Prognostic impact of low allelic ratio FLT3-ITD and NPM1 mutation in acute myeloid leukemia

Author:

Sakaguchi Masahiro1,Yamaguchi Hiroki1,Najima Yuho2,Usuki Kensuke3,Ueki Toshimitsu4,Oh Iekuni5,Mori Sinichiro6,Kawata Eri7,Uoshima Nobuhiko7,Kobayashi Yutaka7,Kako Shinichi8,Tajika Kenji9,Gomi Seiji9,Shono Katsuhiro10,Kayamori Kensuke11,Hagihara Masao12,Kanda Junya13,Uchiyama Hitoji14,Kuroda Junya15,Uchida Naoyuki16,Kubota Yasushi17,Kimura Shinya17,Kurosawa Saiko18,Nakajima Nana1,Marumo Atsushi1,Omori Ikuko1,Fujiwara Yusuke1,Yui Shunsuke1,Wakita Satoshi1,Arai Kunihito1,Kitano Tomoaki1,Kakihana Kazuhiko2ORCID,Kanda Yoshinobu58,Ohashi Kazuteru2,Fukuda Takahiro18,Inokuchi Koiti1

Affiliation:

1. Department of Hematology, Nippon Medical School, Tokyo, Japan;

2. Division of Hematology, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital, Tokyo, Japan;

3. Department of Hematology, NTT Medical Center Tokyo, Tokyo, Japan;

4. Department of Hematology, Nagano Red Cross Hospital, Nagano, Japan;

5. Division of Hematology, Department of Medicine, Jichi Medical University, Tochigi, Japan;

6. Hemato-Oncology Department, St Luke’s International Hospital, Tokyo, Japan;

7. Department of Hematology, Japanese Red Cross Kyoto Daini Hospital, Kyoto, Japan;

8. Division of Hematology, Jichi Medical University Saitama Medical Center, Saitama, Japan;

9. Department of Hematology, Yokohama Minami Kyousai Hospital, Kanagawa, Japan;

10. Department of Hematology, Chiba Aoba Municipal Hospital, Chiba, Japan;

11. Department of Hematology, Chiba University Hospital, Chiba, Japan;

12. Department of Hematology, Eiju General Hopital, Tokyo, Japan;

13. Department of Hematology and Oncology, Graduate School of Medicine, Kyoto University, Kyoto, Japan;

14. Department of Hematology, Japanese Red Cross Kyoto Daiichi Hospital, Kyoto, Japan;

15. Division of Hematology and Oncology, Kyoto Prefectural University of Medicine, Kyoto, Japan;

16. Department of Hematology, Federation of National Public Service Personnel Mutual Aid Associations, Toranomon Hospital, Tokyo, Japan;

17. Division of Hematology, Respiratory Medicine and Oncology, Department of Internal Medicine, Faculty of Medicine, Saga University, Saga, Japan; and

18. Department of Hematopoietic Stem Cell Transplantation, National Cancer Center Hospital, Tokyo, Japan

Abstract

Abstract In the opinion of the European LeukemiaNet (ELN), nucleophosmin member 1 gene mutation (NPM1 mut)–positive acute myeloid leukemia (AML) with an fms-like kinase 3-internal tandem duplication (FLT3-ITD) allele ratio (AR) <0.5 (low AR) has a favorable prognosis, and allogeneic hematopoietic stem cell transplant (allo-HSCT) in the first complete remission (CR1) period is not actively recommended. We studied 147 patients with FLT3-ITD gene mutation–positive AML, dividing them into those with low AR and those with AR of ≥0.5 (high AR), and examined the prognostic impact according to allo-HSCT in CR1. Although FLT3-ITD AR and NPM1 mut are used in the prognostic stratification, we found that NPM1 mut–positive AML with FLT3-ITD low AR was not associated with favorable outcome (overall survival [OS], 41.3%). Moreover, patients in this group who underwent allo-HSCT in CR1 had a significantly more favorable outcome than those who did not (relapse-free survival [RFS] P = .013; OS P = .003). Multivariate analysis identified allo-HSCT in CR1 as the sole favorable prognostic factor (RFS P < .001; OS P < .001). The present study found that prognosis was unfavorable in NPM1 mut–positive AML with FLT3-ITD low AR when allo-HSCT was not carried out in CR1.

Publisher

American Society of Hematology

Subject

Hematology

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