The role of adjuvant chemotherapy in the management of acute promyelocytic leukemia differentiation syndrome
Affiliation
Department of Medicine, University of Arizona National Cancer Institute (NCI) Designated Comprehensive Cancer CenterIssue Date
2022Keywords
Acute Promyelocytic LeukemiaAdjuvant Chemotherapy
All-Trans-Retinoic Acid (ATRA)
Arsenic Trioxide (ATO)
Differentiation Syndrome (DS)
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Frontiers Media S.A.Citation
LaBella, D., Regan, S., Konig, H., Egan, D. N., Bailey, N. A., Mawad, R., Gilbert, M., Pagel, J. M., & Pu, J. J. (2022). The role of adjuvant chemotherapy in the management of acute promyelocytic leukemia differentiation syndrome. Frontiers in Oncology, 12.Journal
Frontiers in OncologyRights
Copyright © 2022 LaBella, Regan, Konig, Egan, Bailey, Mawad, Gilbert, Pagel and Pu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY).Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Acute Promyelocytic Leukemia (APL) is characterized by the t(15;17) chromosomal translocation resulting in a PML-RARA fusion protein. The all-trans-retinoic acid (ATRA) and Arsenic Trioxide (ATO) only regimens have demonstrated success in treating low- and intermediate-risk patients. However, induction with ATRA/ATO only regimens have been showing increased incidence of differentiation syndrome (DS), a potentially lethal complication, traditionally treated with dexamethasone. We conducted a three-institution retrospective study, aiming to evaluate the role of short-term adjuvant chemotherapy in managing moderate DS for patients with low- or intermediate-risk APL initially treated with ATRA/ATO only protocols. We evaluated the difference in incidence and duration of moderate DS in APL patients who were treated with ATRA/ATO with or without adjuvant chemotherapy. 57 low- or intermediate-risk APL patients were retrospectively identified and included for this study; 36 patients received ATRA/ATO only induction treatment, and 21 patients received ATRA/ATO/adjuvant chemotherapy combination induction therapy. Similar proportions of patients experienced DS in both groups (66.7% vs. 81.0%, P = 0.246). The median duration of DS resolution in patients receiving ATRA/ATO only was 17 days (n = 23), and in patients receiving combination therapy was 8 days (n = 16) (P = 0.0001). The lengths of hospital stay in patients receiving ATRO/ATO only was 38 days (n = 7), and in patients receiving combination therapy was 14 days (n = 17) (P = 0.0007). In conclusion, adding adjuvant chemotherapy to ATRA/ATO only protocol may reduce the duration of DS and the length of hospital stay during APL induction treatment. Copyright © 2022 LaBella, Regan, Konig, Egan, Bailey, Mawad, Gilbert, Pagel and Pu.Note
Open access journalISSN
2234-943XVersion
Final published versionae974a485f413a2113503eed53cd6c53
10.3389/fonc.2022.911745
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Except where otherwise noted, this item's license is described as Copyright © 2022 LaBella, Regan, Konig, Egan, Bailey, Mawad, Gilbert, Pagel and Pu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY).

