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
| Author | Affiliation | |
|---|---|---|
Popovic, Lazar | University of Novi Sad | RS |
Barroso-Sousa, Romualdo | Brasilia Hospital | BR |
El Saghir, Nagi S | American University of Beirut Medical Center | LB |
Dent, Rebecca | National Cancer Center Singapore | SG |
Tuzlali, Sitki | Tuzlali Pathology Laboratory | TR |
Akhtar, Saad | King Faisal Specialist Hospital and Research Centre | SA |
LT | ||
Eglitis, Janis | University of Latvia | LV |
Doval, Dinesh C | Rajiv Gandhi Cancer Institute and Research Centre | IN |
Castaneda, Carlos A | Universidad Científica del Sur | PE |
Zirtiloglu, Alisan | F. Hoffmann-La Roche Ltd | CH |
Hartleben, Götz | Roche Pharma AG | DE |
Deurloo, Regula | F. Hoffmann-La Roche Ltd | CH |
Toro, Paula | Roche Diagnostics International AG | CH |
Estaytieh, Iman | Roche Lebanon SARL | LB |
Weber, Enya | Roche Pharma AG | DE |
Mouta, João | Roche Farmacêutica Química | PT |
D'Arrigo, Corrado | Poundbury Cancer Institute for Personalised Medicine | GB |
| Date | Volume | Start Page | End Page |
|---|---|---|---|
2026-02-05 | 86 | 1 | 9 |
Art. no. 104720
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.
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.
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).
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.
| URI | Access Rights |
|---|---|
| PMC | Viso teksto dokumentas (atviroji prieiga) / Full Text Document (Open Access) |
| https://www.sciencedirect.com/science/article/pii/S0960977626000305?via%3Dihub | Viso teksto dokumentas (atviroji prieiga) / Full Text Document (Open Access) |
| https://hdl.handle.net/20.500.12512/257609 |
| Name |
|---|
Roche Holding |