Using MR-Linac for precise radiotherapy in cancer treatment

The Second Affiliated Hospital of Hainan Medical University

Observational The Second Affiliated Hospital of Hainan Medical University · NCT06531681

This study is testing if a new type of radiation therapy using MR-Linac can help cancer patients have better treatment outcomes and improve their quality of life.

Quick facts

Study typeObservational
Enrollment3000 (estimated)
Ages18 Years to 75 Years
SexAll
SponsorThe Second Affiliated Hospital of Hainan Medical University Academic / other
Locations1 site (Haikou)
Trial IDNCT06531681 on ClinicalTrials.gov

What this trial studies

This observational study aims to evaluate the effectiveness of magnetic resonance-guided linear accelerator (MR-Linac) technology in delivering precision radiotherapy for tumors. It will analyze various outcomes including overall response rate, progression-free survival, disease control rate, overall survival, and the incidence of adverse reactions. Additionally, the study will assess the quality of life of patients using standardized measures and evaluate dosimetric parameters related to treatment. The study will involve patients aged 18-75 who have undergone imaging or treatment with MR-Linac.

Who should consider this trial

Good fit: Ideal candidates are patients aged 18-75 with an ECOG score of 0-2 who are undergoing or have undergone treatment with MR-Linac.

Not a fit: Patients with contraindications to MRI or severe comorbidities that prevent them from tolerating radiotherapy may not benefit from this study.

Why it matters

Potential benefit: If successful, this approach could lead to improved tumor response rates and reduced side effects for cancer patients undergoing radiotherapy.

How similar studies have performed: While the use of MR-Linac is a relatively novel approach, preliminary studies have shown promising results in improving precision in radiotherapy.

Eligibility criteria

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patients are undergoing or have undergone imaging or treatment at the MR linac;
* Age 18-75 years, male or female;
* ECOG score 0-2, life expectancy \> 6 months;
* Patients provide written informed consent.

Exclusion Criteria:

* Contraindications to MRI, such as claustrophobia and metallic or electronic implants incompatible with MRI;
* The presence of severe comorbidities that, in the opinion of the investigator, · preclude the toleration or completion of radiotherapy;
* Acute inflammatory disease requiring systemic therapy;
* The presence of active infectious disease;
* Pregnant women, nursing mothers, and patients planning to have children during the study period.

Where this trial is running

Haikou

Study contacts

How to participate

  1. Review the eligibility criteria above with your treating physician.
  2. Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
  3. Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions Overall Response RateOncologyRadiation ToxicityQuality of Life
Last reviewed 2026-06-13 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.