Jessica Cintolo-Gonzalez

ORCID: 0000-0003-0572-5265
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Cutaneous Melanoma Detection and Management
  • BRCA gene mutations in cancer
  • Extracellular vesicles in disease
  • Global Cancer Incidence and Screening
  • T-cell and Retrovirus Studies
  • Ferroptosis and cancer prognosis
  • Cancer Genomics and Diagnostics
  • Animal Disease Management and Epidemiology
  • Nutrition, Genetics, and Disease
  • Sarcoma Diagnosis and Treatment
  • Immunotherapy and Immune Responses
  • Viral-associated cancers and disorders
  • Nonmelanoma Skin Cancer Studies
  • Cancer survivorship and care
  • Vascular Tumors and Angiosarcomas
  • RNA modifications and cancer
  • Global Health Workforce Issues
  • Genetic Associations and Epidemiology
  • Economic and Financial Impacts of Cancer
  • Travel-related health issues
  • Cancer Risks and Factors
  • CAR-T cell therapy research
  • Health and Medical Research Impacts
  • Lung Cancer Diagnosis and Treatment
  • Breast Lesions and Carcinomas

University of Vermont Medical Center
2019-2025

Centre for the Observation and Modelling of Earthquakes, Volcanoes and Tectonics
2024

University of Vermont
2022-2024

Massachusetts General Hospital
2017-2020

Harvard University
2018

MGH Institute of Health Professions
2018

Brigham and Women's Hospital
2017

Hospital of the University of Pennsylvania
2015

University of Pennsylvania
2013

E. Shelley Hwang Terry Hyslop Thomas Lynch Marc D. Ryser Anna Weiss and 95 more Anna Wolf Karen A. Norris Meredith Witten Lars J. Grimm Stuart J. Schnitt Sunil Badve Rachel E. Factor Elizabeth S. Frank Deborah Collyar Desiree Basila Donna Pinto Mark A. Watson Robert B. West Louise Davies Jenny L. Donovan Ayako Shimada Yutong Li Li Yan Antonia V. Bennett Shoshana M. Rosenberg Jeffrey R. Marks Eric Winer Marc Boisvert Armando E. Giuliano Kelsey E. Larson Kathleen J. Yost Priscilla F. McAuliffe Amy Krie Nina P. Tamirisa Lisa A. Carey Alastair M. Thompson Ann H. Partridge Vinay Gudena Akiko Chiba Jessica Bensenhaver Eleni Andreopoulou Elizabeth A. Mittendorf Cindy B. Matsen Rebecca L. Jackson Deba P. Sarma Elie G. Dib Heather B. Neuman Tina Yen Doreen M. Agnese Rachelle Leong Patricia Cronin Ingrid M. Lizarraga Joseph M. Guenther Kristalyn K. Gallagher Reema Batra A. Marilyn Leitch Timothy D. Moore Kimberly Strickland Moira Christoudias Marissa Howard-McNatt Anna M. Higham Anasuya Gunturi John M. Schallenkamp Karng Log Samantha A. Seaward Heather Harris Wright Amy Rivere Eric Feliberti Lisa A. Lai Jessica Cintolo-Gonzalez Kandace P. McGuire Ki Wook Chung Anjali R. Thawani Emily Marcinkowski Jennifer L. Marti Nathalie Johnson Sandhya Pruthi April Phantana-angkool Jessica Maxwell Sangeetha Prabhakaran Douglas Weckstein Mahvish Muzaffar Sarah Sinclair Christopher M. McGreevy Steve Madden Laura Peterson Dan Sotirescu Hannah Hazard‐Jenkins Thomas E. Lad Sarah A. McLaughlin Sheldon Feldman Matthias Weiss Suliat Nurudeen M. Firdos Ziauddin Anthony J. Jaslowski Ivy Abraham Faith Goldman Nicholas J. DiBella Mehra Golshan Tuoc Dao

Importance Active monitoring for low-risk ductal carcinoma in situ (DCIS) of the breast has been proposed as an alternative to guideline-concordant care, but safety this approach is unknown. Objective To compare rates invasive cancer patients with DCIS receiving active vs care. Design, Setting, and Participants Prospective, randomized noninferiority trial enrolling 995 women aged 40 years or older a new diagnosis hormone receptor–positive grade 1 2 without at 100 US Alliance Cancer...

10.1001/jama.2024.26698 article EN JAMA 2024-12-12
Ann H. Partridge Terry Hyslop Shoshana M. Rosenberg Antonia V. Bennett Sarah Drier and 95 more Mattias Jönsson Ayako Shimada Yutong Li Yan Li Thomas Lynch Elizabeth Frank Deborah Collyar Desiree Basila Donna Pinto Anna Weiss Anna Wolf Karen A. Norris Meredith Witten Marc Boisvert Armando E. Giuliano Kelsey E. Larson Kathleen J. Yost Priscilla F. McAuliffe Amy Krie Nina Tamirisa Sonja Darai Lisa A. Carey Alastair M. Thompson E. Shelley Hwang Vinay Gudena Akiko Chiba Jessica Bensenhaver Eleni Andreopoulou Elizabeth A. Mittendorf Cindy B. Matsen Rebecca D. Jackson Deba P. Sarma Elie G. Dib Heather B. Neuman Tina Yen Doreen M. Agnese Rachelle Leong Patricia Cronin Ingrid M. Lizarraga Joseph M. Guenther Kristalyn K. Gallagher Reema Batra A. Marilyn Leitch Timothy M. Moore Kimberly Strickland Moira Christoudias Marissa Howard-McNatt Anna M. Higham Anasuya Gunturi John M. Schallenkamp Karng Log Samantha A. Seaward Heather Wright Amy Rivere Eric Feliberti Lisa A. Lai Jessica Cintolo-Gonzalez Kandace P. McGuire Ki Y. Chung Anjali Thawani Emily Marcinkowski Jennifer L. Marti Nathalie A. Johnson Sandhya Pruthi April Phantana-angkool Jessica Maxwell Sangeetha Prabhakaran Douglas Weckstein Mahvish Muzaffar Sarah Sinclair Christopher M. McGreevy Steve Madden Laura Peterson Dan Sotirescu Hannah Hazard‐Jenkins Thomas E. Lad Sarah A. McLaughlin Sheldon Feldman Matthias Weiss Suliat Nurudeen M. Firdos Ziauddin Anthony J. Jaslowski Ivy Abraham Faith Goldman Nicholas J. DiBella Mehra Golshan Tuoc Dao Howard M. Gross Yolanda Tammaro M. D. Bowie Katharine Yao Theodore Kim Rebecca Aft Alyssa Throckmorton Jose Eugenio Najera

Importance Active monitoring (AM) for low-risk ductal carcinoma in situ (DCIS) has been considered as a potential alternative to guideline-concordant care (GCC; inclusive of surgery with or without radiation). Reported data comparing patient-reported outcomes (PROs) between GCC and AM DCIS are lacking. Objective To compare PROs at baseline over time patients randomized receive either GCC. Design, Setting, Participants This prespecified secondary outcome analysis used prospectively collected...

10.1001/jamaoncol.2024.6556 article EN JAMA Oncology 2024-12-12

Abstract Background Nodal surveillance (NS) has overtaken completion lymphadenectomy as the preferred management for sentinel node-positive (SLN+) melanoma, but requires frequent exams and nodal ultrasound (US). Social determinants of health (SDoH) may affect US adherence in real-world populations, evaluation these potential impacts is needed. Methods Adults with SLN+ melanoma diagnosed from July 2017 to December 2019 who received NS at nine cancer centers were identified retrospectively....

10.1245/s10434-024-16498-w article EN cc-by Annals of Surgical Oncology 2024-11-22

Background The impact of age on breast cancer risk model calculations at the population level has not been well documented. Methods Retrospective analysis formal assessment in 36 542 females ages 40-84 a single institution from 02/2007 to 12/2009. Five-year and lifetime risks were calculated using Gail, Tyrer-Cuzick version 6 (TC6), 7 (TC7), BRCAPRO, Claus models. Risk BRCA mutation was TC6, TC7, Myriad. Eligibility for testing assessed NCCN guidelines. Descriptive analyses performed trends...

10.1111/tbj.12976 article EN The Breast Journal 2018-01-08

Abstract There is a critical need for robust and minimally invasive biomarkers predicting monitoring tumor progression response to treatment. Transcriptomes of plasma-derived exosomes (PDEs) are suitable candidates fulfill such role, since they contain subtranscriptome their cell origin, and, nearly all types secrete exosomes, this allows the potential multiple concurrently. However, major issue preventing widespread adoption exosome as that observed plasma actually result from mixture...

10.1158/1538-7445.am2018-4282 article EN Cancer Research 2018-07-01

Talimogene laherparepvec (T-VEC) is currently the only United States Food and Drug Administration-approved intralesional therapy for advanced melanoma. Recent studies have assessed integration of T-VEC with systemic immunotherapy, though response remains variable. Therefore, we sought to identify factors associated by conducting a retrospective, single-center analysis involving melanoma patients treated T-VEC. In present study, recorded demographic clinicopathological data, details...

10.36922/mi.3445 article EN cc-by Microbes & Immunity 2024-06-04

Abstract Background: Modulation of the PD-1/PD-L1 axis in melanoma is critical importance both setting targeted therapy treatment, as well newer trials combining with checkpoint blocking antibodies. BRAF inhibition has been shown to increase PD-L1 expression tumors. Exosomes are circulating microvesicles that contain a subtranscriptome and/or subproteome their cell origin, including tumor cells and immune cells. We evaluated exosomal protein effect inhibitor (BRAFi) treatment on levels....

10.1158/2326-6074.tumimm17-a35 article EN Cancer Immunology Research 2018-09-01

BACKGROUND Recent advances in diagnostic and therapeutic modalities have made oncologic care ever more challenging, multidisciplinary tumor boards (MTBs) are increasingly being used as a forum to discuss coordinate for complex oncology patients. Literature on the use of MTBs specific cutaneous dermatologic surgery remains limited. OBJECTIVE To share our experiences with at University Vermont Medical Center (UVMMC). METHODS We describe formation, timing, participation, clinical discussion,...

10.1097/dss.0000000000002252 article EN Dermatologic Surgery 2019-11-25

Abstract Background: Over-expression of the receptor tyrosine kinase ErbB2 (HER-2) has been widely implicated in malignant transformation, cell survival, motility and invasion breast cancers. Intermediate expression HER-2 identified luminal cancer stem cells. over-expression down regulates major histocompatibility complex class I molecules (MHCI) Results: We investigated various expressing lines measured HLA A-2 MHC expression. High Her-2 SKBR3 SKOVA3 intermediate MCF7 demonstrated extremely...

10.1158/1557-3125.advbc-b087 article EN Molecular Cancer Research 2013-10-01

Abstract Molecular and immunologic studies analyzing tumor samples have failed to find a robust reliable predictive marker of responsiveness immune checkpoints. Exosomes are circulating microvesicles that contain subtranscriptome their cell origin. They produced by cells been shown be mediators responses in cancer. To examine the role peripheral-blood (PB) derived exosomal transcriptomic signatures, we performed microarray analysis on N=99 from both PB-derived exosomes biopsies N=39 (N=25...

10.1158/2326-6074.tumimm17-b25 article EN Cancer Immunology Research 2018-09-01
Coming Soon ...