Randomized phase III trial of whole-abdominal irradiation versus doxorubicin and cisplatin chemotherapy in advanced endometrial carcinoma: A gynecologic oncology group study

被引:691
作者
Randall, ME
Filiaci, VL
Muss, H
Spirtos, NM
Mannel, RS
Fowler, L
Thigpen, JT
Benda, JA
机构
[1] E Carolina Univ, Brody Sch Med, Leo W Jenkins Canc Ctr, Greenville, NC USA
[2] Roswell Pk Canc Inst, Gynecol Oncol Grp, Stat & Data Ctr, Buffalo, NY 14263 USA
[3] Univ Vermont, Dept Med, Burlington, VT USA
[4] Womens Canc Ctr Community Hosp, Los Gatos, CA USA
[5] Univ Oklahoma, Hlth Sci Ctr, Dept Obstet & Gynecol, Oklahoma City, OK USA
[6] Ohio State Univ, Div Gynecol Oncol, James Canc Hosp & Solove Res Inst, Columbus, OH 43210 USA
[7] Univ Mississippi, Med Ctr, Div Oncol, Dept Med, Jackson, MS 39216 USA
[8] Univ Iowa Hosp & Clin, Dept Pathol, Iowa City, IA 52242 USA
[9] Univ Iowa Hosp & Clin, Dept Obstet & Gynecol, Iowa City, IA 52242 USA
关键词
D O I
10.1200/JCO.2004.00.7617
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose To compare whole-abdominal irradiation (WAI) and doxorubicin-cisplatin (AP) chemotherapy in women with stage III or IV endometrial carcinoma having a maximum of 2 cm of postoperative residual disease. Patients and Methods Four hundred twenty-two patients were entered onto this trial, Of 396 assessable patients, 202 were randomly allocated to receive WAI, and 194 were allocated to receive AP. Irradiation dosage was 30 Gy in 20 fractions, with a 15-Gy boost, Chemotherapy consisted of doxorubicin 60 mg/m(2) and cisplatin 50 mg/m(2) every 3 weeks for seven cycles, followed by one cycle of cisplatin. Results Most patient and tumor characteristics were well balanced. The median patient age was 63 years; 50% had endometrioid tumors, Median follow-up time was 74 months. The hazard ratio for progression adjusted for stage was 0,71 favoring AP (95% Cl, 0,55 to 0.91 P <.01). At 60 months, 50% of patients receiving AP were predicted to be alive and disease free when adjusting for stage compared with 38% of patients receiving WAI, The stage-adjusted death hazard ratio was 0.68 (95% Cl, 0.52 to 0.89; P <.01) favoring AP. Moreover, at 60 months and adjusting for stage, 55% of AP patients were predicted to be alive compared with 42% of WAI patients, Greater acute toxicity was seen with AP. Treatment probably contributed to the deaths of eight patients (4%) on the AP arm and five patients (2%) on the WAI arm. Conclusion Chemotherapy with AP significantly improved progression-free and overall survival compared with WAI. Nevertheless, further advances in efficacy and reduction in toxicity are clearly needed.
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页码:36 / 44
页数:9
相关论文
共 57 条
[1]   Doxorubicin versus doxorubicin and cisplatin in endometrial carcinoma: definitive results of a randomised study (55872) by the EORTC Gynaecological Cancer Group [J].
Aapro, MS ;
van Wijk, FH ;
Bolis, G ;
Chevallier, B ;
van der Burg, MEL ;
Poveda, A ;
de Oliveira, CF ;
Tumolo, S ;
di Palumbo, VS ;
Piccart, M ;
Franchi, M ;
Zanaboni, F ;
Lacave, AJ ;
Fontanelli, R ;
Favalli, G ;
Zola, P ;
Guastalla, JP ;
Rosso, R ;
Marth, C ;
Nooij, M ;
Presti, M ;
Scarabelli, C ;
Splinter, TAW ;
Ploch, E ;
Beex, LVA ;
Huinink, WT ;
Forni, M ;
Melpignano, M ;
Blake, P ;
Kerbrat, P ;
Mendiola, C ;
Cervantes, A ;
Goupil, A ;
Harper, PG ;
Madronal, C ;
Namer, M ;
Scarfone, G ;
Stoot, JEGM ;
Teodorovic, I ;
Coens, C ;
Vergote, I ;
Vermorken, JB .
ANNALS OF ONCOLOGY, 2003, 14 (03) :441-448
[2]   Outcome of endometrial carcinoma patients with involvement of the uterine serosa [J].
Ashman, JB ;
Connell, PP ;
Yamada, D ;
Rotmensch, J ;
Waggoner, SE ;
Mundt, AJ .
GYNECOLOGIC ONCOLOGY, 2001, 82 (02) :338-343
[3]   PARAAORTIC NODE BIOPSY IN CERVICAL AND ENDOMETRIAL CANCERS - DOES IT AFFECT SURVIVAL [J].
BLYTHE, JG ;
HODEL, KA ;
WAHL, TP ;
BAGLAN, RJ ;
LEE, FA ;
ZIVNUSKA, FR .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1986, 155 (02) :306-314
[4]   POSTOPERATIVE ADJUVANT CISPLATIN, DOXORUBICIN, AND CYCLOPHOSPHAMIDE (PAC) CHEMOTHERAPY IN WOMEN WITH HIGH-RISK ENDOMETRIAL CARCINOMA [J].
BURKE, TW ;
GERSHENSON, DM ;
MORRIS, M ;
STRINGER, CA ;
LEVENBACK, C ;
TORTOLEROLUNA, G ;
BAKER, VV .
GYNECOLOGIC ONCOLOGY, 1994, 55 (01) :47-50
[5]   The significance of adnexal involvement in endometrial carcinoma [J].
Connell, PP ;
Rotmensch, J ;
Waggoner, S ;
Mundt, AJ .
GYNECOLOGIC ONCOLOGY, 1999, 74 (01) :74-79
[6]   ENDOMETRIAL CANCER WITH PARAAORTIC ADENOPATHY - PATTERNS OF FAILURE AND OPPORTUNITIES FOR CURE [J].
CORN, BW ;
LANCIANO, RM ;
GREVEN, KM ;
SCHULTZ, DJ ;
REISINGER, SA ;
STAFFORD, PM ;
HANKS, GE .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1992, 24 (02) :223-227
[7]   The relationship of local and distant failure from endometrial cancer: Defining a clinical paradigm [J].
Corn, BW ;
Lanciano, RM ;
DAgostino, R ;
Kiggundu, E ;
Dunton, CJ ;
Purser, P ;
Greven, KM .
GYNECOLOGIC ONCOLOGY, 1997, 66 (03) :411-416
[8]  
COWLES TA, 1985, OBSTET GYNECOL, V66, P413
[9]  
COX DR, 1972, J R STAT SOC B, V34, P187
[10]   Management of aggressive histologic variants of endometrial carcinoma at the Tom Baker Cancer Centre between 1984 and 1994 [J].
Craighead, PS ;
Sait, K ;
Stuart, GC ;
Arthur, K ;
Nation, J ;
Duggan, M ;
Guo, DL .
GYNECOLOGIC ONCOLOGY, 2000, 77 (02) :248-253