Abstract:A series of 115 patients with clinical Stage I non-seminomatous germ cell testicular tumours were managed with orchiectomy and close surveillance (median follow-up 36 months, range 3-119); 34 (29.5%) relapsed, 21 within 6 months, 29 within a year and the latest at 28 months. At relapse all patients were treated with platinum or analogue-based drug combinations, supplemented in 7 by retroperitoneal node dissection; 30 patients achieved durable remissions and 2 have had further relapses successfully treated. Two… Show more
“…These results are similar to those of an earlier report, when the study included only 115 patients with a disease‐specific survival of 98.3% at a median follow‐up of 36 months. The later results confirm our earlier impression that surveillance of Stage I NSGCTT is an appropriate management technique [3]. These results are similar to those reported by others who practise surveillance alone after orchidectomy for clinical Stage I NSGCTT [4,5,16].…”
Section: Discussionsupporting
confidence: 90%
“…The presence or absence or vascular and/or lymphatic invasion (VLI) in the primary tumour was noted, this phenomenon having been identified by ourselves and others as the prognostic factor of greatest significance [3,8,11,12]. VLI were grouped together because of the recognized difficulty experienced by histologists in differentiating vascular channels and lymphatic vessels in such patients.…”
Section: Methodsmentioning
confidence: 99%
“…Since then, many groups have reported the results of surveillance of such patients. This practice has become increasingly popular, with results that match those achieved by RPLND [2–6]. As it is now realized that some patients with stage I disease have a higher risk of relapse, the concept of adjuvant chemotherapy has been proposed for this subgroup.…”
Objective To re-evaluate a national prospective study in for relapse in this series. Only one relapse occurred >28 months after orchidectomy. Despite poor comNew Zealand after 17 years to define whether orchidectomy alone and surveillance for nonseminoma pliance in some patients (12%) their survival was not prejudiced. Three patients died from disease despite germ cell testicular tumour (NSGCTT) is a sound policy and matches the results achieved by other chemotherapy at relapse. At 17 years and a median follow-up of 53 months, 242 of the 248 men are treatment protocols. Patients and methods Between 1980 and 1997, 248 disease-free and the disease-specific survival rate is 98%. men with stage I NSGCTT, from six New Zealand centres, were managed by orchidectomy alone and Conclusions This study shows that orchidectomy alone and treatment of relapses produces excellent longsurveillance, with treatment of relapses using combination chemotherapy.term results without the adverse eCects associated with retroperitoneal node dissection or elective chemoResults Seventy of the 248 patients (28%) relapsed; 42 of 92 (46%) with vascular and/or lymphatic invasion therapy for high-risk cases. Keywords Stage I nonseminoma, testicular cancer, (VLI) in the primary tumour relapsed, whereas only 26 of 151 (17%) without this feature relapsed surveillance, long-term follow-up, orchidectomy (P<0.001). VLI was the only identifiable risk factor ommend that high-risk patients should be oCered adju-
“…These results are similar to those of an earlier report, when the study included only 115 patients with a disease‐specific survival of 98.3% at a median follow‐up of 36 months. The later results confirm our earlier impression that surveillance of Stage I NSGCTT is an appropriate management technique [3]. These results are similar to those reported by others who practise surveillance alone after orchidectomy for clinical Stage I NSGCTT [4,5,16].…”
Section: Discussionsupporting
confidence: 90%
“…The presence or absence or vascular and/or lymphatic invasion (VLI) in the primary tumour was noted, this phenomenon having been identified by ourselves and others as the prognostic factor of greatest significance [3,8,11,12]. VLI were grouped together because of the recognized difficulty experienced by histologists in differentiating vascular channels and lymphatic vessels in such patients.…”
Section: Methodsmentioning
confidence: 99%
“…Since then, many groups have reported the results of surveillance of such patients. This practice has become increasingly popular, with results that match those achieved by RPLND [2–6]. As it is now realized that some patients with stage I disease have a higher risk of relapse, the concept of adjuvant chemotherapy has been proposed for this subgroup.…”
Objective To re-evaluate a national prospective study in for relapse in this series. Only one relapse occurred >28 months after orchidectomy. Despite poor comNew Zealand after 17 years to define whether orchidectomy alone and surveillance for nonseminoma pliance in some patients (12%) their survival was not prejudiced. Three patients died from disease despite germ cell testicular tumour (NSGCTT) is a sound policy and matches the results achieved by other chemotherapy at relapse. At 17 years and a median follow-up of 53 months, 242 of the 248 men are treatment protocols. Patients and methods Between 1980 and 1997, 248 disease-free and the disease-specific survival rate is 98%. men with stage I NSGCTT, from six New Zealand centres, were managed by orchidectomy alone and Conclusions This study shows that orchidectomy alone and treatment of relapses produces excellent longsurveillance, with treatment of relapses using combination chemotherapy.term results without the adverse eCects associated with retroperitoneal node dissection or elective chemoResults Seventy of the 248 patients (28%) relapsed; 42 of 92 (46%) with vascular and/or lymphatic invasion therapy for high-risk cases. Keywords Stage I nonseminoma, testicular cancer, (VLI) in the primary tumour relapsed, whereas only 26 of 151 (17%) without this feature relapsed surveillance, long-term follow-up, orchidectomy (P<0.001). VLI was the only identifiable risk factor ommend that high-risk patients should be oCered adju-
“…Likewise RPLND is still associated with ejaculation problems, as nerve-sparing techniques are not commonly available. We obtained similar survival rates to those reported previously for RPLND and primary chemotherapy [4,13,14].…”
RESULTSThe median (range) follow-up was 38 (6-265) months; the relapse rate was 24% and all occurred before 23 months, with 87% diagnosed within the first year. Platinumbased chemotherapy was given to patients with relapse, and surgery used after chemotherapy in seven. Among all the risk factors, an embryonal carcinoma component was the only significant predictor of relapse. The overall survival rate was 99%.
CONCLUSIONThe presence of embryonal carcinoma in the primary pathology is the only risk factor determining the relapse rate of the present surveillance policy for stage I NSGCTs. The overall survival was no different from those reported for retroperitoneal lymph node dissection and primary chemotherapy. Decreasing the frequency of CT in the first year and totally eliminating it after 1 year reduces the cost of surveillance. The possible compliance problems of patients are also minimized, without changing the overall survival. This surveillance protocol for patients with stage I NSGCT has reduced costs and provided a better quality of life for the patients, without jeopardizing the final outcome.
“…11 The literature review in the present study indicates that 4 years of follow-up is enough for this category of patients with a consequence of improved diagnostic procedures. 9,[12][13][14] If intensive follow-up can be stopped 4 years after orchiectomy, the cost of surveillance will be compatible to primary RPLND. However, physical examination should continue to check for contralateral metachronous testis tumor, which can occur in approximately 3% of the patients.…”
Background: Regardless of the way it is managed, a high cure rate has been achieved for recurrent low-stage testicular cancer. Achieving a balance between survival and the patient's inconvenience and expense during follow-up, has therefore become an important issue. Methods: Prognoses and recurrence patterns were investigated in 39 patients with stage I nonseminomatous germ cell tumor of the testis (NSGCT), and 82 patients with stage I seminomatous germ cell tumor of the testis (SGCT), who underwent high orchiectomy between 1970 and 1997 at our institution. We considered the cost benefits and the risks by reviewing our results together with other reported results.Results: Patients with clinical stage I NSGCT under surveillance showed no progression later than 4 years after orchiectomy. The ability to detect progression using chest X-ray alone appeared very low. There was no infradiaphragmatic recurrence after adjuvant radiotherapy for patients with stage I SGCT. Only two of 204 patients showed progression, which included eight of our patients who underwent two cycles of adjuvant carboplatin therapy. Conclusions: Four years of intensive follow-up is probably sufficient for patients with stage I NSGCT under surveillance, and routine chest X-rays may be required only during the first year of surveillance. The benefit of using adjuvant radiotherapy for patients with stage I SGCT is that we could remove abdominal and pelvic CT scans from the routine follow-up protocol. Randomized trials will clarify whether the adjuvant carboplatin therapy is less toxic, provides better prognosis and is more cost-effective than adjuvant radiotherapy.
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