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Clinical Outcomes Following Dose-Escalated Proton Therapy for Skull-Base Chordoma. | LitMetric

AI Article Synopsis

  • The study aimed to assess how effective external-beam proton therapy is for treating skull-base chordoma and its impact on patient survival and local disease control.
  • Researchers reviewed medical records from 112 patients who received either proton therapy alone or in combination, analyzing various survival rates and the occurrence of radiotherapy-related toxicities.
  • Results showed a high 5-year survival rate and local control rates with minimal severe side effects, suggesting that high-dose proton therapy is a promising treatment option for patients with skull-base chordoma.

Article Abstract

Purpose: To evaluate the effectiveness of external-beam proton therapy (PT) on local control and survival in patients with skull-base chordoma.

Materials And Methods: We reviewed the medical records of patients with skull-base chordoma treated with definitive or adjuvant high-dose PT and updated their follow-up when feasible. We assessed overall survival, disease-specific survival, local control, and freedom from distant metastasis. Radiotherapy toxicities were scored using the Common Terminology Criteria for Adverse Events, version 4.0.

Results: A total 112 patients were analyzed, of whom 105 (94%) received PT and 7 (6%) received combined proton-photon therapy between 2007 and 2019. Eighty-seven patients (78%) underwent a subtotal resection, 22 (20%) a gross total resection, and 3 (3%) a biopsy alone. The median radiotherapy dose was 73.8 Gy radiobiologic equivalent (GyRBE; range, 69.6-74.4). Ninety patients (80%) had gross disease at radiotherapy and 7 (6%) were treated for locally recurrent disease following surgery. Median follow-up was 4.4 years (range, 0.4-12.6); for living patients, it was 4.6 years (range, 0.4-12.6), and for deceased patients, 4.1 years (range, 1.2-11.2). At 5 years after radiotherapy, the actuarial overall survival, disease-specific survival, local control, and freedom from distant metastasis rates were 78% (n = 87), 83% (n = 93), 74% (n = 83), and 99% (n = 111), respectively. The median time to local progression was 2.4 years (range, 0.8-7). Local control and disease-specific survival by resection status was 95% versus 70% ( = 0.28) and 100% versus 80% ( = 0.06) for gross total, versus subtotal, resection or biopsy alone, respectively. There were no serious acute toxicities (grade ≥ 3) related to radiotherapy.

Conclusion: High-dose PT alone or after surgical resection for skull-base chordoma reaffirms the favorable 5-year actuarial local control rate compared with conventional techniques with acceptable late-complication-free survival. Outcomes following gross total resection and adjuvant PT were excellent. Further follow-up of this cohort is necessary to better characterize long-term disease control and late toxicities.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8270096PMC
http://dx.doi.org/10.14338/IJPT-20-00066.1DOI Listing

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