Initial Safety and Tumor Control Results From a 'First-in-Human' Multicenter Prospective Trial Evaluating a Novel Alpha-Emitting Radionuclide for the Treatment of Locally Advanced Recurrent Squamous Cell Carcinomas of the Skin and Head and Neck
| Autor: | G. Feliciani, Anna Sarnelli, L. Deutsch, Eli Rosenfeld, S.R. Bellia, Aron Popovtzer, Yona Keisari, Itzhak Kelson, R. Ben-Hur, Lior Arazi, Aviram Mizrachi |
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| Rok vydání: | 2020 |
| Předmět: |
Male
Cancer Research medicine.medical_specialty Skin Neoplasms Time Factors Erythema medicine.medical_treatment Brachytherapy Pilot Projects Pain Procedural 030218 nuclear medicine & medical imaging 03 medical and health sciences 0302 clinical medicine Skin Ulcer Photography medicine Humans Radiology Nuclear Medicine and imaging Prospective Studies Progression-free survival Prospective cohort study Prior Radiation Therapy Aged Aged 80 and over Radiation business.industry Thorium Common Terminology Criteria for Adverse Events Middle Aged Alpha Particles Progression-Free Survival Radiation therapy Treatment Outcome Oncology Head and Neck Neoplasms Response Evaluation Criteria in Solid Tumors 030220 oncology & carcinogenesis Carcinoma Squamous Cell Feasibility Studies Female Radiology Neoplasm Recurrence Local Safety medicine.symptom business Radium |
| Zdroj: | International Journal of Radiation Oncology*Biology*Physics. 106:571-578 |
| ISSN: | 0360-3016 |
| DOI: | 10.1016/j.ijrobp.2019.10.048 |
| Popis: | Purpose Our purpose was to report the feasibility and safety of diffusing alpha-emitter radiation therapy (DaRT), which entails the interstitial implantation of a novel alpha-emitting brachytherapy source, for the treatment of locally advanced and recurrent squamous cancers of the skin and head and neck. Methods and Materials This prospective first-in-human, multicenter clinical study evaluated 31 lesions in 28 patients. The primary objective was to determine the feasibility and safety of this approach, and the secondary objectives were to evaluate the initial tumor response and local progression-free survival. Eligibility criteria included all patients with biopsy-proven squamous cancers of the skin and head and neck with either primary tumors or recurrent/previously treated disease by either surgery or prior external beam radiation therapy; 13 of 31 lesions (42%) had received prior radiation therapy. Toxicity was evaluated according to the Common Terminology Criteria for Adverse Events version 4.03. Tumor response was assessed at 30 to 45 days at a follow-up visit using the Response Evaluation Criteria in Solid Tumors, version 1.1. Median follow-up time was 6.7 months. Results Acute toxicity included mostly local pain and erythema at the implantation site followed by swelling and mild skin ulceration. For pain and grade 2 skin ulcerations, 90% of patients had resolution within 3 to 5 weeks. Complete response to the Ra-224 DaRT treatment was observed in 22 lesions (22/28; 78.6%); 6 lesions (6/28, 21.4%) manifested a partial response (>30% tumor reduction). Among the 22 lesions with a complete response, 5 (22%) developed a subsequent local relapse at the site of DaRT implantation at a median time of 4.9 months (range, 2.43-5.52 months). The 1-year local progression-free survival probability at the implanted site was 44% overall (confidence interval [CI], 20.3%-64.3%) and 60% (95% CI, 28.61%-81.35%) for complete responders. Overall survival rates at 12 months post-DaRT implantation were 75% (95% CI, 46.14%-89.99%) among all patients and 93% (95% CI, 59.08%-98.96%) among complete responders. Conclusions Alpha-emitter brachytherapy using DaRT achieved significant tumor responses without grade 3 or higher toxicities observed. Longer follow-up observations and larger studies are underway to validate these findings. |
| Databáze: | OpenAIRE |
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