A phase Ib trial evaluating the safety, efficacy, and immunologic effects of pembrolizumab plus paclitaxel or flat-dose capecitabine in 1st/2nd line metastatic triple-negative breast cancer

Author:

Page David1ORCID,Pucilowska Joanna1,Chun Brie2ORCID,Kim Isaac1,Sanchez Katherine1,Moxon Nicole1ORCID,Mellinger Staci1,Wu Yaping1,Koguchi Yoshinobu1,Conrad Valerie1,Redmond William1ORCID,Sun Zhaoyu1,Martel Maritza1,Campbell Mary1,Conlin Alison1,Acheson Anupama1,Basho Reva3,McAndrew Philomena3,El-Masry Mary3,Park Dorothy3,Bennetts Laura1,Seitz Robert4,Nielsen Tyler4ORCID,McGregor Kimberly4,Rajamanickam Venkatesh1,Bernard Brady1,Urba Walter1,McArthur Heather5ORCID

Affiliation:

1. Earle A. Chiles Research Institute / Providence Cancer Institute

2. Providence Portland Medical Center

3. Cedars Sinai Medical Center

4. Oncocyte Corporation

5. University of Texas Southwestern Medical Center

Abstract

Abstract Background Chemoimmunotherapy with anti-programmed cell death 1/ligand 1 and cytotoxic chemotherapy is a promising therapeutic modality for women with triple-negative breast cancer, but questions remain regarding optimal chemotherapy backbone and biomarkers for patient selection. Methods We report final outcomes from a phase Ib trial evaluating pembrolizumab (200mg IV every 3 weeks) with either weekly paclitaxel (80mg/m2 weekly) or flat-dose capecitabine (2000mg orally twice daily for 7 days of every 14-day cycle) in the 1st /2nd line setting. The primary endpoint was safety (receipt of 2 cycles without grade III/IV toxicities requiring discontinuation or ≥ 21-day delays). The secondary endpoint was efficacy (week 12 objective response rate). Exploratory aims were to characterize immunologic effects of treatment over time, and to evaluate novel biomarkers. Results Both regimens met the pre-specified safety endpoint (paclitaxel: 87%; capecitabine: 100%). Objective response rate was 29% for pembrolizumab/paclitaxel and 43% for pembrolizumab/capecitabine. Partial responses were observed in two subjects with chemo-refractory metaplastic carcinoma (both in capecitabine arm). Both regimens were associated with significant peripheral leukocyte contraction over time. Response was associated with clinical PD-L1 score, non-receipt of prior chemotherapy, and the H&E stromal tumor infiltrating lymphocyte score, but also by a novel 27 gene IO score and spatial biomarkers (lymphocyte spatial skewness). Conclusions Pembrolizumab with paclitaxel or capecitabine is safe and clinically active. Both regimens were lymphodepleting, highlighting the competing immunostimulatory versus lymphotoxic effects of cytotoxic chemotherapy. Further exploration of the IO score and spatial TIL biomarkers is warranted. Trial registration: NCT02734290

Publisher

Research Square Platform LLC

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