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Sökning: id:"swepub:oai:gup.ub.gu.se/63494" > Palliative chemothe...

Palliative chemotherapy beyond three courses conveys no survival or consistent quality-of-life benefits in advanced non-small-cell lung cancer

von Plessen, C. (författare)
Bergman, Bengt, 1953 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för medicin, avdelningen för invärtesmedicin,Institute of Medicine, Department of Internal Medicine
Andresen, O. (författare)
visa fler...
Bremnes, R. M. (författare)
Sundström, S. (författare)
Gilleryd, Mona, 1961 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för medicin, avdelningen för invärtesmedicin,Institute of Medicine, Department of Internal Medicine
Stephens, R. (författare)
Vilsvik, J. (författare)
Aasebo, U. (författare)
Sörenson, Sverre, 1941- (författare)
Haukeland University Hospital
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 (creator_code:org_t)
2006-10-03
2006
Engelska.
Ingår i: Br J Cancer. - : Springer Science and Business Media LLC. - 0007-0920 .- 1532-1827. ; 95:8, s. 966-73
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • This randomised multicentre trial was conducted to establish the optimal duration of palliative chemotherapy in advanced non-small-cell lung cancer (NSCLC). We compared a policy of three vs six courses of new-generation platinum-based combination chemotherapy with regard to effects on quality of life (QoL) and survival. Patients with stage IIIB or IV NSCLC and WHO performance status (PS) 0-2 were randomised to receive three (C3) or six (C6) courses of carboplatin (area under the curve (AUC) 4, Chatelut's formula, equivalent to Calvert's AUC 5) on day 1 and vinorelbine 25 mg m(-2) on days 1 and 8 of a 3-week cycle. Key end points were QoL at 18 weeks, measured with EORTC Quality of Life Questionnaire (QLQ)-C30 and QLQ-LC13, and overall survival. Secondary end points were progression-free survival and need of palliative radiotherapy. Two hundred and ninety-seven patients were randomised (C3 150, C6 147). Their median age was 65 years, 30% had PS 2 and 76% stage IV disease. Seventy-eight and 54% of C3 and C6 patients, respectively, completed all scheduled chemotherapy courses. Compliance with QoL questionnaires was 88%. There were no significant group differences in global QoL, pain or fatigue up to 26 weeks. The dyspnoea palliation rate was lower in the C3 arm at 18 and 26 weeks (P<0.05), but this finding was inconsistent across different methods of analysis. Median survival in the C3 group was 28 vs 32 weeks in the C6 group (P=0.75, HR 1.04, 95% CI 0.82-1.31). One- and 2-year survival rates were 25 and 9% vs 25 and 5% in the C3 and C6 arm, respectively. Median progression-free survival was 16 and 21 weeks in the C3 and C6 groups, respectively (P=0.21, HR 0.86, 95% CI 0.68-1.08). In conclusion, palliative chemotherapy with carboplatin and vinorelbine beyond three courses conveys no survival or consistent QoL benefits in advanced NSCLC.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Lungmedicin och allergi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Respiratory Medicine and Allergy (hsv//eng)

Nyckelord

Adult
Aged
Aged
80 and over
dosage/adverse effects/*therapeutic use
Carboplatin/administration & dosage/adverse effects
Carcinoma
Non-Small-Cell Lung/*drug therapy/mortality/pathology
Drug Administration Schedule
Fatigue/chemically induced
Female
Follow-Up Studies
Humans
Lung Neoplasms/*drug therapy/mortality/pathology
Male
Middle Aged
Neoplasm Staging
Pain/chemically induced
Palliative Care
*Quality of Life
Questionnaires
Survival Analysis
Survival Rate
Time Factors
Treatment Outcome
Vinblastine/administration & dosage/adverse effects/analogs & derivatives
MEDICINE

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