Incidence of late-relapse germ cell tumor and outcome to salvage chemotherapy

被引:56
作者
Ronnen, EA
Kondagunta, GV
Bacik, J
Marion, S
Bajorin, DF
Sheinfeld, J
Bosl, GJ
Motzer, RJ
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Med, New York, NY 10021 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Epidemiol & Biostat, Genitourinary Oncol Serv, Div Solid Tumor Oncol, New York, NY USA
[3] Cornell Univ, Joan & Stanford Weill Med Coll 1, Dept Med, Ithaca, NY USA
关键词
PHASE-II TRIAL; HIGH-DOSE CHEMOTHERAPY; LATE RECURRENCE; ANTITUMOR-ACTIVITY; CISPLATIN; IFOSFAMIDE; PACLITAXEL; THERAPY; VINBLASTINE;
D O I
10.1200/JCO.2005.21.956
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose To define the incidence, clinical features, and outcome to salvage chemotherapy in patients with late-relapse germ cell tumor (GCT) after a complete response to first-line chemotherapy. Patients and Methods Two patient populations were examined. First, retrospective analysis of 246 patients treated on a clinical trial with salvage chemotherapy was performed; 29 patients with late-relapse GCT were identified and evaluated for treatment outcome and survival. Salvage regimens included paclitaxel, ifosfamide, and cisplatin, single agents, or a high-dose chemotherapy program. Second, the incidence of late relapse was assessed by retrospective analysis of 551 patients after a complete response (CR) to first-line chemotherapy. Results Twenty-nine patients received salvage chemotherapy on a clinical trial for late relapse GCT. The median survival was 23.9 months. At a median follow-up of 50.6 months, there were nine survivors. The chemotherapy regimens varied, but the only CRs were observed in patients treated with paclitaxel, ifosfamide, and cisplatin. Seven (50%) of 14 patients treated with paclitaxel, ifosfamide, and cisplatin achieved a continuous CR. Among the second population of 551 patients who had previously achieved a CR to a first-line chemotherapy trial, 17 were identified as having a late relapse (3%). The median time to relapse for these 17 patients was 7.8 years. Conclusion Late-relapse GCT is uncommon and is associated with a poor prognosis resulting from a high degree of resistance to chemotherapy. Chemotherapy with paclitaxel, ifosfamide, and cisplatin followed by surgery may be effective in patients with late-relapse GCT who are not considered candidates for primary surgery.
引用
收藏
页码:6999 / 7004
页数:6
相关论文
共 31 条
[1]   LATE RELAPSE OF TESTICULAR CANCER [J].
BANIEL, J ;
FOSTER, RS ;
GONIN, R ;
MESSEMER, JE ;
DONOHUE, JP ;
EINHORN, LH .
JOURNAL OF CLINICAL ONCOLOGY, 1995, 13 (05) :1170-1176
[2]  
Berg WJ, 1999, INVEST NEW DRUG, V16, P337
[3]   High-dose chemotherapy as initial salvage chemotherapy in patients with relapsed testicular cancer [J].
Bhatia, S ;
Abonour, R ;
Porcu, P ;
Seshadri, R ;
Nichols, CR ;
Cornetta, K ;
Einhorn, LH .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (19) :3346-3351
[4]   LATE RECURRENCE OF TESTICULAR TUMOR [J].
BLOM, J .
JOURNAL OF UROLOGY, 1974, 112 (02) :211-211
[5]   LATE RECURRENCE OF TESTICULAR CANCER [J].
BORGE, N ;
FOSSA, SD ;
OUS, S ;
STENWIG, AE ;
LIEN, HH .
JOURNAL OF CLINICAL ONCOLOGY, 1988, 6 (08) :1248-1253
[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]  
DELEO MJ, 1988, CANCER-AM CANCER SOC, V62, P985, DOI 10.1002/1097-0142(19880901)62:5<985::AID-CNCR2820620524>3.0.CO
[8]  
2-8
[9]   Late relapse of germ cell tumors after cisplatin-based chemotherapy [J].
Gerl, A ;
Clemm, C ;
Schmeller, N ;
Hentrich, M ;
Lamerz, R ;
Wilmanns, W .
ANNALS OF ONCOLOGY, 1997, 8 (01) :41-47
[10]   Antitumor activity of paclitaxel after failure of high-dose chemotherapy in a patient with late relapse of a non-seminomatous germ cell tumor [J].
Gerl, A ;
Wilmanns, W .
ANTI-CANCER DRUGS, 1996, 7 (06) :716-718