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Multi-institutional experience of MR-guided stereotactic body radiation therapy for adrenal gland metastases.
Mills, Matthew; Kotecha, Rupesh; Herrera, Roberto; Kutuk, Tugce; Fahey, Matthew; Wuthrick, Evan; Grass, G Daniel; Hoffe, Sarah; Frakes, Jessica; Chuong, Michael D; Rosenberg, Stephen A.
Affiliation
  • Mills M; Department of Radiation Oncology, Moffitt Cancer Center, Tampa, FL, United States.
  • Kotecha R; Department of Radiation Oncology, Miami Cancer Institute, Baptist Health South Florida, Miami, FL, United States.
  • Herrera R; Department of Radiation Oncology, Miami Cancer Institute, Baptist Health South Florida, Miami, FL, United States.
  • Kutuk T; Department of Radiation Oncology, Miami Cancer Institute, Baptist Health South Florida, Miami, FL, United States.
  • Fahey M; University of South Florida Morsani College of Medicine, Tampa, FL, United States.
  • Wuthrick E; Department of Radiation Oncology, Moffitt Cancer Center, Tampa, FL, United States.
  • Grass GD; Department of Radiation Oncology, Moffitt Cancer Center, Tampa, FL, United States.
  • Hoffe S; Department of Radiation Oncology, Moffitt Cancer Center, Tampa, FL, United States.
  • Frakes J; Department of Radiation Oncology, Moffitt Cancer Center, Tampa, FL, United States.
  • Chuong MD; Department of Radiation Oncology, Miami Cancer Institute, Baptist Health South Florida, Miami, FL, United States.
  • Rosenberg SA; Department of Radiation Oncology, Moffitt Cancer Center, Tampa, FL, United States.
Clin Transl Radiat Oncol ; 45: 100719, 2024 Mar.
Article in En | MEDLINE | ID: mdl-38292332
ABSTRACT

Purpose:

While dose escalation is associated with improved local control (LC) for adrenal gland metastases (AGMs), the proximity of gastrointestinal (GI) organs-at-risk (OARs) limits the dose that can be safely prescribed via CT-based stereotactic body radiation therapy (SBRT). The advantages of magnetic resonance-guided SBRT (MRgSBRT), including tumor tracking and online plan adaptation, facilitate safe dose escalation.

Methods:

This is a multi-institutional review of 57 consecutive patients who received MRgSBRT on a 0.35-T MR linac to 61 AGMs from 2019 to 2021. The Kaplan-Meier method was used to estimate overall survival (OS), progression-free survival (PFS), and LC, and the Cox proportional hazards model was utilized for univariate analysis (UVA).

Results:

Median follow up from MRgSBRT was 16.4 months (range [R] 1.1-39 months). Median age was 67 years (R 28-84 years). Primary histologies included non-small cell lung cancer (N = 38), renal cell carcinoma (N = 6), and melanoma (N = 5), amongst others. The median maximum diameter was 2.7 cm (R 0.6-7.6 cm), and most AGMs were left-sided (N = 32). The median dose was 50 Gy (R 30-60 Gy) in 5-10 fractions with a median BED10 of 100 Gy (R 48-132 Gy). 45 cases (74 %) required adaptation for at least 1 fraction (median 4 fractions, R 0-10). Left-sided AGMs required adaptation in at least 1 fraction more frequently than right-sided AGMs (88 % vs 59 %, p = 0.018). There were 3 cases of reirradiation, including 60 Gy in 10 fractions (N = 1) and 40 Gy in 5 fractions (N = 2). One-year LC, PFS, and OS were 92 %, 52 %, and 78 %, respectively. On UVA, melanoma histology predicted for inferior 1-year LC (80 % vs 93 %, p = 0.012). There were no instances of grade 3+ toxicity.

Conclusions:

We demonstrate that MRgSBRT achieves favorable early LC and no grade 3 + toxicity despite prescribing a median BED10 of 100 Gy to targets near GI OARs.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Clin Transl Radiat Oncol Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Clin Transl Radiat Oncol Year: 2024 Document type: Article