2023
DOI: 10.1016/j.modpat.2022.100085
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Grade and Estrogen Receptor Expression Identify a Subset of No Specific Molecular Profile Endometrial Carcinomas at a Very Low Risk of Disease-Specific Death

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Cited by 37 publications
(13 citation statements)
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“…The prognostic value of ER expression has been investigated in recent studies within The Cancer Genome Atlas groups, and remains clinically relevant. 30,31,42 The prognostic value of ER expression appears most relevant in the NSMP group. In the adjuvant treatment setting, a first randomized study is planned to investigate efficacy of adjuvant HT in the NSMP group with advanced EC (ClinicalTrials.gov identifier: NCT05255653).…”
Section: Integration Of Molecular Subgroups With Predictive Biomarkersmentioning
confidence: 99%
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“…The prognostic value of ER expression has been investigated in recent studies within The Cancer Genome Atlas groups, and remains clinically relevant. 30,31,42 The prognostic value of ER expression appears most relevant in the NSMP group. In the adjuvant treatment setting, a first randomized study is planned to investigate efficacy of adjuvant HT in the NSMP group with advanced EC (ClinicalTrials.gov identifier: NCT05255653).…”
Section: Integration Of Molecular Subgroups With Predictive Biomarkersmentioning
confidence: 99%
“…In fact, HT has a good safety profile, whereas chemotherapy is associated with grade 3 treatment-related toxicity in 35% of the patients, compared with only 6.5% with progestin therapy. [29][30][31] On the basis of these facts, we strongly believe that the position of hormonal drugs for preselected groups of patients with EC should be redefined in the context of the molecular classification. To this end, there are a number of considerations and remaining challenges with current data that should be addressed, as discussed in the following part.…”
Section: Introductionmentioning
confidence: 99%
“…In contrast to POLEmut ECs, research focusing specifically on NSMP ECs has shown that additional clinicopathologic and molecular features are strongly associated with outcomes and may aid in prognostic and predictive substratification of this molecular subtype. 50…”
Section: Nsmp Endometrial Cancermentioning
confidence: 99%
“…8,42 Several studies have focused on this NSMP group and showed that based on PTEN/PIK3CA mutation status, histology/grade, chromosome 1q gain/amplification, ER status or chromosomal instability, subgroups with distinct outcomes could be identified. 14,[43][44][45][46][47] Finally, the CN-H/p53abn/TP53abn ECs, associated with the worst outcome among the four molecular subtypes groups, are genetically heterogeneous and several subgroups harboring potentially targetable alterations have been identified across histologic types. 1,19,24,48 An area of active interest is the ERBB2/ HER2-altered subgroup.…”
Section: Therapeutic Implications Of the Ec Molecular Subtypesmentioning
confidence: 99%