Aoki Y, Sato T, Watanabe M, Sasaki M, Tsuneki I, Tanaka K
Department of Obstetrics and Gynecology, Faculty of Medicine, Niigata University, 1-757 Asahimachi dori, Niigata, 951-8510, Japan.
Gynecol Oncol. 2001 Jun;81(3):496-9. doi: 10.1006/gyno.2001.6195.
The goal of this work was to evaluate response rate, toxicity, and survival in treatment with intraarterial 5-fluorouracil (5-FU) and cisplatin in a neoadjuvant setting; this combination was administered to patients with locally advanced cervical adenocarcinoma.
Eleven patients were treated with preoperative neoadjuvant chemotherapy. Those eligible included patients with previously untreated stage IB, II, or III adenocarcinoma with good performance status. Treatment consisted of bilateral internal iliac artery infusion of cisplatin (a total of 10 mg/day) for 30 min, followed by 5-FU (a total of 250 mg/day) given by 24-hour continuous infusion for 10 days. Treatment was repeated every 3 weeks for a total of two or three cycles. All except one patient with progressive disease underwent radical hysterectomy following neoadjuvant chemotherapy. Postoperative radiotherapy was given to the whole pelvis to 6 patients; 3 of the 6 patients with involved common iliac nodes received radiotherapy to a paraaortic field in addition to the whole pelvis.
Among 11 eligible patients, 7 had a partial response (64%). Stable disease was observed in 3 cases (27%) and progressive disease in 1 (9%). Histopathological changes related to chemotherapy, however, revealed only mild effects. Of the 24 treatment cycles administered, no Grade 3 or 4 toxicity was observed and there were no therapy-related deaths. The median follow-up period was 30 months (range, 1-65 months). The mean survival period was 34.7 months and the 5-year survival rate was 21.2%.
Intraarterial neoadjuvant chemotherapy effectively reduced tumor size in patients with locally advanced cervical adenocarcinoma; however, a survival advantage was not clear.
本研究旨在评估新辅助治疗中动脉内注射5-氟尿嘧啶(5-FU)和顺铂的缓解率、毒性及生存率;该联合治疗应用于局部晚期宫颈腺癌患者。
11例患者接受术前新辅助化疗。符合条件的患者包括既往未接受治疗、表现状态良好的IB期、II期或III期腺癌患者。治疗方法为双侧髂内动脉输注顺铂(共10mg/天),持续30分钟,随后持续24小时输注5-FU(共250mg/天),持续10天。每3周重复治疗一次,共进行2或3个周期。除1例疾病进展患者外,所有患者在新辅助化疗后均接受了根治性子宫切除术。6例患者术后接受了全盆腔放疗;6例累及髂总淋巴结的患者中有3例除全盆腔放疗外还接受了腹主动脉旁野放疗。
11例符合条件的患者中,7例部分缓解(64%)。3例病情稳定(27%),1例病情进展(9%)。然而,化疗相关的组织病理学变化仅显示出轻微影响。在24个治疗周期中,未观察到3级或4级毒性反应,也没有与治疗相关的死亡病例。中位随访期为30个月(范围1 - 65个月)。平均生存期为34.7个月,5年生存率为21.2%。
动脉内新辅助化疗有效缩小了局部晚期宫颈腺癌患者的肿瘤大小;然而,生存优势并不明显。