BCR-ABL1 molecular remission after 90Y-epratuzumab tetraxetan radioimmunotherapy in CD22+ Ph+ B-ALL: proof of principle

被引:11
作者
Chevallier, Patrice [1 ,2 ]
Bodet-Milin, Caroline [3 ]
Robillard, Nelly [4 ]
Eugene, Thomas [3 ]
Menard, Audrey [4 ]
Le Houerou, Claire [1 ,2 ]
Guillaume, Thierry [1 ,2 ]
Delaunay, Jacques [1 ,2 ]
Escoffre-Barbe, Martine [5 ]
Wegener, William A. [6 ]
Goldenberg, David M. [6 ]
Kraeber-Bodere, Francoise [3 ]
机构
[1] Univ Nantes, Ctr Invest Clin Cancerol CI2C, CHU Nantes, Hematol Clin, Nantes, France
[2] INSERM, CRNCA UMR 892, Nantes, France
[3] CHU Nantes, Hotel Dieu, Dept Nucl Med, F-44093 Nantes, France
[4] CHU Nantes, Hotel Dieu, Dept Biol Hematol, F-44093 Nantes, France
[5] CHU, Dept Hematol, Rennes, France
[6] Immunomedics Inc, Morris Plains, NJ USA
关键词
B-acute lymphoblastic leukemia; BCR-ABL1; relapse; radioimmunotherapy; epratuzumab; yttrium; CD22; ACUTE LYMPHOBLASTIC-LEUKEMIA; NON-HODGKINS-LYMPHOMA; FRACTIONATED RADIOIMMUNOTHERAPY; MONOCLONAL-ANTIBODY; PHASE-I/II; EPRATUZUMAB; CHEMOIMMUNOTHERAPY; CHEMOTHERAPY; RELAPSE;
D O I
10.1111/ejh.12183
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Although targeted therapies are used increasingly in hematologic malignancies, we are unaware of any prior studies of radioimmunotherapy (RAIT) in B-acute lymphoblastic leukemia (ALL), even though this radiosensitive tumor expresses CD22, potentially a good target for this approach. Here, we report a patient with Philadelphia chromosome-positive B-ALL in third relapse who received RAIT with (90)yttrium (Y-90)-labeled anti-CD22 epratuzumab tetraxetan. Seven weeks after initiating therapy, the patient achieved a BCR-ABL1 molecular remission documented by RT-qPCR, which is now continuing at 6months while awaiting an allogeneic hematopoietic stem cell transplant. Y-90-Epratuzumab tetraxetan may be a promising therapeutic option for CD22(+) B-ALL patients.
引用
收藏
页码:552 / 556
页数:5
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