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Vol. 84, No. 3, 2013
Issue release date: January 2013
Section title: Clinical Study
Oncology 2013;84:158–165
(DOI:10.1159/000341366)

Improved Survival Trends in Platinum-Resistant Patients with Advanced Ovarian, Fallopian or Peritoneal Cancer Treated with First-Line Paclitaxel/Platinum Chemotherapy: The Impact of Novel Agents

Bamias A. · Bamia C. · Zagouri F. · Kostouros E. · Kakoyianni K. · Rodolakis A. · Vlahos G. · Haidopoulos D. · Thomakos N. · Antsaklis A. · Dimopoulos M.-A.
Departments of aClinical Therapeutics, bHygiene and Epidemiology and cObstetrics and Gynaecology, University of Athens, Athens, Greece

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Article / Publication Details

First-Page Preview
Abstract of Clinical Study

Received: 1/24/2012 7:26:24 PM
Accepted: 6/24/2012
Published online: 12/28/2012

Number of Print Pages: 8
Number of Figures: 2
Number of Tables: 4

ISSN: 0030-2414 (Print)
eISSN: 1423-0232 (Online)

For additional information: http://www.karger.com/OCL

Abstract

Objective: The prognosis for patients with platinum-resistant advanced ovarian cancer remains poor. The impact of approved agents on survival has not been clarified during the last decade. We studied survival trends during the last 15 years in platinum-resistant patients treated with cytoreductive surgery followed by paclitaxel/platinum chemotherapy. Methods: Patients with epithelial ovarian, fallopian or peritoneal cancer, stages III/IV and platinum-resistant disease after first-line chemotherapy with paclitaxel/platinum were included. They were grouped according to the period of chemotherapy: group A 31/3/1995–31/12/2001 (n = 56) and Group B 1/1/2002–24/12/2008 (n = 57). In order to compensate for the difference in follow-up between the 2 groups, we performed minimum follow-up (MFU) analyses by considering as cases only women who had an event within 3 years of follow-up. Patients with no events for up to 3 years were censored at that time. Results: MFU analyses showed that median overall survival (OS) was significantly longer in group B: 12.3 vs. 17.5 months (p = 0.012). This was due to a doubling of the median OS after relapse: 5.7 vs. 10.9 months (p = 0.0180). Multivariate Cox regression indicated group and histology as factors statistically significantly associated with OS. Following relapse, patients in group B were predominantly treated with liposomal doxorubicin and gemcitabine, and patients in group A were treated with platinum compounds, docetaxel and oral etoposide (p < 0.001). Conclusions: The introduction of novel agents without cross-resistance to platinum or taxanes has improved the prognosis of platinum-resistant patients.


  

Author Contacts

Flora Zagouri, MD, PhD
Alexandra Hospital, Oncology Unit
80 Vas. Sofias Ave.
GR–115 28 Athens (Greece)
Tel. +30 210 338 1546, E-Mail florazagouri@yahoo.co.uk

  

Article Information

Received: January 24, 2012
Accepted after revision: June 24, 2012
Published online: December 28, 2012
Number of Print Pages : 8
Number of Figures : 2, Number of Tables : 4, Number of References : 23

  

Publication Details

Oncology (International Journal for Cancer Research and Treatment)

Vol. 84, No. 3, Year 2013 (Cover Date: January 2013)

Journal Editor: Markman M. (Philadelphia, Pa.)
ISSN: 0030-2414 (Print), eISSN: 1423-0232 (Online)

For additional information: http://www.karger.com/OCL


Article / Publication Details

First-Page Preview
Abstract of Clinical Study

Received: 1/24/2012 7:26:24 PM
Accepted: 6/24/2012
Published online: 12/28/2012

Number of Print Pages: 8
Number of Figures: 2
Number of Tables: 4

ISSN: 0030-2414 (Print)
eISSN: 1423-0232 (Online)

For additional information: http://www.karger.com/OCL


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