
Locoregional control and overall survival were highest in patients treated with surgery followed by radiotherapy. Definitive chemoradiotherapy provided moderate disease control and survival outcomes in patients unfit for surgery, supporting its use as an alternative treatment strategy.
本研究旨在评估接受根治性放疗(联合或不联合化疗)的淋巴结阳性外阴癌患者的治疗结果,重点关注首次失败模式、局部区域控制和总生存期。
2000年1月至2019年12月期间,在我们机构就诊的组织学诊断为淋巴结阳性外阴癌且接受根治性放疗(联合或不联合化疗)作为主要治疗或在根治性手术后辅助治疗的患者符合入选标准。符合条件的患者从妇科肿瘤病房的前瞻性数据库中选取,该数据库系统收集了临床、组织病理学、治疗和随访数据用于分析。
256例外阴癌患者中,88例(34.4%)符合纳入标准。中位年龄为65岁(范围:33 - 90岁)。62例患者接受了手术及辅助放疗,其中57例(92%)接受了同步化疗。24例患者接受了根治性放化疗,2例仅接受了根治性放疗。根治性治疗时原发部位的中位总剂量为54 Gy,辅助治疗时为45 Gy。腹股沟肿大淋巴结(n = 48)的中位剂量为54 Gy(范围:45 - 60 Gy),原发疾病灶(n = 26)的中位剂量为54 Gy(范围:34 - 64 Gy)。中位随访时间为5.3年(范围:0.1 - 21.8年)。辅助治疗组的5年总生存率为62%,根治性治疗组为50%。88例患者中,46例(52%)复发;46例中的16例(35%)仅在原发部位出现失败。辅助治疗组5年时原发部位和淋巴结的疾病控制率为64%(95% CI:48% - 75%),根治性治疗组为49%(26% - 68%)。
手术加放疗患者的局部区域控制和总生存期最高。根治性放化疗为不适合手术的患者提供了适度的疾病控制和生存结果,支持将其作为一种替代治疗策略。