Short-course adjuvant chemotherapy in high-risk stage I nonseminomatous germ cell tumors of the testis: A medical research council report

被引:246
作者
Cullen, MH
Stenning, SP
Parkinson, MC
Fossa, SD
Kaye, SB
Horwich, AH
Harland, SJ
Williams, MV
Jakes, R
机构
[1] UCL, DEPT HISTOPATHOL, LONDON, ENGLAND
[2] UCL, INST UROL & NEPHROL, LONDON, ENGLAND
[3] ROYAL MARSDEN NHS TRUST, SURREY, ENGLAND
[4] INST CANC RES, SURREY, ENGLAND
[5] ADDENBROOKES HOSP, CLIN ONCOL CTR, CAMBRIDGE, ENGLAND
[6] MRC, CANC TRIALS OFF, CAMBRIDGE, ENGLAND
[7] NORWEGIAN RADIUM HOSP, OSLO, NORWAY
[8] UNIV GLASGOW, CRC, DEPT MED ONCOL, GLASGOW G61 1BD, LANARK, SCOTLAND
关键词
D O I
10.1200/JCO.1996.14.4.1106
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: This United Kingdom Medical Research Council (UK-MRC) study prospectively evaluated efficacy and long-term toxicity of adjuvant chemotherapy in high-risk stage I nonseminomatous germ cell tumors of the testis (NSGCTT). Patients and Methods: Eligible patients were those identified by the local histopathologist as having features confirmed in MRC surveillance studies to indicate an approximate 50% risk of relapse. Central histopathology review was undertaken. Chemotherapy consisted of two courses of cisplatin 100 mg/m(2), bleomycin 30 mg weekly x 3, and etoposide 120 mg/m(2) x 3, every 21 days (BEP). Results: One hundred fourteen eligible cases were enrolled. Median time of follow-up was 4 years, with 93 patients followed-up for at least 2 years. There have been two relapses, including one patient who did not have a germ cell tumor (GCT), according to the reference histopathologist. This patient is alive with active disease, the other has died. There was one death after a cerebrovascular accident during treatment. Assessment of fertility, lung function, and audiometry pretreatment and more than 9 months posttreatment indicated no clinically significant changes. A mean decrease in transfer factor coefficient (KCO) of 15% of the predicted value was noted, but no patient had symptomatic respiratory dysfunction. Conclusion: There have been only two relapses among 114 cases of high-risk stage I NSGCTT treated with two courses of adjuvant BEP chemotherapy. The 95% confidence interval (CI) excludes a true relapse rate of more than 5%. Of 104 patients confirmed on histopathology review to have GCT, there has been only one relapse. Adjuvant chemotherapy is free from significant long-term toxicity, offering an effective alternative to surveillance or retroperitoneal lymph node dissection (RPLND) followed by surveillance, and may be preferred by some patients. (C) 1996 by American Society of Clinical Oncology.
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收藏
页码:1106 / 1113
页数:8
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