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Poster display session: Breast cancer - early stage, locally advanced & metastatic, CNS tumours, Developmental therapeutics, Genitourinary tumours - prostate & non-prostate, Palliative care, Psycho-oncology, Public health policy, Sarcoma, Supportive care

5368 - Multiplex immunoassays analysis of plasma biomarker levels and response to neoadjuvant chemotherapy for locally advanced breast cancer

Date

22 Oct 2018

Session

Poster display session: Breast cancer - early stage, locally advanced & metastatic, CNS tumours, Developmental therapeutics, Genitourinary tumours - prostate & non-prostate, Palliative care, Psycho-oncology, Public health policy, Sarcoma, Supportive care

Topics

Cytotoxic Therapy;  Tumour Immunology

Tumour Site

Breast Cancer

Presenters

Jang Ho Cho

Citation

Annals of Oncology (2018) 29 (suppl_8): viii87-viii89. 10.1093/annonc/mdy271

Authors

J.H. Cho1, K. Park2, E. Lee2, Y. Kim1, S. Park1, S.E. Yoon1, K.K. Lee1, J.Y. Hur1, S.K. Lee3, J.E. Lee3, S.W. Kim3, S.J. Nam3, J. Yu3, J. Kim1, H.H. Jung4, Y.H. Park1

Author affiliations

  • 1 Division Of Hematology-oncology, Department Of Medicine, Samsung Medical Center Sungkyunkwan University School of Medicine, 135-710 - Seoul/KR
  • 2 Samsung Genome Institute, Samsung Medical Center Sungkyunkwan University School of Medicine, Seoul/KR
  • 3 Division Of Breast Surgery, Department Of Surgery, Samsung Medical Center Sungkyunkwan University School of Medicine, Seoul/KR
  • 4 Biomedical Research Institute, Samsung Medical Center Sungkyunkwan University School of Medicine, Seoul/KR

Resources

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Abstract 5368

Background

Neoadjuvant chemotherapy (NAC) has become as the preferred initial therapy for locally advanced breast cancer (LABC) patients. A pathologic complete response (pCR) following NAC correlates strongly with both prolonged disease-free survival and overall survival especially for patients with HER2+ or triple negative breast cancer (TNBC). A lot of modalities and molecular markers for assessing chemotherapy response have been evaluated; however, they have demonstrated only limited predictive value.

Methods

Plasma samples have been collected from 167 patients diagnosed with LABC and received NAC from month, year to month, year prospectively. Samples were collected three times from each patient, prior to NAC (pre-treatment), prior to second cycle of NAC (on-treatment), and after breast surgery (post-treatment). Samples were assayed by multiplex immunoassays for 45 biomarkers. Plasma biomarker levels using Cytokine/Chemokine/Growth Factor 45-Plex Human ProcartaPlexTM Panel were compared with pathologic treatment responses. pCR was defined as the absence of residual tumor both in breast and axillary lymph nodes. This study was approved by the Institutional Review Board of Samsung Medical Center (SMC 2014-11-015-017).

Results

A median age at diagnosis of the 167 patients was 42 (range, 23-68 years). Most of the patients were treated with anthracycline and taxane-based regimen including adriamycin with cyclophosphamide plus docetaxel (AC-T), or AC-T plus trastuzumab. The patients were divided into the following four groups: HR+/HER2- (n = 46, 28%), HR+/HER2 + (n = 26, 16%), HR-/HER2 + (n = 32, 19%), and TNBC (n = 63, 38%). Thirty four patients (20%) achieving a pCR were compared with 133 patients (80%) demonstrating no pCR. Several groups of biomarker expression, BDNF, bNGF, HGF, IFN-gamma, IL-18, IP-10, MCP-1, RANTES, and SCF, were significantly different among pre-treatment, on-treatment and post-treatment. Multivariate analysis on pCR showed that analysis using the multiplex panel has predictive power.

Conclusions

Plasma biomarkers including immune-cytokine may have a role to predict treatment response in the neoadjuvant setting.

Clinical trial identification

Legal entity responsible for the study

Samsung Medical Center.

Funding

Has not received any funding.

Editorial Acknowledgement

Disclosure

All authors have declared no conflicts of interest.

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