92 Near-Infrared Fluorescence Imaging With Indocyanine Green vs Isosulfan Blue for Sentinel Lymph Node Mapping: Comparative Cost Analysis in Early-Stage Breast Cancer

Publication
Article
Miami Breast Cancer Conference® Abstracts Supplement42nd Annual Miami Breast Cancer Conference® - Abstracts
Volume 39
Issue 4
Pages: 68-69

92 Near-Infrared Fluorescence Imaging With Indocyanine Green vs Isosulfan Blue for Sentinel Lymph Node Mapping: Comparative Cost Analysis in Early-Stage Breast Cancer

92 Near-Infrared Fluorescence Imaging With Indocyanine Green vs Isosulfan Blue for Sentinel Lymph Node Mapping: Comparative Cost Analysis in Early-Stage Breast Cancer

Background/Significance

Sentinel lymph node (SLN) mapping is essential in the surgical management of early-stage breast cancer. Isosulfan blue is traditionally used but has drawbacks such as persistent skin staining and allergic reactions. Near-infrared fluorescence (NIRF) imaging with indocyanine green has emerged as a safe, effective, and cost-effective alternative. This study evaluated outpatient revisit costs associated with NIRF with indocyanine green vs isosulfan blue to explore the economic implications of adopting indocyanine green.

Materials and Methods

This retrospective, observational study analyzed data from adult female patients diagnosed with breast cancer undergoing sentinel lymph node mapping with isosulfan blue or NIRF with indocyanine green, indexed to outpatient hospital discharge between July 1, 2017, and August 31, 2022. Data were extracted from the US hospital-based PINC AI Healthcare Database. Patients were grouped based on the SLN mapping method utilized. Costs at 30, 60, and 90 days post procedure were assessed and adjusted to 2022 US dollars using the Medical Care Consumer Price Index.

Results

Among the 1,067,677 patients identified, 5.6% (n = 60,068) underwent SLN, with 11.8% (n = 7,076) meeting inclusion criteria. Outpatient revisit costs to the same hospital for the NIRF with indocyanine green cohort compared with the isosulfan blue cohort were $36 lower at 30 days ($3832 ± $5106 [median, $1,058] vs $3868 ± $4842 [median, $2020], P = NS), $845 lower at 60 days ($7,023 ± $9,360 [median, $3,112] vs $7868 ± $8658 [median, $4740], P <.05, statistically significant), and $774 lower at 90 days ($10,015 ± $13,215 [median, $5,445] vs $10,789 ± $12,166 [median, $5,879], P = NS). A hospital performing 100 SLN mapping procedures annually could save approximately $84,500 per year and $422,500 over 5 years in revisit costs with NIRF with indocyanine green, assuming $845 saved per case.

Conclusion

NIRF with indocyanine green for SLN mapping in breast cancer shows a trend toward cost savings compared with isosulfan blue, particularly at 60 days post procedure. These findings highlight the potential economic benefit of adopting NIRF with indocyanine green in clinical practice and warrant further research into its long-term cost-effectiveness and clinical outcomes.

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17 Salmonella and the Breast: A Literature Review of Salmonella-Induced Breast Abscesses
17 Salmonella and the Breast: A Literature Review of Salmonella-Induced Breast Abscesses
18 Tolerability of First-Line Treatment With Ribociclib for Metastatic Breast Cancer Using 2 Large US Data Sources
18 Tolerability of First-Line Treatment With Ribociclib for Metastatic Breast Cancer Using 2 Large US Data Sources
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20 Impact of Ribociclib Dose Reduction on Efficacy in Patients With Hormone Receptor-Positive/Human Epidermal Growth Factor Receptor 2-Negative Early Breast
21 Distant Disease-Free Survival Across Key Subgroups From the Phase 3 NATALEE Trial of Ribociclib Plus a Nonsteroidal Aromatase Inhibitor in Patients With HR+/HER2− Early Breast Cancer
21 Distant Disease-Free Survival Across Key Subgroups From the Phase 3 NATALEE Trial of Ribociclib Plus a Nonsteroidal Aromatase Inhibitor in Patients With HR+/HER2− Early Breast Cancer
22 Efficacy and Safety of Ribociclib + Nonsteroidal Aromatase Inhibitor in Younger Patients With HR+/HER2− Early Breast Cancer in NATALEE
22 Efficacy and Safety of Ribociclib + Nonsteroidal Aromatase Inhibitor in Younger Patients With HR+/HER2− Early Breast Cancer in NATALEE
23 Clinical Outcomes in Patients With HR+/HER2− Early Breast Cancer By Prior Systemic Treatment: A Subgroup Analysis of the NATALEE Trial
23 Clinical Outcomes in Patients With HR+/HER2− Early Breast Cancer By Prior Systemic Treatment: A Subgroup Analysis of the NATALEE Trial
TPS 24 Phase Ib Dose-Finding Study of [177Lu]Lu-NeoB + Ribociclib + Fulvestrant in Patients With ER+/HER2− Advanced Breast Cancer With GRPR Expression With Early Relapse FromAdjuvant Endocrine Therapy or Progression on ET + CDK4/6i for ABC
TPS 24 Phase Ib Dose-Finding Study of [177Lu]Lu-NeoB + Ribociclib + Fulvestrant in Patients With ER+/HER2− Advanced Breast Cancer With GRPR Expression With Early Relapse FromAdjuvant Endocrine Therapy or Progression on ET + CDK4/6i for ABC
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26 Risk of Recurrence in Real-World NATALEE- and monarchE-Eligible Populations of Patients With HR+/HER2− Early Breast Cancer in an Electronic Health Record-Derived Database
26 Risk of Recurrence in Real-World NATALEE- and monarchE-Eligible Populations of Patients With HR+/HER2− Early Breast Cancer in an Electronic Health Record-Derived Database
27 Elacestrant vs Standard of Care in ER+, HER2- Advanced or Metastatic Breast Cancer With ESR1-Mutated Tumors: ESR1 Allelic Frequencies and Clinical Activity From the Phase 3 EMERALD Trial
27 Elacestrant vs Standard of Care in ER+, HER2- Advanced or Metastatic Breast Cancer With ESR1-Mutated Tumors: ESR1 Allelic Frequencies and Clinical Activity From the Phase 3 EMERALD Trial
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30 Imlunestrant, an Oral Selective Estrogen Receptor Degrader, as Monotherapy and Combined With Abemaciclib, for Patients with ER+, HER2– Advanced Breast Cancer, Pretreated With Endocrine Therapy: Results of the Phase 3 EMBER-3 Trial
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