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Traina Talks TNBC Treatment Evolution

Caroline Seymour
Published: Friday, Mar 23, 2018

Tiffany A. Traina, MD
Tiffany A. Traina, MD
Data from the phase III EMBRACA trial showed the superiority in progression-free survival (PFS) with the PARP inhibitor talazoparib in patients with germline BRCA1/2-mutant metastatic HER2-negative breast cancer, including patients with triple-negative disease (TNBC).

on Breast Cancer, Tiffany A. Traina, MD, a medical oncologist at Memorial Sloan Kettering Cancer Center, discussed the potential for PARP inhibitors, as well as immunotherapy and antibody-drug conjugates, for the treatment of patients with TNBC.

OncLive: What advances have we seen in TNBC? 

Traina: There are 3 advances in TNBC I highlighted from the 2017 San Antonio Breast Cancer Symposium. The first are the data on the PARP inhibitor talazoparib in patients with metastatic disease and germline BRCA1/2 mutations. The second is the interest in immuno-oncology agents and checkpoint inhibitors. The third are the developments in antibody-drug conjugates and the encouraging results of sacituzumab govitecan (IMMU-132). This is the antibody-drug conjugate against Trop-2 that is conjugated to a metabolite of irinotecan.

What is the prevalence of BRCA mutations in TNBC? How have PARP inhibitors affected this population of patients?

The prevalence of germline BRCA mutations is difficult to fully understand because physicians are unclear what the ultimate denominator is. The data presented at the 2017 San Antonio Breast Cancer Symposium showed that there are patients who should undergo clinical genetic testing so they can be aware of their germline BRCA status.

At that meeting, we also saw the data from EMBRACA, a randomized phase III trial of the oral PARP inhibitor talazoparib. While the study populations were slightly different, the hazard ratios were quite comparable in terms of the prevalence of estrogen receptor–positive disease versus TNBC and the portion of patients treated in the first-line versus later line setting. In terms of toxicity, we saw a bit more hematologic toxicity with olaparib compared with chemotherapy. 

Will these data encourage the development of more PARP inhibitors in the space?

There is certainly the opportunity to explore other PARP inhibitors, but we need to understand which patients have germline mutations, as they are the likely candidates for this treatment. We also have trials in development that are looking at the role of PARP inhibitors in non-BRCA germline mutations and BRCA somatic mutations. We need to remind ourselves that these clinical trials underwent central testing; there were specific germline mutations that counted as pathogenic mutations. 

Where do you see immunotherapy fitting into the TNBC treatment paradigm?

There is activity with PD-L1 inhibitors. Prior to the 2017 San Antonio Breast Cancer Symposium, we saw a small signal; several studies reported approximately a 20% to 25% response rate in the first-line setting. It seems that single-agent checkpoint inhibitors have greater activity in the frontline setting. We are most excited by the tail of the curve, which shows that there are some select patients who have durable responses. We would like to think there is an ideal biomarker to select those patients, but I haven't seen reports of that in trials to date. In terms of PD-L1 status, we often don't see dramatic differences in response.

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View Conference Coverage
Online CME Activities
TitleExpiration DateCME Credits
Community Practice Connections™: How Do We Leverage PARP Inhibition Strategies in the Contemporary Treatment of Breast Cancer?May 31, 20191.5
Community Practice Connections™: A Better Way to Stop Pain: Paths Toward Responsible Postsurgical Pain Management for Patients With Breast CancerMay 31, 20191.5
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