High WT1 expression is an early predictor for relapse in patients with acute promyelocytic leukemia in first remission with negative PML-RARa after anthracycline-based chemotherapy: a single-center cohort study

Jae Ho Yoon, Hee Je Kim, Dae Hun Kwak, Sung Soo Park, Young Woo Jeon, Sung Eun Lee, Byung Sik Cho, Ki Seong Eom, Yoo Jin Kim, Seok Lee, Chang Ki Min, Seok Goo Cho, Dong Wook Kim, Jong Wook Lee, Woo Sung Min

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16 Scopus citations

Abstract

Wilms’ tumor gene 1 (WT1) expression is a well-known predictor for relapse in acute myeloid leukemia. We monitored WT1 decrement along the treatment course to identify its significant role as a marker for residual disease in acute promyelocytic leukemia (APL) and tried to suggest its significance for relapse prediction. In this single center retrospective study, we serially measured PML-RARa and WT1 expression from 117 APL patients at diagnosis, at post-induction and post-consolidation chemotherapies, and at every 3 months after starting maintenance therapy. All 117 patients were in molecular remission after treatment of at least 2 consolidation chemotherapies. We used WT1 ProfileQuant™ kit (Ipsogen) for WT1 monitoring. High WT1 expression (>120 copies/104 ABL1) after consolidation and at early period (3 months) after maintenance therapy significantly predicted subsequent relapse. All paired PML-RARa RQ-PCR were not detected except for one sample with early relapse. Patients with high WT1 expression at 3 months after maintenance therapy (n = 40) showed a significantly higher relapse rate (30.5 vs. 6.9%, P < 0.001) and inferior disease free survival (62.8 vs. 91.4%, P < 0.001). Multivariate analysis revealed that high peak leukocyte counts at diagnosis (HR = 6.4, P < 0.001) and high WT1 expression at 3 months after maintenance therapy (HR = 7.1, P < 0.001) were significant factors for prediction of relapse. Our data showed high post-remission WT1 expression was a reliable marker for prediction of subsequent molecular relapse in APL. In this high-risk group, early intervention with ATRA ± ATO, anti-CD33 antibody therapy, and WT1-specific therapy may be used for relapse prevention.

Original languageEnglish
Pages (from-to)1-4
Number of pages4
JournalJournal of Hematology and Oncology
Volume10
Issue number1
DOIs
StatePublished - 23 Jan 2017

Bibliographical note

Publisher Copyright:
© 2017 The Author(s).

Keywords

  • Acute promyelocytic leukemia
  • FLT3 mutation
  • Minimal residual disease
  • WT1

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