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Postirradiation changes in the pelvis: assessment with MR imaging
K Sugimura1, B M Carrington, J M Quivey
1Department of Radiology, University of California, San Francisco 94143.
Radiology
|June 1, 1990
Summary
Magnetic resonance (MR) imaging helps assess pelvic radiation changes. Higher radiation doses correlate with increased tissue toxicity and more severe MR imaging findings in bladder and rectal tissues.
Area of Science:
- Radiology
- Oncology
- Medical Imaging
Background:
- Pelvic radiation therapy can cause significant tissue toxicity.
- Assessing radiation-induced changes and differentiating them from recurrent tumors is clinically important.
Purpose of the Study:
- To evaluate magnetic resonance (MR) imaging features of pelvic radiation changes.
- To correlate MR findings with radiation dose, time post-treatment, and clinical symptoms.
- To assess the accuracy of MR imaging in distinguishing radiation damage from residual/recurrent tumors.
Main Methods:
- Retrospective analysis of MR imaging in 51 patients treated with pelvic radiation.
- Correlation of MR imaging findings with radiation dose (e.g., >4,500 cGy) and clinical data.
- Grading of MR imaging tissue changes and comparison with clinical toxicity.
Main Results:
- Radiation tissue toxicity increased significantly above 4,500 cGy, with marked bladder and rectal changes rising substantially.
- Dose-related MR imaging changes were observed in various pelvic organs.
- MR imaging accurately reflected clinical toxicity, with moderate/severe changes seen in patients with grade 2/3 symptoms.
- Minimal MR changes were noted in asymptomatic patients.
- Diagnostic accuracy for differentiating radiation damage from recurrent tumor varied by primary tumor site (excellent for cervical cancer, less so for rectal carcinoma).
Conclusions:
- MR imaging is valuable for assessing pelvic radiation changes and correlates well with radiation dose and clinical toxicity.
- MR imaging can help differentiate radiation damage from recurrent tumors, though accuracy varies by tumor site.