Is a total dose of 54 Gy with radiochemotherapy sufficient for treatment of intermediate-risk volumes in nasopharyngeal cancer?
Background The mainstay treatment of nasopharyngeal cancer (NPC) is radiation therapy (RT). The doses and volumes may differ from center to center. Most studies and guidelines recommend a total dose of 60 Gy for elective nodal and peritumoral volume treatment. This retrospective analysis aimed to an...
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Veröffentlicht in: | Strahlentherapie und Onkologie 2024-05, Vol.200 (5), p.409-417 |
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Sprache: | eng |
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Zusammenfassung: | Background
The mainstay treatment of nasopharyngeal cancer (NPC) is radiation therapy (RT). The doses and volumes may differ from center to center. Most studies and guidelines recommend a total dose of 60 Gy for elective nodal and peritumoral volume treatment. This retrospective analysis aimed to analyze whether a dose reduction to 54 Gy to this volume would be associated with a higher risk of recurrence.
Methods
A total of 111 patients treated by intensity-modulated radiotherapy (IMRT) and concurrent chemotherapy were retrospectively analyzed. The recurrent tumor volume was classified as “in field” if 95% of the recurrent volume was inside the 95% isodose, as “marginal” if 20–95% of the recurrence was inside the 95% isodose, or as “outside” if less than 20% of the recurrence was inside the 95% isodose.
Results
Median follow-up was 67 months (range 6–142). The 2‑ and 5‑year overall survival (OS) rates were 88.6% and 70%, respectively. The 2‑year locoregional control (LRC), disease-free survival (DFS), and distant metastasis-free survival (DMFS) were 93.3%, 89.3%, and 87.4%, and the 5‑year LRC, DFS, and DMFS were 86.8%, 74%, and 81.1%, respectively. Ten patients (9%) had a local and or regional recurrence. Half of the patients with locoregional failure had in-field recurrences. For primary tumor, there was no recurrence in the volume of 54 Gy. For regional lymph node volume, recurrence was detected in two (1.8%) patients in the volume of 54 Gy.
Conclusion
These retrospective data suggest that a dose reduction may be possible for intermediate-risk volumes, especially for the primary site. |
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ISSN: | 0179-7158 1439-099X |
DOI: | 10.1007/s00066-023-02186-3 |