Abstract

Acute promyelocytic leukemia is a variant of acute myeloid leukemia characterized by t(15;17) and PML/RAR alfa fusion gene. The discovery of the molecular pathogenesis has led to entitle all-trans retinoic acid (ATRA) as the first targeted therapy for acute leukemia. It is usually associated to anthracycline-based chemotherapy with high response rates, but potential long-term sequelae including therapy-related malignancies have been observed. Arsenic trioxide (ATO) was added to obviate these complications and investigational trials aimed to a new strategy with the incorporation of arsenic trioxide (ATO) into initial therapy instead of chemotherapy in selected patients. ATRA plus ATO without chemotherapy was the first attempt to treat low and intermediate-risk patients with APL. Our study aims to describe a monocentric cohort of patients with newly diagnosed APL effectively treated with ATO plus ATRA underlying its efficacy together with the high grade of tolerability of this association. From January 2009 to December 2019 23 APL patients were diagnosed and treated with ATO plus ATRA regimen: 14 males and 9 females patients with a median age of 45 years (range 18-72), for the majority intermediate risk (15 patients, 65%). The treatment was well tolerated and all patients achieved molecular remission after a median time of 3 months (range 1-6 months). All patients proceeded to consolidation phase as outpatients, they maintained complete molecular response at a median time of 44 months (range 15-127) except for 1 patient. All but one patient are alive and in response at a median follow-up of 48 months (range 9-141) without late effects. ATO plus ATRA regimen shows advantages in comparison to chemotherapy; in fact it allowed to treat patients in which chemotherapy could even not be applicable and it did not show secondary hematological diseases. The association of ATO to ATRA as chemo-free regimen enabled to treat APL even without chemotherapy.

Highlights

  • In the setting of acute myeloid leukemia (AML) acute promyelocytic leukemia (APL) is a variant characterized by t(15;17) and PML/RAR alfa

  • Our study aims to describe a monocentric cohort of patients with newly diagnosed APL effectively treated with Arsenic trioxide (ATO) plus all-trans retinoic acid (ATRA) analyzing efficacy and tolerability of this association

  • A possible retinoic acid syndrome was described in 10 cases; even if in many cases it was only suspected ATRA was discontinued for a brief period, patients were treated with steroids and ATRA was restarted without any complications

Read more

Summary

Introduction

In the setting of acute myeloid leukemia (AML) acute promyelocytic leukemia (APL) is a variant characterized by t(15;17) and PML/RAR alfa. All-trans retinoic acid (ATRA) was used as a targeted therapy on the basis of this molecular transcript and was usually associated to anthracycline-based chemotherapy [1] This treatment achieved overall remission rates of up to 95% and cure rates over 80% [2,3,4]. Italian GIMEMA and Spanish PETHEMA trials demonstrated a high antileukemic efficacy of this protocol in terms of complete remission (CR) and disease-free survival rates [1]. All these patients received induction according to AIDA schedule [5], 3 courses of consolidation and maintenance. A minor role for cytarabine and etoposide was suggested in the treatment of newly diagnosed PML/RAR alfa-positive APL patients

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call