Peter A. Kanetsky

ORCID: 0000-0002-5567-9618
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About
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Research Areas
  • Cutaneous Melanoma Detection and Management
  • Skin Protection and Aging
  • melanin and skin pigmentation
  • Testicular diseases and treatments
  • Melanoma and MAPK Pathways
  • BRCA gene mutations in cancer
  • Cancer Genomics and Diagnostics
  • Cancer Immunotherapy and Biomarkers
  • Immunotherapy and Immune Responses
  • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
  • Epigenetics and DNA Methylation
  • Vitamin D Research Studies
  • Genetic Associations and Epidemiology
  • Nutrition, Genetics, and Disease
  • LGBTQ Health, Identity, and Policy
  • Sexual Differentiation and Disorders
  • Climate Change Communication and Perception
  • Allergic Rhinitis and Sensitization
  • Biochemical Analysis and Sensing Techniques
  • Glutathione Transferases and Polymorphisms
  • Cervical Cancer and HPV Research
  • Behavioral Health and Interventions
  • Mast cells and histamine
  • CAR-T cell therapy research
  • Computational Drug Discovery Methods

Moffitt Cancer Center
2016-2025

University of Wisconsin–Madison
2023

University of Pennsylvania
2006-2021

Philadelphia University
2021

University of South Florida
2015-2018

National Institutes of Health
2006-2017

Memorial Sloan Kettering Cancer Center
1992-2016

The University of Sydney
2010-2016

Women's College Hospital
2013-2016

University of North Carolina at Chapel Hill
2016

Increased risk of mortality in patients with CKD has been attributed to inflammation. However, the association between kidney function, albuminuria, and biomarkers inflammation not examined a large cohort patients.This study measured plasma levels IL-1β, IL-1 receptor antagonist (IL-1RA), IL-6, TNF-α, TGF-β, high-sensitivity C-reactive protein (hs-CRP), fibrinogen, serum albumin 3939 participants enrolled Chronic Renal Insufficiency Cohort June 2003 September 2008. An score was established...

10.2215/cjn.03500412 article EN Clinical Journal of the American Society of Nephrology 2012-09-28

Background and objectives CKD is a global public health problem with significant mortality morbidity. Design, setting, participants, & measurements We examined the multivariable association of plasma levels IL-1, IL-1 receptor antagonist, IL-6, TNF- α , TGF- β high–sensitivity C–reactive protein, fibrinogen, serum albumin progression in 3430 Chronic Renal Insufficiency Cohort study participants. Results Over median follow-up time 6.3 years, 899 participants reached composite end point...

10.2215/cjn.13121215 article EN Clinical Journal of the American Society of Nephrology 2016-06-23

Germline variants in MC1R, the gene encoding melanocortin-1 receptor, and sun exposure increase risk for melanoma Caucasians. The majority of melanomas that occur on skin with little evidence chronic sun-induced damage (non-CSD melanoma) have mutations BRAF oncogene, whereas marked CSD (CSD these are less frequent. In two independent Caucasian populations, we show MC1R strongly associated non-CSD melanomas. this tumor subtype, is due to an developing mutations.

10.1126/science.1127515 article EN Science 2006-06-30

<h3>Importance</h3>This study proposes an alternative tumor staging system for cutaneous squamous cell carcinoma (CSCC) that more precisely defines the small subset of tumors with a high risk metastasis and death.<h3>Objective</h3>To identify factors poor outcomes in CSCC evaluate 2010 American Joint Committee on Cancer (AJCC) (T) system's ability to stratify occurrence these outcomes.<h3>Design</h3>Retrospective cohort study.<h3>Setting</h3>A single academic...

10.1001/jamadermatol.2013.2456 article EN JAMA Dermatology 2013-01-16

Although most hospital-based studies suggest more favorable survival with tumor-infiltrating lymphocytes (TILs) present in primary melanomas, it is uncertain whether TILs provide prognostic information beyond existing melanoma staging definitions. We addressed the issue an international population-based study of patients single and multiple melanomas.On basis Genes, Environment Melanoma (GEM) study, we conducted follow-up 2,845 diagnosed from 1998 to 2003 3,330 invasive melanomas centrally...

10.1200/jco.2013.51.3002 article EN Journal of Clinical Oncology 2013-10-15

Abstract In cancer patients, a high pre-treatment neutrophil-to-lymphocyte ratio (NLR) is associated with poorer survival outcomes. Significant variation in the magnitude of this association has been observed between studies, but sources are poorly understood. Here, we explore differences prognostic potential NLR patient subgroups stratified by demographic and clinical characteristics using retrospective cohort 5,363 patients treated at Moffitt Cancer Center (Tampa, FL). We identify for whom...

10.1038/s41598-019-56218-z article EN cc-by Scientific Reports 2019-12-23

Melanoma risk is related to sun exposure; we have investigated variation by tumour site and latitude.We performed a pooled analysis of 15 case-control studies (5700 melanoma cases 7216 controls), correlating patterns exposure, sunburn solar keratoses (three studies) with risk. Pooled odds ratios (pORs) 95% Bayesian confidence intervals (CIs) were estimated using unconditional polytomous logistic random-coefficients models.Recreational exposure was factor for on the trunk (pOR = 1.7; CI:...

10.1093/ije/dyp166 article EN cc-by-nc International Journal of Epidemiology 2009-04-08

NRAS and BRAF mutations in melanoma inform current treatment paradigms, but their role survival from primary has not been established. Identification of patients at high risk melanoma-related death based on characteristics before evidence recurrence could recommendations for patient follow-up eligibility adjuvant trials.

10.1001/jamaoncol.2015.0493 article EN JAMA Oncology 2015-04-09

IMPORTANCE Previous studies have reported that histopathologically amelanotic melanoma is associated with poorer survival than pigmented melanoma; however, small numbers of melanomas, selected populations, lack centralized pathologic review, or no adjustment for stage limit the interpretation generalization results from prior studies.OBJECTIVE To compare melanoma-specific between patients and those in a large international population-based study.DESIGN, SETTING, AND PARTICIPANTS Survival...

10.1001/jamadermatol.2014.1348 article EN JAMA Dermatology 2014-08-27

Purpose.: Somatic mutations in GNAQ, GNA11, SF3B1, EIF1AX, and BAP1 have been identified uveal melanoma (UM). The aim of this study was to determine whether these genes primary tumors were associated with metastases individuals diagnosed UM. Methods.: A total 63 UM cases who developed a metastasis within 48 months treatment 53 controls metastasis-free over similar time period selected for the study. Primary screened BAP1. association tumor characteristics, chromosome 3 copy number,...

10.1167/iovs.14-14550 article EN Investigative Ophthalmology & Visual Science 2014-06-27

Susceptibility to testicular germ cell tumors (TGCT) has a significant heritable component, and genome-wide association studies (GWASs) have identified with variants in several genes, including KITLG , SPRY4 BAK1 TERT DMRT1 ATF7IP . In our GWAS, we genotyped 349 TGCT cases 919 controls replicated top hits an independent set of 439 960 attempt find novel susceptibility loci. We second marker (rs7040024) the doublesex mab-3-related transcription factor 1 ( ) gene that is previously described...

10.1093/hmg/ddr207 article EN Human Molecular Genetics 2011-05-06

PURPOSE To identify potential gaps in attitudes, knowledge, and institutional practices toward lesbian, gay, bisexual, transgender, queer/questioning (LGBTQ) patients, a national survey of oncologists at National Cancer Institute–Designated Comprehensive Centers was conducted to measure these attributes related LGBTQ patients desire for future training education. METHODS A random sample 450 from 45 cancer centers selected the American Medical Association’s Physician Masterfile complete...

10.1200/jco.18.00551 article EN Journal of Clinical Oncology 2019-01-16

The MC1R gene is a key regulator of skin pigmentation. We aimed to evaluate the association between variants and risk sporadic cutaneous melanoma (CM) within M‐SKIP project, an international pooled‐analysis on , cancer phenotypic characteristics. Data included 5,160 cases 12,119 controls from 17 studies. calculated summary odds ratio (SOR) for each nine most studied combined with CM by using random‐effects models. Stratified analysis characteristics were also performed. Melanoma increased...

10.1002/ijc.29018 article EN International Journal of Cancer 2014-06-10
Yan Zhang Amber N. Hurson Haoyu Zhang Parichoy Pal Choudhury Douglas F. Easton and 95 more Roger L. Milne Jacques Simard Per Hall Kyriaki Michailidou Joe Dennis Marjanka K. Schmidt Jenny Chang‐Claude Puya Gharahkhani David C. Whiteman Peter T. Campbell Michael Hoffmeister Mark A. Jenkins Ulrike Peters Li Hsu Stephen B. Gruber Graham Casey Stephanie L. Schmit Tracy A. O’Mara Amanda B. Spurdle Deborah J. Thompson Ian Tomlinson Immaculata De Vivo Maria Teresa Landi Matthew H. Law Mark M. Iles Florence Démenais Rajiv Kumar Stuart MacGregor D. Timothy Bishop Sarah V. Ward Melissa L. Bondy Richard S. Houlston John K. Wiencke Beatrice Melin Jill S. Barnholtz‐Sloan Ben Kinnersley Margaret Wrensch Christopher I. Amos Rayjean J. Hung Paul Brennan James McKay Neil E. Caporaso Sonja I. Berndt Brenda M. Birmann Nicola J. Camp Peter Kraft Nathaniel Rothman Susan L. Slager Andrew Berchuck Paul D.P. Pharoah Thomas A. Sellers Simon A. Gayther Celeste Leigh Pearce Ellen L. Goode Joellen M. Schildkraut Kirsten B. Moysich Laufey T. Ámundadóttir Eric J. Jacobs Alison P. Klein Gloria M. Petersen Harvey A. Risch Rachel Z. Stolzenberg-Solomon Brian M. Wolpin Donghui Li Rosalind A. Eeles Christopher A. Haiman Zsofia Kote‐Jarai Fredrick R. Schumacher Ali Amin Al Olama Mark P. Purdue Ghislaine Scélo Marlene Dalgaard Mark H. Greene Tom Grotmol Peter A. Kanetsky Katherine A. McGlynn Katherine L. Nathanson Clare Turnbull Fredrik Wiklund Douglas F. Easton Roger L. Milne Jacques Simard Per Hall Kyriaki Michailidou Joe Dennis Marjanka K. Schmidt Jenny Chang‐Claude Puya Gharahkhani David C. Whiteman Peter T. Campbell Michael Hoffmeister Mark A. Jenkins Ulrike Peters Li Hsu Stephen B. Gruber

Abstract Genome-wide association studies (GWAS) have led to the identification of hundreds susceptibility loci across cancers, but impact further remains uncertain. Here we analyse summary-level data from GWAS European ancestry fourteen cancer sites estimate number common variants (polygenicity) and underlying effect-size distribution. All cancers show a high degree polygenicity, involving at minimum thousands loci. We project that sample sizes required explain 80% heritability vary 60,000...

10.1038/s41467-020-16483-3 article EN cc-by Nature Communications 2020-07-03
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