재발한 소아 급성림프모구성백혈병에서 blinatumomab 의 초기 치료 반응 및 독성

재발한 소아 급성림프모구성백혈병에서 blinatumomab 의 초기 치료 반응 및 독성

Early treatment response and toxicity of blinatumomab in relapsed/refractory pediatric acute lymphoblastic leukemia

(구연):
Release Date : 2017. 10. 26(목)
Hee Young Ju1, Ji Man Kang1, Byung-Kiu Park1, Hyoung Jin Kang2, Kyung Duk Park2, Hee Young Shin2, Seong-koo Kim33, Jae Wook Lee3, Nack-Gyun Chung3, Bin Cho3, Hack-Ki Kim3, Hyery Kim4, Kyung Nam Koh4, Ho Joon Im4, Jong Jin Seo4, Young Tak Lim5, Meerim Park6 , Hyeon Jin Park1
National Cancer Center Center for Pediatric Cancer1
Seoul National Univesity College of Medicine Department of Pediatrics2
Catholic University College of Medicine Department of Pediatrics3
Ulsan University Asan Medical Center Department of Pediatrics4
Pusan National University Hospital Department of Pediatrics5
Chungbuk National University Hospital Department of Pediatrics6
주희영1, 강지만1, 박병규1, 강형진2, 박경덕2, 신희영2, 김성구3, 이재욱3, 정낙균3, 조빈3, 김학기3, 김혜리4, 고경남4, 임호준4, 서종진4, 임영탁5, 박미림6 , 박현진1
국립암센터 소아청소년암센터1
서울대학교 의과대학 소아청소년과2
가톨릭대학교 의과대학 소아청소년과3
울산의대 서울아산 어린이병원 소아청소년과4
부산대학교병원 소아청소년과5
충북대학교병원 소아청소년과6

Abstract

u>Introduction/u> Blinatumomab is a bispecific T-cell engager antibody construct targeting CD19 on B-cell lymphoblasts. The efficacy of blinatumomab has been reported in adult and pediatric acute lymphoblastic leukemia (ALL) and adult lymphoma, recently. To investigate the treatment response and toxicity, we retrospectively reviewed pediatric ALL cases treated with blinatumomab in multiple Korean pediatric hospitals. u>Patients and methods/u> Clinical data of the patients were collected from 6 Korean pediatric hospitals. Following data were collected; disease status at blinatumomab treatment, early treatment response after blinatumomab first cycle, treatment-related toxicity, continuing treatment, current disease status. u>Results/u> Nine patients were treated with blinatumomab. Median age of the patients was 11.9 years (range, 1.0-23.0), and there were 4 boys and 5 girls. Blinatumomab was treated as 3rd regimen in 5 patients, 4th regimen in 2 patients, and 5th regimen in 2 patients. Two patients were treated with fixed dose (9mcg/day, 1 week followed by 28mcg/day, 3 weeks), and others were treated with calculated dose of 5 mcg/m2/day for 1 week followed by 15mcg/m2/day for 3 weeks. One patient was treated 2 cycles of blinatumomab, and other 8 patients were treated once. Five patients (55.6%) achieved overall response after blinatumomab including three patients with molecular response, and two of the responders were treated with HSCT. Responders showed spontaneous platelet recovery at the end of blinatumomab infusion. There was one patient who discontinued treatment because of no response with aggravating leukocytosis. Seven patients (77.8%) experienced cytokine release syndrome (two grade 2, four grade 1). Three cases were observed neurotoxicity, which were seizure, involuntary movement, and headache. Grade 3 or 4 hematologic toxicities were observed in all patients. One patient experienced repetitive ventricular tachycardia lasting few seconds, which recovered after completion of blinatumomab. u>Conclusion/u> Blinatumomab resulted in overall response in 55.6% of cases with 2 or more leukemia relapses. Toxicity of blinatumomab was tolerable, and there was no treatment-limiting toxicity. Blinatumomab can be an effective treatment for relapsed/refractory pediatric ALL patients with tolerable toxicity.

Keywords: Blinatumomab, acute lymphoblastic leukemia,