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Original Research

Open Access

Weekly paclitaxel/5-fluorouracil followed by platinum retreatment for patients with recurrent ovarian cancer: a single institution experience

  • H. Watari1,*,
  • M. Hosaka1
  • T. Mitamura1
  • M. Moriwaki1
  • Y. Ohba1
  • Y. Todo1
  • M. Takeda1
  • Y. Ebina1
  • N. Sakuragi1

1Department of Obstetrics and Gynecology, Hokkaido University Graduate School of Medicine, Sapporo, Japan

DOI: 10.12892/ejgo200806573 Vol.29,Issue 6,November 2008 pp.573-577

Published: 10 November 2008

*Corresponding Author(s): H. Watari E-mail: watarih@med.hokudai.ac.jp

Abstract

Purpose: Since the prognosis of recurrent ovarian cancer patients is still poor, we need to establish a useful treatment strategy to achieve their long-term survival. We treated recurrent ovarian cancer patients with weekly paclitaxel (PTX)/5-fluorouracil (5-FU) followed by platinum retreatment to investigate its clinical efficacy in a preliminary manner. Methods: Sixteen patients with recurrent ovarian cancer. pretreated with taxane and platinum, were treated with weekly paclitaxel (PTX)/5-fluorouracil (FU). PTX (80 mg/m(2)) on day 1, 8, and 15 was combined with a bolus injection of 5-FU (500 mg/m(2)) on day 2, 9, and 16. Chemotherapy was given every four weeks. Patients with stable disease or progressive disease Were subsequently retreated with a platinum-containing regimen, Response was evaluated by RECIST criteria or CA 1225 criteria. Toxicities were evaluated according to the National Cancer Institute-common toxicity Criteria (NCI-CTC) version 3. Results: Among live patients with sensitive disease, one Of four patients with measurable turner and one without measurable tumor responded to weekly PTX/5-FU. Among 11 patients with resistant disease. none of five patients with measurable tumor and three of six patients without measurable tumor responded to weekly PTX/5-FU, Overall objective response rate by weekly PTX/5-FU was 31.3% (5/16). Among 16 patients, 13 patients who showed no response or progressive disease (three with sensitive disease, ten with resistant disease) received platinum retreatment after weekly PTX/5FU. All three patients with sensitive disease and three of ten patients with resistant disease revealed response to platinum retreatment. Overall objective response rate by platinum retreatment after weekly PTX/5-FU was 46.2% (6/13). Conclusions: Weekly PTX/5FU followed by platinum retreatment Could be a useful treatment strategy for recurrent ovarian cancer patients. We need to establish the standard treatment strategy for recurrent ovarian cancer patients with a poor prognosis.

Keywords

Paclitaxel; 5-fluorouracil; Recurrent disease; Platinum-free interval; Ovarian cancer

Cite and Share

H. Watari,M. Hosaka,T. Mitamura,M. Moriwaki,Y. Ohba,Y. Todo,M. Takeda,Y. Ebina,N. Sakuragi. Weekly paclitaxel/5-fluorouracil followed by platinum retreatment for patients with recurrent ovarian cancer: a single institution experience. European Journal of Gynaecological Oncology. 2008. 29(6);573-577.

References

[1] Amstrong D.K.: “Relapesed ovarian cancer: challenges and management strategies for a chronic disease”. Oncologist, 2002, 7 (suppl. 5), 20.

[2] Jemal A., Thomas A., Murray T., Thun M.: “Cancer statistics, 2002”. CA Cancer J. Clin., 2002, 52, 23.

[3] Markman M., Hall J., Spitz D., Weiner S., Carson L., Le L.V. et al.: “Phase II trial of weekly single-agent paclitaxel in platinum/paclitaxel-refractory ovarian cancer”. J. Clin. Oncol., 2002, 20, 2365.

[4] Gynecologic Oncology Group: Markman M., Blessing J., Rubin S.C., Connor J., Hanjani P.,Waggoner S.: “Phase II trial of weekly paclitaxel (80 mg/m2) in platinum and paclitaxel-resistant ovarian and primary peritoneal cancers: a Gynecologic Oncology Group study”. Gynecol. Oncol., 2006, 101, 436.

[5] Blackledge G., Lawton F., Redman C., Kelly K.: “Response of patients in phase II studies of chemotherapy in ovarian cancer: implications for patient treatment and the design of phase II trials”. Br. J. Cancer, 1989, 59, 650.

[6] Gore M.E., Fryatt I., Wiltshaw E., Dawson T.: “Treatment of relapsed carvinoma of the ovary with cisplatin or carboplatin following initial treatment with these compounds”. Gynecol. Oncol., 1990, 36, 207.

[7] Markman M., Rothman R., Hakes T., Reichman B., Hoskins W., Rubin S. et al.: “Second-line platinum therapy in patients with ovarian cancer previously treated with cisplatin”. J. Clin. Oncol., 1991, 9, 389.

[8] Parmar M.K., Ledermann J.A., Colombo N., du Bois A., Delalovo J.F., Kristensen G.B. et al.: “ICON and AGO Collaborators. Paclitaxel plus platinum-based chemotherapy versus conventional platinum-based chemotherapy in women with relapsed ovarian cancer. The ICON4/SGO-OVAR-2.2 trial”. Lancet, 2003, 361, 2099.

[9] Pfisterer J., Plante M., Vergote I., du Bois A., Hirte H., Lacave A.J. et al.: “AGO-OVAR: NCIC CTG: EORTC GOG. Gemcitabine plus carboplatin compared with carboplatin in patients with platinum- sensitive recurrent ovarian cancer: an intergroup trial of the AGO-OVAR, the NCIC CTG, and the EORTC GOG”. J. Clin. Oncol., 2006, 24, 4699.

[10] Murad A.M., Petroianu A., Guimaraes R.C., Aragao B.C., Cabral L.O., Scalabrini-Neto A.O.: “Phase II trial of the combination of paclitaxel and 5-fluorouracil in the treatment of advanced gastric cancer: a novel, safe, and effective regimen”. Am. J. Clin. Oncol., 1999, 22, 580.

[11] Loesch D.M., Asmar L., Canfield V.A., Parker G.A., Hynes H.E., Ellis P.G. et al.: “A phase II trial of weekly paclitaxel, 5-fluorouracil, and leucovorin as first-line treatment for metastatic breast cancer”. Breast Cancer Res. Treat., 2003, 77, 115.

[12] Sugiyama T., Yakushiji M., Nishida T., Ushijima K., Okura N., Kigawa J. et al.: “Irinotecan (CPT-11) combined with cisplatin in patients with refractory or recurrent ovarian cancer”. Cancer Lett., 1998, 128, 211.

[13] Therasse P., Arbuck S.G., Eisenhauer E.A., Wanders J., Kaplan R.S., Rubinstein L. et al.: “New guideline to evaluate the response to treatment in solid tumors”. J. Natl. Cancer Inst., 2000, 92, 205.

[14] Rustin G.J.S., Nelstrop A.E., McClean P., Brady M.F., McGuire W.P., Hoskins W.J. et al.: “Defining response of ovarian carcinoma to initial chemotherapy according to serum CA-125”. J. Clin. Oncol., 1996, 14, 1545.

[15] Kano Y., Akutsu M., Tsunoda S., Ando J., Matsui J., Suzuki K. et al.: “Schedule-dependent interaction between paclitaxel and 5-fluorouracil in human carcinoma cell lines in vitro”. Br. J. Cancer, 1996, 74, 704.

[16] Cascinu S., Ficarelli R., Safi M.A.A., Graziano F., Catalano G., Cellerino R.: “A phase I study of paclitaxel and 5-fluorouracil in advanced gastric cancer”. Eur. J. Cancer, 1999, 33, 1699.

[17] Nistico C., Bria E., Agostara B., Barni S., Colella E., Frontini L. et al.: “Weekly paclitaxel, 5-fluorouracil and folinic acid with granulocyte colonu-stimulating factor support in metastatic breast cancer patients: a phase II study”. Anticancer Drugs, 2006, 17, 345.

[18] Cesano A., Lane S.R., Poulin R., Ross G., Fields S.Z.: “Stabilization of disease as a useful predictor of survival following secondline chemotherapy in small cell lung cancer and ovarian cancer patients”. Int. J. Oncol., 1999, 15, 1233.

[19] Kavanagh J., Tresukosol D., Edwards C., Freedman R., Gonzalez de Leon C., Fishman A. et al.: “Carboplatin reinduction after taxane in patients with platinum-refractory epithelial ovarian cancer”. J. Clin. Oncol., 1995, 13, 1584.

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