| Literature DB >> 17917880 |
Abstract
MAb have become an important treatment modality in cancer therapy.Genetically engineered chimeric and humanized Ab have demonstrated activity against a variety of tumors. While the humanized anti-CD33MAb lintuzumab has only modest single-agent activity against overt AML, it can eliminate minimal residual disease detectable by reverse transcription-PCR in acute promyelocytic leukemia. Targeted chemotherapy with the anti−CD33−calicheamicin construct gemtuzumab ozogamicin has produced remissions in patients with relapsed AML and appears promising when used in combination with standard chemotherapy in the treatment of newly diagnosed AML.Entities:
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Year: 2008 PMID: 17917880 DOI: 10.1080/14653240701519012
Source DB: PubMed Journal: Cytotherapy ISSN: 1465-3249 Impact factor: 5.414