Volume 21, Issue 4 e12926
ORIGINAL ARTICLE

Impact of post-transplant minimal residual disease on the clinical outcome of pediatric acute leukemia

Katsutsugu Umeda

Corresponding Author

Katsutsugu Umeda

Department of Pediatrics, Graduate School of Medicine, Kyoto University, Kyoto, Japan

Correspondence

Katsutsugu Umeda, Department of Pediatrics, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Email: [email protected]

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Atsushi Iwai

Atsushi Iwai

Department of Pediatrics, Graduate School of Medicine, Kyoto University, Kyoto, Japan

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Koji Kawaguchi

Koji Kawaguchi

Department of Pediatrics, Graduate School of Medicine, Kyoto University, Kyoto, Japan

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Masamitsu Mikami

Masamitsu Mikami

Department of Pediatrics, Graduate School of Medicine, Kyoto University, Kyoto, Japan

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Seishiro Nodomi

Seishiro Nodomi

Department of Pediatrics, Graduate School of Medicine, Kyoto University, Kyoto, Japan

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Satoshi Saida

Satoshi Saida

Department of Pediatrics, Graduate School of Medicine, Kyoto University, Kyoto, Japan

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Hidefumi Hiramatsu

Hidefumi Hiramatsu

Department of Pediatrics, Graduate School of Medicine, Kyoto University, Kyoto, Japan

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Toshio Heike

Toshio Heike

Department of Pediatrics, Graduate School of Medicine, Kyoto University, Kyoto, Japan

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Katsuyuki Ohmori

Katsuyuki Ohmori

Department of Clinical Laboratory, Kyoto University Hospital, Kyoto, Japan

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Souichi Adachi

Souichi Adachi

Human Health Sciences, Graduate School of Medicine, Kyoto University, Kyoto, Japan

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First published: 31 March 2017
Citations: 2

Abstract

This retrospective study examined the clinical significance of FCM-MRD in 36 patients with ALL and 29 patients with AML after their first allogeneic HSCT. Hematological (FCM-MRD ≥5.0%) and molecular relapse (FCM-MRD <5.0%) were first detected in 10 and two patients with ALL and in seven and eight patients with AML, respectively. Eight of 10 patients with molecular relapse eventually progressed to hematological relapse, although most were treated with immunological intervention by aggressive discontinuation of immunosuppressive therapy or donor lymphocyte infusion. Among these 12 patients, four of seven patients that obtained MRDneg CR following post-transplant chemotherapy remain alive and disease-free after their second HSCT; however, all five patients who underwent a second HSCT in non-CR died of disease or treatment-related complications. As the FCM-MRD monitoring system used in the current study was probably not sensitive enough to detect MRD, which could be elucidated by immunological intervention, more sensitive diagnostic tools are mandatory for post-transplant MRD monitoring. Additional studies are required to address the impact of presecond transplant MRD on the clinical outcome of second HSCT.

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