Pan-cancer analysis of mutation and its association with tumor immunogenicity and the efficacy of immune checkpoint blockade.
2/5 보강
TL;DR
It is revealed that the mutation of ALK could enrich infiltration of immune cells, enhance tumor immunogenicity, and improve immune responses, and can be treated as a biomarker for favorable outcomes in pan-cancer immune checkpoint blockade.
PICO 자동 추출 (휴리스틱, conf 2/4)
유사 논문P · Population 대상 환자/모집단
2930 patients with 11 tumor types treated with immune checkpoint inhibitors, the mutation of indicated favorable overall survival (hazard ratio = 0.
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
In conclusion, mutation is associated with promoted cancer immunity and can be treated as a biomarker for favorable outcomes in pan-cancer immune checkpoint blockade.
OpenAlex 토픽 ·
Cancer Immunotherapy and Biomarkers
Lung Cancer Treatments and Mutations
Lung Cancer Research Studies
It is revealed that the mutation of ALK could enrich infiltration of immune cells, enhance tumor immunogenicity, and improve immune responses, and can be treated as a biomarker for favorable outcomes
APA
Zhiyang Huang, Jiajun Chen, et al. (2026). Pan-cancer analysis of mutation and its association with tumor immunogenicity and the efficacy of immune checkpoint blockade.. Genes & diseases, 13(3), 101701. https://doi.org/10.1016/j.gendis.2025.101701
MLA
Zhiyang Huang, et al.. "Pan-cancer analysis of mutation and its association with tumor immunogenicity and the efficacy of immune checkpoint blockade.." Genes & diseases, vol. 13, no. 3, 2026, pp. 101701.
PMID
41716637
Abstract
Anaplastic lymphoma kinase () plays important roles in tumorigenesis and is involved in tumor immunogenicity through various pathways. Here, we conducted a comprehensive bioinformatic and clinical analysis on the characteristics of pan-cancer mutation and its association with tumor immunity and the efficacy of immune checkpoint blockade. In 2930 patients with 11 tumor types treated with immune checkpoint inhibitors, the mutation of indicated favorable overall survival (hazard ratio = 0.69; 95% confidence interval, 0.57-0.83; < 0.001). We further developed and validated a nomogram to estimate the 12-month and 24-month survival probabilities after the initiation of immunotherapy. Moreover, multi-omics analysis on both intrinsic and extrinsic immune landscapes revealed that the mutation of could enrich infiltration of immune cells, enhance tumor immunogenicity, and improve immune responses. In conclusion, mutation is associated with promoted cancer immunity and can be treated as a biomarker for favorable outcomes in pan-cancer immune checkpoint blockade. These results have implications for treatment decision-making and developing immunotherapy for personalized care.
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