Indication
Tumor mutational burden-high solid malignant tumor
Tumor mutational burden-high solid malignant tumor is a tissue-agnostic oncologic indication describing non-hematologic cancers that harbor an elevated frequency of somatic genomic mutations. Read more about Tumor mutational burden-high solid malignant tumor
3 drugs 1 manufacturers
Drugs that treat it
Common Tumor mutational burden-high solid malignant tumor therapies.
KEYTRUDA (pembrolizumab)
KEYTRUDA QLEX (pembrolizumab-berahyaluronidase alfa-pmph)
News & literature
Coming soonRelated codes
Coming soonRelated conditions & guidelines
Coming soonTumor mutational burden-high solid malignant tumor is a tissue-agnostic oncologic indication describing non-hematologic cancers that harbor an elevated frequency of somatic genomic mutations.
Arising in diverse anatomic sites across adult and pediatric populations, these neoplasms are defined by a high mutation density—frequently established as ten or more mutations per megabase through validated genomic sequencing.
Pathophysiologically, the substantial burden of non-synonymous mutations generates an increased repertoire of tumor-specific neoantigens.
This enhances cellular immunogenicity and renders the malignant tissue uniquely recognizable to host tumor-infiltrating lymphocytes, frequently underlying heightened susceptibility to immune checkpoint pathway modulation.
- fda.gov
Tumor mutational burden-high solid malignant tumor is a tissue-agnostic oncologic indication describing non-hematologic cancers that harbor an elevated frequency of somatic genomic mutations Arising in diverse anatomic sites across adult and pediatric populations, these neoplasms are defined by a high mutation density—frequently established as ten or more mutations per megabase through validated genomic sequencing
- oncokb.org
Tumor mutational burden-high solid malignant tumor is a tissue-agnostic oncologic indication describing non-hematologic cancers that harbor an elevated frequency of somatic genomic mutations Arising in diverse anatomic sites across adult and pediatric populations, these neoplasms are defined by a high mutation density—frequently established as ten or more mutations per megabase through validated genomic sequencing This enhances cellular immunogenicity and renders the malignant tissue uniquely re...
- curetoday.com
Pathophysiologically, the substantial burden of non-synonymous mutations generates an increased repertoire of tumor-specific neoantigens This enhances cellular immunogenicity and renders the malignant tissue uniquely recognizable to host tumor-infiltrating lymphocytes, frequently underlying heightened susceptibility to immune checkpoint pathway modulation
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