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Comparative Effectiveness of Sentinel Lymph Node Biopsy for Ductal Carcinoma In Situ

Comparative Effectiveness of Sentinel Lymph Node Biopsy (SLNB) for Ductal Carcinoma In Situ (DCIS)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02908178
Enrollment
28291
Registered
2016-09-20
Start date
2017-01-25
Completion date
2018-06-29
Last updated
2019-05-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ductal Carcinoma In Situ

Keywords

ductal carcinoma in situ (DCIS), sentinel lymph node biopsy (SLNB)

Brief summary

Patients with ductal carcinoma in situ (DCIS) treated with available therapies have experienced excellent outcomes and very low mortality rates due to the disease's non-invasive nature. However, considerable debate exists as to how the DCIS lesion should be treated. As a result, determining strategies to manage DCIS has been identified as a research priority. The role of sentinel lymph node biopsy (SLNB) for DCIS management is controversial in general and needs further scrutiny. Our study addresses this evidence gap as the investigators propose a retrospective cohort study to investigate the outcome of SLNB among DCIS patients. Specifically, the investigators will compare the outcomes, including survival outcomes and treatment side effects, among women older than 67 years of age with DCIS receiving SLNB vs. not receiving SLNB within 6 months of DCIS diagnosis. The investigators have two primary aims in this study: Aim 1: the investigators select our study sample using SEER-Medicare database. The investigators will determine associations between SLNB and acute/subacute side effects, including lymphedema, pain, and limitation of movement of upper extremity from the first breast conserving surgery to 9 months post-diagnosis. Aim 2: the investigators will determine associations between SLNB and long-term outcomes, including breast cancer specific mortality, ipsilateral invasive breast cancer diagnosis, subsequent mastectomy as treated recurrence, and lasting side effects, from \>9 months post-diagnosis to death or the end of this study period. Given the nature of our observational study design, the investigators will apply standard multivariate analyses and propensity score methodology to reduce the influence from confounders. The investigators will control for patient demographics, comorbidities, functional status, tumor characteristics, and prior healthcare utilization. Using distance to the nearest provider that uses SLNB for DCIS or surgeon's tendency in using SLNB for stage I/II breast cancer, the investigators also plan to conduct instrument variable analyses if necessary. Stratifying patients by key DCIS characteristics (including grade, comedonecrosis, and tumor size) and their predicted life expectancy (given their age and comorbidities), the investigators also hope to identify patient subgroups who may safely forgo SLNB. The study would provide evidence on the efficacy and safety outcome of SLNB for DCIS management.

Detailed description

Because of the non-invasive nature of ductal carcinoma in situ (DCIS), patients treated with available therapies have excellent outcomes and very low rates of breast cancer mortality. Considerable debate exists as to how the DCIS lesion should be treated, although there is a movement toward less intensive intervention by the identification of patient subsets with favorable prognoses. Some prospective studies have found that the rate of ipsilateral invasive cancer occurrence is still high after receiving breast conserving surgery (BCS) alone, even among patients with favorable pathologic characteristics. Such findings argue against active surveillance for DCIS treatment. However, evidence exists that older DCIS patients have a lower rate of ipsilateral recurrence because DCIS among older patients tends to be indolent. Identifying suitable subgroups among this lower risk group who may be safe to receive a less aggressive treatment could change the current practice pattern of aggressive treatment. Even when DCIS patients opt to receive a less intensive treatment such as BCS without radiation therapy, they and their providers need to decide whether to undergo sentinel lymph node biopsy (SLNB). A systematic review has shown that evidence gaps exist regarding the benefits of SLNB for DCIS. Given that the likelihood of axillary recurrence is low among DCIS patients who received radiation therapy, routine SLNB is not recommended for DCIS patients. Of note, radiation therapy can control axillary disease if present. If the investigators plan to empower DCIS patients to choose less intensive management options, such as BCS forgoing radiation therapy (RT), it will be crucial for patients and providers to understand the role of SLNB. The overarching goals of this study are to compare side effects and outcomes between receiving SLNB vs. not receiving SLNB among older DCIS patients who received BCS. With this data, the investigators also aim to identify sub-populations for whom less intensive treatments may be appropriate. Using the Surveillance, Epidemiology, and End Result (SEER)-Medicare linked data, our project's overarching aims are: Among older women with DCIS who have received BCS as their first surgery, to compare the outcomes of receiving sentinel lymph node biopsy (SLNB) vs. not receiving SLNB within 6 months of DCIS diagnosis: Aim 1: The investigators will determine associations between SLNB and acute/subacute side effects, including lymphedema, pain, and limitation of movement of upper extremity from the first BCS to 9 months post-diagnosis Aim 2: The investigators will determine associations between SLNB and long-term outcomes, including breast cancer specific mortality, ipsilateral invasive breast cancer diagnosis, subsequent mastectomy as treated recurrence, and lasting side effects, from \> 9 months' post-diagnosis to death or the end of the study period. Our study is a retrospective cohort study with the study population being DCIS patients older than 67 years (hereafter referred to as older women) who were enrolled in a fee-for-service Medicare program and resided in the SEER areas from 1998 to 2011 (2001 to 2013 for Aim 2) and who were followed up to 2012 (2015 for Aim 2). The investigators selected age 67 years as a cut-off value because the investigators plan to use two years of claims data to identify patient comorbidities and control for them in our statistical models, and data is first available at age 65. Given the nature of our observational study design, the investigators will apply standard multivariate analyses and propensity score methodology to reduce the influence from confounders. The investigators will control for patient demographics, comorbidities, functional status, tumor characteristics, and prior healthcare utilization. Using distance to the nearest provider that uses SLNB for DCIS or surgeon's tendency in using SLNB for stage I/II breast cancer, the investigators also plan to conduct instrument variable analyses if necessary. Stratifying patients by key DCIS characteristics (including grade, comedonecrosis, and tumor size) and their predicted life expectancy (given their age and comorbidities), the investigators also hope to identify patient subgroups who may safely forgo SLNB. In comparisons of baseline characteristics between intervention and control groups, the investigators will conduct standard descriptive statistics using chi-square tests for categorical variables and t-tests for continuous variables. The investigators will tabulate the frequencies of outcomes of interests by the intervention vs. control group. For multivariable analyses, the investigators will apply proportional hazards models to test whether the intervention is associated with better outcomes. the investigators plan to control for this issue using propensity score matching methodology. Prior literature has suggested inclusion of either all measured variables or those variables that are associated with treatment selection (SLNB status) when conducting an analysis using the propensity score method. Specifically, our approach to matching will be based on the Mahalanobis distance calculated using age, race, residence in a metropolitan county, comorbidity, prior influenza vaccination or prior visit to a primary care physician (both as proxies for access to care), income, preoperative MRI use, and tumor characteristics. Tumor characteristics include size, grade, comedonecrosis, and estrogen receptor status. By incorporating these factors in matching, the investigators expect to substantially decrease bias and balance the risk for outcomes of interest between the SLNB and non-SLNB groups. The difference in outcomes between the control and intervention groups will be estimated in a Kaplan-Meier curve. The investigators will estimate the relative risk in the propensity score matched sample using the standard method for matched-pair data. The investigators will use the Cox proportional hazards models to investigate the association between various factors (grade, tumor size, and estrogen receptor status) and outcomes.

Interventions

PROCEDURESentinel lymph node biopsy (SLNB)

Intervention is defined as that the DCIS patient has undergone SLNB. Patients in each cohort (group) include those who underwent SLNB (intervention) and those who did not (control).

Sponsors

Patient-Centered Outcomes Research Institute
CollaboratorOTHER
Yale University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
67 Years to 94 Years
Healthy volunteers
No

Inclusion criteria

* Female DCIS patients older than 67 years and younger than 94 years who were enrolled in a fee-for-service Medicare program and resided in the SEER areas. * Aim 1: DCIS patients who received breast conserving surgery (BCS) as their first surgery * Aim 1: DCIS patients who were diagnosed DCIS between January 1998 and December 2011 * Aim 2: DCIS patients who were diagnosed DCIS between January 2001 and December 2013

Exclusion criteria

* Aim 1: DCIS patients who received mastectomy as their first surgery * Aim 2: DCIS patients who received BCS at the beginning yet received mastectomy in the end

Design outcomes

Primary

MeasureTime frameDescription
Side Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or PainFrom the first BCS to 9 months post-diagnosis.Primary outcomes for Aim 1: Acute and subacute side effects include any complication, lymphedema, seroma, wound infection, and pain.

Secondary

MeasureTime frameDescription
Receipt of Radiation Therapy9 months within DCIS diagnosisSecondary outcomes for Aim 1: Receipt of radiation therapy within 9 months of DCIS diagnosis.
Overall SurvivalFrom 9 months post-diagnosis to death/end of study period (up to 1.5 years)Secondary outcomes for Aim 2.
Lasting Side Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or PainFrom 9 months post-diagnosis to death/end of study period (up to 1.5 years)Secondary outcomes for Aim 2: unadjusted side effects (any side effects, lymphedema, any infection, seroma, pain) in the matched sample by use of sentinel lymph node biopsy (SLNB). Any side effects refer to the occurrence of one or more of the following complications since diagnosis of DCIS: lymphedema related complications, any infection, seroma, and any pain.
Receipt of Mastectomy6 months within DCIS diagnosisSecondary outcomes for Aim 1: receipt of mastectomy with and without SLNB after initial BCS through 6 months after DCIS diagnosis.
Ipsilateral Invasive Breast Cancer OccurrenceFrom 9 months post-diagnosis to death/end of study period (up to 1.5 years)Primary outcomes for Aim 2: Ipsilateral invasive breast cancer occurrence after 9 months of a DCIS diagnosis, per SEER reports.
Treated RecurrenceFrom 9 months post-diagnosis to death/end of study period (up to 1.5 years)Primary outcomes for Aim 2: Treated recurrence was defined by the receipt of mastectomy after 9 months of a DCIS diagnosis in the Aim 2 matched cohort.
Breast Cancer Specific MortalityFrom 9 months post-diagnosis to death/end of study period (up to 1.5 years)Primary outcomes for Aim 2: Breast cancer specific mortality from 9 months post-diagnosis to death or the end of the study period (December, 2014).

Countries

United States

Participant flow

Recruitment details

Because this study is 1) secondary data analysis of an existing database, 2) has two aims using the most recent data when conducting the analyses, and 3) uses Mehalanobis matching, the number of participants in Enrollment is the number of patients who are eligible to our inclusion criteria.

Participants by arm

ArmCount
Aim 1 Cohort: No SLNB
The Aim 1 Cohort is constructed to perform analysis to address study objective Aim 1. The cohort population includes patients diagnosed at age 67-94 years with DCIS between January 1998 and December 2011, and had received BCS as their first surgery within 6 months of diagnosis. Only those who did not receive sentinel lymph node biopsy (SLNB) were included (control group).
4,718
Aim 1 Cohort: SLNB
The Aim 1 Cohort is constructed to perform analysis to address study objective Aim 1. The cohort population includes patients diagnosed at age 67-94 years with DCIS between January 1998 and December 2011, and had received BCS as their first surgery within 6 months of diagnosis. Only those who received sentinel lymph node biopsy (SLNB) were included (intervention group).
2,409
Aim 2 Cohort: No SLNB
The Aim 2 Cohort is constructed to perform analysis to address study objective Aim 2.The cohort population includes patients diagnosed at age 67-94 years with DCIS between January 2001 and December 2013, and had received BCS as their first surgery within 6 months of diagnosis. Only those who did not receive sentinel lymph node biopsy (SLNB) were included (control group).
3,965
Aim 2 Cohort: SLNB
The Aim 2 Cohort is constructed to perform analysis to address study objective Aim 2.The cohort population includes patients diagnosed at age 67-94 years with DCIS between January 2001 and December 2013, and had received BCS as their first surgery within 6 months of diagnosis. Only those who received sentinel lymph node biopsy (SLNB) were included (intervention group).
1,992
Total13,084

Baseline characteristics

CharacteristicAim 1 Cohort: SLNBAim 2 Cohort: No SLNBAim 1 Cohort: No SLNBAim 2 Cohort: SLNBTotal
Age, Customized
67-69 years old
573 Participants808 Participants981 Participants478 Participants2840 Participants
Age, Customized
70-74 years old
783 Participants1309 Participants1592 Participants651 Participants4335 Participants
Age, Customized
75-79 years old
614 Participants1110 Participants1263 Participants503 Participants3490 Participants
Age, Customized
80-84 years old
333 Participants567 Participants670 Participants272 Participants1842 Participants
Age, Customized
85+ years old
106 Participants171 Participants212 Participants88 Participants577 Participants
Comedonecrosis
No
2112 Participants3537 Participants4194 Participants1733 Participants11576 Participants
Comedonecrosis
Yes
297 Participants428 Participants524 Participants259 Participants1508 Participants
Elixhauser Comorbidity
1 to 2
935 Participants1548 Participants1914 Participants780 Participants5177 Participants
Elixhauser Comorbidity
3 or more
255 Participants462 Participants575 Participants232 Participants1524 Participants
Elixhauser Comorbidity
None
1219 Participants1955 Participants2229 Participants980 Participants6383 Participants
Ethnicity (NIH/OMB)
Hispanic or Latino
135 Participants190 Participants221 Participants106 Participants652 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
2274 Participants3775 Participants4497 Participants1886 Participants12432 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants0 Participants0 Participants
Geographic Region
Midwest
296 Participants460 Participants583 Participants229 Participants1568 Participants
Geographic Region
Northeast
488 Participants763 Participants979 Participants378 Participants2608 Participants
Geographic Region
South
588 Participants1026 Participants1141 Participants522 Participants3277 Participants
Geographic Region
West
1037 Participants1716 Participants2015 Participants863 Participants5631 Participants
Hormone receptors
ER- and PR-
341 Participants485 Participants631 Participants284 Participants1741 Participants
Hormone receptors
ER+ and PR+
1329 Participants2316 Participants2608 Participants1170 Participants7423 Participants
Hormone receptors
Missing
739 Participants1164 Participants1479 Participants538 Participants3920 Participants
Marital Status
Married
1227 Participants1977 Participants2286 Participants1038 Participants6528 Participants
Marital Status
Other
97 Participants190 Participants236 Participants87 Participants610 Participants
Marital Status
Unmarried
1085 Participants1798 Participants2196 Participants867 Participants5946 Participants
Race/Ethnicity, Customized
Black
170 Participants271 Participants386 Participants129 Participants956 Participants
Race/Ethnicity, Customized
Other
91 Participants200 Participants233 Participants85 Participants609 Participants
Race/Ethnicity, Customized
White
2148 Participants3494 Participants4099 Participants1778 Participants11519 Participants
Region of Enrollment
United States
2409 participants3965 participants4718 participants1992 participants13084 participants
Sex: Female, Male
Female
2409 Participants3965 Participants4718 Participants1992 Participants13084 Participants
Sex: Female, Male
Male
0 Participants0 Participants0 Participants0 Participants0 Participants
Surgeon Volume
1
1140 Participants1986 Participants2182 Participants945 Participants6253 Participants
Surgeon Volume
2
578 Participants969 Participants1099 Participants496 Participants3142 Participants
Surgeon Volume
3
329 Participants465 Participants596 Participants267 Participants1657 Participants
Surgeon Volume
4+
300 Participants509 Participants727 Participants266 Participants1802 Participants
Surgeon Volume
Not assigned
62 Participants36 Participants114 Participants18 Participants230 Participants
Tumor Grade
Moderately differentiated
629 Participants1278 Participants1371 Participants536 Participants3814 Participants
Tumor Grade
Poorly differentiated
802 Participants1262 Participants1449 Participants730 Participants4243 Participants
Tumor Grade
Undifferentiated
321 Participants434 Participants601 Participants226 Participants1582 Participants
Tumor Grade
Unknown
403 Participants567 Participants799 Participants293 Participants2062 Participants
Tumor Grade
Well differentiated
254 Participants424 Participants498 Participants207 Participants1383 Participants
Tumor size
2.0-<5.0 cm
434 Participants550 Participants749 Participants347 Participants2080 Participants
Tumor size
<2.0 cm
1264 Participants2407 Participants2552 Participants1148 Participants7371 Participants
Tumor size
>5.0 cm
89 Participants80 Participants149 Participants42 Participants360 Participants
Tumor size
Missing
622 Participants928 Participants1268 Participants455 Participants3273 Participants
Year of Diagnosis
1998-1999
30 Participants0 Participants63 Participants0 Participants93 Participants
Year of Diagnosis
2000-2003
395 Participants605 Participants806 Participants240 Participants2046 Participants
Year of Diagnosis
2004-2005
431 Participants531 Participants863 Participants264 Participants2089 Participants
Year of Diagnosis
2006-2007
508 Participants647 Participants986 Participants329 Participants2470 Participants
Year of Diagnosis
2008-2009
539 Participants713 Participants1048 Participants380 Participants2680 Participants
Year of Diagnosis
2010-2011
506 Participants753 Participants952 Participants395 Participants2606 Participants
Year of Diagnosis
2012-2013
0 Participants716 Participants0 Participants384 Participants1100 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
0 / 0
other
Total, other adverse events
0 / 0
serious
Total, serious adverse events
0 / 0

Outcome results

Primary

Side Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or Pain

Primary outcomes for Aim 1: Acute and subacute side effects include any complication, lymphedema, seroma, wound infection, and pain.

Time frame: From the first BCS to 9 months post-diagnosis.

Population: Mahalanobis matching was used to adjust for baseline characteristics to account for potential treatment selection bias, where those who received SLNB might be systematically different from those who did not. Matches were assigned by choosing the two best non-SLNB patient matches for each SLNB patient. The final matched cohort was used for analyses.

ArmMeasureGroupValue (COUNT_OF_PARTICIPANTS)
Matched Aim 1 Cohort: No SLNBSide Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or PainNumber of participants with pain365 Participants
Matched Aim 1 Cohort: No SLNBSide Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or PainNumber of participants with any side effects534 Participants
Matched Aim 1 Cohort: No SLNBSide Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or PainNumber of participants with lymphedema23 Participants
Matched Aim 1 Cohort: No SLNBSide Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or PainNumber of participants with wound Infection453 Participants
Matched Aim 1 Cohort: No SLNBSide Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or PainNumber of participants with seroma179 Participants
Matched Aim 1 Cohort: SLNBSide Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or PainNumber of participants with seroma153 Participants
Matched Aim 1 Cohort: SLNBSide Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or PainNumber of participants with wound Infection296 Participants
Matched Aim 1 Cohort: SLNBSide Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or PainNumber of participants with any side effects404 Participants
Matched Aim 1 Cohort: SLNBSide Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or PainNumber of participants with pain237 Participants
Matched Aim 1 Cohort: SLNBSide Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or PainNumber of participants with lymphedema60 Participants
Comparison: Testing the association between use of sentinel lymph node biopsy (SLNB) and any complication in the Aim 1 matched cohort.p-value: <0.00199% CI: [1.18, 1.63]Chi-squared
Comparison: Testing the association between use of sentinel lymph node biopsy (SLNB) and lymphedema in the Aim 1 matched cohort.p-value: <0.00199% CI: [2.27, 8.75]Chi-squared
Comparison: Testing the association between use of sentinel lymph node biopsy (SLNB) and wound infection in the Aim 1 matched cohort.p-value: <0.00199% CI: [1, 1.54]Chi-squared
Comparison: Testing the association between use of sentinel lymph node biopsy (SLNB) and seroma in the Aim 1 matched cohort.p-value: <0.00199% CI: [1.03, 1.91]Chi-squared
Comparison: Testing the association between use of sentinel lymph node biopsy (SLNB) and pain in the Aim 1 matched cohort.p-value: 0.00399% CI: [1.04, 1.65]Chi-squared
Secondary

Breast Cancer Specific Mortality

Primary outcomes for Aim 2: Breast cancer specific mortality from 9 months post-diagnosis to death or the end of the study period (December, 2014).

Time frame: From 9 months post-diagnosis to death/end of study period (up to 1.5 years)

Population: Mahalanobis matching was used to adjust for baseline characteristics and account for potential treatment selection bias, where those who receive SLNB might be systematically different from those who do not. Matches were assigned by choosing the two best non-SLNB patient matches for each SLNB patient. The final matched cohort was used for analyses.

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Matched Aim 1 Cohort: No SLNBBreast Cancer Specific Mortality36 Participants
Matched Aim 1 Cohort: SLNBBreast Cancer Specific Mortality19 Participants
Comparison: Testing the association between between use of sentinel lymph node biopsy (SLNB) and breast cancer specific mortality.p-value: 0.86199% CI: [0.54, 2.35]Chi-squared
Secondary

Ipsilateral Invasive Breast Cancer Occurrence

Primary outcomes for Aim 2: Ipsilateral invasive breast cancer occurrence after 9 months of a DCIS diagnosis, per SEER reports.

Time frame: From 9 months post-diagnosis to death/end of study period (up to 1.5 years)

Population: Mahalanobis matching was used to adjust for baseline characteristics and account for potential treatment selection bias, where those who receive SLNB might be systematically different from those who do not. Matches were assigned by choosing the two best non-SLNB patient matches for each SLNB patient. The final matched cohort was used for analyses.

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Matched Aim 1 Cohort: No SLNBIpsilateral Invasive Breast Cancer Occurrence150 Participants
Matched Aim 1 Cohort: SLNBIpsilateral Invasive Breast Cancer Occurrence70 Participants
Comparison: Testing the association between use of sentinel lymph node biopsy (SLNB) and ipsilateral invasive breast cancer occurrence for the Aim 2 matched cohort.p-value: 0.60399% CI: [0.71, 1.51]Chi-squared
Secondary

Lasting Side Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or Pain

Secondary outcomes for Aim 2: unadjusted side effects (any side effects, lymphedema, any infection, seroma, pain) in the matched sample by use of sentinel lymph node biopsy (SLNB). Any side effects refer to the occurrence of one or more of the following complications since diagnosis of DCIS: lymphedema related complications, any infection, seroma, and any pain.

Time frame: From 9 months post-diagnosis to death/end of study period (up to 1.5 years)

Population: Mahalanobis matching was used to adjust for baseline characteristics and account for potential treatment selection bias, where those who receive SLNB might be systematically different from those who do not. Matches were assigned by choosing the two best non-SLNB patient matches for each patient. The final matched cohort was used for analyses.

ArmMeasureGroupValue (COUNT_OF_PARTICIPANTS)
Matched Aim 1 Cohort: No SLNBLasting Side Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or PainNumber of participants with lymphedema159 Participants
Matched Aim 1 Cohort: No SLNBLasting Side Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or PainNumber of participants with seroma294 Participants
Matched Aim 1 Cohort: No SLNBLasting Side Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or PainNumber of participants with any infection1579 Participants
Matched Aim 1 Cohort: No SLNBLasting Side Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or PainNumber of participants with pain1283 Participants
Matched Aim 1 Cohort: No SLNBLasting Side Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or PainNumber of participants with any side effects2329 Participants
Matched Aim 1 Cohort: SLNBLasting Side Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or PainNumber of participants with pain701 Participants
Matched Aim 1 Cohort: SLNBLasting Side Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or PainNumber of participants with any side effects1204 Participants
Matched Aim 1 Cohort: SLNBLasting Side Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or PainNumber of participants with lymphedema123 Participants
Matched Aim 1 Cohort: SLNBLasting Side Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or PainNumber of participants with any infection751 Participants
Matched Aim 1 Cohort: SLNBLasting Side Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or PainNumber of participants with seroma186 Participants
Comparison: Testing the association between use of sentinel lymph node biopsy (SLNB) and any side effects in the matched Aim 2 cohort.p-value: 0.20799% CI: [1, 1.2]Chi-squared
Comparison: Testing the association between use of sentinel lymph node biopsy (SLNB) and lymphedema related complications in the Aim 2 matched cohort.p-value: <0.00199% CI: [1.12, 2.11]Chi-squared
Comparison: Testing the association between use of sentinel lymph node biopsy (SLNB) and any infection in the Aim 2 matched cohort.p-value: 0.11399% CI: [0.87, 1.1]Chi-squared
Comparison: Testing the association between use of sentinel lymph node biopsy (SLNB) and seroma in the Aim 2 matched cohort.p-value: 0.0199% CI: [0.93, 1.58]Chi-squared
Comparison: Testing the association between use of sentinel lymph node biopsy (SLNB) and pain in the Aim 2 matched cohort.p-value: 0.02999% CI: [0.98, 1.25]Chi-squared
Secondary

Overall Survival

Secondary outcomes for Aim 2.

Time frame: From 9 months post-diagnosis to death/end of study period (up to 1.5 years)

Population: Mahalanobis matching was used to adjust for baseline characteristics and account for potential treatment selection bias, where those who receive SLNB might be systematically different from those who do not. Matches were assigned by choosing the two best non-SLNB patient matches for each SLNB patient. The final matched cohort was used for analyses.

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Matched Aim 1 Cohort: No SLNBOverall Survival727 Participants
Matched Aim 1 Cohort: SLNBOverall Survival287 Participants
Comparison: Testing the association between use of sentinel lymph node biopsy (SLNB) and overall mortality in the Aim 2 matched cohort.p-value: <0.00199% CI: [0.73, 1.05]Chi-squared
Secondary

Receipt of Mastectomy

Secondary outcomes for Aim 1: receipt of mastectomy with and without SLNB after initial BCS through 6 months after DCIS diagnosis.

Time frame: 6 months within DCIS diagnosis

Population: Mahalanobis matching was used to adjust for baseline characteristics and account for potential treatment selection bias, where those who receive SLNB might be systematically different from those who do not. Matches were assigned by choosing the two best non-SLNB patient matches for each SLNB patient. The final matched sample was used for analyses.

ArmMeasureGroupValue (COUNT_OF_PARTICIPANTS)
Matched Aim 1 Cohort: No SLNBReceipt of MastectomyYes237 Participants
Matched Aim 1 Cohort: No SLNBReceipt of MastectomyNo4481 Participants
Matched Aim 1 Cohort: SLNBReceipt of MastectomyYes413 Participants
Matched Aim 1 Cohort: SLNBReceipt of MastectomyNo1996 Participants
Comparison: Testing the association between receipt of SLNB and receipt of mastectomy within 6 months of DCIS diagnosis.p-value: <0.001Chi-squared
Secondary

Receipt of Radiation Therapy

Secondary outcomes for Aim 1: Receipt of radiation therapy within 9 months of DCIS diagnosis.

Time frame: 9 months within DCIS diagnosis

Population: Mahalanobis matching was used to adjust for baseline characteristics and account for potential treatment selection bias, where those who receive SLNB might be systematically different from those who do not. Matches were assigned by choosing the two best non-SLNB patient matches for each SLNB patient. The final matched cohort was used for analyses.

ArmMeasureGroupValue (COUNT_OF_PARTICIPANTS)
Matched Aim 1 Cohort: No SLNBReceipt of Radiation TherapyYes2814 Participants
Matched Aim 1 Cohort: No SLNBReceipt of Radiation TherapyNo1904 Participants
Matched Aim 1 Cohort: SLNBReceipt of Radiation TherapyYes1416 Participants
Matched Aim 1 Cohort: SLNBReceipt of Radiation TherapyNo993 Participants
Comparison: Testing the association between receipt of SLNB and receipt of radiation therapy within 9 months of DCIS diagnosis.p-value: 0.48Chi-squared
Secondary

Treated Recurrence

Primary outcomes for Aim 2: Treated recurrence was defined by the receipt of mastectomy after 9 months of a DCIS diagnosis in the Aim 2 matched cohort.

Time frame: From 9 months post-diagnosis to death/end of study period (up to 1.5 years)

Population: Mahalanobis matching was used to adjust for baseline characteristics and account for potential treatment selection bias, where those who receive SLNB might be systematically different from those who do not. Matches were assigned by choosing the two best non-SLNB patient matches for each SLNB patient. The final matched cohort was used for analyses.

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Matched Aim 1 Cohort: No SLNBTreated Recurrence145 Participants
Matched Aim 1 Cohort: SLNBTreated Recurrence78 Participants
Comparison: Testing the association between use of sentinel lymph node biopsy (SLNB) and treated recurrence in the Aim 2 matched cohort.p-value: 0.6299% CI: [0.81, 1.69]Chi-squared

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026