Abstract 268P
Background
Previous research in early-stage BC has established the association of a 14-gene immunoglobulin/B-cell (IGG) signature (sig) with a reduced risk of distant metastasis. However, the relationship between this signature and patient longevity, in the absence of a BC recurrence, is unknown.
Methods
We employed competing risk analyses to test the association between the IGG sig, age, and longevity, where the competing event was prior relapse. Longevity was defined as survival or death without a documented BC relapse. The analysis was performed in 3 BC cohorts: METABRIC (n=1,133), SCAN-B (n=4,470), and TCGA (n=936). We conducted spatial proteomics on 39 immune-related proteins within the tumor stroma and assessed the presence of tertiary lymphoid structures (TLS) in 132 FFPE BC tumors with varying IGG levels. We performed single-cell RNA sequencing (scRNAseq) of CD45-positive cells from 6 fresh BC samples, and characterized B-cell and T-cell receptors (BCR and TCR) across different IGG levels using the immunoSEQ assay in 33 FFPE BC tumors and analyzing bulk RNAseq data of the CALGB-40601 BC trial (n=264).
Results
The IGG sig was significantly linked to increased longevity across all cohorts (p<0.001). A moderate inverse correlation was found between the IGG sig and age. Notably, in patients aged 40-70 years, the IGG sig was significantly associated with longevity independently of age (p<0.001). IGG-high tumors showed enrichment in TLS+ and higher expression of plasma cell and memory B cell marker (CD27), activated T cells (ICOS), antigen-presenting cells (CD40), and lower levels of stromal fibronectin. ImmunoSEQ, bulk and scRNAseq analyses showed that IGG high tumors had a tendency towards higher B cell infiltration and demonstrated a TCR and BCR polyclonal repertoire, compared to IGG low tumors (Simpson, Shannon p<0.001).
Conclusions
The IGG sig serves as a prognostic biomarker for both recurrence and extended longevity of patients with early-stage BC. Its association with longevity might rely on the detection of enhanced immune fitness, which could better protect against infections and other cancers. Our results open potential new avenues for develop tailored therapy strategies, enhancing patient outcomes and quality of life.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Instituto de Salud Carlos III and Breast cancer research foundation.
Disclosure
L. Pare Brunet: Financial Interests, Institutional, Full or part-time Employment: Reveal Genomics S.L.; Financial Interests, Institutional, Other, Patent pending: In vitro method for the prognosis of patients suffering from HER2-positive breast cancer - 905333: SOLTI; Financial Interests, Institutional, Other, Patent filed: EP23382703: Reveal Genomics S.L.; Financial Interests, Institutional, Other, Patent filed: EP23383369: Reveal Genomics S.L. E. Segui Solis: Financial Interests, Personal, Invited Speaker: Novartis, Veracyte, Pfizer, Daiichi Sankyo, Eisai; Financial Interests, Personal, Advisory Board: Pfizer, Seagen; Financial Interests, Personal, Full or part-time Employment: SOLTI; Financial Interests, Personal, Research Grant: Amgen. G. Villacampa: Financial Interests, Personal, Invited Speaker, Invited speaker in a course: MSD; Financial Interests, Personal, Advisory Board: AstraZeneca; Financial Interests, Personal, Invited Speaker, Invited speaker in an internal training: Pierre Fabrer, GSK; Financial Interests, Personal, Invited Speaker, Internal discussion about the interpretation of some published results: Pfizer; Financial Interests, Personal, Other, Collaborations with specific projects: Reveal Genomics. W. Buckingham: Financial Interests, Institutional, Full or part-time Employment, Employed by Reveal Genomics SL: Reveal Genomics SL; Financial Interests, Personal, Stocks/Shares, Spouse stock ownership: Natera Inc. A. Vivancos: Financial Interests, Personal, Advisory Board: Roche, Bristol Myers Squibb, Guardant Health, Bayer, Incyte; Financial Interests, Personal, Stocks/Shares: Reveal Genomics; Financial Interests, Institutional, Research Grant, Preclinical Research Grant: Bristol Myers Squibb, Roche, Incyte. P. Villagrasa Gonzalez: Financial Interests, Personal, Full or part-time Employment, CEO and co-founder of the company: Reveal Genomics S.L.; Financial Interests, Personal, Ownership Interest: Reveal Genomics S.L.; Financial Interests, Personal, Royalties, PCT/EP2021/086493 - In Vitro Method For The Prognosis Of Patients Suffering From HER2-Positive Breast Cancer: Reveal Genomics S.L. C.M. Perou: Financial Interests, Personal, Other, consultant: GeneCentric Therapeutics, Bioclassifier LLC, Reveal Genomics; Financial Interests, Personal, Member of Board of Directors: GeneCentric Therapeutics; Financial Interests, Personal, Ownership Interest: GeneCentric Therapeutics, Bioclassifier LLC, Reveal Genomics; Financial Interests, Personal, Royalties: Bioclassifier LLC. A. Prat: Financial Interests, Personal, Invited Speaker: Roche; Financial Interests, Personal, Invited Speaker, Lecture fees: Novartis, Daiichi Sankyo; Financial Interests, Personal, Advisory Board, Advisory role/consultancy: Novartis, Pfizer, Peptomyc; Financial Interests, Institutional, Invited Speaker, Clinical trials: Daiichi Sankyo; Financial Interests, Institutional, Other, Contracted research: Boehringer, Medica Scientia inno. Research; Financial Interests, Personal, Advisory Board: AstraZeneca, Reveal Genomics, 1TRIALSP, S.L.; Financial Interests, Personal, Member of Board of Directors, Leadership role: Reveal Genomics, SL.; Financial Interests, Personal, Stocks/Shares: Reveal Genomics; Financial Interests, Personal, Royalties: Reveal Genomics, International Oncology Bureau, S.L.,; Financial Interests, Institutional, Local PI: Roche, AstraZeneca; Financial Interests, Personal and Institutional, Steering Committee Member: Daiichi Sankyo; Financial Interests, Institutional, Coordinating PI: Novartis; Financial Interests, Institutional, Funding: Reveal Genomics; Non-Financial Interests, Institutional, Other, Leadership roles: Patronage committee: Actitud Frente al Cáncer Foundation; Non-Financial Interests, Personal, Other, Asociación Española de Investigación sobre el Cáncer: ASEICA; Non-Financial Interests, Personal, Other, Research Foundation that gives grants to researchers: FERO. F. Braso Maristany: Non-Financial Interests, Personal and Institutional, Other, Consulting fees: Reveal Genomics. All other authors have declared no conflicts of interest.
Resources from the same session
259P - Relationship between initial tumor burden and the probability of pathological complete response within molecular subtypes of early breast cancer treated with neoadjuvant chemotherapy
Presenter: Nicolas Roussot
Session: Poster session 14
260P - Impact of HER2-low status on clinicopathological characteristics and pathological complete response in luminal and triple-negative early breast cancer
Presenter: Katarzyna Pogoda
Session: Poster session 14
261P - Subtyping of residual disease (RD) following neoadjuvant chemotherapy (NACT) for triple negative breast cancer (TNBC): Evolution and prognostic impact
Presenter: Isabel Echavarria Diaz-Guardamino
Session: Poster session 14
262P - Predictive clinico-biological factors of toxicity associated to neo-adjuvant chemo- immunotherapy in early-stage triple-negative breast cancer
Presenter: Elsa Volant
Session: Poster session 14
263P - Association between clinicopathological characteristics and pathological complete response in patients with triple negative breast cancer treated by neoadjuvant chemo-immunotherapy
Presenter: Clara Helal
Session: Poster session 14
264P - Neuropsychological and morphological effects of simultaneous exercise during neo-/adjuvant chemotherapy in breast cancer patients: The Exercise Cancer and Cognition (ECCO) study
Presenter: David Kiesl
Session: Poster session 14
265P - Association of clinical benefit of adjuvant capecitabine and RCB class in triple negative breast cancer (TNBC) patients with residual disease following neoadjuvant chemotherapy
Presenter: Shinyoung Lee
Session: Poster session 14
266P - Association of RAD51 and efficacy outcomes in patients with HER2-negative breast cancer (BC) and homologous recombination deficiency (HRD): Post-hoc analysis of the GeparOla trial
Presenter: Guillermo Villacampa
Session: Poster session 14
267P - The tumour microenvironment influences long-term tamoxifen treatment response in breast cancer patients
Presenter: Paula Camargo Romera
Session: Poster session 14
269P - Her2-low/HRR proficient early triple negative breast cancer is characterized by good prognosis
Presenter: Benedetta Pellegrino
Session: Poster session 14