The role of adjuvant chemotherapy in the management of acute promyelocytic leukemia differentiation syndrome
dc.contributor.author | LaBella, Dominic | |
dc.contributor.author | Regan, Samuel | |
dc.contributor.author | Konig, Heiko | |
dc.contributor.author | Egan, Daniel N. | |
dc.contributor.author | Bailey, Neil A. | |
dc.contributor.author | Mawad, Raya | |
dc.contributor.author | Gilbert, Morgan | |
dc.contributor.author | Pagel, John M. | |
dc.contributor.author | Pu, Jeffrey J. | |
dc.contributor.department | Medicine, School of Medicine | |
dc.date.accessioned | 2023-08-09T14:48:12Z | |
dc.date.available | 2023-08-09T14:48:12Z | |
dc.date.issued | 2022-08-03 | |
dc.description.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. | |
dc.eprint.version | Final published version | |
dc.identifier.citation | LaBella D, Regan S, Konig H, et al. The role of adjuvant chemotherapy in the management of acute promyelocytic leukemia differentiation syndrome. Front Oncol. 2022;12:911745. Published 2022 Aug 3. doi:10.3389/fonc.2022.911745 | |
dc.identifier.uri | https://hdl.handle.net/1805/34809 | |
dc.language.iso | en_US | |
dc.publisher | Frontiers Media | |
dc.relation.isversionof | 10.3389/fonc.2022.911745 | |
dc.relation.journal | Frontiers in Oncology | |
dc.rights | Attribution 4.0 International | en |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.source | PMC | |
dc.subject | Acute Promyelocytic Leukemia | |
dc.subject | All-Trans-Retinoic Acid (ATRA) | |
dc.subject | Arsenic Trioxide (ATO) | |
dc.subject | Differentiation Syndrome (DS) | |
dc.subject | Adjuvant Chemotherapy | |
dc.title | The role of adjuvant chemotherapy in the management of acute promyelocytic leukemia differentiation syndrome | |
dc.type | Article |