Multimodal therapy including neoadjuvant methotrexate, vinblastine, doxorubicin, and cisplatin (MVAC) for stage IIB to IV cervical cancer

被引:9
作者
Dowdy, SC
Boardman, CH
Wilson, TO
Podratz, KC
Hartmann, LC
Long, HJ
机构
[1] Mayo Clin, Sect Gynecol Surg, Rochester, MN 55905 USA
[2] Mayo Clin, Div Med Oncol, Rochester, MN 55905 USA
关键词
cervical cancer; chemotherapy; neoadjuvant;
D O I
10.1067/mob.2002.123820
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
OBJECTIVE: The purpose of this study was to determine the survival rates and toxicity levels that are associated with multimodal therapy (including neoadjuvant methotrexate, vinblastine, doxorubicin, and cisplatin [MVAC]) in patients with stage IIB to IVB cervical cancer. STUDY DESIGN: We retrospectively reviewed the cases of 49 patients who were treated between 1989 and 1997 with neoadjuvant MVAC for advanced cervical cancer. RESULTS: The clinical response rate was 90% (27 partial responders, 17 complete responders). Grade 3 or greater toxicity was mostly limited to neutropenia; no deaths were attributed to MVAC. Combined therapy after MVAC included operation in 34 patients (69%) and radiation in 41 patients (84%). Twenty-one patients (43%) had <2 cm residual tumor at histologic evaluation. Pelvic control was achieved in 86% of patients. Five-year disease-specific survival for patients with stage III disease was 60%. CONCLUSION: For patients with advanced cervical cancer, neoadjuvant MVAC had a high response rate (90%) and an acceptable toxicity level. Compared with historic control subjects, multimodal treatment may be associated with improved rates of pelvic control.
引用
收藏
页码:1167 / 1173
页数:7
相关论文
共 17 条
[1]   COMBINATION BLEOMYCIN, IFOSFAMIDE, AND CISPLATIN CHEMOTHERAPY IN CERVICAL-CANCER [J].
BUXTON, EJ ;
MEANWELL, CA ;
HILTON, C ;
MOULD, JJ ;
SPOONER, D ;
CHETIYAWARDANA, A ;
LATIEF, T ;
PATERSON, M ;
REDMAN, CW ;
LUESLEY, DM ;
BLACKLEDGE, GR .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1989, 81 (05) :359-361
[2]  
EIFEL PJ, 1990, CANCER, V65, P2507, DOI 10.1002/1097-0142(19900601)65:11<2507::AID-CNCR2820651120>3.0.CO
[3]  
2-9
[4]   Cancer statistics, 2000 [J].
Greenlee, RT ;
Murray, T ;
Bolden, S ;
Wingo, PA .
CA-A CANCER JOURNAL FOR CLINICIANS, 2000, 50 (01) :7-33
[5]  
Jemal A, 2011, CA-CANCER J CLIN, V61, P134, DOI [10.3322/caac.21492, 10.3322/caac.20107, 10.3322/caac.20115]
[6]   Cisplatin, radiation, and adjuvant hysterectomy compared with radiation and adjuvant hysterectomy for bulky stage IB cervical carcinoma [J].
Keys, HM ;
Bundy, BN ;
Stehman, FB ;
Muderspach, LI ;
Chafe, WE ;
Suggs, CL ;
Walker, JL ;
Gersell, D .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 340 (15) :1154-1161
[7]   PHASE-II TRIAL OF METHOTREXATE, VINBLASTINE, DOXORUBICIN, AND CISPLATIN IN ADVANCED RECURRENT CARCINOMA OF THE UTERINE CERVIX AND VAGINA [J].
LONG, HJ ;
CROSS, WG ;
WIEAND, HS ;
WEBB, MJ ;
MAILLIARD, JA ;
KUGLER, JW ;
TSCHETTER, LK ;
KARDINAL, CG ;
EBBERT, LP ;
RAYSON, S .
GYNECOLOGIC ONCOLOGY, 1995, 57 (02) :235-239
[8]  
LONG HJ, 1990, P AN M AM SOC CLIN, V9, P158
[9]   Pelvic radiation with concurrent chemotherapy compared with pelvic and para-aortic radiation for high-risk cervical cancer [J].
Morris, M ;
Eifel, PJ ;
Lu, JD ;
Grigsby, PW ;
Levenback, C ;
Stevens, RE ;
Rotman, M ;
Gershenson, DM ;
Mutch, DG .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 340 (15) :1137-1143
[10]  
MUSCATO MS, 1982, SEMIN ONCOL, V9, P373