Incidence, description, and timing of serious and opportunistic infections in patients with hairy cell leukemia

Hairy cell leukemia is an uncommon B-cell malignancy with excellent response to purine analogs and to targeted therapies such as ibrutinib and vemurafenib. However, purine analogs are known to be highly immunosuppressive and the infection burden in this patient population with current therapies is unknown. We therefore conducted a retrospective cohort study following 149 patients. Median follow-up time was 6.9 years. Thirty-six percent developed an opportunistic or serious infection requiring hospitalization. Most cases were bacterial and most coincided with neutropenia and/or CD4 T-lymphopenia. No single treatment agent was significantly associated with increased or decreased incidence of infection. Reassuringly, the cumulative incidence of infections plateaued 2 months after initial treatment suggesting clinically significant immune recovery. Only one patient in our cohort passed away due to infection. Estimated 10-year overall survival was 99% suggesting that infections may not cause as much mortality as was seen prior to current therapies.

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Publication Details

Journal
eJHaem
Published
2024-08-30
DOI
https://doi.org/10.1002/jha2.982
Citations
3
Primary Topic
Chronic Lymphocytic Leukemia Research
Type
article
Field-Weighted Citation Impact
1.31

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article

Incidence, description, and timing of serious and opportunistic infections in patients with hairy cell leukemia

Andrew Stiff, Zeinab El Boghdadly, Leslie A. Andritsos, Kerry Anne Rogers et al.
3 citations
eJHaem
Chronic Lymphocytic Leukemia Research
1.31
article

Incidence, description, and timing of serious and opportunistic infections in patients with hairy cell leukemia

Andrew Stiff, Zeinab El Boghdadly, Leslie A. Andritsos, Kerry Anne Rogers, Nilesh Kapoor, Seema Ali Bhat, Michael R. Grever, Mirela Anghelina, Qiuhong Zhao, James S. Blachly, Narendranath Epperla
article en
3 citations

Abstract

Hairy cell leukemia is an uncommon B-cell malignancy with excellent response to purine analogs and to targeted therapies such as ibrutinib and vemurafenib. However, purine analogs are known to be highly immunosuppressive and the infection burden in this patient population with current therapies is unknown. We therefore conducted a retrospective cohort study following 149 patients. Median follow-up time was 6.9 years. Thirty-six percent developed an opportunistic or serious infection requiring hospitalization. Most cases were bacterial and most coincided with neutropenia and/or CD4 T-lymphopenia. No single treatment agent was significantly associated with increased or decreased incidence of infection. Reassuringly, the cumulative incidence of infections plateaued 2 months after initial treatment suggesting clinically significant immune recovery. Only one patient in our cohort passed away due to infection. Estimated 10-year overall survival was 99% suggesting that infections may not cause as much mortality as was seen prior to current therapies.

eJHaemVol. 5(5)
University of New Mexico (US), The Ohio State University (US), The University of Texas Southwestern Medical Center (US)
Leukemia and Lymphoma Society, Ohio State University, National Institutes of Health
Good health and well-being
Openalex Percentile: Top 18%
Chronic Lymphocytic Leukemia Research
1.31
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