Abstract PS3-08-17: HR+ HER2- Early Breast Cancer (EBC) Patients ≥70 with High Risk 70-gene signature benefit from (Neo)adjuvant chemotherapy (CT): Real World FLEX Study

Abstract BACKGROUND: Women ≥70 are less likely to receive CT due to quality-of-life concerns and comorbidities. These patients (pts) are underrepresented in studies assessing the utility of genomic profiling to guide CT decisions. To identify the utility of a 70-gene recurrence risk assay MammaPrint (MP) we examined the relationship of age (≥70 vs <70), comorbidities, and treatment outcomes stratified by MP result in pts with HR+HER2- EBC. METHODS: The FLEX Study (NCT03053193) includes stage I-III pts with EBC who had MP performed and consented to full transcriptome and clinical data collection. Clinical characteristic differences between age groups were assessed by Chi-squared, Fisher’s exact, or Wilcoxon-Mann-Whitney tests. 4-year (yr) DRFS was assessed using Kaplan-Meier survival analysis. Log-rank tests assessed differences in endpoints between treatment groups. Comorbidity scoring assigned conditions into 7 categories. Pts were assigned 1 point for each category with a reported condition; multiple conditions in a single category counted as 1 point (Table). A multivariate Cox regression model evaluated predictors of DRFS in pts ≥70, adjusting for treatment-genomic risk interactions. Results: A total of 6237 HR+HER2- EBC pts were included. 1145 were ≥70 (18%) and 4792 <70 (82%). MP results showed higher rates of low-risk tumors in the ≥70 vs <70 group (Ultralow 15.2% vs 14.6%, Low 41.5% vs 39.5%, High 1 (H1) 37.4% vs 36.7%, and High 2 (H2) 6.0% vs 9.2%, p = 0.013). Pts ≥70 vs <70 were less likely to receive (neo)adjuvant CT (26.0% vs 42.5%, p<0.001). 16.7% of pts ≥70 had no comorbidities, vs 42.0% of those <70 (p<0.001). A larger proportion of ≥70 pts vs <70 had a comorbidity score of 2 (25.2% vs 13.1%, p<0.001). Scores of 3+ were rare at 2.2% in both groups. Pts aged ≥70 with High -Risk cancers were less likely to receive CT than those <70 (H1: 49.4% vs 77.1%, H2: 72.1% vs 90.9%, p<0.001). The 4-year DRFS for pts ≥70 with High -Risk cancers trended toward superiority for those treated with CT vs endocrine thx alone, especially in H2 cancers (H1 88.5% vs 84.8%, p=.031, H2 88.1% vs 78.3%, p=.064). In multivariate analysis, CT was associated with improved DRFS in H1 (HR=0.51, p=0.015) and H2 (HR=0.35, p=0.009) pts ≥70. CONCLUSION: This Real-World Evidence study demonstrates that pts ≥70 with HR+HER2− EBC are less likely to receive CT than younger pts, despite a substantial number being classified as MP High. Among pts ≥70 with MP High, CT use was associated with improved DRFS, even in the presence of comorbidities. While the unadjusted difference in 4-year DRFS for the H2 subgroup did not reach significance, multivariate analysis showed a significant association between CT and reduced recurrence risk. These findings suggest that MP may provide additional risk information supporting individualized treatment decisions in pts ≥70 with HR+HER2- EBC even with underlying comorbidities. Citation Format: R. Mahtani, H. Wildiers, S. Lin, S. Ana, A. Schreiber, L. Carcas, N. Dempsey, V. Poillucci, M. Landon, C. Dreezen, H. Ramaswamy, W. Audeh, J. O'Shaughnessy. HR+ HER2- Early Breast Cancer (EBC) Patients ≥70 with High Risk 70-gene signature benefit from (Neo)adjuvant chemotherapy (CT): Real World FLEX Study [abstract]. In: Proceedings of the San Antonio Breast Cancer Symposium 2025; 2025 Dec 9-12; San Antonio, TX. Philadelphia (PA): AACR; Clin Cancer Res 2026;32(4 Suppl):Abstract nr PS3-08-17.

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Clinical Cancer Research
Published
2026-02-17
DOI
https://doi.org/10.1158/1557-3265.sabcs25-ps3-08-17
Primary Topic
Breast Cancer Treatment Studies
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article

Abstract PS3-08-17: HR+ HER2- Early Breast Cancer (EBC) Patients ≥70 with High Risk 70-gene signature benefit from (Neo)adjuvant chemotherapy (CT): Real World FLEX Study

Christa Dreezen, Anna Schreiber, Michelle Landon, Lauren Carcas et al.
Clinical Cancer Research
Breast Cancer Treatment Studies
article

Abstract PS3-08-17: HR+ HER2- Early Breast Cancer (EBC) Patients ≥70 with High Risk 70-gene signature benefit from (Neo)adjuvant chemotherapy (CT): Real World FLEX Study

Christa Dreezen, Anna Schreiber, Michelle Landon, Lauren Carcas, Harshini Ramaswamy, R. Mahtani, S. Lin, N. Dempsey, J. A. O'Shaughnessy, V. Poillucci, H. Wildiers, W. Audeh, S. Ana
article en

Abstract

Abstract BACKGROUND: Women ≥70 are less likely to receive CT due to quality-of-life concerns and comorbidities. These patients (pts) are underrepresented in studies assessing the utility of genomic profiling to guide CT decisions. To identify the utility of a 70-gene recurrence risk assay MammaPrint (MP) we examined the relationship of age (≥70 vs <70), comorbidities, and treatment outcomes stratified by MP result in pts with HR+HER2- EBC. METHODS: The FLEX Study (NCT03053193) includes stage I-III pts with EBC who had MP performed and consented to full transcriptome and clinical data collection. Clinical characteristic differences between age groups were assessed by Chi-squared, Fisher’s exact, or Wilcoxon-Mann-Whitney tests. 4-year (yr) DRFS was assessed using Kaplan-Meier survival analysis. Log-rank tests assessed differences in endpoints between treatment groups. Comorbidity scoring assigned conditions into 7 categories. Pts were assigned 1 point for each category with a reported condition; multiple conditions in a single category counted as 1 point (Table). A multivariate Cox regression model evaluated predictors of DRFS in pts ≥70, adjusting for treatment-genomic risk interactions. Results: A total of 6237 HR+HER2- EBC pts were included. 1145 were ≥70 (18%) and 4792 <70 (82%). MP results showed higher rates of low-risk tumors in the ≥70 vs <70 group (Ultralow 15.2% vs 14.6%, Low 41.5% vs 39.5%, High 1 (H1) 37.4% vs 36.7%, and High 2 (H2) 6.0% vs 9.2%, p = 0.013). Pts ≥70 vs <70 were less likely to receive (neo)adjuvant CT (26.0% vs 42.5%, p<0.001). 16.7% of pts ≥70 had no comorbidities, vs 42.0% of those <70 (p<0.001). A larger proportion of ≥70 pts vs <70 had a comorbidity score of 2 (25.2% vs 13.1%, p<0.001). Scores of 3+ were rare at 2.2% in both groups. Pts aged ≥70 with High -Risk cancers were less likely to receive CT than those <70 (H1: 49.4% vs 77.1%, H2: 72.1% vs 90.9%, p<0.001). The 4-year DRFS for pts ≥70 with High -Risk cancers trended toward superiority for those treated with CT vs endocrine thx alone, especially in H2 cancers (H1 88.5% vs 84.8%, p=.031, H2 88.1% vs 78.3%, p=.064). In multivariate analysis, CT was associated with improved DRFS in H1 (HR=0.51, p=0.015) and H2 (HR=0.35, p=0.009) pts ≥70. CONCLUSION: This Real-World Evidence study demonstrates that pts ≥70 with HR+HER2− EBC are less likely to receive CT than younger pts, despite a substantial number being classified as MP High. Among pts ≥70 with MP High, CT use was associated with improved DRFS, even in the presence of comorbidities. While the unadjusted difference in 4-year DRFS for the H2 subgroup did not reach significance, multivariate analysis showed a significant association between CT and reduced recurrence risk. These findings suggest that MP may provide additional risk information supporting individualized treatment decisions in pts ≥70 with HR+HER2- EBC even with underlying comorbidities. Citation Format: R. Mahtani, H. Wildiers, S. Lin, S. Ana, A. Schreiber, L. Carcas, N. Dempsey, V. Poillucci, M. Landon, C. Dreezen, H. Ramaswamy, W. Audeh, J. O'Shaughnessy. HR+ HER2- Early Breast Cancer (EBC) Patients ≥70 with High Risk 70-gene signature benefit from (Neo)adjuvant chemotherapy (CT): Real World FLEX Study [abstract]. In: Proceedings of the San Antonio Breast Cancer Symposium 2025; 2025 Dec 9-12; San Antonio, TX. Philadelphia (PA): AACR; Clin Cancer Res 2026;32(4 Suppl):Abstract nr PS3-08-17.

Clinical Cancer ResearchVol. 32(4_Supplement)
University of Colorado Hospital (US), Baylor University Medical Center (US), Agendia (Netherlands) (NL), Florida Cancer Care (US), University of Colorado Denver (US), KU Leuven (BE)
Good health and well-being
Openalex Percentile: Top 54%
Breast Cancer Treatment Studies
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