Effects of neoadjuvant chemotherapy (NAC) on tumor infiltrating lymphocytes (TIL) and PD-L1 expression in the SWOG S0800 clinical trial.

Authors

null

Vasiliki Pelekanou

Yale School of Medicine, New Haven, CT

Vasiliki Pelekanou , William E. Barlow , Marie-Kristin von Wahlde , Brad Wasserman , Ying-Chun Lo , Daniel F. Hayes , Gabriel N. Hortobagyi , Julie Gralow , Debu Tripathy , Robert B. Livingston , Peggy Porter , Zeina A. Nahleh , David L. Rimm , Lajos Pusztai

Organizations

Yale School of Medicine, New Haven, CT, Cancer Research and Biostatistics, Seattle, WA, Universitätsklinikum Münster, Munchen, Germany, Yale University, New Haven, CT, University of Michigan Comprehensive Cancer Center, Ann Arbor, MI, The University of Texas MD Anderson Cancer Center, Houston, TX, Seattle Cancer Care Alliance, Seattle, WA, Arizona Cancer Center, Tucson, AZ, Fred Hutchinson Cancer Research Center, Seattle, WA, Texas Tech University Health Science Center, El Paso, TX, Yale Cancer Center, New Haven, CT

Research Funding

Other

Background: Higher baseline TILs and PD-L1 expression are associated with greater pathologic complete response (pCR) rates, but how chemotherapy affects these immune parameters is unknown. The goal of this study was to examine TIL and PD-L1 expression in pre- and post-NAC tumor specimens from the S0800 clinical trial that compared weekly nab-paclitaxel/bevacizumab + dose-dense doxorubicin and cyclophosphamide (AC) with nab-paclitaxel + AC as NAC for HER2-negative cases. Association between immune parameters, pCR and NAC-induced changes were tested using ER and NAC-arm adjusted logistic regression. Methods: TILs were assessed on H&E stained full sections of 120 pre- and 62 post-NAC tissues (tumor bed of pCR) including 59 matched samples. PD-L1 immunohistochemistry was performed using the FDA cleared 22C3 assay and results were available for 121 baseline and 43 matched post-NAC samples. Results: At baseline, the mean TIL count was 18%; 16% had no TILs and 9% had > 50% TILs. Higher baseline TILs were associated with higher pCR rate (p = 0.043, trend test p = 0.014) but there was no interaction with NAC arm. Post-NAC, the mean TIL counts was 11%; 5% had no TILs and 1.6% had > 50% TILs. In the matching post-NAC samples, the mean change was 15% decrease in TILs, but in 32% of cases TILs increased. Cases with residual disease (n=44) had lesser average decrease (p=0.029) than cases with pCR (n=15). The post-NAC decrease in TILs was also observed after excluding cases with pCR. At baseline, PD-L1 expression either in the stroma or on epithelial cells or in both was detected in 52 (43%) of 121 cases (5 tumor only, 29 stroma only, 18 tumor + stroma). Those with baseline PD-L1 expression had higher pCR (63% vs. 37%; p=0.008). Post-NAC, PD-L1 expression was seen in 14 of 43 (33%) cases (7 stroma only, 7 tumor + stroma). In the 39 matching pre- and post-NAC samples, PD-L1 expression was negative in both in 20, positive in both in 10 cases and 6 patients had PD-L1 expression at baseline but not in the post-NAC sample. Conclusions: TIL counts and PD-L1 expression generallydecreased, but in a minority of cases increased after NAC. The decrease in TIL was significantly greater in cases achieving pCR. Clinical trial information: NCT00856492

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Abstract Details

Meeting

2017 ASCO Annual Meeting

Session Type

Poster Discussion Session

Session Title

Breast Cancer—Local/Regional/Adjuvant

Track

Breast Cancer

Sub Track

Neoadjuvant Therapy

Clinical Trial Registration Number

NCT00856492

Citation

J Clin Oncol 35, 2017 (suppl; abstr 519)

DOI

10.1200/JCO.2017.35.15_suppl.519

Abstract #

519

Poster Bd #

119

Abstract Disclosures