Ductal Carcinoma In Situ
Conditions
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
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
Study design
Eligibility
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
| Measure | Time frame | Description |
|---|---|---|
| Side Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or Pain | From 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
| Measure | Time frame | Description |
|---|---|---|
| Receipt of Radiation Therapy | 9 months within DCIS diagnosis | Secondary outcomes for Aim 1: Receipt of radiation therapy within 9 months of DCIS diagnosis. |
| Overall Survival | From 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 Pain | From 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 Mastectomy | 6 months within DCIS diagnosis | Secondary outcomes for Aim 1: receipt of mastectomy with and without SLNB after initial BCS through 6 months after DCIS diagnosis. |
| Ipsilateral Invasive Breast Cancer Occurrence | From 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 Recurrence | From 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 Mortality | From 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
| Arm | Count |
|---|---|
| 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 |
| Total | 13,084 |
Baseline characteristics
| Characteristic | Aim 1 Cohort: SLNB | Aim 2 Cohort: No SLNB | Aim 1 Cohort: No SLNB | Aim 2 Cohort: SLNB | Total |
|---|---|---|---|---|---|
| Age, Customized 67-69 years old | 573 Participants | 808 Participants | 981 Participants | 478 Participants | 2840 Participants |
| Age, Customized 70-74 years old | 783 Participants | 1309 Participants | 1592 Participants | 651 Participants | 4335 Participants |
| Age, Customized 75-79 years old | 614 Participants | 1110 Participants | 1263 Participants | 503 Participants | 3490 Participants |
| Age, Customized 80-84 years old | 333 Participants | 567 Participants | 670 Participants | 272 Participants | 1842 Participants |
| Age, Customized 85+ years old | 106 Participants | 171 Participants | 212 Participants | 88 Participants | 577 Participants |
| Comedonecrosis No | 2112 Participants | 3537 Participants | 4194 Participants | 1733 Participants | 11576 Participants |
| Comedonecrosis Yes | 297 Participants | 428 Participants | 524 Participants | 259 Participants | 1508 Participants |
| Elixhauser Comorbidity 1 to 2 | 935 Participants | 1548 Participants | 1914 Participants | 780 Participants | 5177 Participants |
| Elixhauser Comorbidity 3 or more | 255 Participants | 462 Participants | 575 Participants | 232 Participants | 1524 Participants |
| Elixhauser Comorbidity None | 1219 Participants | 1955 Participants | 2229 Participants | 980 Participants | 6383 Participants |
| Ethnicity (NIH/OMB) Hispanic or Latino | 135 Participants | 190 Participants | 221 Participants | 106 Participants | 652 Participants |
| Ethnicity (NIH/OMB) Not Hispanic or Latino | 2274 Participants | 3775 Participants | 4497 Participants | 1886 Participants | 12432 Participants |
| Ethnicity (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Geographic Region Midwest | 296 Participants | 460 Participants | 583 Participants | 229 Participants | 1568 Participants |
| Geographic Region Northeast | 488 Participants | 763 Participants | 979 Participants | 378 Participants | 2608 Participants |
| Geographic Region South | 588 Participants | 1026 Participants | 1141 Participants | 522 Participants | 3277 Participants |
| Geographic Region West | 1037 Participants | 1716 Participants | 2015 Participants | 863 Participants | 5631 Participants |
| Hormone receptors ER- and PR- | 341 Participants | 485 Participants | 631 Participants | 284 Participants | 1741 Participants |
| Hormone receptors ER+ and PR+ | 1329 Participants | 2316 Participants | 2608 Participants | 1170 Participants | 7423 Participants |
| Hormone receptors Missing | 739 Participants | 1164 Participants | 1479 Participants | 538 Participants | 3920 Participants |
| Marital Status Married | 1227 Participants | 1977 Participants | 2286 Participants | 1038 Participants | 6528 Participants |
| Marital Status Other | 97 Participants | 190 Participants | 236 Participants | 87 Participants | 610 Participants |
| Marital Status Unmarried | 1085 Participants | 1798 Participants | 2196 Participants | 867 Participants | 5946 Participants |
| Race/Ethnicity, Customized Black | 170 Participants | 271 Participants | 386 Participants | 129 Participants | 956 Participants |
| Race/Ethnicity, Customized Other | 91 Participants | 200 Participants | 233 Participants | 85 Participants | 609 Participants |
| Race/Ethnicity, Customized White | 2148 Participants | 3494 Participants | 4099 Participants | 1778 Participants | 11519 Participants |
| Region of Enrollment United States | 2409 participants | 3965 participants | 4718 participants | 1992 participants | 13084 participants |
| Sex: Female, Male Female | 2409 Participants | 3965 Participants | 4718 Participants | 1992 Participants | 13084 Participants |
| Sex: Female, Male Male | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Surgeon Volume 1 | 1140 Participants | 1986 Participants | 2182 Participants | 945 Participants | 6253 Participants |
| Surgeon Volume 2 | 578 Participants | 969 Participants | 1099 Participants | 496 Participants | 3142 Participants |
| Surgeon Volume 3 | 329 Participants | 465 Participants | 596 Participants | 267 Participants | 1657 Participants |
| Surgeon Volume 4+ | 300 Participants | 509 Participants | 727 Participants | 266 Participants | 1802 Participants |
| Surgeon Volume Not assigned | 62 Participants | 36 Participants | 114 Participants | 18 Participants | 230 Participants |
| Tumor Grade Moderately differentiated | 629 Participants | 1278 Participants | 1371 Participants | 536 Participants | 3814 Participants |
| Tumor Grade Poorly differentiated | 802 Participants | 1262 Participants | 1449 Participants | 730 Participants | 4243 Participants |
| Tumor Grade Undifferentiated | 321 Participants | 434 Participants | 601 Participants | 226 Participants | 1582 Participants |
| Tumor Grade Unknown | 403 Participants | 567 Participants | 799 Participants | 293 Participants | 2062 Participants |
| Tumor Grade Well differentiated | 254 Participants | 424 Participants | 498 Participants | 207 Participants | 1383 Participants |
| Tumor size 2.0-<5.0 cm | 434 Participants | 550 Participants | 749 Participants | 347 Participants | 2080 Participants |
| Tumor size <2.0 cm | 1264 Participants | 2407 Participants | 2552 Participants | 1148 Participants | 7371 Participants |
| Tumor size >5.0 cm | 89 Participants | 80 Participants | 149 Participants | 42 Participants | 360 Participants |
| Tumor size Missing | 622 Participants | 928 Participants | 1268 Participants | 455 Participants | 3273 Participants |
| Year of Diagnosis 1998-1999 | 30 Participants | 0 Participants | 63 Participants | 0 Participants | 93 Participants |
| Year of Diagnosis 2000-2003 | 395 Participants | 605 Participants | 806 Participants | 240 Participants | 2046 Participants |
| Year of Diagnosis 2004-2005 | 431 Participants | 531 Participants | 863 Participants | 264 Participants | 2089 Participants |
| Year of Diagnosis 2006-2007 | 508 Participants | 647 Participants | 986 Participants | 329 Participants | 2470 Participants |
| Year of Diagnosis 2008-2009 | 539 Participants | 713 Participants | 1048 Participants | 380 Participants | 2680 Participants |
| Year of Diagnosis 2010-2011 | 506 Participants | 753 Participants | 952 Participants | 395 Participants | 2606 Participants |
| Year of Diagnosis 2012-2013 | 0 Participants | 716 Participants | 0 Participants | 384 Participants | 1100 Participants |
Adverse events
| Event type | EG000 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
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.
| Arm | Measure | Group | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|---|
| Matched Aim 1 Cohort: No SLNB | Side Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or Pain | Number of participants with pain | 365 Participants |
| Matched Aim 1 Cohort: No SLNB | Side Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or Pain | Number of participants with any side effects | 534 Participants |
| Matched Aim 1 Cohort: No SLNB | Side Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or Pain | Number of participants with lymphedema | 23 Participants |
| Matched Aim 1 Cohort: No SLNB | Side Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or Pain | Number of participants with wound Infection | 453 Participants |
| Matched Aim 1 Cohort: No SLNB | Side Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or Pain | Number of participants with seroma | 179 Participants |
| Matched Aim 1 Cohort: SLNB | Side Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or Pain | Number of participants with seroma | 153 Participants |
| Matched Aim 1 Cohort: SLNB | Side Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or Pain | Number of participants with wound Infection | 296 Participants |
| Matched Aim 1 Cohort: SLNB | Side Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or Pain | Number of participants with any side effects | 404 Participants |
| Matched Aim 1 Cohort: SLNB | Side Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or Pain | Number of participants with pain | 237 Participants |
| Matched Aim 1 Cohort: SLNB | Side Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or Pain | Number of participants with lymphedema | 60 Participants |
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.
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Matched Aim 1 Cohort: No SLNB | Breast Cancer Specific Mortality | 36 Participants |
| Matched Aim 1 Cohort: SLNB | Breast Cancer Specific Mortality | 19 Participants |
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.
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Matched Aim 1 Cohort: No SLNB | Ipsilateral Invasive Breast Cancer Occurrence | 150 Participants |
| Matched Aim 1 Cohort: SLNB | Ipsilateral Invasive Breast Cancer Occurrence | 70 Participants |
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.
| Arm | Measure | Group | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|---|
| Matched Aim 1 Cohort: No SLNB | Lasting Side Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or Pain | Number of participants with lymphedema | 159 Participants |
| Matched Aim 1 Cohort: No SLNB | Lasting Side Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or Pain | Number of participants with seroma | 294 Participants |
| Matched Aim 1 Cohort: No SLNB | Lasting Side Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or Pain | Number of participants with any infection | 1579 Participants |
| Matched Aim 1 Cohort: No SLNB | Lasting Side Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or Pain | Number of participants with pain | 1283 Participants |
| Matched Aim 1 Cohort: No SLNB | Lasting Side Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or Pain | Number of participants with any side effects | 2329 Participants |
| Matched Aim 1 Cohort: SLNB | Lasting Side Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or Pain | Number of participants with pain | 701 Participants |
| Matched Aim 1 Cohort: SLNB | Lasting Side Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or Pain | Number of participants with any side effects | 1204 Participants |
| Matched Aim 1 Cohort: SLNB | Lasting Side Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or Pain | Number of participants with lymphedema | 123 Participants |
| Matched Aim 1 Cohort: SLNB | Lasting Side Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or Pain | Number of participants with any infection | 751 Participants |
| Matched Aim 1 Cohort: SLNB | Lasting Side Effects (Claim-based Measure), Including Lymphedema, Seroma, Wound Infection, or Pain | Number of participants with seroma | 186 Participants |
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.
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Matched Aim 1 Cohort: No SLNB | Overall Survival | 727 Participants |
| Matched Aim 1 Cohort: SLNB | Overall Survival | 287 Participants |
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.
| Arm | Measure | Group | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|---|
| Matched Aim 1 Cohort: No SLNB | Receipt of Mastectomy | Yes | 237 Participants |
| Matched Aim 1 Cohort: No SLNB | Receipt of Mastectomy | No | 4481 Participants |
| Matched Aim 1 Cohort: SLNB | Receipt of Mastectomy | Yes | 413 Participants |
| Matched Aim 1 Cohort: SLNB | Receipt of Mastectomy | No | 1996 Participants |
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.
| Arm | Measure | Group | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|---|
| Matched Aim 1 Cohort: No SLNB | Receipt of Radiation Therapy | Yes | 2814 Participants |
| Matched Aim 1 Cohort: No SLNB | Receipt of Radiation Therapy | No | 1904 Participants |
| Matched Aim 1 Cohort: SLNB | Receipt of Radiation Therapy | Yes | 1416 Participants |
| Matched Aim 1 Cohort: SLNB | Receipt of Radiation Therapy | No | 993 Participants |
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.
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Matched Aim 1 Cohort: No SLNB | Treated Recurrence | 145 Participants |
| Matched Aim 1 Cohort: SLNB | Treated Recurrence | 78 Participants |