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Circulating CD8+CD28- suppressor T cells tied to poorer prognosis among metastatic breast cancer patients receiving adoptive T-cell therapy: A cohort study.

Publication ,  Journal Article
Song, Q; Ren, J; Zhou, X; Wang, X; Song, G; Hobeika, A; Yuan, Y; Lyerly, HK
Published in: Cytotherapy
January 2018

BACKGROUND AIMS: This study aimed to determine the prognostic value of circulating CD8+CD28- T lymphocytes among breast cancer patients treated with adoptive T-lymphocyte immunotherapy after chemotherapy. METHODS: Two hundred and thirty-two breast cancer patients underwent adoptive T-cell immunotherapy. Circulating CD8+CD28- proportion was measured by flow cytometry. Median proportion of CD8+CD28- was 24.2% and set as the categorical cutoff value for further analysis. The median survival was estimated by Kaplan-Meier curve, with difference detection and hazard ratio estimation by log-rank test and Cox hazard proportion regression model. RESULTS: With adoptive T-cell therapy, patients with higher CD8+CD28- levels experienced median progression-free and overall survival of 7.1 months and 26.9 months, respectively-significantly shorter than patients with lower levels (11.8 and 36.2 months). CD8+CD28- proportion >24.2% demonstrated a hazard ratio (HR) of 2.06 (95% confidence interval [CI] 1.31-3.12) for progression and an HR of 1.97 (95% CI 1.06-3.67) for death. Among patients who had received previous first-line chemotherapy, CD8+CD28- proportion >24.2% demonstrated an HR of 2.66 (95% CI 1.45-4.88) for progression. Among patients exposed to previous second-line or higher chemotherapy, CD8+CD28- proportion >24.2% demonstrated a 486% higher risk for death (HR = 5.86, 95% CI 1.77-19.39). A 1% increase in suppressive T cells was associated with a 5% increased risk of death. DISCUSSION: Elevated peripheral blood CD8+CD28- was associated with poorer prognosis for metastatic breast cancer, especially for higher risk of progression among patients with first-line chemotherapy and higher risk of death among patients with more than second-line chemotherapy.

Duke Scholars

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Published In

Cytotherapy

DOI

EISSN

1477-2566

Publication Date

January 2018

Volume

20

Issue

1

Start / End Page

126 / 133

Location

England

Related Subject Headings

  • Progression-Free Survival
  • Prognosis
  • Multivariate Analysis
  • Middle Aged
  • Immunotherapy, Adoptive
  • Immunology
  • Humans
  • Female
  • Cohort Studies
  • CD8-Positive T-Lymphocytes
 

Citation

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MLA
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Song, Q., Ren, J., Zhou, X., Wang, X., Song, G., Hobeika, A., … Lyerly, H. K. (2018). Circulating CD8+CD28- suppressor T cells tied to poorer prognosis among metastatic breast cancer patients receiving adoptive T-cell therapy: A cohort study. Cytotherapy, 20(1), 126–133. https://doi.org/10.1016/j.jcyt.2017.08.018
Song, Qingkun, Jun Ren, Xinna Zhou, Xiaoli Wang, Guohong Song, Amy Hobeika, Yanhua Yuan, and Herbert Kim Lyerly. “Circulating CD8+CD28- suppressor T cells tied to poorer prognosis among metastatic breast cancer patients receiving adoptive T-cell therapy: A cohort study.Cytotherapy 20, no. 1 (January 2018): 126–33. https://doi.org/10.1016/j.jcyt.2017.08.018.
Song, Qingkun, et al. “Circulating CD8+CD28- suppressor T cells tied to poorer prognosis among metastatic breast cancer patients receiving adoptive T-cell therapy: A cohort study.Cytotherapy, vol. 20, no. 1, Jan. 2018, pp. 126–33. Pubmed, doi:10.1016/j.jcyt.2017.08.018.
Song Q, Ren J, Zhou X, Wang X, Song G, Hobeika A, Yuan Y, Lyerly HK. Circulating CD8+CD28- suppressor T cells tied to poorer prognosis among metastatic breast cancer patients receiving adoptive T-cell therapy: A cohort study. Cytotherapy. 2018 Jan;20(1):126–133.
Journal cover image

Published In

Cytotherapy

DOI

EISSN

1477-2566

Publication Date

January 2018

Volume

20

Issue

1

Start / End Page

126 / 133

Location

England

Related Subject Headings

  • Progression-Free Survival
  • Prognosis
  • Multivariate Analysis
  • Middle Aged
  • Immunotherapy, Adoptive
  • Immunology
  • Humans
  • Female
  • Cohort Studies
  • CD8-Positive T-Lymphocytes