Neoadjuvant chemotherapy using low-dose consecutive intraarterial infusions of cisplatin combined with 5-fluorouracil for locally advanced cervical adenocarcinoma

被引:31
作者
Aoki, Y [1 ]
Sato, T [1 ]
Watanabe, M [1 ]
Sasaki, M [1 ]
Tsuneki, I [1 ]
Tanaka, K [1 ]
机构
[1] Niigata Univ, Fac Med, Dept Obstet & Gynecol, Niigata 9518510, Japan
关键词
cervical adenocarcinoma; neoadjuvant chemotherapy; low-dose intraarterial infusion; cisplatin and 5-fluorouracil;
D O I
10.1006/gyno.2001.6195
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective. 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. Methods. 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. Results. 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%. Conclusions. Intraarterial neoadjuvant chemotherapy effectively reduced tumor size in patients with locally advanced cervical adenocarcinoma; however, a survival advantage was not clear. (C) 2001 Academic Press.
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收藏
页码:496 / 499
页数:4
相关论文
共 16 条
[1]  
[Anonymous], 1993, INT J CANCER, DOI DOI 10.1002/ijc.2910540413
[2]   High-risk group in node-positive patients with stage IB, IIA, and IIB cervical carcinoma after radical hysterectomy and postoperative pelvic irradiation [J].
Aoki, Y ;
Sasaki, M ;
Watanabe, M ;
Sato, T ;
Tsuneki, I ;
Aida, H ;
Tanaka, K .
GYNECOLOGIC ONCOLOGY, 2000, 77 (02) :305-309
[3]   Locally advanced cervical adenocarcinoma: Is there a place for chemo-surgical treatment? [J].
BenedettiPanici, P ;
Greggi, S ;
Scambia, G ;
Salerno, MG ;
Amoroso, M ;
Maneschi, F ;
Cutillo, G ;
Caruso, A ;
Capelli, A ;
Mancuso, S .
GYNECOLOGIC ONCOLOGY, 1996, 61 (01) :44-49
[4]   Randomized trial of neoadjuvant cisplatin, vincristine, bleomycin, and radical hysterectomy versus radiation therapy for bulky stage IB and IIA cervical cancer [J].
Chang, TC ;
Lai, CH ;
Hong, JH ;
Hsueh, S ;
Huang, KG ;
Chou, HH ;
Tseng, CJ ;
Tsai, CS ;
Chang, JT ;
Lin, CT ;
Chang, HH ;
Chao, PJ ;
Ng, KK ;
Tang, SGJ ;
Soong, YK .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (08) :1740-1747
[5]   Prognostic factors of primary adenocarcinoma of the uterine cervix [J].
Chen, RJ ;
Chang, DY ;
Yen, ML ;
Lee, EF ;
Huang, SC ;
Chow, SN ;
Hsieh, CY .
GYNECOLOGIC ONCOLOGY, 1998, 69 (02) :157-164
[6]   Decrease in tumor volume and histologic response to intraarterial neoadjuvant chemotherapy in patients with cervical and endometrial adenocarcinoma [J].
Fujiwaki, R ;
Takahashi, K ;
Kitao, M .
GYNECOLOGIC ONCOLOGY, 1997, 65 (02) :258-264
[7]   Neoadjuvant chemotherapy with mitomycin C, etoposide, and cisplatin for adenocarcinoma of the cervix [J].
Iwasaka, T ;
Fukuda, K ;
Hara, K ;
Yokoyama, M ;
Nakao, Y ;
Uchiyama, M ;
Sugimori, H .
GYNECOLOGIC ONCOLOGY, 1998, 70 (02) :236-240
[8]   COMBINATION CHEMOTHERAPY FOR METASTATIC OR RECURRENT ADENOCARCINOMA OF THE CERVIX [J].
KAVANAGH, JJ ;
GERSHENSON, D ;
COPELAND, L ;
ROBERTS, WS .
JOURNAL OF CLINICAL ONCOLOGY, 1987, 5 (10) :1621-1623
[9]   STAGE IB ADENOCARCINOMA OF THE CERVIX - METASTATIC POTENTIAL AND PATTERNS OF DISSEMINATION [J].
KJORSTAD, KE ;
BOND, B .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1984, 150 (03) :297-299
[10]   Ovarian metastasis in stage IB and II cervical adenocarcinoma [J].
Natsume, N ;
Aoki, Y ;
Kase, H ;
Kashima, K ;
Sugaya, S ;
Tanaka, K .
GYNECOLOGIC ONCOLOGY, 1999, 74 (02) :255-258