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.

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27 CARDIAC-STAR: Prevalence of Cardiovascular (CV) Comorbidities in Hormone Receptor–Positive/ Human Epidermal Growth Factor Receptor 2–Negative (HR+/HER2–) Metastatic Breast Cancer (mBC)
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28 Enhancing the Interpretation of Real-World Quality of Life (QoL) in Patients With Hormone Receptor– Positive/Human Epidermal Growth Factor Receptor 2–Negative (HR+/HER2-) Advanced Breast Cancer (ABC) Enrolled in the POLARIS Trial
29 ELEVATE: A Phase 1b/2, Open-Label, Umbrella Study Evaluating Elacestrant in Various Combinations in Patients (pts) With Estrogen Receptor–Positive (ER+), HER2-Negative (HER2–) Locally Advanced or Metastatic Breast Cancer (mBC)
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30 Datopotamab Deruxtecan (Dato-DXd) vs Chemotherapy in Previously-Treated Inoperable or Metastatic Hormone Receptor–Positive, HER2-Negative (HR+/HER2–) Breast Cancer (BC): Primary Results From the Randomised Phase 3 TROPION-Breast01 Trial
31 Adjuvant Abemaciclib Plus Endocrine Therapy for HR+, HER2–, High-Risk Early Breast Cancer: Results From a Preplanned MonarchE Overall Survival Interim Analysis, Including 5-Year Efficacy Outcomes
31 Adjuvant Abemaciclib Plus Endocrine Therapy for HR+, HER2–, High-Risk Early Breast Cancer: Results From a Preplanned MonarchE Overall Survival Interim Analysis, Including 5-Year Efficacy Outcomes
32 Neoadjuvant Pembrolizumab or Placebo Plus Chemotherapy Followed by Adjuvant Pembrolizumab or Placebo for Early-Stage Triple- Negative Breast Cancer: Updated Event-Free Survival Results From the Phase 3 KEYNOTE-522 Study
32 Neoadjuvant Pembrolizumab or Placebo Plus Chemotherapy Followed by Adjuvant Pembrolizumab or Placebo for Early-Stage Triple- Negative Breast Cancer: Updated Event-Free Survival Results From the Phase 3 KEYNOTE-522 Study
33 MammaPrint® and BluePrint® Predict Anthracycline Chemosensitivity in Patients With HR+HER2– Early-Stage Breast Cancer Enrolled in FLEX
33 MammaPrint® and BluePrint® Predict Anthracycline Chemosensitivity in Patients With HR+HER2– Early-Stage Breast Cancer Enrolled in FLEX
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36 MONARCH 3: Final Overall Survival Results of Abemaciclib Plus a Nonsteroidal Aromatase Inhibitor as First-Line Therapy for HR+/HER2– Advanced Breast Cancer
37 Estimating the Direct and Indirect Resource Burden of Treatment Management With Current Standard of Care or Elacestrant for ER+, HER2–, ESR1-Mutated Advanced or Metastatic Breast Cancer Patients: A Population- Level Provider Model
37 Estimating the Direct and Indirect Resource Burden of Treatment Management With Current Standard of Care or Elacestrant for ER+, HER2–, ESR1-Mutated Advanced or Metastatic Breast Cancer Patients: A Population- Level Provider Model
38 Influence of Race on Attainment of Textbook Oncologic Outcome Following Modified Radical Mastectomy for Breast Cancer
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40 Ethnic Disparities in Complication Rates and Outcomes  of Nipple-Sparing Mastectomy:  A Comprehensive Analysis
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41 A Case Series of Sarcomas
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