Brief Article
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World J Clin Oncol. Oct 10, 2012; 3(10): 137-141
Published online Oct 10, 2012. doi: 10.5306/wjco.v3.i10.137
Pegylated liposomal doxorubicin/carboplatin combination in ovarian cancer, progressing on single-agent pegylated liposomal doxorubicin
Alberto Gabizon, Yevgeni Plotkin, Rut Isacson, Ora Rosengarten, Tal Grenader
Tal Grenader, Ora Rosengarten, Rut Isacson, Yevgeni Plotkin, Alberto Gabizon, Department of Oncology, Sha’are Zedek Medical Center, Jerusalem 91031, Israel
Author contributions: Grenader T and Gabizon A contributed to the conception and design; Grenader T, Gabizon A, Rosengarten O and Isacson R contributed to acquisition of data; Grenader T, Rosengarten O and Gabizon A contributed to analysis and interpretation of data; Grenader T, Rosengarten O, Isacson R, Gabizon A and Plotkin Y contributed to drafting and revising the article; Grenader T, Rosengarten O, Isacson R, Gabizon A and Plotkin Y approved the final version of publication.
Correspondence to: Tal Grenader, MD, Department of Oncology, Sha’are Zedek Medical Center, PO Box 3235, Jerusalem 91031, Israel. talgrenader65@hotmail.com
Telephone: +972-2-6666378 Fax: +972-2-6666731
Received: June 26, 2012
Revised: September 14, 2012
Accepted: September 28, 2012
Published online: October 10, 2012
Abstract

AIM: To assess the efficacy and safety of the combination of pegylated liposomal doxorubicin (PLD) and carboplatin in patients with recurrent epithelial ovarian carcinoma (ROC), following disease progression on single agent PLD.

METHODS: An analysis of the medical records of 10 patients with ROC, treated in our institution with a combination of PLD and carboplatin following progression on single-agent PLD therapy was performed. The median age was 59.1 years (range, 45 to 77 years). All diagnoses were histological-proven. Eight of the 10 patients were platinum-resistant. Following disease progression on single-agent PLD treatment, carboplatin area under the curve (AUC)-5 was added to PLD in all 10 patients. In order to assess disease status, Ca-125 was assessed before each PLD/carboplatin treatment. Relative changes in Ca-125 values were calculated, and response defined as a greater than 50% reduction in Ca-125 from baseline. Radiographic studies were re-evaluated and responses to therapy based on computer tomography (CT) scans carried out on a regular basis every 2-3 mo in each patient. Statistical analysis was performed using SPSS (V19).

RESULTS: A median of 10 cycles (range, 2-26) of the carboplatin-PLD combination was given. Of the 10 treated patients, 6 had > 50% reduction in Ca-125 levels from baseline, 4 of these had a partial response according to Response Evaluation Criteria in Solid Tumors (RECIST) criteria, and the other 2 patients had no measurable disease. In a further 2 patients with a best response of disease stabilization and < 50% reduction of Ca-125 levels, one had progression of disease after 26 cycles, and the second progressed with brain metastases following 12 cycles. Seven of the eight patients who were platinum-resistant showed evidence of clinical benefit on carboplatin-PLD combination therapy; 5 of these had > 50% reduction in Ca-125 level, 4 also showed a partial response on CT scan. The treatment was generally well-tolerated by the patients.

CONCLUSION: Addition of carboplatin to PLD, after disease progression on single-agent PLD therapy, is both effective and safe in patients with ROC, even in those with Platinum-resistant disease.

Keywords: Pegylated liposomal doxorubicin; Carboplatin; Ovarian cancerchemotherapy; Platinum-resistant ovarian cancer; Platinum sensitive ovarian cancer