Associations between etiologic factors and mortality after endometrial cancer diagnosis: The NRG Oncology/Gynecologic Oncology Group 210 trial Journal Article


Authors: Felix, A. S.; Scott McMeekin, D.; Mutch, D.; Walker, J. L.; Creasman, W. T.; Cohn, D. E.; Ali, S.; Moore, R. G.; Downs, L. S.; Ioffe, O. B.; Park, K. J.; Sherman, M. E.; Brinton, L. A.
Article Title: Associations between etiologic factors and mortality after endometrial cancer diagnosis: The NRG Oncology/Gynecologic Oncology Group 210 trial
Abstract: Background Few studies have analyzed relationships between risk factors for endometrial cancer, especially with regard to aggressive (non-endometrioid) histologic subtypes, and prognosis. We examined these relationships in the prospective NRG Oncology/Gynecologic Oncology Group 210 trial. Methods Prior to surgery, participants completed a questionnaire assessing risk factors for gynecologic cancers. Pathology data were derived from clinical reports and central review. We used the Fine and Gray subdistribution hazards model to estimate subhazard ratios (HRs) and 95% confidence intervals (CIs) for associations between etiologic factors and cause-specific subhazards in the presence of competing risks. These models were stratified by tumor subtype and adjusted for stage and socioeconomic status indicators. Results Median follow-up was 60 months after enrollment (range: 1 day-118 months). Among 4609 participants, a total of 854 deaths occurred, of which, 582 deaths were attributed to endometrial carcinoma. Among low-grade endometrioid cases, endometrial carcinoma-specific subhazards were significantly associated with age at diagnosis (HR = 1.04, 95% CI = 1.01-1.06 per year, P-trend) and BMI (class II obesity vs. normal BMI: HR = 2.29, 95% CI = 1.06-4.98, P-trend = 0.01). Among high-grade endometrioid cases, endometrial carcinoma-specific subhazards were associated with age at diagnosis (HR = 1.05, 95% CI = 1.02-1.07 per year, P-trend < 0.001). Among non-endometrioid cases, endometrial carcinoma-specific subhazards were associated with parity relative to nulliparity among serous (HR = 0.55, 95% CI = 0.36-0.82) and carcinosarcoma cases (HR = 2.01, 95% CI = 1.00-4.05). Discussion Several endometrial carcinoma risk factors are associated with prognosis, which occurs in a tumor-subtype specific context. If confirmed, these results would suggest that factors beyond histopathologic features and stage are related to prognosis. ClinicalTrials.gov Identifier: NCT00340808.
Keywords: adult; cancer chemotherapy; controlled study; major clinical study; histopathology; multimodality cancer therapy; cancer patient; cancer radiotherapy; cancer staging; follow up; endometrial cancer; antineoplastic agent; cancer diagnosis; endometrioid carcinoma; endometrium carcinoma; hysterectomy; endometrium cancer; prospective study; salpingooophorectomy; breast cancer; clinical assessment; estrogen; obesity; risk factor; cancer mortality; confidence interval; social status; body mass; tamoxifen; hazard ratio; trend study; chemoradiotherapy; gestagen; female genital tract cancer; gog; parity; nullipara; cancer prognosis; prognosis; human; female; priority journal; article; etiologic factors; nrg
Journal Title: Gynecologic Oncology
Volume: 139
Issue: 1
ISSN: 0090-8258
Publisher: Elsevier Inc.  
Date Published: 2015-10-01
Start Page: 70
End Page: 76
Language: English
DOI: 10.1016/j.ygyno.2015.08.022
PROVIDER: scopus
PMCID: PMC4587355
PUBMED: 26341710
DOI/URL:
Notes: Export Date: 2 November 2015 -- Source: Scopus
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  1. Kay Jung Park
    308 Park