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Circulating T cell subsets are associated with clinical outcome of anti-VEGF-based 1st-line treatment of metastatic colorectal cancer patients: a prospective study with focus on primary tumor sidedness
B. Bencsikova, E. Budinska, I. Selingerova, K. Pilatova, L. Fedorova, K. Greplova, R. Nenutil, D. Valik, R. Obermannova, MA. Sheard, L. Zdrazilova-Dubska,
Language English Country Great Britain
Document type Journal Article
Grant support
AZV 16-31966A
Ministerstvo Zdravotnictví Ceské Republiky (CZ)
AZV 16-31966A
Ministerstvo Zdravotnictví Ceské Republiky
DRO 00209805
Ministerstvo Zdravotnictví Ceské Republiky
DRO 00209805
Ministerstvo Zdravotnictví Ceské Republiky
AZV 16-31966A
Ministerstvo Zdravotnictví Ceské Republiky
DRO 00209805
Ministerstvo Zdravotnictví Ceské Republiky
AZV 16-31966A
Ministerstvo Zdravotnictví Ceské Republiky
LO1413
Ministerstvo Školství, Mládeže a Tělovýchovy
LM2015089
Ministerstvo Školství, Mládeže a Tělovýchovy
LM2015089
Ministerstvo Školství, Mládeže a Tělovýchovy
LO1413
Ministerstvo Školství, Mládeže a Tělovýchovy
NV16-31966A
MZ0
CEP Register
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- MeSH
- Adenocarcinoma blood drug therapy mortality pathology MeSH
- Bevacizumab administration & dosage therapeutic use MeSH
- T-Lymphocytes, Cytotoxic metabolism MeSH
- Progression-Free Survival MeSH
- Adult MeSH
- Angiogenesis Inhibitors administration & dosage therapeutic use MeSH
- Colorectal Neoplasms blood drug therapy mortality pathology MeSH
- Middle Aged MeSH
- Humans MeSH
- Neoplasm Metastasis drug therapy MeSH
- Survival Rate MeSH
- Biomarkers, Tumor metabolism MeSH
- Follow-Up Studies MeSH
- Lymphocyte Count MeSH
- Prospective Studies MeSH
- Proto-Oncogene Proteins p21(ras) analysis MeSH
- T-Lymphocytes, Regulatory metabolism MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Vascular Endothelial Growth Factor A antagonists & inhibitors MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
BACKGROUND: In a prospective study with long-term follow-up, we analyzed circulating T cell subsets in patients with metastatic colorectal cancer (mCRC) in the context of primary tumor sidedness, KRAS status, and clinical outcome. Our primary goal was to investigate whether baseline levels of circulating T cell subsets serve as a potential biomarker of clinical outcome of mCRC patients treated with an anti-VEGF-based regimen. METHODS: The study group consisted of 36 patients with colorectal adenocarcinoma who started first-line chemotherapy with bevacizumab for metastatic disease. We quantified T cell subsets including Tregs and CD8+ T cells in the peripheral blood prior to therapy initiation. Clinical outcome was evaluated as progression-free survival (PFS), overall survival (OS), and objective response rate (ORR). RESULTS: 1) mCRC patients with KRAS wt tumors had higher proportions of circulating CD8+ cytotoxic T cells among all T cells but also higher measures of T regulatory (Treg) cells such as absolute count and a higher proportion of Tregs in the CD4+ subset. 2) A low proportion of circulating Tregs among CD4+ cells, and a high CD8:Treg ratio at initiation of VEGF-targeting therapy, were associated with favorable clinical outcome. 3) In a subset of patients with primarily right-sided mCRC, superior PFS and OS were observed when the CD8:Treg ratio was high. CONCLUSIONS: The baseline level of circulating immune cells predicts clinical outcome of 1st-line treatment with the anti-VEGF angio/immunomodulatory agent bevacizumab. Circulating immune biomarkers, namely the CD8:Treg ratio, identified patients in the right-sided mCRC subgroup with favorable outcome following treatment with 1st-line anti-VEGF treatment.
Department of Laboratory Medicine Masaryk Memorial Cancer Institute Brno Czech Republic
Regional Centre for Applied Molecular Oncology Masaryk Memorial Cancer Institute Brno Czech Republic
References provided by Crossref.org
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