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A phase 2 trial of oral imatinib in patients with epithelial ovarian, fallopian tube, or peritoneal carcinoma in second or greater remission
1Gynecologic Medical Oncology Service, Department of Medicine, USA
2Gynecologic Surgical Oncology Service, Department of Surgery, USA
3Department of Epidemiology and Biostatistics, USA
4Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York, NY, USA
*Corresponding Author(s): P. Sabbatini E-mail: sabbatip@mskcc.org
Purpose of investigation: To determine the effect of imatinib on progression-free survival in patients with epithelial ovarian cancer in second or greater complete clinical remission (CCR). Methods: 35 patients were enrolled between 10/2002 and 1/2005. Eligible patients received imatinib at 400 mg daily orally. Results: One patient withdrew consent, and two patients received protocol therapy in first remission and were excluded. Five patients were removed for possibly related toxicity. No associations were seen between PDGF-R staining and PFS. Conclusions: Treatment with imatinib for patients with ovarian cancer in second CCR or greater did not prolong the PFS beyond the historical estimate.
Imatinib; Ovarian cancer; Peritoneal; Remission
M. Juretzka,M.L. Hensley,W. Tew,J. Konner,C. Aghajanian,M. Leitao,A. Iasonos,R. Soslow,K. Park,P. Sabbatini. A phase 2 trial of oral imatinib in patients with epithelial ovarian, fallopian tube, or peritoneal carcinoma in second or greater remission. European Journal of Gynaecological Oncology. 2008. 29(6);568-572.
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