Adverse events after adjuvant radiation therapy for Dupuytren’s disease in the DEPART randomized trial

This study reports adverse events after adjuvant radiotherapy in patients with Dupuytren's disease. Patients for planned limited fasciectomy, collagenase injection or percutaneous needle fasciotomy were enrolled in a randomized controlled trial. Sixty patients were randomized to observation or radiotherapy (30 Gy, 10 fractions) starting within 4 days of the procedure. During a follow-up period of up to 4 years, 114 adverse events were reported. Of 102 (89%) mild adverse events, 45 (44.1%) were attributed to radiotherapy. Of the 12 moderate to severe, three were attributed to radiotherapy. By 6 months, most moderate to severe adverse events had resolved. Between 12 and 36 month follow-ups, the only persistent adverse event attributed to radiotherapy was reduced sweating. In this trial of adjuvant radiotherapy for Dupuytren's disease, adverse events are generally mild and self-limiting, suggesting that adjuvant radiotherapy is well tolerated.<b>Level of evidence:</b> Level 2, individual RCT.

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Publication Details

Journal
Journal of Hand Surgery (European Volume)
Published
2025-02-28
DOI
https://doi.org/10.1177/17531934251321393
Citations
4
Primary Topic
Dupuytren's Contracture and Treatments
Type
article
Field-Weighted Citation Impact
6.67
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article

Adverse events after adjuvant radiation therapy for Dupuytren’s disease in the DEPART randomized trial

Paul M. N. Werker, Jarad Martin, Eric Wegener, Brett McClelland et al.
4 citations
Journal of Hand Surgery (European Volume)
Dupuytren's Contracture and Treatments
6.67
article

Adverse events after adjuvant radiation therapy for Dupuytren’s disease in the DEPART randomized trial

Paul M. N. Werker, Jarad Martin, Eric Wegener, Brett McClelland, Tanya Burgess, David J. Hunter‐Smith
article en
4 citations

Abstract

This study reports adverse events after adjuvant radiotherapy in patients with Dupuytren's disease. Patients for planned limited fasciectomy, collagenase injection or percutaneous needle fasciotomy were enrolled in a randomized controlled trial. Sixty patients were randomized to observation or radiotherapy (30 Gy, 10 fractions) starting within 4 days of the procedure. During a follow-up period of up to 4 years, 114 adverse events were reported. Of 102 (89%) mild adverse events, 45 (44.1%) were attributed to radiotherapy. Of the 12 moderate to severe, three were attributed to radiotherapy. By 6 months, most moderate to severe adverse events had resolved. Between 12 and 36 month follow-ups, the only persistent adverse event attributed to radiotherapy was reduced sweating. In this trial of adjuvant radiotherapy for Dupuytren's disease, adverse events are generally mild and self-limiting, suggesting that adjuvant radiotherapy is well tolerated.<b>Level of evidence:</b> Level 2, individual RCT.

Journal of Hand Surgery (European Volume)Vol. 50(7)
University Medical Center Groningen (NL), University of Groningen (NL), The Alfred Hospital (AU), Monash Alfred Psychiatry Research centre (AU), Hunter Genetics (AU), Lake Macquarie Private Hospital (AU), Monash University (AU), University of Newcastle Australia (AU)
Good health and well-being
Openalex Percentile: Top 4%
Dupuytren's Contracture and Treatments
6.67
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