Indication
Mismatch repair proficient endometrial cancer
Mismatch repair proficient endometrial cancer is a molecularly defined subtype of uterine malignancy originating in the endometrium, accounting for the majority of endometrial carcinomas. Read more about Mismatch repair proficient endometrial cancer
3 drugs 1 manufacturers
Drugs that treat it
Common Mismatch repair proficient endometrial cancer therapies.
KEYTRUDA (pembrolizumab)
KEYTRUDA QLEX (pembrolizumab-berahyaluronidase alfa-pmph)
News & literature
Coming soonRelated codes
Coming soonRelated conditions & guidelines
Coming soonMismatch repair proficient endometrial cancer is a molecularly defined subtype of uterine malignancy originating in the endometrium, accounting for the majority of endometrial carcinomas.
It affects adult females and is characterized pathophysiologically by functional cellular DNA mismatch repair machinery—demonstrated by intact immunohistochemical nuclear expression of the core mismatch repair proteins MLH1, MSH2, MSH6, and PMS2—and an associated microsatellite stable (MSS) or low microsatellite instability (MSI-L) phenotype.
Because these tumors typically exhibit lower mutation rates, fewer neoantigens, and a less immunogenic microenvironment than mismatch repair deficient variants, mismatch repair proficient status serves as a critical prognostic and predictive biomarker that informs oncologic risk stratification and dictates eligibility for tailored systemic regimens.
- mypathologyreport.ca
Mismatch repair proficient endometrial cancer is a molecularly defined subtype of uterine malignancy originating in the endometrium It affects adult females and is characterized pathophysiologically by functional cellular DNA mismatch repair machinery—demonstrated by intact immunohistochemical nuclear expression of the core mismatch repair proteins MLH1, MSH2, MSH6, and PMS2—and an associated microsatellite stable (MSS) or low microsatellite instability (MSI-L) phenotype Because these tumors typ...
- nih.gov
It affects adult females and is characterized pathophysiologically by functional cellular DNA mismatch repair machinery—demonstrated by intact immunohistochemical nuclear expression of the core mismatch repair proteins MLH1, MSH2, MSH6, and PMS2—and an associated microsatellite stable (MSS) or low microsatellite instability (MSI-L) phenotype
- jsafog.com
Because these tumors typically exhibit lower mutation rates, fewer neoantigens, and a less immunogenic microenvironment than mismatch repair deficient variants, mismatch repair proficient status serves as a critical prognostic and predictive biomarker that informs oncologic risk stratification and dictates eligibility for tailored systemic regimens
- onclive.com
Because these tumors typically exhibit lower mutation rates, fewer neoantigens, and a less immunogenic microenvironment than mismatch repair deficient variants, mismatch repair proficient status serves as a critical prognostic and predictive biomarker that informs oncologic risk stratification and dictates eligibility for tailored systemic regimens
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