Literature DB >> 28688082

Circulating myeloid-derived suppressor cells increase in patients undergoing neo-adjuvant chemotherapy for breast cancer.

Robert Wesolowski1, Megan C Duggan2, Andrew Stiff2, Joseph Markowitz2,3, Prashant Trikha2, Kala M Levine2, Lynn Schoenfield4, Mahmoud Abdel-Rasoul5, Rachel Layman1,6, Bhuvaneswari Ramaswamy1, Erin R Macrae1, Maryam B Lustberg1, Raquel E Reinbolt1, Ewa Mrozek1, John C Byrd2, Michael A Caligiuri2, Thomas A Mace2, William E Carson7.   

Abstract

This study sought to evaluate whether myeloid-derived suppressor cells (MDSC) could be affected by chemotherapy and correlate with pathologic complete response (pCR) in breast cancer patients receiving neo-adjuvant chemotherapy. Peripheral blood levels of granulocytic (G-MDSC) and monocytic (M-MDSC) MDSC were measured by flow cytometry prior to cycle 1 and 2 of doxorubicin and cyclophosphamide and 1st and last administration of paclitaxel or paclitaxel/anti-HER2 therapy. Of 24 patients, 11, 6 and 7 patients were triple negative, HER2+ and hormone receptor+, respectively. 45.8% had pCR. Mean M-MDSC% were <1. Mean G-MDSC% and 95% confidence intervals were 0.88 (0.23-1.54), 5.07 (2.45-7.69), 9.32 (4.02-14.61) and 1.97 (0.53-3.41) at draws 1-4. The increase in G-MDSC by draw 3 was significant (p < 0.0001) in all breast cancer types. G-MDSC levels at the last draw were numerically lower in patients with pCR (1.15; 95% CI 0.14-2.16) versus patients with no pCR (2.71; 95% CI 0-5.47). There was no significant rise in G-MDSC from draw 1 to 3 in African American patients, and at draw 3 G-MDSC levels were significantly lower in African Americans versus Caucasians (p < 0.05). It was concluded that G-MDSC% increased during doxorubicin and cyclophosphamide therapy, but did not significantly differ between patients based on pathologic complete response.

Entities:  

Keywords:  Breast cancer; Chemotherapy; Cytokines; Myeloid-derived suppressor cells

Mesh:

Substances:

Year:  2017        PMID: 28688082      PMCID: PMC5647220          DOI: 10.1007/s00262-017-2038-3

Source DB:  PubMed          Journal:  Cancer Immunol Immunother        ISSN: 0340-7004            Impact factor:   6.968


  28 in total

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