69 The Importance of Tri-Modality Therapy for De Novo Stage IV Invasive Lobular Carcinoma (ILC) Presenting With Bone-Only Metastases

Publication
Article
Miami Breast Cancer Conference® Abstracts Supplement41st Annual Miami Breast Cancer Conference® - Abstracts
Volume 38
Issue 4
Pages: 63-64

Systemic Therapy Only vs Locoregional Therapy With Systemic Therapy in Patients With Stage IV ILC With Bone-Only Metastases

Systemic Therapy Only vs Locoregional Therapy With Systemic Therapy in Patients With Stage IV ILC With Bone-Only Metastases

Background

Locoregional therapy (LRT) of the primary breast carcinoma (BC) in the setting of de novo oligometastatic stage IV disease is strongly debated, despite both retrospective data and prospective trials supporting it. This study aims to determine the overall survival (OS) benefit of LRT combined with systemic therapy (ST) vs ST only in the management of invasive lobular carcinoma (ILC) presenting with de novo stage IV bone-only metastases.

Methods

Patients who presented from 2014 to 2022 with bone-only metastases were retrospectively identified from a prospectively maintained multi-institutional cohort of patients with oligometastases. Univariable and multivariable Cox proportional hazards models were used to identify factors associated with OS. The Kaplan-Meier method was used to estimate time-to-event outcomes. Groups were compared using the log-rank test. Variables included demographics, tumor size, histology, receptor status, use of endocrine therapy, chemotherapy, bisphosphonates, and ovarian suppression.

Results

Of 744 patients identified, 83 (11%) had ILC. Patients with ILC were older (58.9 years vs 52.6 years; P < .05), had a higher number of multiple tumors (81% vs 61%; P < .05), and had lower HER2-positive frequency (12% vs 29%; P < .05) than those with IDC. Hazard of death was 63% higher in ILC vs IDC (HR, 1.63; 95% CI, 1.1-2.24; P = .003). Median OS was 69 months and 49 months in IDC and ILC, respectively. For patients with ILC, baseline characteristics of age, body mass index, T stage, hormone receptor status, ST, and intervention to metastatic sites did not differ between those who had LRT plus ST (n = 25; 30%) vs ST only (P > .05). At a median follow-up of 36 months (IQR, 26-57), 48% (n = 40) of patients with ILC had died. In the ILC group, Kaplan-Meier OS estimates demonstrated longer OS among patients who underwent LRT+ST (median 78 months) vs 38 months with ST only, log-rank P = .008; Figure). Hazard of death was 63% lower with LRT+ST vs ST only (HR, 0.37; 95% CI, 0.18-0.79; P = .01). LRT plus ST was the only factor contributing to OS at 36 months (OR, 3.64; 95% CI, 1.33-11.20; P = .02).

Conclusion

Patients with ILC and de novo bone-only metastases have a worse prognosis compared to those with IDC, but those who have LRT plus ST have a better OS than those who receive ST only. While there may be selection biases in our multi-institutional retrospective cohort, patients with ILC should be considered for LRT for the primary tumor combined with ST.

Articles in this issue

1 Centrally Located Breast Cancer Is More Aggressive in Bahraini Patients
1 Centrally Located Breast Cancer Is More Aggressive in Bahraini Patients
2 Is Laterality in Breast Cancer Still Worth Studying? Local Experience in Bahrain
2 Is Laterality in Breast Cancer Still Worth Studying? Local Experience in Bahrain
3 Gender Disparities in the  National Institutes of Health  Funding for Breast Cancer
3 Gender Disparities in the National Institutes of Health Funding for Breast Cancer
4 Bacopaside: Exploring Its Potential in Addressing Chemoresistance and Modulating Doxorubicin Accumulation in Triple-Negative Breast Cancer Cells
4 Bacopaside: Exploring Its Potential in Addressing Chemoresistance and Modulating Doxorubicin Accumulation in Triple-Negative Breast Cancer Cells
5 Predictors of Axillary Complete Pathologic Response in Hormone Receptor–Positive, HER2-Negative, Clinically Node-Positive Breast Cancer
5 Predictors of Axillary Complete Pathologic Response in Hormone Receptor–Positive, HER2-Negative, Clinically Node-Positive Breast Cancer
6 Treatment Outcomes of the KEYNOTE-522 Regimen in an Ethnically Diverse Patient Population
6 Treatment Outcomes of the KEYNOTE-522 Regimen in an Ethnically Diverse Patient Population
7 Real-World Efficacy and Adverse Events of Neoadjuvant Immunotherapy in Early-Stage Triple-Negative Breast Cancer Patients: A Multicenter Experience
7 Real-World Efficacy and Adverse Events of Neoadjuvant Immunotherapy in Early-Stage Triple-Negative Breast Cancer Patients: A Multicenter Experience
8 Using a Liquid Biopsy Mediated Approach for Determination of HER2 Amplification Status in Patient Samples
8 Using a Liquid Biopsy Mediated Approach for Determination of HER2 Amplification Status in Patient Samples
9 Elacestrant (ELA) vs Standard-of-Care (SOC) in ER+/HER2–Advanced (adv) or Metastatic Breast Cancer (mBC) with ESR1 Mutation (ESR1-mut): Key Biomarkers and Clinical Subgroup Analyses From the Phase 3 EMERALD Trial
9 Elacestrant (ELA) vs Standard-of-Care (SOC) in ER+/HER2–Advanced (adv) or Metastatic Breast Cancer (mBC) with ESR1 Mutation (ESR1-mut): Key Biomarkers and Clinical Subgroup Analyses From the Phase 3 EMERALD Trial
10 Real-World Effectiveness of Palbociclib (PAL) Plus Aromatase Inhibitors (AI) in Patients With Metastatic Breast Cancer (MBC) and Cardiovascular Diseases (CVD)
10 Real-World Effectiveness of Palbociclib (PAL) Plus Aromatase Inhibitors (AI) in Patients With Metastatic Breast Cancer (MBC) and Cardiovascular Diseases (CVD)
11 Phase 3 Study of Neoadjuvant Pembrolizumab or Placebo Plus Chemotherapy, Followed by Adjuvant Pembrolizumab or Placebo Plus Endocrine Therapy for Early-Stage High-Risk ER+/HER2– Breast Cancer: KEYNOTE-756
11 Phase 3 Study of Neoadjuvant Pembrolizumab or Placebo Plus Chemotherapy, Followed by Adjuvant Pembrolizumab or Placebo Plus Endocrine Therapy for Early-Stage High-Risk ER+/HER2– Breast Cancer: KEYNOTE-756
12 EMERALD Trial Analysis of Patient-Reported Outcomes (PROs) in Patients (pts) With ER+/HER2- Advanced or Metastatic Breast  Cancer (mBC) Comparing Oral Elacestrant vs Standard-of-Care (SoC) Endocrine Therapy
12 EMERALD Trial Analysis of Patient-Reported Outcomes (PROs) in Patients (pts) With ER+/HER2- Advanced or Metastatic Breast Cancer (mBC) Comparing Oral Elacestrant vs Standard-of-Care (SoC) Endocrine Therapy
13 The Cause and Eradication of Breast Cancer
13 The Cause and Eradication of Breast Cancer
14 Outcomes With First-Line (1L) Ribociclib (RIB) + Endocrine Therapy (ET) vs Physician’s Choice Combination Chemotherapy (combo CT) by Age in Pre/Perimenopausal Patients (pts) With Aggressive HR+/HER2– Advanced Breast Cancer (ABC): A Subgroup Analysis of the RIGHT Choice Trial
14 Outcomes With First-Line (1L) Ribociclib (RIB) + Endocrine Therapy (ET) vs Physician’s Choice Combination Chemotherapy (combo CT) by Age in Pre/Perimenopausal Patients (pts) With Aggressive HR+/HER2– Advanced Breast Cancer (ABC): A Subgroup Analysis of the RIGHT Choice Trial
15 Concurrent Use of Abemaciclib and Radiation Therapy (RT) Among Patients With HR+, HER2– Metastatic Breast Cancer (MBC): Real-World Utilization and Safety
15 Concurrent Use of Abemaciclib and Radiation Therapy (RT) Among Patients With HR+, HER2– Metastatic Breast Cancer (MBC): Real-World Utilization and Safety
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