A phase I/II study of docetaxel and gemcitabine combination for chemotherapy-resistant ovarian cancer.

Abstract:

BACKGROUND:A phase I/II study of docetaxel (DOC) and gemcitabine (GEM) combination for treatment-resistant ovarian cancer (OC) was conducted. MATERIALS AND METHODS:Eligible patients exhibited recurrent OC within 12 months after initial treatment, or after more than 2 chemotherapy regimens. Planned dose levels (DL) were as follows: DOC 70 mg/m(2), GEM 800 mg/m(2) (DL1); DOC 70 mg/m(2), GEM 1000 mg/m(2) (DL2). DOC was administered on day 1 combined with GEM on days 1 and 8 every 3 weeks. Adverse events were assessed by NCI-CTC2.0J. Response was evaluated by RECIST or Rustin's criteria. RESULTS:The recommended dose was DL1. For all enrolled patients, the median interval from last chemotherapy was 2.5 (1-11) months and 32 patients were assessable for response. One complete response, 6 partial responses and 6 stable disease were noted. Median time to progression was 4.8 months. Toxicities were mainly hematological and manageable. CONCLUSION:This combination could be an acceptable treatment option before palliation.

journal_name

Anticancer Res

journal_title

Anticancer research

authors

Itani Y,Hosokawa K,Ito K,Takeuchi S,Tabata T,Tsubamoto H,Fujita H,Akiyama M,Adachi S

subject

Has Abstract

pub_date

2009-05-01 00:00:00

pages

1521-6

issue

5

eissn

0250-7005

issn

1791-7530

pii

29/5/1521

journal_volume

29

pub_type

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