Abstract:The results obtained with primary retroperitoneal lymph-node dissection (RPLND) in 464 patients with clinical stage A nonseminomatous germ-cell (NSGC) testicular cancer over a period of 25 years were reviewed. Results were analyzed in clinical terms and subdivided into early (1965)(1966)(1967)(1968)(1969)(1970)(1971)(1972)(1973)(1974)(1975)(1976)(1977)(1978) and contemporary (1979)(1980)(1981)(1982)(1983)(1984)(1985)(1986)(1987)(1988)(1989) findings so as to be comparable with series using radiotherapy or sur… Show more
“…The disadvantages of RPLND are that, even with modifical techniques, the operation may result in a considerable morbidity rate of 11-23% and in a mortality rate of approximately 0.3% [23]. Despite a previous RPLND, tumour recurrences in the retro peritoneum occurred in 7-12% of patients after 2 years [24][25][26], and despite major improvements in nervesparing techniques, still has some risk of ejaculation loss depending on the surgeon's expertise [27]. Thus, these patients can benefit from earlier chemotherapy with 2-3 cycles and optimal chance for cure [9].…”
Testis cancer is the most common cancer in young men and its incidence continues to rise. Even if prognosis is considered as good, a group with bad prognosis still remains. We aimed to evaluate whether two courses of chemotherapy after orchiectomy in patients with clinical stage I, non-seminomatous germ cell testicular tumour at high risk of relapse, will spare patients additional chemotherapy or surgery. High-risk patients had one or more of the following: preorchiectomy alpha-fetoprotein level of 80 ng/dl, 80% embryonal cell carcinoma or greater, vessel invasion in the primary tumour and tumour stage pT2 or greater. Low-risk patients had none of these factors or had 50% teratoma or more without vessel invasion. High-risk patients were offered two 21-day courses of outpatient chemotherapy consisting cisplatin, etoposide and bleomycin (BEP). Low-risk patients were observed. Of the 108 patients, we classified 71 as high risk and 37 as low risk of relapse. All of the high-risk patients received two courses of BEP chemotherapy. Low-risk patients were kept on close-up. The median follow-up was 26 months (range 10-60). Of the 71 patients in high-risk group, 3 relapsed with viable cancer and required additional chemotherapy and 1 patient with normal biomarkers and a late-appearing mass underwent retroperitoneal lympadenectomy for mature teratoma. All 4 relapsed patients were in high-risk group and presently they are free of disease. None of the 37 patients at low risk of recurrences developed relapse. We recommend two courses of adjuvant chemotherapy after postorchiectomy for high-risk patients with stage I non-seminomatous germ cell tumour of the testis. Adjuvant chemotherapy for these patients results in a low relapse and morbidity, wich compares favourably with the results of surveillance or RPLND. This well-tolerated approach may spare patients additional surgery or protracted chemotherapy, reduce the cost and eliminate the compliance problems associated with intensive follow up of high-risk patients.
“…The disadvantages of RPLND are that, even with modifical techniques, the operation may result in a considerable morbidity rate of 11-23% and in a mortality rate of approximately 0.3% [23]. Despite a previous RPLND, tumour recurrences in the retro peritoneum occurred in 7-12% of patients after 2 years [24][25][26], and despite major improvements in nervesparing techniques, still has some risk of ejaculation loss depending on the surgeon's expertise [27]. Thus, these patients can benefit from earlier chemotherapy with 2-3 cycles and optimal chance for cure [9].…”
Testis cancer is the most common cancer in young men and its incidence continues to rise. Even if prognosis is considered as good, a group with bad prognosis still remains. We aimed to evaluate whether two courses of chemotherapy after orchiectomy in patients with clinical stage I, non-seminomatous germ cell testicular tumour at high risk of relapse, will spare patients additional chemotherapy or surgery. High-risk patients had one or more of the following: preorchiectomy alpha-fetoprotein level of 80 ng/dl, 80% embryonal cell carcinoma or greater, vessel invasion in the primary tumour and tumour stage pT2 or greater. Low-risk patients had none of these factors or had 50% teratoma or more without vessel invasion. High-risk patients were offered two 21-day courses of outpatient chemotherapy consisting cisplatin, etoposide and bleomycin (BEP). Low-risk patients were observed. Of the 108 patients, we classified 71 as high risk and 37 as low risk of relapse. All of the high-risk patients received two courses of BEP chemotherapy. Low-risk patients were kept on close-up. The median follow-up was 26 months (range 10-60). Of the 71 patients in high-risk group, 3 relapsed with viable cancer and required additional chemotherapy and 1 patient with normal biomarkers and a late-appearing mass underwent retroperitoneal lympadenectomy for mature teratoma. All 4 relapsed patients were in high-risk group and presently they are free of disease. None of the 37 patients at low risk of recurrences developed relapse. We recommend two courses of adjuvant chemotherapy after postorchiectomy for high-risk patients with stage I non-seminomatous germ cell tumour of the testis. Adjuvant chemotherapy for these patients results in a low relapse and morbidity, wich compares favourably with the results of surveillance or RPLND. This well-tolerated approach may spare patients additional surgery or protracted chemotherapy, reduce the cost and eliminate the compliance problems associated with intensive follow up of high-risk patients.
“…Thus, the approach of adjuvant chemotherapy to high risk clinical Stage I patients constitutes over-treatment in at least half of cases. On the other hand, however, by using this approach almost 50% of patients who would in fact have relapsed are cured with two cycles of chemotherapy instead of at least three that would be required at relapse [7,33].…”
Section: Primary Chemotherapy For High-risk Clinical Stage I Nstgctmentioning
confidence: 99%
“…Over the past 2 decades, several modifications of surgical techniques by down-scaling the surgical template and development of nerve-sparing techniques have considerably reduced the morbidity of primary RPLND without comprising the high cure rate. In centers in the U.S. that have a strong urological surgical tradition, primary RPLND is still recommended as standard approach to clinical Stage I NSTGCT [7].…”
“…Tatsache ist aber, daß es sich noch niemals in der Geschichte der Onkologie als vorteilhaft erwiesen hat, einen bösartigen Tumor eher später und nicht so früh wie möglich zu behandeln [15]. Die Rate der falsch-negativen Befunde liegt im Promillebereich.…”
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