| Literature DB >> 26628884 |
W Cao1, K Vyboh2, B Routy3, M Chababi-Atallah4, B Lemire5, J P Routy2.
Abstract
Kaposi sarcoma (ks) is a vascular tumour caused by oncogenic human herpesvirus type 8; it often occurs with hiv-associated immunosuppression. Numerous cellular signalling pathways are involved in the pathogenesis of ks, among which receptor tyrosine kinases such as the c-Kit and platelet-derived growth factor receptors play an important role. Imatinib mesylate, a tyrosine kinase inhibitor, has resulted in partial regression of ks lesions in one third of treated patients, but its mechanism of action remains unclear. Here, we report the case of a white man with recurrent ks despite well-suppressed hiv infection and multiple chemotherapies who received imatinib and showed a complete and sustained tumour response. To our knowledge, this report is the first showing the value of imatinib in the management of ks in the context of long-lasting hiv control with adequate quantitative CD4 recovery. Our case indicates that imatinib can be a treatment option for highly chemoresistant recurrent ks in patients on long-term antiretroviral therapy.Entities:
Keywords: Kaposi sarcoma; autophagy; hiv-1; imatinib
Year: 2015 PMID: 26628884 PMCID: PMC4608417 DOI: 10.3747/co.22.2635
Source DB: PubMed Journal: Curr Oncol ISSN: 1198-0052 Impact factor: 3.677