Risk Factors for Concurrent Endometrial Carcinoma in Patients With a Curettage Diagnosis of Endometrial Hyperplasia
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Purpose
Objective: To examine the risk factors for coexisting endometrial carcinoma in patients with endometrial hyperplasia.
Method: Seventy-seven patients who received hysterectomy for endometrial hyperplasia were enrolled and divided into the non-endometrial carcinoma group (57) and the endometrial carcinoma group (20) depending on the final pathology. Clinical variables were analyzed.
| Condition |
|---|
|
Endometrial Carcinoma |
| Study Type: | Observational |
| Study Design: | Observational Model: Case-Only Time Perspective: Retrospective |
| Official Title: | Concurrent Endometrial Cancer With Endometrial Hyperplasia or Endometrial Intraepithelial Neoplasia - Focus on Risk Factors Analysis |
- The prognosis of patients diagnosed as endometrial carcinoma after hysterectomy. [ Time Frame: From carcinoma diagnosed to the last patient follow-up or death till June, 2011 ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 100 |
| Study Start Date: | January 2005 |
| Estimated Study Completion Date: | June 2011 |
| Estimated Primary Completion Date: | January 2006 (Final data collection date for primary outcome measure) |
We retrospectively reviewed the cases of seventy-seven patients who had hysterectomies for endometrial hyperplasia between January 1996 and September 2006 at the Department of Obstetrics and Gynecology, National Taiwan University Hospital. A preoperative pathologic diagnosis of endometrial hyperplasia was obtained by D&C (dilation and curettage) in all patients. Twenty of them were diagnosed as having endometrial carcinoma in their hysterectomy specimens. All of the specimens were reviewed by a gynecologic pathologist.
Depending on the final pathologic reports of hysterectomy, we divided the seventy-seven patients into two groups - the non-endometrial carcinoma group and the endometrial carcinoma group. Fifty-seven of the studied patients were in the non-endometrial carcinoma group and twenty were in the endometrial carcinoma group. As already mentioned above, we investigated them by clinical parameters including age, menopausal status, obstetrical history, medical history of diabetes and hypertension, BMI (body mass index) and preoperative pathology of D&C.
The clinical and pathologic characteristics of the twenty patients diagnosed as having endometrial carcinoma postoperatively were also reviewed. Initial manifestation, histological grading of the carcinoma, the depth of myometrial invasion, with or without adjuvant radiotherapy and recurrence were included. The histological grading of endometrial carcinoma was based on FIGO ( International Federation of Gynecology and Obstetrics ) definitions. The BMIs of the patients with endometrial carcinoma were also analyzed by the receiver operating characteristic curve. The Research and Ethics Committee of National Taiwan University Hospital approved this study.
Statistical analyses were performed with the Independent-Samples T test and the Mann-Whitney test. Subsequently, multivariate analysis of risk factors was also employed with Binary logistic regression model to obtain the adjusted odds ratio (OR) and 95% confidence interval (CI) for selective variables. P<0.05 was defined as significant.
Eligibility| Ages Eligible for Study: | 30 Years to 70 Years |
| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
We retrospectively reviewed the cases of seventy-seven patients who had hysterectomies for endometrial hyperplasia between January 1996 and September 2006 at the Department of Obstetrics and Gynecology, National Taiwan University Hospital. A preoperative pathologic diagnosis of endometrial hyperplasia was obtained in all patients.
Inclusion Criteria:
- Endometrial hyperplasia patient having hysterectomy with or without bilateral salpingo-oophorectomy
Exclusion Criteria:
- none
Contacts and Locations| Contact: Chi-An Chen, Professor | 886-2-23123456 ext 5166 | chianchen@ntu.edu.tw |
| Taiwan | |
| Chi-An Chen | Recruiting |
| Taipei, Taiwan | |
| Contact: Yu-Li Chen, M.D, 886-2-23123456 ext 5166 uly1007@yahoo.com.tw | |
| Chi-An Chen | Recruiting |
| Taipei, Taiwan, 100 | |
| Contact: Yu-Li Chen, M.D 886-2-23123456 ext 5166 uly1007@yahoo.com.tw | |
| Study Chair: | Chi An Chen, M.D. | Department of Obstetrics and Gynecology, National Taiwan University Hospital |
More Information
No publications provided
| Responsible Party: | Chi-An Chen/Professor, National Taiwan Unviersity Hospital |
| ClinicalTrials.gov Identifier: | NCT01273636 History of Changes |
| Other Study ID Numbers: | 200712018R |
| Study First Received: | August 14, 2008 |
| Last Updated: | January 6, 2011 |
| Health Authority: | Taiwan: Department of Health |
Keywords provided by National Taiwan University Hospital:
|
Endometrial hyperplasia Hysterectomy Endometrial carcinoma |
Additional relevant MeSH terms:
|
Carcinoma Endometrial Hyperplasia Hyperplasia Adenoma Endometrial Neoplasms Neoplasms, Glandular and Epithelial Neoplasms by Histologic Type Neoplasms |
Uterine Diseases Genital Diseases, Female Pathologic Processes Uterine Neoplasms Genital Neoplasms, Female Urogenital Neoplasms Neoplasms by Site |
ClinicalTrials.gov processed this record on May 23, 2013