Clinical benefit and quality of life in patients with advanced pancreatic cancer receiving gemcitabine plus capecitabine versus gemcitabine alone: a randomized multicenter phase III clinical trial--SAKK 44/00-CECOG/PAN.1.3.001.

Details

Serval ID
serval:BIB_AE6B77264841
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Clinical benefit and quality of life in patients with advanced pancreatic cancer receiving gemcitabine plus capecitabine versus gemcitabine alone: a randomized multicenter phase III clinical trial--SAKK 44/00-CECOG/PAN.1.3.001.
Journal
Journal of Clinical Oncology
Author(s)
Bernhard J., Dietrich D., Scheithauer W., Gerber D., Bodoky G., Ruhstaller T., Glimelius B., Bajetta E., Schüller J., Saletti P., Bauer J., Figer A., Pestalozzi B.C., Köhne C.H., Mingrone W., Stemmer S.M., Tàmas K., Kornek G.V., Koeberle D., Herrmann R.
Working group(s)
Central European Cooperative Oncology Group
ISSN
1527-7755 (Electronic)
ISSN-L
0732-183X
Publication state
Published
Issued date
2008
Volume
26
Number
22
Pages
3695-3701
Language
english
Notes
Publication types: Clinical Trial, Phase III ; Comparative Study ; Journal Article ; Multicenter Study ; Randomized Controlled Trial ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Abstract
PURPOSE: To compare clinical benefit response (CBR) and quality of life (QOL) in patients receiving gemcitabine (Gem) plus capecitabine (Cap) versus single-agent Gem for advanced/metastatic pancreatic cancer.
PATIENTS AND METHODS: Patients were randomly assigned to receive GemCap (oral Cap 650 mg/m(2) twice daily on days 1 through 14 plus Gem 1,000 mg/m(2) in a 30-minute infusion on days 1 and 8 every 3 weeks) or Gem (1,000 mg/m(2) in a 30-minute infusion weekly for 7 weeks, followed by a 1-week break, and then weekly for 3 weeks every 4 weeks) for 24 weeks or until progression. CBR criteria and QOL indicators were assessed over this period. CBR was defined as improvement from baseline for >or= 4 consecutive weeks in pain (pain intensity or analgesic consumption) and Karnofsky performance status, stability in one but improvement in the other, or stability in pain and performance status but improvement in weight.
RESULTS: Of 319 patients, 19% treated with GemCap and 20% treated with Gem experienced a CBR, with a median duration of 9.5 and 6.5 weeks, respectively (P < .02); 54% of patients treated with GemCap and 60% treated with Gem had no CBR (remaining patients were not assessable). There was no treatment difference in QOL (n = 311). QOL indicators were improving under chemotherapy (P < .05). These changes differed by the time to failure, with a worsening 1 to 2 months before treatment failure (all P < .05).
CONCLUSION: There is no indication of a difference in CBR or QOL between GemCap and Gem. Regardless of their initial condition, some patients experience an improvement in QOL on chemotherapy, followed by a worsening before treatment failure.
Keywords
Adenocarcinoma/complications, Adenocarcinoma/drug therapy, Administration, Oral, Adult, Aged, Aged, 80 and over, Analgesics/therapeutic use, Antineoplastic Combined Chemotherapy Protocols/therapeutic use, Body Weight/drug effects, Deoxycytidine/administration & dosage, Deoxycytidine/analogs & derivatives, Drug Administration Schedule, Europe, Female, Fluorouracil/administration & dosage, Fluorouracil/analogs & derivatives, Humans, Infusions, Parenteral, Karnofsky Performance Status, Male, Middle Aged, Pain/drug therapy, Pain/etiology, Pain Measurement, Pancreatic Neoplasms/complications, Pancreatic Neoplasms/drug therapy, Prospective Studies, Quality of Life, Time Factors, Treatment Failure
Pubmed
Web of science
Create date
04/03/2009 17:20
Last modification date
20/08/2019 16:18
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