NCT04386993Completed
De-escalated Conformal Radiation Expedited Sequentially With Chemotherapy for Endometrial Cancer
De-escalated Conformal Radiation Expedited Sequentially With Chemotherapy for Endometrial Cancer (DeCRESCEndo)
Source: ClinicalTrials.gov · Last updated 20 Oct 2025
Brief summary (registry, in English)
The goal of this study is to evaluate short course radiation in the post-operative female pelvis after hysterectomy in stage III-IVA endometrial adenocarcinoma patients, or any stage patients with uterine serous or carcinosarcoma histology. The investigators hypothesize that short course pelvic radiation will have an acute and late grade 3-4 toxicity rate \< 10%, and patients will benefit from both convenient and effective loco-regional control comparable to the traditional 5-6 weeks of radiation.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 25 (actual)
- First submitted
- 8 May 2020
- Start date
- 7 Jul 2020
- Primary completion date
- 13 Oct 2025
- Lead sponsor
- Washington University School of Medicine
- Diseases
- Endometrial cancer
- NCT number
- NCT04386993
What you commit to
- Study type: Interventional
- Participants enrolled: 25
- From 7 Jul 2020 to the primary completion date, 13 Oct 2025
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Prior radiation to the pelvis.
- Currently receiving any investigational agents.
Other illness
- Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, inflammatory bowel disease, or irritable bowel disease.
Lab values
- Patients with HIV are eligible unless their CD4+ T-cell counts are \< 350 cells/mcL or they have a history of AIDS-defining opportunistic infection within the 12 months prior to registration. Concurrent treatment with effective ART according to DHHS treatment guidelines is recommended.
Who the study is looking for
- Histologically or cytologically confirmed stage IIIA-IVA endometrial cancer, or any stage I-IVA where any proportion of the tumor is uterine serous, clear cell, de-differentiated, or carcinosarcoma histology.
- Must have already undergone radical hysterectomy. Hysterectomy may have occurred no more than one year prior to enrollment.
- At least 18 years of age.
- ECOG performance status ≤ 2
- Minimal bone marrow and organ function as defined below:
- Leukocytes ≥ 1,000 cumm
- Absolute neutrophil count ≥ 500 cumm
- Platelets ≥ 50,000 cumm
- Hemoglobin ≥ 7g/dL
- Ability to understand and willingness to sign an IRB approved written informed consent document (or that of legally authorized representative, if applicable).
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Washington University School of Medicine Coordinator of this site? Confirm its status | St Louis | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.