Findings Support Retesting for MMRD at Uterine Cancer Recurrence
Patients who have mismatch repair proficiency in the primary setting may have mismatch repair deficiency at recurrence.
Patients who have mismatch repair proficiency in the primary setting may have mismatch repair deficiency at recurrence.
In a real-world study, more than 54% of patients had at least 1 potentially actionable genomic alteration.
A subanalysis of the GOG 252 trial revealed factors associated with longer survival among patients with stage II-III epithelial ovarian cancer.
Niraparib reduced the risk of progression or death by 55%.
In one patient, progression would have been detected up to 143 days earlier with ctDNA than with conventional surveillance methods.
The response rate observed with mirvetuximab soravtansine was nearly triple the benchmark set in prior studies.
Open radical hysterectomy was associated with better outcomes at a median follow-up of 4.5 years.
The median overall survival was 147.8 months for patients with MAPK-mutated tumors and 89.5 months for patients without MAPK mutations.
In the first wave, 59% of respondents met criteria for low professional fulfillment, and 41% met criteria for burnout.
In a study of more than 5000 patients with advanced ovarian cancer, 56% received first-line maintenance therapy.