4.6 Review

Epidemiological characteristics and genetic alterations in adult diffuse glioma in East Asian populations

Journal

CANCER BIOLOGY & MEDICINE
Volume 19, Issue 10, Pages 1440-1459

Publisher

CHINA ANTI-CANCER ASSOC
DOI: 10.20892/j.issn.2095-3941.2022.0418

Keywords

Glioma; East Asian; epidemiology; germline; somatic

Funding

  1. Excellent Young Scientists Fund (Hong Kong, China and Macau, China) [31922088]
  2. RGC [26102719]
  3. ITC [MHP/004/19, ITCPD/17-9]
  4. Department of Science and Technology of Guangdong Province [2020A0505090007]
  5. Project of Hetao Shenzhen-Hong Kong Science and Technology Innovation Cooperation Zone [HZQB-KCZYB-2020083]

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Understanding the racial specificities of diseases, such as adult diffuse glioma, is crucial for precision medicine. This comprehensive review examines the epidemiology and genomic characteristics of gliomas in East Asian populations and other ancestry groups. The study reveals lower glioma incidence in East Asians compared to Whites, as well as differences in age of onset, overall survival, and genetic risk loci between the two populations.
Understanding the racial specificities of diseases-such as adult diffuse glioma, the most common primary malignant tumor of the central nervous system-is a critical step toward precision medicine. Here, we comprehensively review studies of gliomas in East Asian populations and other ancestry groups to clarify the racial differences in terms of epidemiology and genomic characteristics. Overall, we observed a lower glioma incidence in East Asians than in Whites; notably, patients with glioblastoma had significantly younger ages of onset and longer overall survival than the Whites. Multiple genome-wide association studies of various cohorts have revealed single nucleotide polymorphisms associated with overall and subtype-specific glioma susceptibility. Notably, only 3 risk loci-5p15.33, 11q23.3, and 20q13.33-were shared between patients with East Asian and White ancestry, whereas other loci predominated only in particular populations. For instance, risk loci 12p11.23, 15q15-21.1, and 19p13.12 were reported in East Asians, whereas risk loci 8q24.21, 1p31.3, and 1q32.1 were reported in studies in White patients. Although the somatic mutational profiles of gliomas between East Asians and non-East Asians were broadly consistent, a lower incidence of EGFR amplification in glioblastoma and a higher incidence of 1p19q-IDH-TERT triple-negative low-grade glioma were observed in East Asian cohorts. By summarizing large-scale disease surveillance, germline, and somatic genomic studies, this review reveals the unique characteristics of adult diffuse glioma among East Asians, to guide clinical management and policy design focused on patients with East Asian ancestry.

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