6533b826fe1ef96bd1284833

RESEARCH PRODUCT

Management of acute promyelocytic leukemia: updated recommendations from an expert panel of the European LeukemiaNet

Giuseppe AvvisatiFarhad RavandiUwe PlatzbeckerAlan K. BurnettPau MontesinosElihu H. EsteyMiguel A. SanzMiguel A. SanzHarry J. IlandPierre FenauxEduardo Magalhães RegoEva LengfelderHagop M. KantarjianHartmut DöhnerBob LöwenbergVikram MathewsLionel AdèsNigel H. RussellMartin S. TallmanTomoki NaoeSai Juan ChenFrancesco Lo-coco

subject

Acute promyelocytic leukemiamedicine.medical_specialtymedicine.medical_treatmentImmunologyMEDLINETretinoinDiseaseHemorrhagic DisordersBiochemistryHemorrhagic disorderEuropean LeukemiaNetArsenic TrioxideLeukemia Promyelocytic AcutePregnancyRecurrenceHumansMedicineDisease management (health)Intensive care medicineSpecial ReportNeoadjuvant therapyAPL Differentiation SyndromeAgedbusiness.industryDisease ManagementCell BiologyHematologymedicine.diseasePractice Guidelines as TopicFemalebusiness

description

Abstract Since the comprehensive recommendations for the management of acute promyelocytic leukemia (APL) reported in 2009, several studies have provided important insights, particularly regarding the role of arsenic trioxide (ATO) in frontline therapy. Ten years later, a European LeukemiaNet expert panel has reviewed the recent advances in the management of APL in both frontline and relapse settings in order to develop updated evidence- and expert opinion–based recommendations on the management of this disease. Together with providing current indications on genetic diagnosis, modern risk-adapted frontline therapy, and salvage treatment, the review contains specific recommendations for the identification and management of the most important complications such as the bleeding disorder APL differentiation syndrome, QT prolongation, and other all-trans retinoic acid– and ATO-related toxicities, as well as recommendations for molecular assessment of the response to treatment. Finally, the approach to special situations is also discussed, including management of APL in children, elderly patients, and pregnant women. The most important challenges remaining in APL include early death, which still occurs before and during induction therapy, and optimizing treatment in patients with high-risk disease.

10.1182/blood-2019-01-894980https://doi.org/10.1182/blood-2019-01-894980