2001
DOI: 10.1016/s0093-7754(01)80003-8
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A Prospective Study of Gemcitabine and Carboplatin as First-Line Therapy in Advanced Non-Small Cell Lung Cancer: Toxicity of a Three- Versus a Four-Week Schedule

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Cited by 11 publications
(5 citation statements)
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“…The results of this retrospective analysis suggest that this schedule seems to be active and well tolerated. Our data are comparable with those already published [9][10][11][12][13][14][15] . Unfortunately, the number of elderly patients is too small (n = 27) to demonstrate that the regimen is a good option in this patient setting.…”
Section: Discussionsupporting
confidence: 92%
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“…The results of this retrospective analysis suggest that this schedule seems to be active and well tolerated. Our data are comparable with those already published [9][10][11][12][13][14][15] . Unfortunately, the number of elderly patients is too small (n = 27) to demonstrate that the regimen is a good option in this patient setting.…”
Section: Discussionsupporting
confidence: 92%
“…The combination of gemcitabine and carboplatin has been used in the treatment of patients with advanced NSCLC in phase I and II trials, using 3-week as well 4week schedules [7][8][9][10][11][12][13][14] . The combination has been shown to be feasible and effective in several randomized trials 6,15 .…”
Section: Introductionmentioning
confidence: 99%
“…However, the number of reductions and omissions of the day 15 gemcitabine dose was quite high in these trials. Several trials showed that a 3‐week regimen was better tolerated and equally effective in NSCLC 34–36 . Various doses of gemcitabine (1000 mg/m 2 , 1200 mg/m 2 and 1250 mg/m 2 ) have been used in the 21‐day regimen.…”
Section: Discussionmentioning
confidence: 99%
“…The question of 3-versus 4-weekly scheduling was addressed in two trials that comprised 58 previously untreated patients with unresectable advanced/metastatic NSCLC [28] . In the first trial 30 patients received carboplatin AUC 5 on day 1 and gemcitabine 1000 mg/m 2 on day 1, 8 every 21 days.…”
Section: Clinical Effi Cacy: Phase I and Ii Trialsmentioning
confidence: 99%