Comparison of gemcitabine and carboplatin versus cisplatin and etoposide for patients with poor-prognosis small cell lung cancer

被引:47
作者
Lee, S. M. [1 ]
James, L. E. [2 ]
Qian, W. [3 ]
Spiro, S.
Eisen, T. [4 ]
Gower, N. H. [2 ]
Ferry, D. R. [5 ]
Gilligan, D. [6 ]
Harper, P. G. [7 ]
Prendiville, J. [7 ]
Hocking, M. [8 ]
Rudd, R. M. [9 ]
机构
[1] Univ Coll Hosp, Dept Oncol, London NW1 2PG, England
[2] UCL, Canc Trials Ctr, London, England
[3] MRC, Clin Trials Unit, London, England
[4] Royal Marsden Hosp, London SW3 6JJ, England
[5] Birmingham Heartlands NHS Trust, Birmingham, W Midlands, England
[6] Addenbrookes NHS Trust, Cambridge CB2 2QQ, England
[7] Guys & St Thomas NHS Trust, London, England
[8] Walsgrave Hosp NHS Trust, Coventry, W Midlands, England
[9] St Bartholomews Hosp, London, England
关键词
PHASE-II; PLUS GEMCITABINE; RANDOMIZED-TRIAL; CLINICAL-TRIALS; CHEMOTHERAPY; METAANALYSIS; CARCINOMA; AGENT;
D O I
10.1136/thx.2007.093872
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: The combination of cisplatin and etoposide (PE) has been a standard treatment for patients with poor-prognosis small cell lung cancer (SCLC). This non-inferiority design trial aimed to determine whether the combination of gemcitabine and carboplatin (GC) results in similar survival but is less toxic with better quality of life. Methods: Previously untreated patients with SCLC with extensive disease or limited stage with poor prognostic factors were randomly assigned to six 3-weekly cycles of GC or PE. Results: 241 patients (121 GC, 120 PE) were recruited, of which 216 (90%) had died. There was no difference in overall survival (HR 1.01, 95% CI 0.77 to 1.32). Median survival with GC and PE was 8.0 and 8.1 months, respectively. Median progression-free survival was 5.9 months with GC and 6.3 months with PE. Grade 3 or 4 myelosuppressions were more frequent with GC (anaemia: 14% GC vs 2% PE; leucopenia: 32% GC vs 13% PE; thrombocytopenia: 22% GC vs 4% PE), but these were not associated with increased hospital admissions, infections or fatalities. Grade 2-3 alopecia (68% PE vs 17% GC) and nausea (43% PE vs 26% GC) were more frequent with PE. Patients given GC received more chemotherapy as outpatients (89% GC vs 66% PE of treatment cycles). In QoL questionnaires, more patients receiving PE reported being upset by hair loss (p = 0.004) and impaired cognitive functioning (p = 0.04). Conclusions: GC is as effective as PE in terms of overall survival and progression-free survival and has a toxicity profile more acceptable to patients. Trial registration number: ISRCTN 39679215
引用
收藏
页码:75 / 80
页数:6
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