Literature DB >> 15613105

Thalidomide in combination with vincristine, epirubicin and dexamethasone (VED) for previously untreated patients with multiple myeloma.

P Schütt1, P Ebeling, U Buttkereit, D Brandhorst, B Opalka, M Hoiczyk, M Flasshove, J Hense, P Bojko, K Metz, T Moritz, S Seeber, M R Nowrousian.   

Abstract

The present study aimed to evaluate the side-effects and efficacy of thalidomide in combination with an anthracycline-containing chemotherapy regimen in previously untreated myeloma patients. Thalidomide (400 mg/d) was combined with bolus injections of vincristine and epirubicin and oral dexamethasone (VED). Chemotherapy cycles were repeated every 3 wk until no further reduction in myeloma protein was observed, whereas the treatment with thalidomide was continued until disease progression. Thirty-one patients were enrolled, 12 patients were exclusively treated with thalidomide in combination with VED and 19 patients additionally received high-dose melphalan, for consolidation. Adverse events and response to therapy were assessed prior to treatment with high-dose chemotherapy. Response to thalidomide combined with VED was complete remission in six patients (19%), partial remission in 19 patients (61%), stable disease in five patients (16%), and progressive disease in one patient (3.2%). Grade 3 and 4 adverse events consisted of leukocytopenia in 10 patients (32%), and thrombocytopenia and anemia in one patient each (3.2%). Neutropenic infections grade 3 and 4 occurred in seven (23%) and three patients (9.7%), respectively, including two patients (6.5%) who died from septic shock. Deep vein thrombosis occurred in eight patients (26%), constipation in 20 patients (65%), and polyneuropathy in 20 patients (65%). The probability of event-free survival and overall survival in the whole group of patients at 36 months were 26 and 62%, respectively. In conclusion, the combination of thalidomide with VED appears to be highly effective in previously untreated patients with multiple myeloma, but it is associated with a high rate of thrombotic events, polyneuropathy, and neutropenic infections.

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Year:  2005        PMID: 15613105     DOI: 10.1111/j.1600-0609.2004.00349.x

Source DB:  PubMed          Journal:  Eur J Haematol        ISSN: 0902-4441            Impact factor:   2.997


  3 in total

1.  Arterial thrombosis and thalidomide.

Authors:  Mustafa Goz; M Nesimi Eren; Omer Cakir
Journal:  J Thromb Thrombolysis       Date:  2008-04       Impact factor: 2.300

2.  Venous thromboembolism in myelodysplastic syndrome patients receiving lenalidomide: results from postmarketing surveillance and data mining techniques.

Authors:  Xionghu Yang; Nancy A Brandenburg; John Freeman; Maria Luisa Salomon; Jerome B Zeldis; Robert D Knight; Robert Bwire
Journal:  Clin Drug Investig       Date:  2009       Impact factor: 2.859

3.  Review of thalidomide in the treatment of newly diagnosed multiple myeloma.

Authors:  Federica Cavallo; Mario Boccadoro; Antonio Palumbo
Journal:  Ther Clin Risk Manag       Date:  2007-08       Impact factor: 2.423

  3 in total

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