Literature DB >> 12141952

Fludarabine combination therapy for the treatment of chronic lymphocytic leukemia.

Barbara Schmitt1, Clemens M Wendtner, Manuela Bergmann, Raymonde Busch, Astrid Franke, Rita Pasold, Rudolf Schlag, Georg Hopfinger, Wolfgang Hiddemann, Bertold Emmerich, Michael Hallek.   

Abstract

Fludarabine combination therapies have attained an increased popularity in the treatment of chronic lymphocytic leukemia (CLL). Among them, the combination of fludarabine/cyclophosphamide (FC) is by far the best regimen studied. Patients receiving FC at relapse show response rates (RRs) of 70%-94% with 11%-34% complete remission (CR) rates. In previously untreated patients with CLL, RRs of 64%-88% with 21%-46% CR rates were observed. The main side effects of FC are myelotoxicity and infections; most complications are reported as fever of unknown origin, infections of the upper respiratory tract, or herpes virus infection. There is probably a correlation between the higher dose of cyclophosphamide (> 750 mg/m2 per treatment course) and an increase in the number of severe infectious complications. Similar results were reported regarding the RRs and side effects of the combination of fludarabine/epirubicin. The triple combination of fludarabine/cyclophosphamide/mitoxantrone and fludarabine combinations with anti-CD20 (rituximab) or anti-CD52 (Campath-1H) antibody, might be even be more promising, since a relevant number of complete molecular remissions are achieved with these drugs. The precise role of fludarabine combinations within the overall treatment strategy remains to be determined. Our current recommendation is to use these combinations at relapse, while their use in first-line therapy should be investigated in clinical protocols. It remains to be shown whether patients with CLL achieve improved overall survival with these combination chemotherapies.

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Year:  2002        PMID: 12141952     DOI: 10.3816/clm.2002.n.008

Source DB:  PubMed          Journal:  Clin Lymphoma        ISSN: 1526-9655


  5 in total

1.  Combination chemoimmunotherapy with pentostatin, cyclophosphamide, and rituximab shows significant clinical activity with low accompanying toxicity in previously untreated B chronic lymphocytic leukemia.

Authors:  Neil E Kay; Susan M Geyer; Timothy G Call; Tait D Shanafelt; Clive S Zent; Diane F Jelinek; Renee Tschumper; Nancy D Bone; Gordon W Dewald; Thomas S Lin; Nyla A Heerema; Lisa Smith; Michael R Grever; John C Byrd
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Review 2.  Trial watch: Tumor-targeting monoclonal antibodies for oncological indications.

Authors:  Erika Vacchelli; Jonathan Pol; Norma Bloy; Alexander Eggermont; Isabelle Cremer; Wolf Hervé Fridman; Jérôme Galon; Aurélien Marabelle; Holbrook Kohrt; Laurence Zitvogel; Guido Kroemer; Lorenzo Galluzzi
Journal:  Oncoimmunology       Date:  2015-02-03       Impact factor: 8.110

3.  Fludarabine modulates composition and function of the T cell pool in patients with chronic lymphocytic leukaemia.

Authors:  Franz Josef Gassner; Lukas Weiss; Roland Geisberger; Josefina Piñón Hofbauer; Alexander Egle; Tanja Nicole Hartmann; Richard Greil; Inge Tinhofer
Journal:  Cancer Immunol Immunother       Date:  2010-09-21       Impact factor: 6.968

4.  VDAC1-based peptides: novel pro-apoptotic agents and potential therapeutics for B-cell chronic lymphocytic leukemia.

Authors:  T Prezma; A Shteinfer; L Admoni; Z Raviv; I Sela; I Levi; V Shoshan-Barmatz
Journal:  Cell Death Dis       Date:  2013-09-19       Impact factor: 8.469

Review 5.  Trial Watch: Tumor-targeting monoclonal antibodies in cancer therapy.

Authors:  Erika Vacchelli; Fernando Aranda; Alexander Eggermont; Jérôme Galon; Catherine Sautès-Fridman; Laurence Zitvogel; Guido Kroemer; Lorenzo Galluzzi
Journal:  Oncoimmunology       Date:  2014-01-01       Impact factor: 8.110

  5 in total

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