Event-free survival by residual cancer burden after neoadjuvant pembrolizumab + chemotherapy versus placebo + chemotherapy for early TNBC: Exploratory analysis from KEYNOTE-522.

Authors

null

Lajos Pusztai

Yale School of Medicine, Yale Cancer Center, New Haven, CT

Lajos Pusztai , Carsten Denkert , Joyce O'Shaughnessy , Javier Cortes , Rebecca Alexandra Dent , Heather L. McArthur , Sherko Kuemmel , Jonas C. S. Bergh , Yeon Hee Park , Rina Hui , Nadia Harbeck , Masato Takahashi , Michael Untch , Peter A. Fasching , Fatima Cardoso , Yalin Zhu , Wilbur Pan , Konstantinos Tryfonidis , Peter Schmid

Organizations

Yale School of Medicine, Yale Cancer Center, New Haven, CT, Institute of Pathology, Philipps-University Marburg and University Hospital Marburg, Marburg, Germany, Baylor University Medical Center, Texas Oncology, US Oncology Network, Dallas, TX, International Breast Cancer Center, Quironsalud Group, Barcelona, Spain and Universidad Europea de Madrid, Madrid, Spain, National Cancer Center Singapore, Duke–National University of Singapore Medical School, Singapore, Singapore, University of Texas Southwestern Medical Center, Dallas, TX, Breast Unit, Kliniken Essen-Mitte, Essen, Germany and Charité– Universitätsmedizin Berlin, Department of Gynecology with Breast Center, Berlin, Germany, Department of Oncology-Pathology, Karolinska Institutet and Breast Cancer Centre, Cancer Theme, Karolinska University Hospital, Karolinska Comprehensive Cancer Center, Stockholm, Sweden, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea, Westmead Breast Cancer Institute, Westmead Hospital and the University of Sydney, Sydney, NSW, Australia, Breast Center, LMU University Hospital, Munich, Germany, Hokkaido Cancer Center, Sapporo, Japan, Breast Cancer Center, Helios Klinikum Berlin-Buch, Berlin, Germany, University Hospital Erlangen, Comprehensive Cancer Center Erlangen-EMN, Erlangen, Germany, Champalimaud Clinical Center, Lisbon, Portugal, Oncology, Merck & Co., Inc., Kenilworth, NJ, Centre for Experimental Cancer Medicine, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom

Research Funding

Pharmaceutical/Biotech Company

Background: KEYNOTE-522 (NCT03036488) tested the benefit from adding pembrolizumab (pembro) to chemotherapy (chemo) in patients (pts) with early TNBC. The primary results showed statistically significant and clinically meaningful improvements in pCR and EFS with pembro.Prior studies have shown the prognostic value of the residual cancer burden (RCB) method to quantify the extent of residual disease after neoadjuvant chemo. In this exploratory analysis, we assessed EFS by RCB in KEYNOTE-522. Methods: 1174 pts with previously untreated, nonmetastatic, stage T1c/N1-2 or T2-4/N0-2 TNBC were randomized 2:1 to pembro 200 mg Q3W or placebo (pbo) given with 4 cycles of paclitaxel + carboplatin, then 4 cycles of doxorubicin or epirubicin + cyclophosphamide. After definitive surgery, pts received pembro or pbo for 9 cycles or until recurrence or unacceptable toxicity. Dual primary endpoints are pCR and EFS. RCB was assessed by the local pathologist at the time of surgery. The association between RCB categories (RCB-0, -1, -2, -3, corresponding to increasingly larger residual cancer) and EFS was assessed based on a Cox regression model with treatment as a covariate. Results: Median follow-up was 39.1 months at data cutoff (23 MAR 2021). Pembro shifted RCB to lower categories across the entire spectrum (Table). The HRs (95% CI) for EFS were 0.70 (0.38 - 1.31) for RCB-0 (equivalent to pCR), 0.92 (0.39 - 2.20) for RCB-1, 0.52 (0.32 - 0.82) for RCB-2, and 1.24 (0.69 - 2.23) for RCB-3. The most common EFS event in both arms was distant recurrence, which occurred in fewer pts in the pembro arm in all RCB categories. Conclusions: Increased RCB score was associated with worse EFS. Pts with residual disease had lower RCB values in the pembro arm, including fewer pts with RCB-3. Pembro + chemo prolonged EFS vs chemo alone in the RCB-0, -1, and -2 categories; the small sample size limits interpretation in the RCB-3 category. The small subset of pts with extensive residual disease (RCB-3) in both arms, 5.1% and 6.7%, respectively, had a poor prognosis. These results highlight the importance of neoadjuvant treatment with pembro for improving survival in pts with early TNBC, and identified a subset of pts for whom additional therapies will be needed. Clinical trial information: NCT03036488.

RCB-0
Pembro
RCB-0
Pbo
RCB-1
Pembro
RCB-1
Pbo
RCB-2
Pembro
RCB-2
Pbo
RCB-3
Pembro
RCB-3
Pbo
Frequency,
n/N (%)
497/784 (63.4)
219/390 (56.2)
69/784 (8.8)
45/390 (11.5)
145/784 (18.5)
79/390 (20.3)
40/784 (5.1)
26/390 (6.7)
Any EFS event,
n/N (%)
26/497 (5.2)
16/219 (7.3)
12/69 (17.4)
9/45 (20.0)
37/145 (25.5)
35/79 (44.3)
29/40 (72.5)
18/26 (69.2)
Distant recurrence,
n (%)
16 (3.2)
12 (5.5)
6 (8.7)
4 (8.9)
22 (15.2)
18 (22.8)
14 (35.0)
14 (53.8)
36-mo EFS, %
(95% CI)
94.7
(92.2 - 96.4)
92.6
(88.2 - 95.4)
83.8
(72.6 - 90.7)
84.4
(70.1 - 92.3)
75.7
(67.8 - 81.9)
55.9
(44.1 - 66.2)
26.2
(13.5 - 41.0)
34.6
(17.5 - 52.5)

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Abstract Details

Meeting

2022 ASCO Annual Meeting

Session Type

Oral Abstract Session

Session Title

Breast Cancer—Local/Regional/Adjuvant

Track

Breast Cancer

Sub Track

Neoadjuvant Therapy

Clinical Trial Registration Number

NCT03036488

Citation

J Clin Oncol 40, 2022 (suppl 16; abstr 503)

DOI

10.1200/JCO.2022.40.16_suppl.503

Abstract #

503

Abstract Disclosures