Pascual T, Villacampa G, Oliveira M, Escrivá-de-Romaní S, Pernas S, Paré L, Adamo B, Martínez E, Cortés J, Perelló A, Galan M, Melé M, Villanueva L, Gonzalez-Rodriguez M, Tolosa P, González-Farré B, Galván P, Canes J, Nuciforo P, Ferrero-Cafiero J M, González-Farré X, Villagrasa P, Prat A, Ciruelos E
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.
SOLTI Cancer Research Group, Barcelona, Spain; Statistics Unit, Vall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain.
ESMO Open. 2025 Sep 1;10(9):105572. doi: 10.1016/j.esmoop.2025.105572.
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 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.
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.
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.
SOLTI-1303-PATRICIA试验(NCT02448420)是一项II期研究,旨在调查哌柏西利和曲妥珠单抗联合或不联合内分泌治疗用于激素受体(HR)阳性/人表皮生长因子受体2(HER2)阳性转移性乳腺癌(MBC)的疗效。本手稿展示了最终的总生存期(OS)结果和生物标志物分析。
曾接受曲妥珠单抗治疗且接受过两至四种治疗方案的患者符合条件。对于雌激素受体(ER)阴性疾病(A组),患者接受哌柏西利和曲妥珠单抗治疗。对于ER阳性疾病,患者按1:1随机分组至B1组(不接受额外治疗)或B2组(来曲唑)。OS和长期无进展生存期(PFS)是预先定义的次要终点。采用Kaplan-Meier曲线和分层Cox模型。
71例患者中,中位OS为29.8个月[95%置信区间(CI)20.9 - 38.0个月];4年OS率分别为13.3%(A组)、35.7%(B1组)和32.3%(B2组)。PAM50管腔亚型的OS优于非管腔亚型(38.0个月对26.6个月)。探索性生物标志物分析发现,与管腔相关的基因与更好的长期生存相关,而基底和增殖相关基因与耐药相关。较高的管腔A、管腔B以及先前报道的化疗 - 内分泌评分与良好预后相关。
这些发现突出了基因表达谱在HER2阳性乳腺癌中的相关性,并支持基于生物标志物的患者选择。PATRICIA试验的长期结果验证了基于非化疗方法在HR阳性/HER2阳性MBC中的潜力。