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Poster session 04

879P - Whole-genome landscape of head and neck melanomas in East Asia (China)

Date

10 Sep 2022

Session

Poster session 04

Topics

Pathology/Molecular Biology;  Genetic and Genomic Testing

Tumour Site

Melanoma

Presenters

Xuan Wang

Citation

Annals of Oncology (2022) 33 (suppl_7): S356-S409. 10.1016/annonc/annonc1059

Authors

X. Wang1, W. Wu2, X. Wu1, L. Si1, Z. Chi1, X. Sheng1, L. li3, W. Han3, H. Li3, B. Lian1, L. Zhou1, L. Mao1, X. Bai1, T. Bixia1, X. Wei1, C. Cui1, Y. Kong1, J. Guo1

Author affiliations

  • 1 Department Of Renal Cell Carcinoma & Melanoma, Peking University Cancer Hospital and Institute, 100142 - Beijing/CN
  • 2 Clinical Research Division, Berry Oncology Corporation, 350200 - Fuzhou/CN
  • 3 Na, Berry Oncology Corporation, 350200 - Fuzhou/CN

Resources

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Abstract 879P

Background

Head and neck melanomas are a heterogeneous group of tumors that may arise from abnormal melanocytes in various sites, such as scalp of the head, conjunctiva, nasal pharyngeal and oral cavity.Despite their close anatomical location, melanomas from different sites of the head and neck have widely different histological structures, biological behaviors, genetic characteristics, and prognosis. However, researches on genomic landscape of head and neck melanoma in East Asian patients are still sparse.

Methods

We performed whole-genome sequencing (WES) and clinical profiling on 40 head and neck melanoma samples, including 8 conjunctival melanoma of the eyes, 7 scalp of the head, 10 nasal and 15 oral cavity. All the samples were derived from East Asian populations.

Results

We show that tumors from eyes and head tended to harbor more substitution/indel (SNVs) than those from nasal and oral. Percent of the genome affected by copy number variants was no significant differences among the four sites. Head and neck melanomas samples had more genetic aberations in genes within the RTK-RAS pathway and NOTCH pathway. BRAF, NRAS were identified as significantly mutated genes (SMGs).Eyes and head tumors had consistent mutational signature, while the oral and nasal tumors had similar mutationnal signature. The number and type of structural rearrangements varied dramatically among the four sites, suggesting the implication of distinctive mutational processes. Somatic arm level CNV alterations including amplification at chromosomes 1q, 6p, 7 and deletions at chromosomes 6q, 10, 13q, 16q, 18p, 19.Significantly amplified regions, included those containing 1q22(MUC1), 3p13(MITF), 4q12(KIT), 5p15.33 (TERT), 6p23, 7p22.1(RAC1), 8q24.3(MYC), 9q34.3(NOTCH1),11q14.1(PAK1,GAB2), 12q14.1(CDK4), 17q25.1, 20q13.2. as well as deleted regions 3q22.2, 6q26, 9p21.3-24.3(CDKN2A,CDKN2B), 10q26.13, 11q23.3, 16p12.1, 11q22.3(ATM).

Conclusions

Here, we provided a detailed view of the genomic landscape of East Asian head and neck melanomas at different sites, which might extend our current understanding of head and neck melanoma.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

Peking University Cancer Hospital and Institute.

Funding

Has not received any funding.

Disclosure

X. Wang: Financial Interests, Personal, Advisory Board: Oriengene. W. Wu: Financial Interests, Personal, Full or part-time Employment: Berry Oncology Corporation. L. Si: Financial Interests, Personal, Advisory Board: MSD, Roche, Novartis, Shanghai Junshi Biosciences; Financial Interests, Personal, Invited Speaker: Oriengene. L. li: Financial Interests, Personal, Full or part-time Employment: Berry Oncology Corporation. W. Han: Financial Interests, Personal, Full or part-time Employment: Berry Oncology Corporation. H. Li: Financial Interests, Personal, Full or part-time Employment: Berry Oncology Corporation. J. Guo: Financial Interests, Personal, Advisory Board: MSD, Roche, Bayer, Novartis, Simcere Pharmaceutical Group, Shanghai Junshi Biosciences, Oriengene; Non-Financial Interests, Member: ASCO; Non-Financial Interests, Leadership Role: CSCO. All other authors have declared no conflicts of interest.

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