Systemic inflammatory status predict the outcome of k-RAS WT metastatic colorectal cancer patients receiving the thymidylate synthase poly-epitope-peptide anticancer vaccine

TSPP is an anticancer poly-epitope peptide vaccine to thymidylate synthase, recently investigated in the multi-arm phase Ib TSPP/VAC1 trial. TSPP vaccination induced immune-biological effects and showed antitumor activity in metastatic colorectal cancer (mCRC) patients and other malignancies. Progre...

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Veröffentlicht in:Oncotarget 2018-04, Vol.9 (29), p.20539-20554
Hauptverfasser: Correale, Pierpaolo, Botta, Cirino, Staropoli, Nicoletta, Nardone, Valerio, Pastina, Pierpaolo, Ulivieri, Cristina, Gandolfo, Claudia, Baldari, Tatiana Cosima, Lazzi, Stefano, Ciliberto, Domenico, Giannicola, Rocco, Fioravanti, Antonella, Giordano, Antonio, Zappavigna, Silvia, Caraglia, Michele, Tassone, Pierfrancesco, Pirtoli, Luigi, Cusi, Maria Grazia, Tagliaferri, Pierosandro
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Sprache:eng
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Zusammenfassung:TSPP is an anticancer poly-epitope peptide vaccine to thymidylate synthase, recently investigated in the multi-arm phase Ib TSPP/VAC1 trial. TSPP vaccination induced immune-biological effects and showed antitumor activity in metastatic colorectal cancer (mCRC) patients and other malignancies. Progression-free and overall survival of 41 mCRC patients enrolled in the study correlated with baseline levels of CEA, immune-inflammatory markers (neutrophil/lymphocyte ratio, CRP, ESR, LDH, ENA), IL-4 and with post-treatment change in p-ANCA and CD56 CD16 NKs ( < 0.04). A subset of 19 patients with activating k-ras mutations showed a different immune-inflammatory response to TSPP as compared to patients with k-ras/wt and a worse outcome in term of PFS ( = 0.048). In patients with k-ras/mut, inflammatory markers lost their predictive value and their survival directly correlated with the baseline levels of IL17/A over the median value ( = 0.01). These results provide strong hints for the design of further clinical trials aimed to test TSPP vaccination in mCRC patients.
ISSN:1949-2553
1949-2553
DOI:10.18632/oncotarget.24993