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Article: Oral arsenic trioxide, all‐trans retinoic acid, and ascorbic acid maintenance after first complete remission in acute promyelocytic leukemia: Long‐term results and unique prognostic indicators

TitleOral arsenic trioxide, all‐trans retinoic acid, and ascorbic acid maintenance after first complete remission in acute promyelocytic leukemia: Long‐term results and unique prognostic indicators
Authors
Keywordsacute promyelocytic leukemia
arsenic trioxide
first completion remission
maintenance
oral
Issue Date2020
PublisherJohn Wiley & Sons, Inc. The Journal's web site is located at http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1097-0142
Citation
Cancer, 2020, v. 126 n. 14, p. 3244-3254 How to Cite?
AbstractBackground: The role of arsenic trioxide (As2O3) in the maintenance of first complete remission (CR1) in acute promyelocytic leukemia (APL) is unclear. Methods: A total of 129 consecutive adult patients with APL of all risk categories who achieved CR1 with conventional induction (all‐trans retinoic acid [ATRA]/daunorubicin) and consolidation (daunorubicin/cytarabine [induction daunorubicin and consolidation omitted for age ≥70 years]) underwent maintenance comprising ATRA (45 mg/m2/day), oral As2O3 (10 mg/day), and ascorbic acid (1 g/day) (AAA) for 2 weeks every 2 months for 2 years. Results: Over a 17‐year period from August 1, 2002, to July 31, 2019, 63 men and 66 women (median age, 46 years [range, 18‐82 years]) received AAA maintenance, which was already completed in 117 patients. At a median follow‐up of 100 months (range, 8‐215 months), 17 patients (13%) developed first relapse (R1) (hematologic, n = 14; molecular, n = 3) after a median of 19 months (range, 7‐96 months) from CR1. Two R1 patients had concomitant central nervous system (CNS) involvement. All patients achieved CR2 with oral As2O3‐based salvage. Five patients had a subsequent relapse and died. Eight patients died of unrelated causes while still in CR1. The 5‐year and 10‐year rates of relapse‐free survival (RFS) were 89% and 85%, respectively. The 5‐year and 10‐year rates of overall survival (OS) were 94% and 87%, respectively. Multivariate analysis showed that inferior RFS was associated with FLT3‐ITD (P = .005) and CNS involvement on presentation (P = .004), and inferior OS was associated with therapy‐related APL (P = .03), FLT3‐ITD (P = .03), and relapse (P = .03). The safety profile was favorable, with no grade 3/4 organ toxicities. Conclusion: CR1 maintenance with AAA is safe and results in favorable long‐term survival in patients with APL.
Persistent Identifierhttp://hdl.handle.net/10722/282528
ISSN
2021 Impact Factor: 6.921
2020 SCImago Journal Rankings: 3.052
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorSingh, HSG-
dc.contributor.authorYim, RY-
dc.contributor.authorKumana, CR-
dc.contributor.authorTse, E-
dc.contributor.authorKwong, Y-L-
dc.date.accessioned2020-05-15T05:29:17Z-
dc.date.available2020-05-15T05:29:17Z-
dc.date.issued2020-
dc.identifier.citationCancer, 2020, v. 126 n. 14, p. 3244-3254-
dc.identifier.issn0008-543X-
dc.identifier.urihttp://hdl.handle.net/10722/282528-
dc.description.abstractBackground: The role of arsenic trioxide (As2O3) in the maintenance of first complete remission (CR1) in acute promyelocytic leukemia (APL) is unclear. Methods: A total of 129 consecutive adult patients with APL of all risk categories who achieved CR1 with conventional induction (all‐trans retinoic acid [ATRA]/daunorubicin) and consolidation (daunorubicin/cytarabine [induction daunorubicin and consolidation omitted for age ≥70 years]) underwent maintenance comprising ATRA (45 mg/m2/day), oral As2O3 (10 mg/day), and ascorbic acid (1 g/day) (AAA) for 2 weeks every 2 months for 2 years. Results: Over a 17‐year period from August 1, 2002, to July 31, 2019, 63 men and 66 women (median age, 46 years [range, 18‐82 years]) received AAA maintenance, which was already completed in 117 patients. At a median follow‐up of 100 months (range, 8‐215 months), 17 patients (13%) developed first relapse (R1) (hematologic, n = 14; molecular, n = 3) after a median of 19 months (range, 7‐96 months) from CR1. Two R1 patients had concomitant central nervous system (CNS) involvement. All patients achieved CR2 with oral As2O3‐based salvage. Five patients had a subsequent relapse and died. Eight patients died of unrelated causes while still in CR1. The 5‐year and 10‐year rates of relapse‐free survival (RFS) were 89% and 85%, respectively. The 5‐year and 10‐year rates of overall survival (OS) were 94% and 87%, respectively. Multivariate analysis showed that inferior RFS was associated with FLT3‐ITD (P = .005) and CNS involvement on presentation (P = .004), and inferior OS was associated with therapy‐related APL (P = .03), FLT3‐ITD (P = .03), and relapse (P = .03). The safety profile was favorable, with no grade 3/4 organ toxicities. Conclusion: CR1 maintenance with AAA is safe and results in favorable long‐term survival in patients with APL.-
dc.languageeng-
dc.publisherJohn Wiley & Sons, Inc. The Journal's web site is located at http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1097-0142-
dc.relation.ispartofCancer-
dc.rightsPreprint This is the pre-peer reviewed version of the following article: [FULL CITE], which has been published in final form at [Link to final article using the DOI]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. Postprint This is the peer reviewed version of the following article: [FULL CITE], which has been published in final form at [Link to final article using the DOI]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.-
dc.subjectacute promyelocytic leukemia-
dc.subjectarsenic trioxide-
dc.subjectfirst completion remission-
dc.subjectmaintenance-
dc.subjectoral-
dc.titleOral arsenic trioxide, all‐trans retinoic acid, and ascorbic acid maintenance after first complete remission in acute promyelocytic leukemia: Long‐term results and unique prognostic indicators-
dc.typeArticle-
dc.identifier.emailSingh, HSG: gillhsh@hku.hk-
dc.identifier.emailYim, RY: ritayim@hku.hk-
dc.identifier.emailTse, E: ewctse@hku.hk-
dc.identifier.emailKwong, Y-L: ylkwong@hkucc.hku.hk-
dc.identifier.authoritySingh, HSG=rp01914-
dc.identifier.authorityTse, E=rp00471-
dc.identifier.authorityKwong, Y-L=rp00358-
dc.description.naturelink_to_OA_fulltext-
dc.identifier.doi10.1002/cncr.32937-
dc.identifier.scopuseid_2-s2.0-85085075442-
dc.identifier.hkuros309886-
dc.identifier.volume126-
dc.identifier.issue14-
dc.identifier.spage3244-
dc.identifier.epage3254-
dc.identifier.isiWOS:000530436100001-
dc.publisher.placeUnited States-
dc.identifier.issnl0008-543X-

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