CD30: an important new target in hematologic malignancies

被引:61
作者
Deutsch, Yehuda E. [1 ,2 ]
Tadmor, Tamar [3 ]
Podack, Eckhard R. [4 ]
Rosenblatt, Joseph D. [1 ,2 ,4 ]
机构
[1] Univ Miami, Sylvester Comprehens Canc Ctr, Miami, FL 33136 USA
[2] Univ Miami, Miller Sch Med, Dept Med, Div Hematol Oncol, Miami, FL 33136 USA
[3] Bnai Zion Med Ctr, Hematol Oncol Unit, Haifa, Israel
[4] Univ Miami, Miller Sch Med, Dept Microbiol & Immunol, Miami, FL 33136 USA
关键词
Lymphoma and Hodgkin disease; antibody-based immunotherapy; CD30; brentuximab vedotin; LARGE-CELL LYMPHOMA; ANTI-CD30; ANTIBODY; 5F11; REED-STERNBERG CELLS; FACTOR-KAPPA-B; REFRACTORY HODGKINS-DISEASE; RETRACTED ARTICLE. SEE; HIGH SERUM-LEVEL; CD4(+) T-CELLS; SOLUBLE CD30; ANTITUMOR-ACTIVITY;
D O I
10.3109/10428194.2011.574761
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
CD30 is abundantly and selectively expressed on the surface of Hodgkin Reed-Sternberg cells, anaplastic large cell lymphomas (ALCLs), and other lymphoid malignancies as well as on several non-lymphoid malignancies including selected germ cell tumors. Expression of CD30 on normal cells is highly restricted, thereby allowing differential targeting of malignant cells. CD30, a member of the tumor necrosis factor (TNF)-receptor family has pleiotropic biologic functions, and antibodies targeting CD30 and other TNF family receptors can exhibit both agonistic and antagonistic signaling functions. Recently, antibody-drug conjugates targeting CD30, such as brentuximab vedotin, have shown striking activity in phase I and II trials, with manageable toxicity. This has defined an important emerging role for targeting of CD30 in the setting of Hodgkin lymphoma, ALCL, and possibly other CD30+ malignancies.
引用
收藏
页码:1641 / 1654
页数:14
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