Small-cell carcinoma of the cervix: Fourteen years of experience at a single institution using a combined-modality regimen of involved-field irradiation and platinum-based combination chemotherapy

被引:132
作者
Hoskins, PJ
Swenerton, KD
Pike, JA
Lim, P
Aquino-Parsons, C
Wong, F
Lee, N
机构
[1] British Columbia Canc Agcy, Div Med Oncol, Vancouver, BC V5Z 4E6, Canada
[2] British Columbia Canc Agcy, Div Radiat Oncol, Vancouver, BC V5Z 4E6, Canada
[3] British Columbia Canc Agcy, Canc Control Res, Vancouver, BC V5Z 4E6, Canada
关键词
D O I
10.1200/JCO.2003.01.501
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose : To determine the efficacy and toxicity of a combined-modality regimen of irradiation with platinum-based combination chemotherapy in small-cell carcinoma of the cervix (SCCC). Patients and Methods: Thirty-four patients with SCCC were seen and treated at the British Columbia Cancer Agency between May 1988 and November 2002. Two protocols were used, SMCC (May 1988 to December 1995) and SMCC2 (January 1996 to November 2002). Both protocols used cisplatin, etoposide, and involved-field irradiation (essentially pelvis plus or minus para-aortics) with concurrent chemotherapy. In addition, SMCC2 included carboplatin and paclitaxel, and the para-aortics were irradiated routinely. Results: Thirty-one patients received either SMCC (n = 17) or SMCC2 (n 14), and three patients did not (disease too extensive, n 1; patient refusal, n = 1; and alternative regimen, n = 1). For the 31 patients treated on one of the protocols, the 3-year overall and failure-free survival (FFS) rates were 60% and 57%, respectively. The results were equivalent for SMCC and SMCC2. Radiologic stage was the only independent predictor for FFS (80% at 3 years for stage I and II patients v 38% at 3 years for stage III and IV patients). Distant failure (28%) was the most common cause of failure, with local failure occurring in 13% of patients. The switch to SMCC2 did not improve efficacy but did lessen the toxicity. Conclusion: SCCC can be successfully treated in approximately 55% of patients with a combination of irradiation and platinum-based chemotherapy. Disease extent predicts for chance of curability.
引用
收藏
页码:3495 / 3501
页数:7
相关论文
共 31 条
[1]  
ABELER VM, 1994, CANCER, V73, P672, DOI 10.1002/1097-0142(19940201)73:3<672::AID-CNCR2820730328>3.0.CO
[2]  
2-R
[3]  
ALBORESSAAVEDRA J, 1976, CANCER, V38, P2328, DOI 10.1002/1097-0142(197612)38:6<2328::AID-CNCR2820380620>3.0.CO
[4]  
2-J
[5]  
Benedet JK, 2000, STAGING CLASSIFICATI
[6]  
CHANG TC, 1993, P 4 INT C ANTIC CHEM
[7]  
ETTINGER DS, 1993, P AN M AM SOC CLIN, V12, P329
[8]   RANDOMIZED TRIAL OF CYCLOPHOSPHAMIDE, DOXORUBICIN, AND VINCRISTINE VERSUS CISPLATIN AND ETOPOSIDE VERSUS ALTERNATION OF THESE REGIMENS IN SMALL-CELL LUNG-CANCER [J].
FUKUOKA, M ;
FURUSE, K ;
SAIJO, N ;
NISHIWAKI, Y ;
IKEGAMI, H ;
TAMURA, T ;
SHIMOYAMA, M ;
SUEMASU, K .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1991, 83 (12) :855-861
[9]   SMALL-CELL UNDIFFERENTIATED CARCINOMA OF THE CERVIX - A CLINICOPATHOLOGIC, ULTRASTRUCTURAL, AND IMMUNOCYTOCHEMICAL STUDY OF 15 CASES [J].
GERSELL, DJ ;
MAZOUJIAN, G ;
MUTCH, DG ;
RUDLOFF, MA .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1988, 12 (09) :684-698
[10]   SMALL-CELL CARCINOMA OF THE CERVIX TREATED WITH CONCURRENT RADIOTHERAPY, CISPLATIN, AND ETOPOSIDE [J].
HOSKINS, PJ ;
WONG, F ;
SWENERTON, KD ;
PIKE, JA ;
MANJI, M ;
MCMURTRIE, E ;
ACKER, B ;
LERICHE, J .
GYNECOLOGIC ONCOLOGY, 1995, 56 (02) :218-225