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Efficacy and safety of blinatumomab treatment in adult Korean patients with relapsed/refractory acute lymphoblastic leukemia on behalf of the Korean Society of Hematology ALL Working Party

  • Sung Hoon Jung
  • , Se ryeon Lee
  • , Deok Hwan Yang
  • , Seok Lee
  • , Jae Ho Yoon
  • , Hyewon Lee
  • , Soo Mee Bang
  • , Youngil Koh
  • , Silvia Park
  • , Dae Sik Kim
  • , Ho Young Yhim
  • , Sung Hyun Kim
  • , Ji Hyun Lee
  • , Sang Kyun Sohn
  • , Ik Chan Song
  • , Hong ghi Lee
  • , Jung Won Cheong
  • , Yunsuk Choi
  • , Ho Jin Shin*
  • *Corresponding author for this work
  • Chonnam National University
  • Korea University
  • The Catholic University of Korea
  • National Cancer Center Korea
  • Seoul National University
  • Samsung Medical Center, Sungkyunkwan university
  • Dong-A Medical Center
  • Kyungpook National University
  • Chungnam National University
  • Konkuk University
  • Yonsei University
  • University of Ulsan
  • Pusan National University

Research output: Contribution to journalJournal articlepeer-review

Abstract

Blinatumomab, a bispecific T cell-engaging antibody, has demonstrated efficacy for relapsed or refractory acute lymphoblastic leukemia (ALL). In this study, we evaluated the efficacy and toxicity of blinatumomab in adult Korean patients with relapsed or refractory Philadelphia-negative B cell precursor ALL. A total of 50 patients received blinatumomab treatment between June 2016 and August 2017 in Korea. The median number of prior therapy was one (range, 1–4). Among the 49 evaluable patients, 22 (44.9%) achieved complete response (CR) or CR with incomplete blood count recovery, and 16 of whom subsequently underwent allogenic stem cell transplantation. Although no statistically significant differences were observed, patients with extramedullary disease and poor performance status had lower responses to blinatumomab treatment. In addition, the use of high-dose dexamethasone prior to blinatumomab treatment did not affect the response to blinatumomab. The median event-free survival and overall survival of the responders were 7.5 and 8.1 months, respectively. For non-hematologic toxicities, the most common toxicity was infection. The incidences of severe cytokine release syndrome and neurologic toxicity each was 4%. In conclusion, blinatumomab was an effective and tolerable therapy in adult Korean patients with relapsed or refractory Philadelphia-negative B cell precursor ALL.

Original languageEnglish
Pages (from-to)151-158
Number of pages8
JournalAnnals of Hematology
Volume98
Issue number1
DOIs
StatePublished - 2019.01.30

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Acute lymphoblastic leukemia
  • Blinatumomab
  • Predictor

Quacquarelli Symonds(QS) Subject Topics

  • Medicine

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