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Treatment patterns and clinical outcomes according to PD-L1 status in >2000 patients with early-stage or metastatic triple-negative breast cancer treated in the real-world setting: VANESSA study results

  • Lazar Popovic(corresponding author)
    ,
  • Romualdo Barroso-Sousa
    ,
  • Nagi S. El Saghir
    ,
  • Rebecca Dent
    ,
  • Sitki Tuzlali
    ,
  • Saad Akhtar
*Corresponding author for this work
  • Faculty of Medicine, University of Novi Sad
    ,
  • Rede Américas
    ,
  • American University of Beirut
    ,
  • National Cancer Centre Singapore
    ,
  • Tuzlali Pathology Laboratory
    ,
  • King Faisal Specialist Hospital and Research Center
Research Output:
Contribution to journal
Article
Peer-review

Open access

Publication Information

Output type

Research Output:
Contribution to journal
Article
Peer-review

Original language

English

Article number

104720

Journal (Volume, Issue Number)

Breast (Volume 86)

Publication milestones

  • Published - 04/2026

Publication status

Published - 04/2026

ISSN

0960-9776

Publication IDs

  • Scopus: 105029637889

Abstract

Background: The prognostic effect of PD-L1 status in triple-negative breast cancer (TNBC) is uncertain and little is known about PD-L1-positive prevalence and outcomes in the real-world setting. Patients and methods: The multicentre retrospective observational VANESSA study evaluated the prevalence and impact of PD-L1-positive status in 2054 patients receiving systemic therapy for early-stage or metastatic (e/m)TNBC between 2014 and 2017. PD-L1 expression was assessed locally and centrally on archival samples. Descriptive analyses of demographic and clinicopathological characteristics, treatment patterns and clinical outcomes (extracted from patients’ medical records) according to PD-L1 status were prespecified. Results: Among 1902 patients with eTNBC, 681 (36%) received neoadjuvant chemotherapy and 1261 (66%) adjuvant chemotherapy. Demographic characteristics were generally similar regardless of PD-L1 status, but lower-risk tumour characteristics were more common in the PD-L1-positive subgroup. Invasive disease-free and overall survival were more favourable in PD-L1-positive eTNBC. In the mTNBC cohort, 120/145 (83%) patients had de novo mTNBC. Median progression-free survival on first-line treatment was 7.6 months (95% CI: 4.1–15.0) in PD-L1-positive mTNBC (n = 30) and 4.9 months (95% CI: 3.6–6.1) in PD-L1-negative mTNBC (n = 83). Conclusion: In eTNBC and mTNBC, PD-L1-positive status was associated with more favourable long-term outcomes, possibly due to tumour-intrinsic characteristics and/or the host immune response. The high proportion with de novo mTNBC may suggest enrolment bias and/or geographic variations in stage at diagnosis.

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