Moore D H, Thomas G M, Montana G S, Saxer A, Gallup D G, Olt G
Department of Gynecologic Oncology, Indiana University Medical Center, Indianapolis 46202, USA.
Int J Radiat Oncol Biol Phys. 1998 Aug 1;42(1):79-85. doi: 10.1016/s0360-3016(98)00193-x.
To determine the feasibility of using preoperative chemoradiotherapy to avert the need for more radical surgery for patients with T3 primary tumors, or the need for pelvic exenteration for patients with T4 primary tumors, not amenable to resection by standard radical vulvectomy.
Seventy-three evaluable patients with clinical Stage III-IV squamous cell vulvar carcinoma were enrolled in this prospective, multi-institutional trial. Treatment consisted of a planned split course of concurrent cisplatin/5-fluorouracil and radiation therapy followed by surgical excision of the residual primary tumor plus bilateral inguinal-femoral lymph node dissection. Radiation therapy was delivered to the primary tumor volume via anterior-posterior-posterior-anterior (AP-PA) fields in 170-cGy fractions to a dose of 4760 cGy. Patients with inoperable groin nodes received chemoradiation to the primary vulvar tumor, inguinal-femoral and lower pelvic lymph nodes.
Seven patients did not undergo a post-treatment surgical procedure: deteriorating medical condition (2 patients); other medical condition (1 patient); unresectable residual tumor (2 patients); patient refusal (2 patients). Following chemoradiotherapy, 33/71 (46.5%) patients had no visible vulvar cancer at the time of planned surgery and 38/71 (53.5%) had gross residual cancer at the time of operation. Five of the latter 38 patients had positive resection margins and underwent: further radiation therapy to the vulva (3 patients); wide local excision and vaginectomy necessitating colostomy (1 patient); no further therapy (1 patient). Using this strategy of preoperative, split-course, twice-daily radiation combined with cisplatin plus 5-fluorouracil chemotherapy, only 2/71 (2.8%) had residual unresectable disease. In only three patients was it not possible to preserve urinary and/or gastrointestinal continence. Toxicity was acceptable, with acute cutaneous reactions to chemoradiotherapy and surgical wound complications being the most common adverse effects.
Preoperative chemoradiotherapy in advanced squamous cell carcinoma of the vulva is feasible, and may reduce the need for more radical surgery including primary pelvic exenteration.
确定对于T3期原发性肿瘤患者,采用术前放化疗避免进行更根治性手术的可行性;或对于T4期原发性肿瘤患者,避免进行盆腔脏器清除术的可行性,这些患者无法通过标准根治性外阴切除术切除肿瘤。
73例可评估的临床III-IV期鳞状细胞外阴癌患者参加了这项前瞻性、多机构试验。治疗包括计划分疗程同步顺铂/5-氟尿嘧啶和放射治疗,随后手术切除残留的原发性肿瘤并进行双侧腹股沟-股淋巴结清扫。通过前后-后前(AP-PA)野对原发性肿瘤体积进行放射治疗,每次分割剂量为170 cGy,总剂量为4760 cGy。腹股沟淋巴结无法切除的患者接受针对原发性外阴肿瘤、腹股沟-股及下盆腔淋巴结的放化疗。
7例患者未接受治疗后手术:病情恶化(2例);其他疾病(1例);残留肿瘤无法切除(2例);患者拒绝(2例)。放化疗后,33/71(46.5%)患者在计划手术时未见外阴癌,38/71(53.5%)患者在手术时有肉眼可见的残留癌。后38例患者中有5例切缘阳性,接受了以下治疗:对外阴进一步放疗(3例);广泛局部切除及阴道切除术并需行结肠造口术(1例);未进一步治疗(1例)。采用这种术前分疗程、每日两次放疗联合顺铂加5-氟尿嘧啶化疗的策略,仅2/71(2.8%)患者有残留无法切除的疾病。仅3例患者无法保留尿控和/或胃肠控。毒性反应可接受,放化疗引起的急性皮肤反应和手术伤口并发症是最常见的不良反应。
晚期鳞状细胞外阴癌的术前放化疗是可行的,且可能减少包括原发性盆腔脏器清除术在内的更根治性手术的需求。