TCR diversity - a universal cancer immunotherapy biomarker?
- PMID: 27879971
- PMCID: PMC5109785
- DOI: 10.1186/s40425-016-0175-4
TCR diversity - a universal cancer immunotherapy biomarker?
Abstract
Sipuleucel-T was approved as a treatment for men with advanced metastatic, castration-resistant prostate cancer on the basis of improved survival in randomized clinical trials. A major challenge for this therapy, as well as other newer cancer immunotherapy agents, has been to identify markers that can identify patients who benefit from these therapies. In a recent manuscript by Sheikh and colleagues, the investigators evaluated changes in T cell clonality in the peripheral blood and tumors of patients treated with sipuleucel-T using next generation sequencing of T cell receptor Vß CDR3 sequences. Their findings are discussed in the context of this trial and other cancer immunotherapies.
Keywords: Prostate cancer; Sipuleucel-T; T-cell diversity; TCR sequencing; Tumor vaccine.
Comment on
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Clonotypic Diversification of Intratumoral T Cells Following Sipuleucel-T Treatment in Prostate Cancer Subjects.Cancer Res. 2016 Jul 1;76(13):3711-8. doi: 10.1158/0008-5472.CAN-15-3173. Epub 2016 May 23. Cancer Res. 2016. PMID: 27216195 Free PMC article. Clinical Trial.
References
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- Hall SJ, Klotz L, Pantuck AJ, George DJ, Whitmore JB, Frohlich MW, Sims RB. “Integrated safety data from 4 randomized, double-blind, controlled trials of autologous cellular immunotherapy with sipuleucel-T in patients with prostate cancer.”. J Urol. 2011;186:877–81. doi: 10.1016/j.juro.2011.04.070. - DOI - PubMed
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