Abstract
Treatment of refractory or relapsed classical Hodgkin lymphoma (HL) remains challenging, but targeted immunotherapy has recently emerged as a potential treatment option for these patients. Although first-generation monoclonal anti-CD30 antibodies proved disappointing, current efforts to modify anti-CD30 antibodies to improve binding of effector cells and enhance activity appears more promising, as does the development of novel antibody-drug conjugates (ADCs). ADCs offer the potential to deliver potent therapies with minimal toxicity. One highly active ADC, brentuximab vedotin (SGN-35), combines an anti-CD30 monoclonal antibody and the antitubulin agent monomethyl auristatin E. Initial phase 1 studies of brentuximab vedotin showed a 52% overall response rate in relapsed HL, with minimal toxicity. This article highlights the development of anti-CD30 antibodies and ADCs for relapsed or refractory classical HL.
Original language | English |
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Pages (from-to) | 140-147 |
Number of pages | 8 |
Journal | Current Hematologic Malignancy Reports |
Volume | 5 |
Issue number | 3 |
DOIs | |
State | Published - Jul 2010 |
Keywords
- Anti-CD30 antibodies
- Brentuximab vedotin
- Hodgkin lymphoma
- SGN-35