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Showing papers by "Roger Stupp published in 2000"


Journal Article
TL;DR: In this paper, the anti CD-20 monoclonal antibody Rituximab has been reported in patients with follicular lymphoma and mantle-cell lymphoma (MCL).

117 citations


Journal ArticleDOI
TL;DR: Rituximab is an active agent for the treatment of FL, while its efficacy is modest in MCL, and the effect in reducing minimal residual disease is more pronounced on the blood than it is on the bone marrow.

111 citations


Journal ArticleDOI
TL;DR: It was possible to confirm the efficacy of docetaxel as a single agent for first- and second-line chemotherapy in a large patient population treated in a community setting.

21 citations



Journal ArticleDOI
TL;DR: The alternating schedule produced response, toxicity and survival figures that compared favorable with those using the concomitant schedule, and could serve as a model for future studies of non-cisplatin-containing regimens, in which full doses of docetaxel could alternate withFull doses of other new agents active against NSCLC.
Abstract: The objective of this study was to evaluate a regimen of full doses of docetaxel and cisplatin, using an alternating schedule, as first-line therapy for patients with inoperable non-small cell lung cancer (NSCLC) The standard concomitant schedule does not allow full doses of both drugs to be administered We wanted to see if there was an advantage to be gained by administering full doses of both docetaxel and cisplatin, using a different schedule Docetaxel 100 mg/m2 was given once every 6 weeks from week 1 and cisplatin (120 mg/m2 for two doses and 100 mg/m2 thereafter) once every 6 weeks from week 4, for six cycles (three docetaxel and three cisplatin) Thirty-six of the 44 patients enrolled were evaluable for efficacy Forty-eight percent of the patients had good (KPS 90-100%) performance status A median of five cycles was administered, for which no dose reductions were necessary There were 13 of 36 partial responses (36%; 95% CI 21-54%) and 15 of 36 patients achieved stable disease (42%) The median duration of response was 105 months, the median time to progression was 45 months and the median survival was 9 months The 1 and 2 year survival rates were 39 and 16%, respectively The most frequent grade 3-4 toxicities were nausea (23% of patients), vomiting (18%) and neutropenia (77%) Infections were also common, but not severe The alternating schedule produced response, toxicity and survival figures that compared favorable with those using the concomitant schedule This study could serve as a model for future studies of non-cisplatin-containing regimens, in which full doses of docetaxel could alternate with full doses of other new agents active against NSCLC

6 citations