Evidence map›Paper›PMID 42554864›Full record

ArticleBreast cancer research and treatment2026

First-line treatment patterns and real-world survival outcomes in PD-L1-negative locally recurrent inoperable or metastatic triple-negative breast cancer in the United States.

Tiffany A Traina, Elizabeth Serra, Jerome Bedard, Mohira Levesque-Leroux, Patrick Gagnon-Sanschagrin, Annie Guérin, Silke Guenther, George Joseph, Victoria Guan, Jonathan Salcedo

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Article in Breast cancer research and treatment, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Tiffany A TrainaDepartment of Medicine, Evelyn H. Lauder Breast Center, Memorial Sloan Kettering Cancer Center, New York, NY, USA. trainat@mskcc.org.
Elizabeth SerraAnalysis Group ULC, Montréal, QC, Canada.
Jerome BedardAnalysis Group ULC, Montréal, QC, Canada.
Mohira Levesque-LerouxAnalysis Group ULC, Montréal, QC, Canada.
Patrick Gagnon-SanschagrinAnalysis Group ULC, Montréal, QC, Canada.
Annie GuérinAnalysis Group ULC, Montréal, QC, Canada.
Silke GuentherBioNTech SE, Mainz, Germany.
George JosephBioNTech US, Inc., Cambridge, MA, USA.
Victoria GuanBioNTech US, Inc., Cambridge, MA, USA.
Jonathan SalcedoBioNTech US, Inc., Cambridge, MA, USA.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

purposeContemporary real-world data on treatment patterns and clinical outcomes in patients with programmed death ligand 1 (PD-L1)-negative locally recurrent inoperable or metastatic triple-negative breast cancer (lr/mTNBC) are sparse. We describe first-line (1L) systemic therapies and real-world survival outcomes in this population in the United States (US).

methodsAdults with PD-L1-negative lr/mTNBC initiating 1L systemic treatment in the US were identified using the Komodo Research Data (KRD+; 1/1/2016-12/31/2023). Treatment patterns, including treatment durations and sequences from 1L through three lines of therapy, real-world overall survival (rwOS) and progression-free survival (rwPFS) from 1L, were analyzed. rwOS and rwPFS were summarized using Kaplan-Meier methods in subgroups of patients with ≥ 18 months and ≥ 6 months of potential follow-up, respectively.

resultsOverall, 929 patients were included (median age 59.0 years, 60.1% White, 26.4% Black or African American, 64.9% commercially insured). Most common 1L treatments included cyclophosphamide + doxorubicin-based regimens (28.1%), capecitabine (12.7%), and paclitaxel (10.4%); 44.5% were observed to receive a second-line treatment, and 16.0% a third-line treatment. Treatment sequences were heterogeneous, with 329 unique sequences captured. Median rwOS and rwPFS (95% confidence interval) were 12.2 (10.7, 14.4) months and 4.7 (4.5, 5.2) months, respectively.

conclusionIn this large real-world US cohort of patients with PD-L1-negative lr/mTNBC, 1L treatment regimens were highly heterogeneous and often diverged from guideline recommendations. Despite treatment, survival outcomes remain poor within this patient population. These findings highlight the need for more effective therapeutic options for this population.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsB7-H1 AntigenNeoplasm Recurrence, LocalTriple Negative Breast NeoplasmsAdultAgedFemaleHumansKaplan-Meier EstimateMiddle AgedNeoplasm MetastasisTreatment OutcomeUnited StatesB7-H1 AntigenCD274 protein, humanBreast cancerOverall survivalProgressionTreatment patternsTriple-negative breast cancer

Identifiers

PMID42554864
PMCPMC13442314

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.