| Literature DB >> 31264788 |
Sarah Elitzur1,2, Nira Arad-Cohen3, Shlomit Barzilai-Birenboim1,2, Miriam Ben-Harush4, Bella Bielorai2,5, Ronit Elhasid2,6, Tamar Feuerstein1, Gil Gilad1,2, Alexander Gural7, Mira Kharit8, Naomi Litichever1, Ronit Nirel9, Sigal Weinreb10, Ofir Wolach2,11, Amos Toren2,5, Shai Izraeli1,2, Elad Jacoby2,5.
Abstract
Tremendous progress in the therapy of pediatric acute lymphoblastic leukemia (ALL) has been achieved through combination cytotoxic chemotherapy, leading to high cure rates, at the cost of significant life-threatening toxicity. The bispecific T-cell engager blinatumomab, recently approved for relapsed/refractory ALL, has a unique nonmyelotoxic toxicity profile. As blinatumomab causes B-cell depletion, the safety of its use during severe chemotherapy-induced toxicity is unclear. We report 11 pediatric patients with ALL, treated with blinatumomab following overwhelming chemotherapy-associated toxicity, with recovery of all patients and successful bridging to further antileukemia therapy. Blinatumomab can be considered for rare patients who cannot tolerate cytotoxic therapy.Entities:
Keywords: blinatumomab; childhood acute lymphoblastic leukemia; immunotherapy; treatment-related toxicity
Year: 2019 PMID: 31264788 DOI: 10.1002/pbc.27898
Source DB: PubMed Journal: Pediatr Blood Cancer ISSN: 1545-5009 Impact factor: 3.167