Skip Navigation

This Article
Right arrow Full Text (PDF)
Right arrow E-letters: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when E-letters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (69)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Bergmann, L.
Right arrow Articles by Hoelzer, D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bergmann, L.
Right arrow Articles by Hoelzer, D.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Annals of Oncology 4:371-375, 1993
© 1993 European Society for Medical Oncology


research-article

Immunosuppressive effects and clinical response of fludarabine in refractory chronic lymphocytic leukemia

L. Bergmann, K. Fenchel, B. Jahn, P. S. Mitrou and D. Hoelzer

Division of Hematology, Department of Internal Medicine, J. W. Goethe University Frankfurt/M., FRG

Correspondence to: L. Bergmann, M.D., Div. of Hematology, Dept. of Internal Medicine, University Hospital, Theodor-Stern-Kai 7, D-6000 Frankfurt/M, FRG

BACKGROUND:: Fludarabine monophosphate is a new adenine nucleoside analogue with a promising efficacy in B-cell chronic lymphocytic leukemia (B-CLL) with response rates, including hematological complete remissions, of 50%–60% in previously treated and 75%–80% in previously untreated patients.

PATIENTS AND METHODS:: Here, the clinical experience with and side effects of fludarabine are reported in 19 patients with refractory CLL (17 B-CLL, 2 T-CLL). All patients were pretreated with one to four different regimens and had progressive disease. Fludarabine was administered at a dosage of 25 mg/m2 daily for 5 days as a 30-minute intravenous infusion. This course was repeated every fifth week. Dosage and time course were adapted to toxicity.

RESULTS:: 12/18 (67%) evaluable patients achieved partial remissions (PR), 1/18 (6%) had stable disease (SD) and 5/18 (28%) were progressive. The median duration of partial remission until relapse or death was 6 months. Most responses to fludarabine occurred within two treatment courses. Major toxic effects included infections in 11 patients and nausea in 8 (mainly grade 1). Meanwhile, three patients died of progressive disease and 8 of pneumonias or other infections. Two patients had pneumocystis carinii pneumonias and one an aspergillus pneumonia. The high infection rate may be due not only to hypogammaglobulinaemia or fludarabine-induced granulocytopenia but also to a remarkable decrease of CD4+-cells during fludarabine therapy. In one case a tumor lysis syndrome was observed. No CNS toxicity was noted.

CONCLUSION:: It is concluded that fludarabine is effective even in patients with advanced chronic lymphocytic leukemia refractory to multiple chemotherapy regimens. However, fludarabine has a remarkable suppressive effect on T-lymphocytes, predominantly CD4+-lymphocytes. Long-term antibiotic prophylaxis is recommended.

fludarabine, chronic lymphocytic leukemia, immunosuppression, infection rate


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Clin. Cancer Res.Home page
Y. L. Kasamon, I. W. Flinn, M. R. Grever, L. F. Diehl, E. Garrett-Mayer, S. N. Goodman, M. S. Lucas, and J. C. Byrd
Phase I Study of Low-Dose Interleukin-2, Fludarabine, and Cyclophosphamide for Previously Untreated Indolent Lymphoma and Chronic Lymphocytic Leukemia
Clin. Cancer Res., December 1, 2005; 11(23): 8413 - 8417.
[Abstract] [Full Text] [PDF]


Home page
ASH Education BookHome page
S. N. O'Brien, N. M.A. Blijlevens, T. H. Mahfouz, and E. J. Anaissie
Infections in Patients with Hematological Cancer: Recent Developments
Hematology, January 1, 2003; 2003(1): 438 - 472.
[Abstract] [Full Text] [PDF]


Home page
JCOHome page
V. A. Morrison, K. R. Rai, B. L. Peterson, J. E. Kolitz, L. Elias, F. R. Appelbaum, J. D. Hines, L. Shepherd, R. E. Martell, R. A. Larson, et al.
Impact of Therapy With Chlorambucil, Fludarabine, or Fludarabine Plus Chlorambucil on Infections in Patients With Chronic Lymphocytic Leukemia: Intergroup Study Cancer and Leukemia Group B 9011
J. Clin. Oncol., August 15, 2001; 19(16): 3611 - 3621.
[Abstract] [Full Text] [PDF]


Home page
The OncologistHome page
N. Kalil and B. D. Cheson
Chronic Lymphocytic Leukemia
Oncologist, October 1, 1999; 4(5): 352 - 369.
[Abstract] [Full Text]


Home page
BloodHome page
U. Consoli, I. El-Tounsi, A. Sandoval, V. Snell, H.-D. Kleine, W. Brown, J. R. Robinson, F. DiRaimondo, W. Plunkett, and M. Andreeff
Differential Induction of Apoptosis by Fludarabine Monophosphate in Leukemic B and Normal T Cells in Chronic Lymphocytic Leukemia
Blood, March 1, 1998; 91(5): 1742 - 1748.
[Abstract] [Full Text] [PDF]


Home page
The OncologistHome page
P. Fidias, B. A. Chabner, and M. L. Grossbard
Purine Analogs for the Treatment of Low-Grade Lymphoproliferative Disorders
Oncologist, June 1, 1996; 1(3): 125 - 139.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.