2004
DOI: 10.1093/annonc/mdh260
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Front-line paclitaxel–vinorelbine versus paclitaxel–carboplatin in patients with advanced non-small-cell lung cancer: a randomized phase III trial

Abstract: PCT combined with VRL produces similar (non-significant) response rates, survival and toxicity (except for neutropenia, as noted above) to standard CRP-PCT treatment in untreated advanced-stage NSCLC.

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Cited by 55 publications
(33 citation statements)
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“…The proportion of males varied within the range of 51%-93%. Most patients had stage IIIB or IV NSCLC; inoperable stage IIIA disease was also admitted in three studies [35,45,62], whereas stage IIIB disease was excluded in one trial [47].…”
Section: Patient Characteristicsmentioning
confidence: 99%
See 1 more Smart Citation
“…The proportion of males varied within the range of 51%-93%. Most patients had stage IIIB or IV NSCLC; inoperable stage IIIA disease was also admitted in three studies [35,45,62], whereas stage IIIB disease was excluded in one trial [47].…”
Section: Patient Characteristicsmentioning
confidence: 99%
“…Reasons for exclusion were not stated in eight studies [30,31,40,42,43,48,57,64], whereas we were unable to assess if any exclusion criteria were applied in a trial published in Chinese only [46]. Response was assessed according to the World Health Organization standard criteria [72] in 19 trials [22,23,25,29,32,34,35,39,44,45,47,49,50,52,53,59,62,65,68], according to the Southwest Oncology Group guidelines [73] in two studies [21,24], and according to the Response Evaluation Criteria in Solid Tumors [74] in four trials [60,61,66,67].…”
Section: Patient Characteristicsmentioning
confidence: 99%
“…Paclitaxel was given biweekly (once every 2 weeks) at a dose of 135 mg m À2 , in combination with a second agent, and toxicity was well-tolerated (Stathopoulos et al, 2004). The dose of irinotecan combined with another agent, administered on days 1 and 8, repeated every 21 days, varied from 60 to 110 mg m À2 (Kakolyris et al, 2000(Kakolyris et al, , 2001Keresztes et al, 2004).…”
Section: Treatment Planmentioning
confidence: 99%
“…We intended to increase the latter to a higher dose if it was well tolerated. The dose of paclitaxel remained at 135 mg m À2 , as this had been tested in a biweekly administration in combination with other myelotoxic agents such as carboplatin or navelbine (Stathopoulos et al, 2004). Table 1 shows dose escalation.…”
Section: Treatment Planmentioning
confidence: 99%
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