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DCIS is a noninvasive cancer, not a risk factor for breast cancer [Meeting Abstract]
Guth, A; Montes, J; Schnabel, F; Chun, J; Schwartz, S; Kamen, E; Shapiro, R; Axelrod, D
Introduction: Ductal carcinoma in situ (DCIS) and invasive breast cancer have long been viewed as representing two points on the spectrum of one disease. A recent study published by Narod et al. found that women diagnosed with DCIS who developed an invasive recurrence were 18.1 times more likely to die of breast cancer than women who did not. In light of this controversial topic, we investigated DCIS in a contemporary cohort of newly diagnosed women at our institution spanning a five year period. Methods: The institutional Breast Cancer Database was queried for all women with newly diagnosed breast cancer from 2010-2015. Variables included age, race, body mass index (BMI), risk factors, tumor characteristics and outcomes. Statistical analyses included Pearson's Chi Square and Fisher's Exact Tests. Results: Out of a total of 2190 patients, 475 (22%) had pure DCIS while 1715 (78%) had invasive cancer. The median follow up was 3 years. The median age was 59 years (range 22-95). Of the patients with invasive cancer, 36 (2%) had any recurrence. Similarly, of the patients with DCIS, 9 (2%) developed recurrent disease (ipsilateral or contralateral), with 4 patients diagnosed with invasive recurrence (44%). Of the 36 recurrences in patients with invasive cancer, 33% presented with chest wall or distant metastasis. Patients with pure DCIS had a slightly higher proportion of African Americans and Hispanics (11% v. 8%) and higher proportion of women with BMI>30 who developed an invasive recurrence (78% v. 50%). All recurrences in the pure DCIS cohort were detected by routine screening surveillance, with a majority detected by mammography (89%). Conclusions: Within a relatively short follow up period, we found that the rates of in-breast recurrences were the same in women with pure DCIS compared to women with invasive breast cancer. Also, 44% of women developed invasive breast cancer recurrence after an initial DCIS diagnosis, potentially altering their long term survival. These findings suggest that women with all breast cancers, including DCIS, requires intensive surveillance after initial treatment, as consequences of delayed diagnosis may impact on their long term survival
EMBASE:72203400
ISSN: 1068-9265
CID: 2014912
Cost Analysis of Intraoperative Subareolar Frozen Section During Nipple-Sparing Mastectomy
Alperovich, Michael; Reis, Scott M; Choi, Mihye; Karp, Nolan S; Frey, Jordan D; Chang, Jessica B; Axelrod, Deborah M; Shapiro, Richard L; Guth, Amber A
BACKGROUND: Permanent paraffin subareolar biopsy during nipple-sparing mastectomy (NSM) tests for occult cancer at the nipple-areolar complex. Intraoperative subareolar frozen section can provide earlier detection intraoperatively. Cost analysis for intraoperative subareolar frozen section has never been performed. METHODS: NSM cases from 2006-2013 were reviewed. Patient records including financial charges were analyzed. RESULTS: Of 480 subareolar biopsies for NSM from 2006-2013, 21 were abnormal (4.4 %). A total of 307 of the subareolar biopsies included intraoperative frozen section. Of the 307, 12 (3.9 %) were abnormal with 7 of 12 detected on intraoperative frozen section. The median baseline charge for an intraoperative subareolar frozen section was $309 for an estimated total cost of $94,863 in 307 breasts. The median baseline charge for interval operative resection of a nipple-areolar complex following an abnormal subareolar pathology result was $11,021. Intraoperative subareolar biopsy avoided an estimated six return trips to the operating room for savings of $66,126. At our institution, routine use of intraoperative frozen section resulted in an additional $28,737 in healthcare charges or $95 per breast. CONCLUSIONS: We present the first cost analysis to evaluate intraoperative subareolar frozen section in NSM. This practice obviated an estimated six return trips to the operating room. With our institutional frequency of abnormal subareolar pathology, intraoperative frozen sections resulted in a marginal increased charge per mastectomy.
PMID: 26438436
ISSN: 1534-4681
CID: 1794552
Nipple-sparing Mastectomy and Sub-areolar Biopsy: To Freeze or not to Freeze? Evaluating the Role of Sub-areolar Intraoperative Frozen Section
Alperovich, Michael; Choi, Mihye; Karp, Nolan S; Singh, Baljit; Ayo, Diego; Frey, Jordan D; Roses, Daniel F; Schnabel, Freya R; Axelrod, Deborah M; Shapiro, Richard L; Guth, Amber A
Use of nipple-sparing mastectomy (NSM) for risk-reduction and therapeutic breast cancer resection is growing. The role for intraoperative frozen section of the nipple-areolar complex remains controversial. Records of patients undergoing NSM at our institution from 2006 to 2013 were reviewed. Records from 501 nipple-sparing mastectomies were reviewed (216 therapeutic, 285 prophylactic). Of the 480 breasts with sub-areolar biopsies, 307 had intraoperative frozen sections and 173 were evaluated with permanent paraffin section only. Among the 307 intraoperative frozen sections, 12 biopsies were positive on permanent paraffin section (3.9% or 12/307). Of the 12 positive permanent biopsies, five were false negative and the remaining seven concordant intraoperatively. Sensitivity and specificity of sub-areolar frozen section were 0.58 and 1, respectively. Positive sub-areolar biopsies consisted primarily of ductal carcinoma in situ (62% or 13/21). The nipples or nipple-areolar complex were resected in a separate procedure following mastectomy (10/21), intraoperatively following frozen section results (7/21) or during second-stage breast reconstruction (3/21; 1 additional scheduled). Only 30% (6/20) of resected specimens had abnormal residual pathology. Intraoperative frozen section is highly specific and moderately sensitive for the detection of positive sub-areolar biopsies in NSM. Its use can help guide intraoperative reconstructive planning. The presence of positive sub-areolar biopsies in both contralateral and high-risk prophylactic mastectomy specimens emphasizes the need to perform sub-areolar biopsies in all nipple-sparing mastectomies.
PMID: 26510917
ISSN: 1524-4741
CID: 1817532
Oncologic outcomes after nipple-sparing mastectomy: A single-institution experience
Frey, Jordan D; Alperovich, Michael; Kim, Jennifer Chun; Axelrod, Deborah M; Shapiro, Richard L; Choi, Mihye; Schnabel, Freya R; Karp, Nolan S; Guth, Amber A
INTRODUCTION: Long-term oncologic outcomes in nipple-sparing mastectomy (NSM) continue to be defined. Rates of locoregional recurrence for skin-sparing mastectomy (SSM) and NSM in the literature range from 0% to 14.3%. We investigated the outcomes of NSM at our institution. METHODS: Patients undergoing NSM at our institution from 2006 to 2014 were identified and outcomes were analyzed. RESULTS: From 2006 to 2014, 319 patients (555 breasts) underwent NSM. One-hundered and fourty-one patients (237 breasts) had long-term follow-up available. Average patient age and BMI were 47.78 and 24.63. Eighty-four percent of patients underwent mastectomy primarily for a therapeutic indication. Average tumor size was 1.50 cm with the most common histologic type being invasive ductal carcinoma (62.7%) followed by DCIS (23.7%). Average patient follow-up was 30.73 months. There was one (0.8%) incidence of ipsilateral chest-wall recurrence. There were 0.37 complications per patient. CONCLUSIONS: We examined our institutional outcomes with NSM and found a locoregional recurrence rate of 0.8% with no nipple-areolar complex recurrence. This rate is lower than published rates for both NSM and SSM. J. Surg. Oncol. (c) 2015 Wiley Periodicals, Inc.
PMID: 26628318
ISSN: 1096-9098
CID: 1863442
MarginProbe device use and re-excision rates for breast conservation surgeries [Meeting Abstract]
Schnabel, F; Guth, A; Axelrod, D; Chun, J; Schwartz, S; Shapiro, R
ISI:000375622403424
ISSN: 1538-7445
CID: 2146972
Breast Density and Positive Lumpectomy Margins [Meeting Abstract]
Schnabel, Freya; Chun, Jennifer; Schwartz, Shira; Axelrod, Deborah; Guth, Amber; Shapiro, Richard; Daniel, Roses; Hiotis, Karen; Radzio, Agnes
ISI:000384566800141
ISSN: 1068-9265
CID: 2283912
Genomic characterization of acral lentiginous melanoma: Identification of altered metabolism as a potential therapeutic target. [Meeting Abstract]
Weiss, Sarah Ann; Martinez, Carlos N.; de Miera, Eleazar Vega-Saenz; Dolgalev, Igor; Shapiro, Richard L.; Heguy, Adriana; Hernando, Eva; Kirchhoff, Tomas; Osman, Iman
ISI:000404711507146
ISSN: 0732-183x
CID: 5236632
Oncologic outcomes after nipple-sparing mastectomy: A single-institution experience [Meeting Abstract]
Guth, A A; Frey, J D; Alperovich, M; Kim, J C; Axelrod, D M; Shapiro, R L; Choi, M; Karp, N S; Schnabel, F R
Introduction: Nipple-sparing mastectomy (NSM) is the latest advancement in the treatment of breast cancer. Long-term oncologic outcomes in nipple-sparing mastectomy (NSM) continue to be defined. Rates of locoregional recurrence for skin-sparing mastectomy (SSM) and NSM in the literature range from 0 to 14.3%. We investigated the outcomes of NSM at our institution. Methods: Patients undergoing NSM at our institution from 2006 to 2014 were identified. Patient demographics, tumor characteristics, and outcomes were collected. Locoregional recurrence was compared to previously published NSM and SSM results compiled from 14 and 11 studies in the literature. Institutional review board approval was obtained prior to the initiation of this study. Results: From 2006 to 2014, 319 patients (555 breasts) underwent NSM. 149 patients (248 breasts) had long-term follow-up available. Average patient age and BMI were 47.4 and 24.28. Eighty-five percent of patients underwent mastectomy primarily for a therapeutic indication. Average tumor size was 1.41 centimeters with the most common histologic type being invasive ductal carcinoma (66.7%) followed by DCIS (23.8%). Nodal disease was present in 14.8% of patients. Average patient follow-up was 30.72 months. There was one (0.7%) incidence of ipsilateral chest-wall recurrence in a 44 year-old (p<0.0001, compared to aggregate NSM and SSM data). There were 0.36 complications per patient. There were 3 incidences of nipple-areola complex (NAC) necrosis: 2 partial thickness necrosis and 1 full thickness necrosis. (Table Presented) Conclusions: We examined our institutional outcomes with NSM and found a locoregional recurrence rate of 0.7% with no nipple-areolar complex recurrence. This rate is significantly lower than aggregate published rates for both NSM and SSM
EMBASE:72247810
ISSN: 0008-5472
CID: 2096172
Impact of Socioeconomic Status and Ethnicity on Melanoma Presentation and Recurrence in Caucasian Patients
Salvaggio, Christine; Han, Sung Won; Martires, Kathryn; Robinson, Eric; Madankumar, Reshmi; Gumaste, Priyanka; Polsky, David; Stein, Jennifer; Berman, Russell; Shapiro, Richard; Zhong, Judy; Osman, Iman
OBJECTIVES: The impact of ethnicity and the socioeconomic status (SES) among Caucasians is not well studied. Here, we examine the impact of income on melanoma presentation and prognosis within a Caucasian cohort, accounting for ethnicity, as some reports suggest increased melanoma incidence in Ashkenazi Jewish (AJ) BRCA mutation carriers. METHODS: We studied prospectively enrolled primary melanoma patients at New York University. SES data were estimated using United States' Census Bureau data and patient zip codes. We evaluated associations between ethnicity, SES, and baseline characteristics using the x03C7;2 test and multivariate logistic regression. We compared survival distributions using Kaplan-Meier curves, log-rank tests, and Cox proportional hazard ratios. RESULTS: Of the 1,339 enrolled patients, AJ represented 32% (n = 423). Apart from AJ being older at presentation (p < 0.001), no significant differences were observed in baseline characteristics between ethnic groups. Patients with a median household income (MHI) lower than the median of the cohort were significantly more likely to present with advanced stages (p < 0.001) compared to patients with a higher MHI. Shorter overall (p = 0.016) and post-recurrence survival (p = 0.042) was also observed in patients from lower-income households. CONCLUSION: Data suggest that disparities in melanoma presentation in Caucasians stratify according to income independent of ethnic background.
PMID: 26840790
ISSN: 1423-0232
CID: 1933532
Somatic and germline analyses of a long term melanoma survivor with a recurrent brain metastasis
Weiss, Sarah; Darvishian, Farbod; Tadepalli, Jyothi; Shapiro, Richard; Golfinos, John; Pavlick, Anna; Polsky, David; Kirchhoff, Tomas; Osman, Iman
BACKGROUND: Median overall survival (OS) of patients with melanoma brain metastases (MBM) is usually 6 months or less. There are rare reports of patients with treated MBM who survived for years. These outlier cases represent valuable opportunities to study the somatic and germline factors that may have influenced patient outcome and led to extended survival. CASE PRESENTATION: Here we report the clinical scenario of a 67 year old man with a recurrent brain metastasis from melanoma who has survived over 12 years post-resection. We review the literature relating to clinical and molecular variables associated with long term survival post-brain metastasis. We present the somatic characteristics of this individual patient's tumor as well as an analysis of inherited genetic variants related to immune function. The patient's resected brain tumor is BRAF V600E mutated, NRAS wild type (WT), and TERT C250T mutated. The patient is a carrier of germline variants in immunomodulatory loci associated with prolonged survival. CONCLUSIONS: Our data suggest that genetic variants in immunomodulatory loci may partially contribute to this patient's unusually favorable outcome and should not be overlooked. With further and future investigation, knowledge of inherited single nucleotide polymorphisms (SNPs) may provide clinicians with more individualized prognostic information for melanoma patients, with potential implications for surveillance strategies and therapeutic interventions.
PMCID:4657192
PMID: 26597176
ISSN: 1471-2407
CID: 1856342