Novel immunotherapies for adult patients with B-lineage acute lymphoblastic leukemia
Abstract The past decade witnessed the rapid development of adult B-lineage acute lymphoblastic leukemia (ALL) treatment. Beyond the development of chemotherapy regimens, immunotherapy is starting a new era with unprecedented complete remission (CR) rate. Targeting B-lineage-specific surface markers...
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2017-08-01
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doaj-ef2c03d5f08b4f99b3feca6e2b80713b2020-11-25T02:19:06ZengBMCJournal of Hematology & Oncology1756-87222017-08-0110111310.1186/s13045-017-0516-xNovel immunotherapies for adult patients with B-lineage acute lymphoblastic leukemiaGuoqing Wei0Jiasheng Wang1He Huang2Yanmin Zhao3Bone Marrow Transplantation Center, The First Affiliated Hospital, School of Medicine, Zhejiang UniversityBone Marrow Transplantation Center, The First Affiliated Hospital, School of Medicine, Zhejiang UniversityBone Marrow Transplantation Center, The First Affiliated Hospital, School of Medicine, Zhejiang UniversityBone Marrow Transplantation Center, The First Affiliated Hospital, School of Medicine, Zhejiang UniversityAbstract The past decade witnessed the rapid development of adult B-lineage acute lymphoblastic leukemia (ALL) treatment. Beyond the development of chemotherapy regimens, immunotherapy is starting a new era with unprecedented complete remission (CR) rate. Targeting B-lineage-specific surface markers such as CD19, CD20, CD22, or CD52, immunotherapy has been demonstrating promising clinical results. Among the immunotherapeutic methods, naked monoclonal antibodies (mAbs), antibody-drug conjugate (ADC), bispecific T cell engager (BiTE), and chimeric antigen receptor (CAR) T cells are the main types. In this review, we will examine the emerging preclinical and clinical development on (1) anti-CD20 naked mAbs rituximab, ofatumumab, and obinutuzumab; (2) anti-CD19 ADCs SAR3419 and SGN-CD19A and anti-CD19 BiTE blinatumomab; (3) anti-CD22 naked mAb epratuzumab and anti-CD22 ADC inotuzumab ozogamicin; (4) anti-CD52 naked mAb alemtuzumab; and (5) anti-CD19 CAR T cells. We will discuss their efficacy, adverse effects, as well as future development.http://link.springer.com/article/10.1186/s13045-017-0516-x |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Guoqing Wei Jiasheng Wang He Huang Yanmin Zhao |
spellingShingle |
Guoqing Wei Jiasheng Wang He Huang Yanmin Zhao Novel immunotherapies for adult patients with B-lineage acute lymphoblastic leukemia Journal of Hematology & Oncology |
author_facet |
Guoqing Wei Jiasheng Wang He Huang Yanmin Zhao |
author_sort |
Guoqing Wei |
title |
Novel immunotherapies for adult patients with B-lineage acute lymphoblastic leukemia |
title_short |
Novel immunotherapies for adult patients with B-lineage acute lymphoblastic leukemia |
title_full |
Novel immunotherapies for adult patients with B-lineage acute lymphoblastic leukemia |
title_fullStr |
Novel immunotherapies for adult patients with B-lineage acute lymphoblastic leukemia |
title_full_unstemmed |
Novel immunotherapies for adult patients with B-lineage acute lymphoblastic leukemia |
title_sort |
novel immunotherapies for adult patients with b-lineage acute lymphoblastic leukemia |
publisher |
BMC |
series |
Journal of Hematology & Oncology |
issn |
1756-8722 |
publishDate |
2017-08-01 |
description |
Abstract The past decade witnessed the rapid development of adult B-lineage acute lymphoblastic leukemia (ALL) treatment. Beyond the development of chemotherapy regimens, immunotherapy is starting a new era with unprecedented complete remission (CR) rate. Targeting B-lineage-specific surface markers such as CD19, CD20, CD22, or CD52, immunotherapy has been demonstrating promising clinical results. Among the immunotherapeutic methods, naked monoclonal antibodies (mAbs), antibody-drug conjugate (ADC), bispecific T cell engager (BiTE), and chimeric antigen receptor (CAR) T cells are the main types. In this review, we will examine the emerging preclinical and clinical development on (1) anti-CD20 naked mAbs rituximab, ofatumumab, and obinutuzumab; (2) anti-CD19 ADCs SAR3419 and SGN-CD19A and anti-CD19 BiTE blinatumomab; (3) anti-CD22 naked mAb epratuzumab and anti-CD22 ADC inotuzumab ozogamicin; (4) anti-CD52 naked mAb alemtuzumab; and (5) anti-CD19 CAR T cells. We will discuss their efficacy, adverse effects, as well as future development. |
url |
http://link.springer.com/article/10.1186/s13045-017-0516-x |
work_keys_str_mv |
AT guoqingwei novelimmunotherapiesforadultpatientswithblineageacutelymphoblasticleukemia AT jiashengwang novelimmunotherapiesforadultpatientswithblineageacutelymphoblasticleukemia AT hehuang novelimmunotherapiesforadultpatientswithblineageacutelymphoblasticleukemia AT yanminzhao novelimmunotherapiesforadultpatientswithblineageacutelymphoblasticleukemia |
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