Volume 21, Issue 4 e12918
CASE REPORT

Haploidentical peripheral blood stem cell transplantation without irradiation or busulfan after reduced‐intensity conditioning for KMT2A(MLL)‐rearranged infant B‐cell precursor acute lymphoblastic leukemia: Report of two cases

Ai Yoshimi

Corresponding Author

Division of Pediatric Hematology and Oncology, Ibaraki Children's Hospital, Mito, Japan

Correspondence

Ai Yoshimi, Division of Pediatric Hematology and Oncology, Ibaraki Children's Hospital, Mito, Japan.

Email: yoshimi-tuk@umin.ac.jp

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Keisuke Kato

Division of Pediatric Hematology and Oncology, Ibaraki Children's Hospital, Mito, Japan

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Sho Hosaka

Department of Pediatrics, Institute of Clinical Medicine, University of Tsukuba, Tsukuba, Japan

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Ryoko Suzuki

Department of Pediatrics, Institute of Clinical Medicine, University of Tsukuba, Tsukuba, Japan

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Hiroko Fukushima

Department of Pediatrics, Institute of Clinical Medicine, University of Tsukuba, Tsukuba, Japan

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Tomohei Nakao

Department of Pediatrics, Institute of Clinical Medicine, University of Tsukuba, Tsukuba, Japan

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Chie Kobayashi

Division of Pediatric Hematology and Oncology, Ibaraki Children's Hospital, Mito, Japan

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Takashi Fukushima

Department of Pediatrics, Institute of Clinical Medicine, University of Tsukuba, Tsukuba, Japan

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Kazutoshi Koike

Division of Pediatric Hematology and Oncology, Ibaraki Children's Hospital, Mito, Japan

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Ryo Sumazaki

Department of Pediatrics, Institute of Clinical Medicine, University of Tsukuba, Tsukuba, Japan

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Masahiro Tsuchida

Division of Pediatric Hematology and Oncology, Ibaraki Children's Hospital, Mito, Japan

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First published: 22 March 2017

Abstract

We present two infants with KMT2A(MLL)‐gene‐R‐associated BCP‐ALL, who received HLA haploidentical PBSCT after RIC. The patients developed ALL at age 6 months and 3 months, respectively. Case 1 underwent PBSCT at the second CR with detectable KMT2A‐AFF1(MLL‐AF4) fusion gene transcript at 11 months of age, and Case 2 at the first CR without KMT2A‐MLLT1(MLL‐ENL) fusion gene transcript at 8 months of age. Both patients received G‐CSF‐mobilized unmanipulated peripheral blood mononuclear cells from their HLA haploidentical mothers after administration of FLU, MEL, and ATG. Tacrolimus, methotrexate, and mPSL were administered as prophylaxis against GVHD. Engraftment was rapidly obtained with complete chimerism in both patients. Acute adverse events included acute GVHD in Case 1 and bacterial sepsis in Case 2. At last clinical check at age 5 years and 4 years, respectively, both patients were recurrence‐free and attained normal growth and development. We conclude that PBSCT from an HLA haploidentical mother with non‐TBI and non‐BU regimen seems feasible and efficacious, offering favorable life quality for infants.

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