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Originally published as JCO Early Release 10.1200/JCO.2007.15.9103 on October 20 2008

Journal of Clinical Oncology, Vol 26, No 33 (November 20), 2008: pp. 5416-5421
© 2008 American Society of Clinical Oncology.

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Chemotherapy As an Alternative to Radiotherapy in the Treatment of Stage IIA and IIB Testicular Seminoma: A Spanish Germ Cell Cancer Group Study

Xavier Garcia-del-Muro, Pablo Maroto, Josep Gumà, Javier Sastre, Marta López Brea, José A. Arranz, Nuria Lainez, Diego Soto de Prado, Jorge Aparicio, José M. Piulats, Xavier Pérez, Josep R. Germá-Lluch

From the Institut Català d’Oncología, Institut d’Investigació Biomèdica de Bellvitge; Hospital de Sant Pau, Barcelona; Hospital Universitari Sant Joan, Reus; Hospital Universitario San Carlos; Hospital Gregorio Marañón, Madrid; Hospital Marqués de Valdecilla, Santander; Hospital de Navarra, Pamplona; Hospital Clínico, Valladolid; and Hospital La Fe, Valencia, Spain

Corresponding author: Xavier Garcia-del-Muro, MD, Genitourinary Tumors and Sarcoma Unit, Department of Medical Oncology, Institut Català d’Oncologia L’Hospitalet, Avda Gran Via Km 2.7, 08907 L’Hospitalet, Barcelona, Spain; e-mail: garciadelmuro{at}iconcologia.net

Purpose To assess the long-term efficacy and toxicity of front-line cisplatin-based chemotherapy in patients with stage IIA or IIB testicular seminoma.

Patients and Methods Untreated patients with pure seminoma of the testis after orchiectomy, with clinical stage IIA or IIB, were considered eligible for this prospective observational study. Chemotherapy consisted of either four cycles of cisplatin and etoposide or three cycles of cisplatin, etoposide, and bleomycin.

Results Between April 1994 and March 2003, 72 patients were entered onto the study at 26 participating centers. Eighteen patients had stage IIA disease, and 54 patients had stage IIB disease. Eighty-three percent of patients achieved complete response, and 17% achieved partial response with residual mass. After a median follow-up time of 71.5 months, six patients with stage IIB disease experienced relapse, and one of these patients died as a result of seminoma. Three patients experienced non–seminoma-related deaths (two died from a further esophageal carcinoma, and one died from an upper digestive hemorrhage). The estimated 5-year progression-free survival rates for patients with stage IIA or IIB disease were 100% and 87% (95% CI, 77.5% to 97%), respectively. Five-year progression-free and overall survival rates for the whole group were 90% (95% CI, 82% to 98%) and 95% (95% CI, 89% to 100%), respectively. Severe granulocytopenia and thrombocytopenia were observed in eight and two patients, respectively. Mild to moderate emesis, stomatitis, and diarrhea were the most common nonhematologic effects.

Conclusion Chemotherapy is a highly effective and well-tolerated treatment for patients with stage IIA or IIB seminoma and represents an available alternative that could avoid some of the serious late effects associated with radiotherapy. Further studies focusing on long-term toxicities of different treatment modalities are needed.

published online ahead of print at www.jco.org on October 20, 2008.

Presented in part at the 40th Annual Meeting of the American Society of Clinical Oncology, June 5-8, 2004, New Orleans, LA.

Authors’ disclosures of potential conflicts of interest and author contributions are found at the end of this article.


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Related Correspondence

  • Treating IIA/B Seminoma With Combination Carboplatin and Radiotherapy
    Duncan C. Gilbert, Nicholas J. VanAs, Sharon Beesley, David Bloomfield, Julian Money-Kyrle, Andy Norman, David Dearnaley, Alan Horwich, and Robert A. Huddart
    JCO 2009 27: 2101-2102 [Full Text]


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D. C. Gilbert, N. J. VanAs, S. Beesley, D. Bloomfield, J. Money-Kyrle, A. Norman, D. Dearnaley, A. Horwich, and R. A. Huddart
Treating IIA/B Seminoma With Combination Carboplatin and Radiotherapy
J. Clin. Oncol., April 20, 2009; 27(12): 2101 - 2102.
[Full Text] [PDF]


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X. Garcia-del-Muro and J. R. Germa-Lluch
In Reply
J. Clin. Oncol., April 20, 2009; 27(12): 2102 - 2103.
[Full Text] [PDF]



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