A 14-gene B-cell immune signature in early-stage triple-negative breast cancer (TNBC): a pooled analysis of seven studies

被引:9
作者
Conte, Benedetta [1 ,2 ]
Braso-Maristany, Fara [1 ,2 ,3 ]
Hernandez, Adela Rodriguez [1 ,2 ]
Pascual, Tomas [1 ,2 ,4 ]
Villacampa, Guillermo [3 ,4 ,5 ]
Schettini, Francesco [1 ,2 ,6 ]
Losada, Maria J. Vidal [1 ,2 ,4 ,6 ,7 ]
Segui, Elia [1 ,2 ,4 ]
Angelats, Laura [1 ,2 ]
Garcia-Fructuoso, Isabel [1 ,2 ]
Gomez-Bravo, Raquel [1 ,2 ]
Lorman-Carbo, Natalia [1 ]
Pare, Laia [3 ]
Marin-Aguilera, Mercedes [3 ]
Martinez-Saez, Olga [1 ,2 ]
Adamo, Barbara [1 ,2 ]
Sanfeliu, Esther [1 ,8 ]
Fratini, Beatrice [1 ]
Falato, Claudette [1 ,4 ]
Chic, Nuria [1 ,2 ]
Vivancos, Ana [3 ,9 ]
Villagrasa, Patricia [3 ]
Staaf, Johan [10 ]
Parker, Joel S. [11 ]
Perou, Charles M. [11 ,12 ]
Prat, Aleix [1 ,2 ,3 ,6 ,7 ]
机构
[1] August Pi i Sunyer Biomed Res Inst IDIBAPS, Translat Genom & Targeted Therapies Solid Tumors G, Barcelona, Spain
[2] Hosp Clin Barcelona, Canc Inst & Blood Dis, Barcelona, Spain
[3] Reveal Genom, Barcelona, Spain
[4] SOLTI Cooperat Grp, Barcelona, Spain
[5] Vall dHebron Inst Oncol, Oncol Data Sci, Barcelona, Spain
[6] Univ Barcelona, Dept Med, Barcelona, Spain
[7] Hosp QuironSalud, Inst Oncol IOB, Barcelona, Spain
[8] Hosp Clin Barcelona, Pathol Dept, Barcelona, Spain
[9] Vall dHebron Inst Oncol VHIO, Canc Genom Grp, Barcelona, Spain
[10] Lund Univ, Dept Lab Med, Div Translat Canc Res, Lund, Sweden
[11] Univ N Carolina, Dept Genet, Chapel Hill, NC USA
[12] Univ N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC USA
来源
EBIOMEDICINE | 2024年 / 102卷
关键词
Triple-negative breast cancer (TNBC); Pathological complete response (pCR); Event-free survival (EFS); Overall survival (OS); B-cell/immunoglobulin signature (IGG); Prognostic biomarkers; Predictive biomarkers; Gene expression; TUMOR-INFILTRATING LYMPHOCYTES; STANDARD NEOADJUVANT CHEMOTHERAPY; PATHOLOGICAL COMPLETE RESPONSE; RANDOMIZED PHASE-II; PROGNOSTIC VALUE; PREDICTIVE-VALUE; CARBOPLATIN; PACLITAXEL; RISK; DOXORUBICIN;
D O I
10.1016/j.ebiom.2024.105043
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Early -stage triple -negative breast cancer (TNBC) displays clinical and biological diversity. From a biological standpoint, immune infiltration plays a crucial role in TNBC prognosis. Currently, there is a lack of genomic tools aiding in treatment decisions for TNBC. This study aims to assess the effectiveness of a B -cell/ immunoglobulin signature (IGG) alone, or in combination with tumor burden, in predicting prognosis and treatment response in patients with TNBC. Methods Genomic and clinical data were retrieved from 7 cohorts: SCAN -B (N = 874), BrighTNess (n = 482), CALGB40603 (n = 389), METABRIC (n = 267), TCGA (n = 118), GSE58812 (n = 107), GSE21653 (n = 67). IGG and a risk score integrating IGG with tumor/nodal staging (IGG-Clin) were assessed for event -free survival (EFS) and overall survival (OS) in each cohort. Random effects model was used to derive pooled effect sizes. Association of IGG with pathological complete response (pCR) was assessed in CALGB-40603 and BrighTNess. Immune significance of IGG was estimated through CIBERSORTx and EcoTyper. Findings IGG was associated with improved EFS (pooled HR = 0.77, [95% CI = 0.70-0.85], I2 = 18%) and OS (pooled HR = 0.79, [0.73-0.85], I2 = 0%) across cohorts, and was predictive of pCR in CALGB-40603 (OR 1.25, [1.10-1.50]) and BrighTNess (OR 1.57 [1.25-1.98]). IGG-Clin was predictive of recurrence (pooled HR = 2.11, [1.75-2.55], I2 = 0%) and death (pooled HR = 1.99, 95% [0.84-4.73], I2 = 79%) across cohorts. IGG was associated with adaptive immune response at CIBERSORTx and EcoTyper analysis. Interpretation IGG is linked to improved prognosis and pCR in early -stage TNBC. The integration of IGG alongside tumor and nodal staging holds promise as an approach to identify patients benefitting from intensified or deintensified treatments. Agencia de Gesto d'Ajuts Universitaris i de Recerca, Instituto de Salud Carlos III, Fundacion Contigo, Asociacion Cancer de Mama Metastasico IV, Breast Cancer Research Foundation, RESCUER, Fundacion cientifica AECC and FSEOM. Copyright (c) 2024 The Author(s). Published by Elsevier B.V. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
引用
收藏
页数:15
相关论文
共 50 条
[31]   Neoadjuvant, Anthracycline-Free Chemotherapy with Carboplatin and Docetaxel in Triple-Negative, Early-Stage Breast Cancer: A Multicentric Analysis of Feasibility and Rates of Pathologic Complete Response [J].
Kern, Peter ;
Kalisch, Anne ;
Kolberg, Hans-Christian ;
Kimmig, Rainer ;
Otterbach, Friederich ;
von Minckwitz, Gunter ;
Sikov, William M. ;
Pott, Dirk ;
Kurbacher, Christian .
CHEMOTHERAPY, 2013, 59 (05) :387-394
[32]   Immunotherapy in Early-Stage Triple-Negative Breast Cancer: Where Are We Now and Where Are We Headed? [J].
Dixon-Douglas, Julia ;
Loi, Sherene .
CURRENT TREATMENT OPTIONS IN ONCOLOGY, 2023, 24 (08) :1004-1020
[33]   Homologous Recombination Deficiency (HRD) and BRCA 1/2 Gene Mutation for Predicting the Effect of Platinum-Based Neoadjuvant Chemotherapy of Early-Stage Triple-Negative Breast Cancer (TNBC): A Systematic Review and Meta-Analysis [J].
Chai, Yue ;
Chen, Yujie ;
Zhang, Di ;
Wei, Yuce ;
Li, Zhijun ;
Li, Qiao ;
Xu, Binghe .
JOURNAL OF PERSONALIZED MEDICINE, 2022, 12 (02)
[34]   Adjuvant addition of capecitabine to early-stage triple-negative breast cancer patients receiving standard chemotherapy: a meta-analysis [J].
Li, Yan ;
Zhou, Yidong ;
Mao, Feng ;
Lin, Yan ;
Zhang, Xiaohui ;
Shen, Songjie ;
Sun, Qiang .
BREAST CANCER RESEARCH AND TREATMENT, 2020, 179 (03) :533-542
[35]   Management of patients with early-stage triple-negative breast cancer following pembrolizumab-based neoadjuvant therapy: What are the evidences? [J].
Bonadio, Renata Colombo ;
Tarantino, Paolo ;
Testa, Laura ;
Punie, Kevin ;
Pernas, Sonia ;
Barrios, Carlos ;
Curigliano, Giuseppe ;
Tolaney, Sara M. ;
Barroso-Sousa, Romualdo .
CANCER TREATMENT REVIEWS, 2022, 110
[36]   A novel immune checkpoint-related gene signature for predicting overall survival and immune status in triple-negative breast cancer [J].
Liu, Jingyi ;
Ling, Yuwei ;
Su, Ning ;
Li, Yan ;
Tian, Siyuan ;
Hou, Bingxin ;
Luo, Shanquan ;
Zhao, Lina ;
Shi, Mei .
TRANSLATIONAL CANCER RESEARCH, 2022, 11 (01) :181-+
[37]   Predictors of Pathologic Complete Response with Neoadjuvant Chemo-Immunotherapy in Early-Stage Triple-Negative Breast Cancer [J].
Perry, Lauren M. ;
Sevilimedu, Varadan ;
Polidorio, Natalia ;
Abuhadra, Nour ;
Morrow, Monica ;
Plitas, George ;
Downs-Canner, Stephanie .
ANNALS OF SURGICAL ONCOLOGY, 2025, 32 (06) :3991-4001
[38]   A Novel Prognostic Model Based on the Serum Iron Level for Patients With Early-Stage Triple-Negative Breast Cancer [J].
Hua, Xin ;
Duan, Fangfang ;
Huang, Jiajia ;
Bi, Xiwen ;
Xia, Wen ;
Song, Chenge ;
Wang, Li ;
Jiang, Chang ;
Yuan, Zhongyu .
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, 2021, 9
[39]   Homologous recombination deficiency predicts the response to platinum-based neoadjuvant chemotherapy in early-stage triple-negative breast cancer patients: a systematic review and meta-analysis [J].
Zhang, Liulu ;
Chen, Yuanqi ;
Cheng, Min-Yi ;
Zhuang, Xiaosheng ;
Zou, Jiachen ;
Wei, Dannuo ;
Lin, Ying-Yi ;
Zhang, Yi ;
Wang, Kun .
THERAPEUTIC ADVANCES IN MEDICAL ONCOLOGY, 2022, 14
[40]   Automated mitotic spindle hotspot counts are highly associated with clinical outcomes in systemically untreated early-stage triple-negative breast cancer [J].
Leon-Ferre, Roberto A. ;
Carter, Jodi M. ;
Zahrieh, David ;
Sinnwell, Jason P. ;
Salgado, Roberto ;
Suman, Vera J. ;
Hillman, David W. ;
Boughey, Judy C. ;
Kalari, Krishna R. ;
Couch, Fergus J. ;
Ingle, James N. ;
Balkenhol, Maschenka ;
Ciompi, Francesco ;
van der Laak, Jeroen ;
Goetz, Matthew P. .
NPJ BREAST CANCER, 2024, 10 (01)