Grant Details
Grant Number: |
5R01CA233524-05 Interpret this number |
Primary Investigator: |
Thomas, Nancy |
Organization: |
Univ Of North Carolina Chapel Hill |
Project Title: |
Identification of Lethal Melanomas at the Time of Diagnosis |
Fiscal Year: |
2024 |
Abstract
PROJECT SUMMARY/ABSTRACT
Melanoma incidence rates continue to increase, whereas rates for most other cancers have
declined. Emerging systemic therapies for patients who have progressed to metastatic melanoma
are extending survival, but can be toxic, immensely costly and have variable efficacy. There are
efforts to extend the use of new agents to earlier disease stages as adjuvant therapies. Better
prediction of lethal melanoma at time of diagnosis is important to determine those who would
benefit from adjuvant therapies and, conversely, avoid toxicity in those whose melanomas are
unlikely to recur. Our central hypothesis is that it is possible to determine the combinations of
genetic alterations and immune responses in tumor samples that define a melanoma likely to be
ultimately lethal if not treated early. Conversely, we hypothesize that it will be possible to identify
somatic profiles of the tumors that indicate a very low risk of recurrence and ultimate death of the
patient, obviating the need for expensive, toxic treatments in such patients. We also hypothesize
that host characteristics, including germline variants in multiple genes, will be associated with
lethal melanoma. In Aim 1, we will test whether common somatic mutations in 104 genes/gene
regions in tumors are associated with death from melanoma. These genes include known
oncogenic drivers (BRAF, NRAS and TERT) and tumor suppressors (NF1, CDKN2A/CDKN2B,
PTEN and TP53). We will also test the hypothesis that measuring the immune cell milieu will add
information to survival prediction beyond conventional grading of tumor-infiltrating lymphocytes.
We will then explore how best to combine the genetic alterations, immune measures and 2018
American Joint Committee on Cancer (AJCC) tumor stage to identify those melanomas highly
likely to be ultimately lethal. In Aim 2, we will determine the extent to which the host characteristics
of germline variants, phenotypic characteristics, sun exposure, age and gender differ among
melanoma cases characterized as potentially lethal vs. nonlethal, leading to the identification of
a subset of the population at high risk for lethal melanoma. This research will be undertaken using
a resource that is uniquely suited to addressing these issues, the international, population-based
Genes, Environment and Melanoma (GEM) Study, which collected epidemiologic data, pathology
and tumor sections for a large cohort of incident primary cutaneous melanoma cases diagnosed
in the year 2000. We have available a minimum of 10 years of follow-up of vital status and cause
of death for all cases. GEM is an ideal resource because the end of the follow-up period precedes
the targeted and immune therapy era, allowing us to study factors affecting the natural history of
the disease. The vast majority of GEM cases (more than 85%) presented with local disease, and
we project that at least 80% of the deaths will occur in cases initially presenting with local or
regional disease. The results should enhance our ability to identify lethal melanomas at an early
stage when treatments may be more effective and, conversely, to identify melanomas with a very
low risk of recurrence for which unnecessary and potentially toxic treatments can be confidently
avoided.
Publications
Region of Interest Detection in Melanocytic Skin Tumor Whole Slide Images-Nevus and Melanoma.
Authors: Cui Y.
, Li Y.
, Miedema J.R.
, Edmiston S.N.
, Farag S.W.
, Marron J.S.
, Thomas N.E.
.
Source: Cancers, 2024-07-23 00:00:00.0; 16(15), .
EPub date: 2024-07-23 00:00:00.0.
PMID: 39123344
Related Citations
Region of Interest Detection in Melanocytic Skin Tumor Whole Slide Images - Nevus & Melanoma.
Authors: Cui Y.
, Li Y.
, Miedema J.R.
, Edmiston S.N.
, Farag S.
, Marron J.S.
, Thomas N.E.
.
Source: Arxiv, 2024-05-16 00:00:00.0; , .
EPub date: 2024-05-16 00:00:00.0.
PMID: 38800658
Related Citations
Genetic Variants Associated With Hidradenitis Suppurativa.
Authors: Sun Q.
, Broadaway K.A.
, Edmiston S.N.
, Fajgenbaum K.
, Miller-Fleming T.
, Westerkam L.L.
, Melendez-Gonzalez M.
, Bui H.
, Blum F.R.
, Levitt B.
, et al.
.
Source: Jama Dermatology, 2023-09-01 00:00:00.0; 159(9), p. 930-938.
PMID: 37494057
Related Citations
Association of functional, inherited vitamin D-binding protein variants with melanoma-specific death.
Authors: Gibbs D.C.
, Thomas N.E.
, Kanetsky P.A.
, Luo L.
, Busam K.J.
, Cust A.E.
, Anton-Culver H.
, Gallagher R.P.
, Zanetti R.
, Rosso S.
, et al.
.
Source: Jnci Cancer Spectrum, 2023-08-31 00:00:00.0; 7(5), .
PMID: 37494457
Related Citations
Sex-Specific Associations of MDM2 and MDM4 Variants with Risk of Multiple Primary Melanomas and Melanoma Survival in Non-Hispanic Whites.
Authors: Ward S.V.
, Autuori I.
, Luo L.
, LaPilla E.
, Yoo S.
, Sharma A.
, Busam K.J.
, Olilla D.W.
, Dwyer T.
, Anton-Culver H.
, et al.
.
Source: Cancers, 2023-05-11 00:00:00.0; 15(10), .
EPub date: 2023-05-11 00:00:00.0.
PMID: 37345045
Related Citations
Pathway Alterations in Stage II/III Primary Melanoma.
Authors: Kostrzewa C.E.
, Luo L.
, Arora A.
, Seshan V.E.
, Ernstoff M.S.
, Edmiston S.N.
, Conway K.
, Gorlov I.
, Busam K.
, Orlow I.
, et al.
.
Source: Jco Precision Oncology, 2023 Mar; 7, p. e2200439.
PMID: 36926987
Related Citations
Methylation of nonessential genes in cutaneous melanoma - Rule Out hypothesis.
Authors: Gorlov I.P.
, Conway K.
, Edmiston S.N.
, Parrish E.A.
, Hao H.
, Amos C.I.
, Tsavachidis S.
, Gorlova O.Y.
, Begg C.
, Hernando E.
, et al.
.
Source: Melanoma Research, 2023-02-20 00:00:00.0; , .
EPub date: 2023-02-20 00:00:00.0.
PMID: 36805567
Related Citations
Landscape of mutations in early stage primary cutaneous melanoma: An InterMEL study.
Authors: Luo L.
, Shen R.
, Arora A.
, Orlow I.
, Busam K.J.
, Lezcano C.
, Lee T.K.
, Hernando E.
, Gorlov I.
, Amos C.
, et al.
.
Source: Pigment Cell & Melanoma Research, 2022-07-25 00:00:00.0; , .
EPub date: 2022-07-25 00:00:00.0.
PMID: 35876628
Related Citations
Minimally invasive microbiopsy for genetic profiling of melanocytic lesions: A case series.
Authors: Jain M.
, Autuori I.
, Everett N.
, Harris U.
, Yamada M.
, Prow T.
, Busam K.
, Marchetti M.A.
, Halpern A.C.
, Orlow I.
.
Source: Journal Of The American Academy Of Dermatology, 2021-12-16 00:00:00.0; , .
EPub date: 2021-12-16 00:00:00.0.
PMID: 34922919
Related Citations
Characterization of the CpG island hypermethylated phenotype (CIMP) subclass in primary melanomas.
Authors: Conway K.
, Tsai Y.S.
, Edmiston S.N.
, Parker J.S.
, Parrish E.A.
, Hao H.
, Kuan P.F.
, Scott G.A.
, Frank J.S.
, Googe P.
, et al.
.
Source: The Journal Of Investigative Dermatology, 2021-11-26 00:00:00.0; , .
EPub date: 2021-11-26 00:00:00.0.
PMID: 34843679
Related Citations
Association of Melanoma-Risk Variants with Primary Melanoma Tumor Prognostic Characteristics and Melanoma-Specific Survival in the GEM Study.
Authors: Davari D.R.
, Orlow I.
, Kanetsky P.A.
, Luo L.
, Busam K.J.
, Sharma A.
, Kricker A.
, Cust A.E.
, Anton-Culver H.
, Gruber S.B.
, et al.
.
Source: Current Oncology (toronto, Ont.), 2021-11-16 00:00:00.0; 28(6), p. 4756-4771.
EPub date: 2021-11-16 00:00:00.0.
PMID: 34898573
Related Citations
Disease-Associated Risk Variants in ANRIL are Associated with Tumor-Infiltrating Lymphocytes Presence in Primary Melanomas in the Population-Based GEM Study.
Authors: Davari D.R.
, Orlow I.
, Kanetsky P.A.
, Luo L.
, Edmiston S.N.
, Conway K.
, Parrish E.A.
, Hao H.
, Busam K.J.
, Sharma A.
, et al.
.
Source: Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology, 2021-10-04 00:00:00.0; , .
EPub date: 2021-10-04 00:00:00.0.
PMID: 34607836
Related Citations
Comparison of community pathologists with expert dermatopathologists evaluating Breslow thickness and histopathologic subtype in a large international population-based study of melanoma.
Authors: Yardman-Frank J.M.
, Bronner B.
, Rosso S.
, From L.
, Busam K.
, Groben P.
, Tucker P.
, Cust A.
, Armstrong B.
, Kricker A.
, et al.
.
Source: Jaad International, 2021 Sep; 4, p. 25-27.
EPub date: 2021-06-01 00:00:00.0.
PMID: 34409386
Related Citations
Differences in Melanoma Between Canada and New South Wales, Australia: A Population-Based Genes, Environment, and Melanoma (GEM) Study.
Authors: Yardman-Frank J.M.
, Glassheim E.
, Kricker A.
, Armstrong B.K.
, Marrett L.D.
, Luo L.
, Cust A.E.
, Busam K.J.
, Orlow I.
, Gallagher R.P.
, et al.
.
Source: Jid Innovations, 2021 Mar; 1(1), .
EPub date: 2021-01-25 00:00:00.0.
PMID: 33768212
Related Citations
Non-Cell-Autonomous Activity of the Hemidesmosomal Protein BP180/Collagen XVII in Granulopoiesis in Humanized NC16A Mice.
Authors: Lin L.
, Hwang B.J.
, Li N.
, Googe P.
, Diaz L.A.
, Miao E.
, Vilen B.
, Thomas N.E.
, Ting J.
, Liu Z.
.
Source: Journal Of Immunology (baltimore, Md. : 1950), 2020-09-30 00:00:00.0; , .
EPub date: 2020-09-30 00:00:00.0.
PMID: 32998984
Related Citations
Association of Known Melanoma Risk Factors with Primary Melanoma of the Scalp and Neck.
Authors: Wood R.P.
, Heyworth J.S.
, McCarthy N.S.
, Mauguen A.
, Berwick M.
, Thomas N.E.
, Millward M.J.
, Anton-Culver H.
, Cust A.E.
, Dwyer T.
, et al.
.
Source: Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology, 2020-08-20 00:00:00.0; , .
EPub date: 2020-08-20 00:00:00.0.
PMID: 32856602
Related Citations
Human genes differ by their UV sensitivity estimated through analysis of UV-induced silent mutations in melanoma.
Authors: Gorlov I.P.
, Amos C.I.
, Tsavachidis S.
, Begg C.
, Hernando E.
, Cheng C.
, Shen R.
, Orlow I.
, Luo L.
, Ernstoff M.S.
, et al.
.
Source: Human Mutation, 2020-07-09 00:00:00.0; , .
EPub date: 2020-07-09 00:00:00.0.
PMID: 32643855
Related Citations
Association of IRF4 single-nucleotide polymorphism rs12203592 with melanoma-specific survival.
Authors: Ward S.V.
, Gibbs D.C.
, Orlow I.
, Thomas N.E.
, Kanetsky P.A.
, Luo L.
, Cust A.E.
, Anton-Culver H.
, Gruber S.B.
, Gallagher R.P.
, et al.
.
Source: The British Journal Of Dermatology, 2020-01-20 00:00:00.0; , .
EPub date: 2020-01-20 00:00:00.0.
PMID: 31958143
Related Citations
Inherited Melanoma Risk Variants Associated with Histopathologically Amelanotic Melanoma.
Authors: Gibbs D.C.
, Orlow I.
, Vernali S.
, Powell H.B.
, Kanetsky P.A.
, Luo L.
, Busam K.J.
, Sharma A.
, Kricker A.
, Armstrong B.K.
, et al.
.
Source: The Journal Of Investigative Dermatology, 2019-09-27 00:00:00.0; , .
EPub date: 2019-09-27 00:00:00.0.
PMID: 31568773
Related Citations
A risk prediction model for development of subsequent primary melanoma in a population-based cohort.
Authors: Cust A.E.
, Badcock C.
, Smith J.
, Thomas N.E.
, Haydu L.E.
, Armstrong B.K.
, Law M.H.
, Thompson J.F.
, Kanetsky P.A.
, Begg C.B.
, et al.
.
Source: The British Journal Of Dermatology, 2019-09-14 00:00:00.0; , .
EPub date: 2019-09-14 00:00:00.0.
PMID: 31520533
Related Citations
Utility of TERT Promoter Mutations for Cutaneous Primary Melanoma Diagnosis.
Authors: Thomas N.E.
, Edmiston S.N.
, Tsai Y.S.
, Parker J.S.
, Googe P.B.
, Busam K.J.
, Scott G.A.
, Zedek D.C.
, Parrish E.A.
, Hao H.
, et al.
.
Source: The American Journal Of Dermatopathology, 2018-09-11 00:00:00.0; , .
EPub date: 2018-09-11 00:00:00.0.
PMID: 30211730
Related Citations