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Inotuzumab Ozogamicin for Acute Lymphoblastic Leukemia: Clinical Pharmacology and Therapeutic Results

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Chemotherapy for Leukemia
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Abstract

CD22 antigen is a B-cell lineage-restricted type I transmembrane protein, a member of Siglec family of cell surface receptors. Expression of CD22 is found in almost all the B cells and most B-lymphoid malignancies including non-Hodgkin lymphoma (NHL) and acute lymphoblastic leukemia (ALL).

Inotuzumab ozogamicin (INO) is one of the antibody-drug conjugates (ADCs) that consists of a cytotoxic drug, calicheamicin, attached to a humanized monoclonal anti-CD22 antibody. Based upon clinical trials, INO was shown to be effective for relapsed/refractory ALL as well as B-cell NHL. Single-agent treatment of INO (1.8 mg/m2 once every 3–4 weeks or fractionated weekly, 0.8 mg/m2 on day 1, and 0.5 mg/m2 on day 8 and 15 every 3–4 weeks) provided an objective response rate of 60% in the treatment of relapsed/refractory CD22-positive ALL patients. Combination of INO with rituximab and low-intensive conventional chemotherapy for patients with relapsed/refractory ALL showed better objective response. This review summarizes the clinical efficacy and safety of INO in the treatment of relapsed/refractory ALL, based on currently available data in the literature.

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Conflict of Interest Disclosure

Dr. Usui has received research grants and honoraria from CIMIC, Takeda, Eli Lilly Japan, Pfizer, Nippon Boehringer-Ingelheim, Sysmex, Janssen Pharmaceutical, Zenyaku Kogyo, Kyowa Hakko Kirin, Astellas Pharma, Otsuka Pharmaceutical, Celgene, SymBio Pharmaceuticals, Huya Bioscience International, Chugai Pharmaceutical, Bristol-Myers Squibb, and Solasia Pharma.

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Usui, N. (2017). Inotuzumab Ozogamicin for Acute Lymphoblastic Leukemia: Clinical Pharmacology and Therapeutic Results. In: Ueda, T. (eds) Chemotherapy for Leukemia. Springer, Singapore. https://doi.org/10.1007/978-981-10-3332-2_7

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  • DOI: https://doi.org/10.1007/978-981-10-3332-2_7

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