| dc.contributor | Vall d'Hebron Barcelona Hospital Campus |
| dc.contributor.author | PERNAS SIMON, SONIA |
| dc.contributor.author | Pascual, Tomás |
| dc.contributor.author | Villacampa Javierre, Guillermo |
| dc.contributor.author | Oliveira, Mafalda |
| dc.contributor.author | Escriva de Romani, Santiago |
| dc.contributor.author | Paré, Laia |
| dc.contributor.author | Nuciforo, Paolo |
| dc.date.accessioned | 2025-11-04T12:08:38Z |
| dc.date.available | 2025-11-04T12:08:38Z |
| dc.date.issued | 2025-09 |
| dc.identifier.citation | Pascual T, Villacampa G, Oliveira M, Escrivá-de-Romaní S, Pernas S, Paré L, et al. Palbociclib and trastuzumab for HER2-positive metastatic breast cancer: final overall survival results of cohort A and B of SOLTI-1303-PATRICIA trial. ESMO Open. 2025 Sep;10(9):105572. |
| dc.identifier.issn | 2059-7029 |
| dc.identifier.uri | http://hdl.handle.net/11351/14011 |
| dc.description | HR-positive/HER2-positive; Biomarkers; Gene expression profiling |
| dc.description.abstract | Background
The SOLTI-1303-PATRICIA trial (NCT02448420) is a phase II study investigating palbociclib and trastuzumab, with or without endocrine therapy, in hormone receptor (HR)-positive/human epidermal growth factor receptor 2 (HER2)-positive metastatic breast cancer (MBC). This manuscript presents final overall survival (OS) results and biomarker analyses.
Patients and methods
Patients previously treated with trastuzumab and two to four regimens were eligible. For estrogen receptor (ER)-negative disease (cohort A), patients received palbociclib and trastuzumab. For ER-positive disease, patients were randomized 1 : 1 to cohort B1 (no additional therapy) or B2 (letrozole). OS and long-term progression-free survival (PFS) were pre-defined secondary endpoints. Kaplan–Meier curves and stratified Cox models were used.
Results
Among 71 patients, median OS was 29.8 months [95% confidence interval (CI) 20.9-38.0 months]; 4-year OS rates were 13.3% (A), 35.7% (B1), and 32.3% (B2). PAM50 luminal subtypes showed better OS than non-luminal subtypes (38.0 versus 26.6 months). Exploratory biomarker analyses found luminal-related genes associated with better long-term survival, while basal and proliferation-related genes were linked to resistance. Higher luminal A, luminal B, and previously reported chemo-endocrine scores correlated with favorable prognoses.
Conclusions
These findings highlight the relevance of gene expression profiling in HER2-positive breast cancer and support biomarker-driven patient selection. Long-term PATRICIA results validate the potential of non-chemotherapy-based approaches in HR-positive/HER2-positive MBC. |
| dc.language.iso | eng |
| dc.publisher | Elsevier |
| dc.relation.ispartofseries | ESMO Open;10(9) |
| dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 International |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ |
| dc.source | Scientia |
| dc.subject | Metàstasi |
| dc.subject | Mama - Càncer - Tractament |
| dc.subject | Quimioteràpia combinada |
| dc.subject | Marcadors tumorals |
| dc.subject.mesh | Breast Neoplasms |
| dc.subject.mesh | /drug therapy |
| dc.subject.mesh | Antineoplastic Combined Chemotherapy Protocols |
| dc.subject.mesh | Neoplasm Metastasis |
| dc.subject.mesh | Biomarkers, Tumor |
| dc.title | Palbociclib and trastuzumab for HER2-positive metastatic breast cancer: final overall survival results of cohort A and B of SOLTI-1303-PATRICIA trial |
| dc.type | info:eu-repo/semantics/article |
| dc.identifier.doi | 10.1016/j.esmoop.2025.105572 |
| dc.subject.decs | neoplasias de la mama |
| dc.subject.decs | /farmacoterapia |
| dc.subject.decs | protocolos de quimioterapia antineoplásica combinada |
| dc.subject.decs | metástasis neoplásica |
| dc.subject.decs | marcadores tumorales |
| dc.relation.publishversion | https://doi.org/10.1016/j.esmoop.2025.105572 |
| dc.type.version | info:eu-repo/semantics/publishedVersion |
| dc.audience | Professionals |
| dc.contributor.organismes | Institut Català de la Salut |
| dc.contributor.authoraffiliation | [Pascual T] SOLTI Cancer Research Group, Barcelona, Spain. Department of Medical Oncology, Cancer Institute and Blood Disorders, Hospital Clínic de Barcelona, Barcelona, Spain. Translational Genomics and Targeted Therapies in Solid Tumors, August Pi I Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain. Medicine Department, University of Barcelona, Barcelona, Spain. [Villacampa G] SOLTI Cancer Research Group, Barcelona, Spain. Statistics Unit, Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. [Oliveira M, Escrivá-de-Romaní S] SOLTI Cancer Research Group, Barcelona, Spain. Servei d’Oncologia Mèdica, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Breast Cancer Group, Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. [Pernas S] SOLTI Cancer Research Group, Barcelona, Spain. Institut Catala d’Oncologia-IDIBELL, L’Hospitalet, Barcelona, Spain. [Paré L] SOLTI Cancer Research Group, Barcelona, Spain. Reveal Genomics, Barcelona, Spain. [Nuciforo P] Molecular Oncology Group, Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain |
| dc.identifier.pmid | 40896880 |
| dc.identifier.wos | 001568022300003 |
| dc.rights.accessrights | info:eu-repo/semantics/openAccess |