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MASTEC trial

MR-guided adaptive stereotactic radiotherapy for endometrial cancer - MASTEC trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON58512
Enrollment
61
Registered
2025-11-18
Start date
2026-04-01
Completion date
Unknown
Last updated
2026-07-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

endometrial cancer

Interventions

MRI-guided radiotherapy: A hypofractionated schedule (5x6Gy) with reduced margins will be given twice weekly, with adaptation of the radiotherapy plan before each fraction on the MR-Linac (a linear ac

Sponsors

Radboud Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Women aged 18 years or older with histologically proven carcinoma of the endometrium, treated with curative hysterectomy with or without bilateral salpingo-oophorectomy. All histologies may be included (endometrioid, clear cell carcinoma, de-/undifferentiated carcinoma, carcinosarcoma, other non-endometrioid)Candidate for adjuvant EBRT: FIGO IB grade 3 endometrioid carcinomaFIGO stage II endometrioid carcinomaFIGO stage IIIA-C1 endometrioid carcinomaFIGO IB-II clear cell carcinomaFIGO IA-III carcinosarcinomaPatients receiving adjuvant systemic therapy are eligible as these therapies will not be administered concurrentlyPatients receiving vaginal vault radiotherapy are eligibleCapable of giving informed consent

Exclusion criteria

Exclusion criteria: Contra-indications for MRI according to the guidelines of the local department of Radiology, inability to lay on a treatment table for 45-60 minutes or severe claustrofobiaWHO performance score > 2Presence of para-aortic lymph node metastases (FIGO stage IIIC2)Prior pelvic radiotherapy

Design outcomes

Primary

MeasureTime frame
The primary endpoint is acute gastrointestinal and genitourinary toxicity, scored by the Common Terminology Criteria Adverse Events version 5.0. Secondary endpoints are late gastrointestinal and genitourinary toxicity, quality of life and biochemical disease free survival (defined by the Phoenix consensus definition); disease-specific survival; overall survival and metastasis-free survival.

Secondary

MeasureTime frame
Secondary endpoints are late gastrointestinal and genitourinary toxicity, quality of life and biochemical disease free survival (defined by the Phoenix consensus definition); disease-specific survival; overall survival and metastasis-free survival.

Countries

Netherlands

Contacts

Public ContactC. Reijnen

Radboud Universitair Medisch Centrum

casper.reijnen@radboudumc.nl024 361 4505

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Jul 23, 2026