Inotuzumab ozogamicin in infants and young children with relapsed or refractory acute lymphoblastic leukaemia: a case series

Erica Brivio(Princess Máxima Center), Christophe Chantrain(Centre Hospitalier Chrétien), Tanja A. Grüber(Stanford Medicine), Adriana Thano(Princess Máxima Center), Fanny Rialland(Centre Hospitalier Universitaire de Nantes), Audrey Contet(Centre Hospitalier Régional et Universitaire de Nancy), Sarah Elitzur(Tel Aviv University), Luciano Dalla‐Pozza(Children's Hospital at Westmead), Krisztián Kállay, Chi Kong Li(Chinese University of Hong Kong), Motohiro Kato(National Center For Child Health and Development), Inna V. Markova(First Pavlov State Medical University of St. Petersburg), Kjeld Schmiegelow(University of Copenhagen), Nicole Bodmer(University Children's Hospital Zurich), Erin H. Breese(Cincinnati Children's Hospital Medical Center), Raoull Hoogendijk(Princess Máxima Center), Rob Pieters(Princess Máxima Center), C. Michel Zwaan(Princess Máxima Center)
British Journal of Haematology
February 2, 2021
Cited by 24Open Access
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Abstract

Summary No data on inotuzumab ozogamicin (InO) in infant acute lymphoblastic leukaemia (ALL) have been published to date. We collected data internationally on infants/young children (<3 years) with ALL treated with InO. Fifteen patients (median 4.4 months at diagnosis) received InO due to relapsed or refractory (R/R) disease. Median percentage of CD22 + blasts was 72% (range 40–100%, n = 9). The median dose in the first course was 1.74 mg/m 2 (fractionated). Seven patients (47%) achieved complete remission; one additional minimal residual disease (MRD)‐positive patient became MRD‐negative. Six‐month overall survival was 47% (95% confidence interval [CI] 27–80%). Two patients developed veno‐occlusive disease after transplant. Further evaluation of InO in this subgroup of ALL is justified.


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