Journal of Clinical Oncology, Vol 23, No 27 (September 20), 2005: pp. 6549-6555
© 2005 American Society of Clinical Oncology.
DOI: 10.1200/JCO.2005.19.638
Combination of Paclitaxel, Ifosfamide, and Cisplatin Is an Effective Second-Line Therapy for Patients With Relapsed Testicular Germ Cell Tumors
G. Varuni Kondagunta,
Jennifer Bacik,
Alessia Donadio,
Dean Bajorin,
Stephanie Marion,
Joel Sheinfeld,
George J. Bosl,
Robert J. Motzer
From the Genitourinary Oncology Service, Division of Solid Tumor Oncology, Department of Medicine, Memorial Sloan-Kettering Cancer Center; and the Department of Medicine, Joan and Sanford I. Weill Medical College of Cornell University, New York, NY
Address reprint requests to G. Varuni Kondagunta, MD, Memorial Sloan-Kettering Cancer Center, 1275 York Ave, New York, NY 10021; e-mail: kondaguv{at}mskcc.org
PURPOSE: The efficacy of paclitaxel was evaluated in combination with ifosfamide and cisplatin as second-line chemotherapy for patients with relapsed testicular germ cell tumors (GCTs).
PATIENTS AND METHODS: Forty-six patients with progressive metastatic GCTs were treated with paclitaxel and ifosfamide plus cisplatin (TIP) as second-line therapy. Eligibility required that patients have both a testis primary tumor site and a prior complete response (CR) to a first-line chemotherapy program, which had been identified previously as favorable prognostic factors to conventional-dose salvage chemotherapy.
RESULTS: Thirty-two (70%) of 46 patients achieved a CR to treatment. Three patients (7%) who achieved a CR relapsed after TIP chemotherapy. Twenty-nine patients are continuously disease free at a median follow-up time of 69 months, resulting in a 63% durable CR rate and a 2-year progression-free survival rate of 65% (95% CI, 51% to 79%).
CONCLUSION: Four cycles of TIP as second-line therapy achieved a durable CR rate in a high proportion of patients with relapsed testicular GCT. The high CR rate emphasizes the importance of patient selection according to prognostic factors to achieve a favorable outcome to conventional-dose salvage therapy.
Supported by Bristol Myers Squibb, National Institutes of Health Grants No. K24 CA-82431 and 5T32-CA-09207-26, and the Craig D. Tifford Foundation.
Presented at the 39th Annual Meeting of the American Society of Clinical Oncology, Chicago, IL, May 31-June 3, 2003.
Authors' disclosures of potential conflicts of interest are found at the end of this article.

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