Literature DB >> 16260698

Risk-adapted management for patients with clinical stage I seminoma: the Second Spanish Germ Cell Cancer Cooperative Group study.

Jorge Aparicio1, José R Germà, Xavier García del Muro, Pablo Maroto, José A Arranz, Alberto Sáenz, Agustín Barnadas, Joan Dorca, Josep Gumà, David Olmos, Romá Bastús, Joan Carles, Daniel Almenar, Miguel Sánchez, Luis Paz-Ares, Juan J Satrústegui, Begoña Mellado, Ana Balil, Marta López-Brea, Alfredo Sánchez.   

Abstract

PURPOSE: To assess the efficacy of a risk-adapted treatment policy for patients with stage I seminoma by using universally accepted risk criteria. PATIENTS AND METHODS: Between 1999 and 2003, 314 patients with clinical stage I seminoma after orchiectomy were prospectively included. One hundred patients (31.8%) presented no risk factors and were managed with surveillance. In contrast, 131 patients (41.7%) had tumors larger than 4 cm, 33 patients (10.5%) had rete testis involvement, and 50 patients (15.9%) had both risk factors. All the latter received two courses of adjuvant carboplatin.
RESULTS: Chemotherapy was well tolerated, as only 17 patients (7.9%) presented grade 3 to 4 toxicity. Relapses were observed in six patients (6.0%) on surveillance and in seven patients (3.3%) treated with carboplatin (0.8% of tumors larger than 4 cm, 9.1% of those involving the rete testis, and 6.0% of patients with both risk criteria). All were located at the retroperitoneum, except for one at the spermatic cord. Median tumor size was 25 mm (range, 11 to 70 mm), and median time to relapse was 9 months (range, 4 to 28 months). All patients were rendered disease-free with chemotherapy (etoposide plus cisplatin). Median follow-up was 34 months (range, 12 to 72 months). The actuarial 5-year disease-free survival rate was 93.4% for patients on surveillance and 96.2% for patients treated with adjuvant chemotherapy. Overall 5-year survival was 100%.
CONCLUSION: Adjuvant carboplatin is effective in reducing the relapse rate in patients with stage I seminoma and risk factors. A risk-adapted strategy is safe and feasible and should be considered an alternative to systematic approaches, such as irradiation, chemotherapy, or surveillance.

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Year:  2005        PMID: 16260698     DOI: 10.1200/JCO.2005.01.9810

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  32 in total

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4.  [Testicular cancer--is there an indication for adjuvant or neoadjuvant systemic therapy?].

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Review 5.  Controversies in the management of early-stage germ cell tumors.

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Journal:  Curr Oncol Rep       Date:  2009-05       Impact factor: 5.075

6.  [Risk of second malignancies after platinum-based chemotherapy of testicular cancer].

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Journal:  Strahlenther Onkol       Date:  2019-02       Impact factor: 3.621

7.  Predictive value of preoperative neutrophil-to-lymphocyte ratio on the prognosis of germ cell testicular tumors.

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8.  Controversies in the Management of Clinical Stage I Seminoma: Carboplatin a Decade in-Time to Start Backing Out.

Authors:  Rune A W van de Wetering; Stefan Sleijfer; Darren R Feldman; Samuel A Funt; George J Bosl; Ronald de Wit
Journal:  J Clin Oncol       Date:  2018-02-01       Impact factor: 44.544

Review 9.  Clinical stage I seminoma: the case for surveillance.

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Journal:  World J Urol       Date:  2009-06-11       Impact factor: 4.226

10.  Update on management of seminoma.

Authors:  Emma J Alexander; Ingrid M White; Alan Horwich
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