Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where Andrea Hestley is active.

Publication


Featured researches published by Andrea Hestley.


Annals of Surgical Oncology | 2003

The Amount of Metastatic Melanoma in a Sentinel Lymph Node: Does It Have Prognostic Significance?

Grant W. Carlson; Douglas R. Murray; Robert H. Lyles; Charles A. Staley; Andrea Hestley; Cynthia Cohen

Background: The amount of metastatic disease in the sentinel lymph node (SLN) is examined as a prognostic factor in malignant melanoma.Methods: SLN mapping was performed on 592 patients with stage I and II malignant melanoma from March 1, 1994, through December 31, 1999. One hundred four patients were found to have 134 sentinel SLNs containing metastatic melanoma. The slides were reviewed, and the size of the metastatic melanoma in each SLN was measured. The size of the metastatic deposit was defined as macrometastasis (>2 mm), micrometastasis (≤2 mm), a cluster of cells (10–30 grouped cells) in the subcapsular space or interfollicular zone, or isolated melanoma cells (1 to ≥20 individual cells) in subcapsular sinuses.Results: The number of metastases in each SLN was isolated melanoma cells, n = 5 (3.7%); cluster of cells, n = 35 (26.1%); ≤2 mm, n = 45 (33.6%); and >2 mm, n = 49 (36.7%). Seventy-nine patients (76%) had a single positive SLN. The size of the largest nodal metastasis was used to stratify patients with multiple positive SLNs. The overall 3-year survival for patients with SLN micrometastases was 90%, versus 58% for patients with SLN macrometastases (P = .004).Conclusions: The amount of metastatic melanoma in an SLN is an independent predictor of survival. Patients with SLN metastatic deposits >2 mm in diameter have significantly decreased survival.


Annals of Surgical Oncology | 2003

Sentinel Lymph Node Mapping for Thick (≥4-mm) Melanoma: Should We Be Doing It?

Grant W. Carlson; Douglas R. Murray; Andrea Hestley; Charles A. Staley; Robert H. Lyles; Cynthia Cohen

Background: Thick (≥4-mm) primary melanomas are believed to be associated with a high incidence of occult distant metastases. The use of sentinel lymph node (SLN) mapping and biopsy in the treatment lesions has been questioned.Methods: A retrospective review of a computerized database identified 114 patients who underwent successful SLN mapping and biopsy from January 1, 1994, to December 31, 1999. Records were reviewed for clinicopathologic features of the patients and their tumors. Survival curves were constructed from Kaplan-Meier estimates and analyzed with log-rank tests and Cox proportional hazards modeling.Results: There were 75 men and 39 women with a mean age of 57 years (range, 24–85 years). The primary tumor sites were head and neck (n = 29; 25.4%), trunk (n = 44; 38.6%), and extremities (n = 41; 36%). Tumor thickness ranged from 4 to 17 mm (median, 5.2 mm; mean, 6.3 mm). Ulceration was present in 40 (35.1%) tumors. Thirty-seven patients (32.5%) had a positive SLN biopsy, and 18 of these patients (48.6%) had a single tumor-positive lymph node after dissection. The mean follow-up was 37.8 months. The overall 3-year survival for SLN-negative patients was 82%, versus 57% for SLN-positive patients (P = .006). Lymph node status and tumor ulceration were independent predictors of overall survival in multivariate Cox regression analysis.Conclusions:The pathologic status of the SLN in patients with thick melanomas is a strong independent prognostic factor for survival, and SLN mapping should be routinely performed.


Annals of Surgery | 2008

Regional recurrence after negative sentinel lymph node biopsy for melanoma.

Grant W. Carlson; Andrew J. Page; Cynthia Cohen; Douglas Parker; Ron Yaar; Anya Li; Andrea Hestley; Keith A. Delman; Douglas R. Murray

Objective:Sentinel lymph node (SLN) biopsy has shown great utility in the management of melanoma. An analysis of regional recurrence in previously mapped negative SLN basins as the first site of relapse is performed. Methods:A retrospective query of a prospective melanoma database from 1994 to 2006 identified 1287 patients who underwent successful SLN biopsy. One thousand sixty patients (82.4%) were SLN negative and 227 (17.6%) patients SLN positive. Clinical variables were examined for the impact on regional recurrence by multivariate analysis. Results:Mean follow-up was 44.3 months (range 3–155 months). Thirty-five patients (3.3%) presented with false-negative (FN) SLN biopsy. Pathologic review of the SLNs harvested from these basins found 7 (20.0%) samples positive for metastatic melanoma. Multivariate analysis found head and neck site [hazard ratio 3.67; 95% confidence interval (CI), 1.77–7.60, P < 0.001] and tumor thickness (hazard ratio 1.16; 95% CI, 1.04–1.30, P = 0.01) to be predictive of FN SLN biopsy. The 5-year melanoma specific survival calculated from the date of the SLN biopsy was 57.6% (95%CI, 35.7–41.9) in the FN group, which was not statistically different than the SLN positive group 60.0% (95% CI, 29.6–40.1; P = 0.14). Conclusions:Head and neck tumor site and tumor thickness are predictors of a FN SLN biopsy. Mechanisms other than pathologic SLN sampling error may contribute to the failure of the SLN biopsy in some patients. Patients with regional recurrence after negative SLN biopsy have a similar 5-year survival compared with patients with positive SLNs.


Plastic and Reconstructive Surgery | 2005

Sentinel lymph node biopsy in the management of cutaneous head and neck melanoma.

Grant W. Carlson; Douglas R. Murray; Robert H. Lyles; Andrea Hestley; Cynthia Cohen

Sentinel lymph node biopsy has revolutionized the surgical management of primary malignant melanoma. Most series on sentinel lymph node mapping have concentrated on extremity and truncal melanomas. The head and neck region has a rich and unpredictable lymphatic system. The use of sentinel lymph node mapping in the management of head and neck melanoma is evaluated. The authors conducted a retrospective review of patients treated for clinical stage I and stage II malignant melanoma of the head and neck with dynamic lymphoscintigraphy and gamma probe–guided sentinel lymph node biopsy. One hundred thirty-two patients (99 male patients and 33 female patients) were identified. The primary melanoma sites were the scalp (n = 54), ear (n = 14), face (n = 37), and neck (n = 27). Primary tumor staging was as follows: T1, 11; T2, 38; T3, 39; and T4, 44. Dynamic lymphoscintigraphy visualized sentinel lymph nodes in 128 patients (97 percent). In 71 cases (55 percent), a single draining nodal basin was identified, and in 57 cases there were multiple draining nodal basins (two basins, 55; three basins, two). Sentinel lymph nodes were successfully identified in 176 of 186 nodal basins (95 percent). Positive sentinel lymph nodes were identified in 22 patients (17.6 percent). Sentinel lymph node positivity by tumor staging was as follows: T2, 10.8 percent; T3, 19.4 percent; and T4, 26.8 percent. Completion lymphadenectomy revealed residual disease in seven patients (33.3 percent). Sentinel lymph node mapping for head and neck melanoma can be performed with results comparable to those of other anatomical sites.


Annals of Surgical Oncology | 2002

The definition of the sentinel lymph node in melanoma based on radioactive counts.

Grant W. Carlson; Douglas R. Murray; Vinod H. Thourani; Andrea Hestley; Cynthia Cohen

BackgroundThere is no consensus on the definition of a hot, nonblue sentinel lymph node (SLN), despite the widespread use of radiocolloid in SLN mapping.MethodsA retrospective review of 592 patients with malignant melanoma who underwent SLN mapping was performed. Ex vivo SLN counts and nodal bed counts were obtained by using a gamma probe. The size of each metastatic deposit in an SLN was defined as macrometastases (>2 mm), micrometastases (≤2 mm), a cluster of cells, or isolated melanoma cells.ResultsA total of 1175 SLNs (SLN−, n=1041; SLN+, n=134) were evaluated. The mean SLN count/bed counts were SLN−, 322±980 and SLN+, 450±910 (not significant [NS]) (>2 mm, 270±792 [NS]; ≤2 mm, 446±693 [NS]; isolated melanoma cells/cluster of cells, 677±1189 [P=.036]). Overall, 16 (1.4%) of the SLNs collected had an overall ratio of ≤2. This included two positive SLNs (1.5%), both of which contained macrometatic disease. Forty-seven positive nodal basins had at least one negative SLN. The hottest SLNs in these basins were negative for metastatic disease in nine cases (19.1%). In one basin (2.1%), the positive SLN count was <10% of the hottest lymph node count.ConclusionsRemoval of lymph nodes until the bed count is 10% of the hottest lymph node will remove 98% of positive SLNs. Lymph node tumor burden influences radioactive counts.


Head and Neck-journal for The Sciences and Specialties of The Head and Neck | 2013

Analysis of regional recurrence after negative sentinel lymph node biopsy for head and neck melanoma.

Kelly McDonald; Andrew J. Page; Sumanas W. Jordan; Carrie K. Chu; Andrea Hestley; Keith A. Delman; Douglas R. Murray; Grant W. Carlson

The head and neck have a rich lymphatic drainage and complex anatomy, which complicate sentinel lymph node (SLN) biopsy for melanoma. The incidence of regional recurrence after a negative SLN biopsy has been shown to be higher than that at other sites. Compounding factors in this scenario were analyzed to determine their impact on both SLN status and survival.


International Journal of Surgical Oncology | 2012

Increasing Age Is Associated with Worse Prognostic Factors and Increased Distant Recurrences despite Fewer Sentinel Lymph Node Positives in Melanoma

Andrew J. Page; Anya Li; Andrea Hestley; Douglas R. Murray; Grant W. Carlson; Keith A. Delman

Background. Advanced age is associated with a poorer prognosis in patients with melanoma. Despite this established finding, a decreased incidence of positive sentinel lymph nodes (SLNs) with advancing age has paradoxically been described. Methods. Using a single-institution database of melanoma patients between 1994 and 2009, the relationship between standard clinicopathologic variables and recurrence based on age was evaluated. Results. 1244 patients who underwent successful SLN biopsies were analyzed (mean followup 80.3 months). Increasing age was independently associated with worse survival on multivariable analysis (P = 0.02). SLN status was more likely to be negative if the patient was older (P = 0.01). Conclusions. Our data supports the paradox that increasing age is associated with a lower frequency of positive-SLN biopsies despite age itself being a poor prognostic factor. We propose that age-dependent variations in the primary tumor and the patient may predispose to a hematogenous route of spread for the older population, leading to worse survival.


Journal of Surgical Oncology | 2010

Routine biopsy of cloquet's node is of limited value in sentinel node positive melanoma patients†‡

Carrie K. Chu; Jonathan S. Zager; Suroosh S. Marzban; Mark I. Gimbel; Douglas R. Murray; Andrea Hestley; Jane L. Messina; Vernon K. Sondak; Grant W. Carlson; Keith A. Delman

Biopsy of Cloquets node (CN) during groin dissection has been used to indicate need for pelvic dissection. With earlier detection of microscopic regional disease in the era of sentinel node biopsy (SNB), frequency of positive CN may be so low that routine biopsy is unwarranted.


Journal of Surgical Oncology | 2015

Tanning beds: A call to action for further educational and legislative efforts

Clara R. Farley; Yewande Alimi; Lauren R. Espinosa; Sebastian D. Perez; William Knechtle; Andrea Hestley; Grant W. Carlson; Maria C. Russell; Keith A. Delman; Monica Rizzo

Melanoma is steadily increasing over the past decade. Recent studies confirmed a link between tanning bed use and melanoma. We sought to determine the prevalence and frequency of tanning bed among young patients with melanoma.


Archives of Otolaryngology-head & Neck Surgery | 2000

Management of Malignant Melanoma of the Head and Neck Using Dynamic Lymphoscintigraphy and Gamma Probe–Guided Sentinel Lymph Node Biopsy

Grant W. Carlson; Douglas R. Murray; Robert Greenlee; Naomi P. Alazraki; Cynthia Fry-Spray; Rufus Poole; Michel Blais; Andrea Hestley; John P. Vansant

Collaboration


Dive into the Andrea Hestley's collaboration.

Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Researchain Logo
Decentralizing Knowledge