ADVANCED SEMINOMA - TREATMENT RESULTS, SURVIVAL, AND PROGNOSTIC FACTORS IN 142 PATIENTS

被引:117
作者
MENCEL, PJ
MOTZER, RJ
MAZUMDAR, M
VLAMIS, V
BAJORIN, DF
BOSL, GJ
机构
[1] CORNELL UNIV, MED CTR, COLL MED, NEW YORK, NY 10021 USA
[2] MEM SLOAN KETTERING CANC CTR, DEPT MED, DIV SOLID TUMOR ONCOL, GENITOURINARY ONCOL SERV, NEW YORK, NY 10021 USA
[3] MEM SLOAN KETTERING CANC CTR, DEPT EPIDEMIOL & BIOSTAT, DIV BIOSTAT, NEW YORK, NY 10021 USA
关键词
D O I
10.1200/JCO.1994.12.1.120
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To investigate the efficacy of chemotherapy and to assess the relationship between selected pretreatment characteristics and survival in patients with advanced seminoma. Patients and Methods: One hundred forty-two patients with advanced seminoma treated with platinum-based chemotherapy were the subject of this study. Treatment regimens included cisplatin, vinblastine, bleomycin, cyclophosphamide, and dactinomycin (VAB-6) (45 patients), a six-cycle regimen of VAB-6 alternating with etoposide and cisplatin (two patients), cisplatin and etoposide (60 patients), and etoposide and carboplatin (35 patients). Results: One hundred thirty of 140 (93%) assessable patients treated with platinum-based therapy achieved a favorable response (complete response or a partial response with negative serum tumor markers). One hundred twenty-five patients (88%) are alive and 120 (86%) remain progression-free at a median follow-up duration of 43 months. Fifty-seven of 60 patients (95%) who were treated with cisplatin and etoposide achieved a favorable response; 55 (92%) remain progression-free. The relative risks of death or of an event (death or relapse) related to human chorionic gonadotropin (HCG) elevation were 1.8 (P = .04) and 1.96 (P = .001), respectively. The relative risks of death or of an event associated with lactate dehydrogenase (LDH) elevation were 2.6 (P = .05) and 2.7 (P = .02), respectively. All 19 patients with a mediastinal primary tumor site achieved a complete response, and 18 of 19 (95%) remain progression-free. Conclusion: Four cycles of cisplatin and etoposide is highly effective therapy for seminoma and is the standard therapy at our center. Elevation of the serum markers HCG and LDH were of prognostic significance, while an extragonadal primary tumor site was not associated with an adverse prognosis. Studies of tumor biology, including genetic analysis, are ongoing to determine other parameters that may correlate with response and survival.
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页码:120 / 126
页数:7
相关论文
共 36 条
[1]  
AMATO R, 1992, P AN M AM SOC CLIN, V11, pA623
[2]   RANDOMIZED TRIAL OF ETOPOSIDE AND CISPLATIN VERSUS ETOPOSIDE AND CARBOPLATIN IN PATIENTS WITH GOOD-RISK GERM-CELL TUMORS - A MULTIINSTITUTIONAL STUDY [J].
BAJORIN, DF ;
SAROSDY, MF ;
PFISTER, DG ;
MAZUMDAR, M ;
MOTZER, RJ ;
SCHER, HI ;
GELLER, NL ;
FAIR, WR ;
HERR, H ;
SOGANI, P ;
SHEINFELD, J ;
RUSSO, P ;
VLAMIS, V ;
CAREY, R ;
VOGELZANG, NJ ;
CRAWFORD, ED ;
BOSL, GJ .
JOURNAL OF CLINICAL ONCOLOGY, 1993, 11 (04) :598-606
[3]  
BAJORIN DF, 1993, P AN M AM SOC CLIN, V12, P234
[4]  
BAJORIN DF, 1992, PPO UPDATES, V6, P1
[5]  
BOSL GJ, 1983, CANCER RES, V43, P3403
[6]   VAB-6 - AN EFFECTIVE CHEMOTHERAPY REGIMEN FOR PATIENTS WITH GERM-CELL TUMORS [J].
BOSL, GJ ;
GLUCKMAN, R ;
GELLER, NL ;
GOLBEY, RB ;
WHITMORE, WF ;
HERR, H ;
SOGANI, P ;
MORSE, M ;
MARTINI, N ;
BAINS, M ;
MCCORMACK, P .
JOURNAL OF CLINICAL ONCOLOGY, 1986, 4 (10) :1493-1499
[7]  
BOSL GJ, 1988, CANCER RES, V48, P3524
[8]   ALTERNATING CYCLES OF ETOPOSIDE PLUS CISPLATIN AND VAB-6 IN THE TREATMENT OF POOR-RISK PATIENTS WITH GERM-CELL TUMORS [J].
BOSL, GJ ;
GELLER, NL ;
VOGELZANG, NJ ;
CAREY, R ;
AUMAN, J ;
WHITMORE, WF ;
HERR, H ;
MORSE, M ;
SOGANI, P ;
CHAN, E .
JOURNAL OF CLINICAL ONCOLOGY, 1987, 5 (03) :436-440
[9]   A RANDOMIZED TRIAL OF ETOPOSIDE + CISPLATIN VERSUS VINBLASTINE + BLEOMYCIN + CISPLATIN + CYCLOPHOSPHAMIDE + DACTINOMYCIN IN PATIENTS WITH GOOD-PROGNOSIS GERM-CELL TUMORS [J].
BOSL, GJ ;
GELLER, NL ;
BAJORIN, D ;
LEITNER, SP ;
YAGODA, A ;
GOLBEY, RB ;
SCHER, H ;
VOGELZANG, NJ ;
AUMAN, J ;
CAREY, R ;
FAIR, WR ;
HERR, H ;
MORSE, M ;
SOGANI, P ;
WHITMORE, W .
JOURNAL OF CLINICAL ONCOLOGY, 1988, 6 (08) :1231-1238
[10]  
CLEMM C, 1989, P EUROPEAN C CLIN ON, V5, pP813