Adjuvant volumetric modulated arc therapy compared to 3D conformal radiation therapy for newly diagnosed soft tissue sarcoma of the extremities: outcome and toxicity evaluation

Author:

Di Brina Lucia1,Fogliata Antonella1ORCID,Navarria Pierina1,D'Agostino Giuseppe1,Franzese Ciro1,Franceschini Davide1,De Rose Fiorenza1,Comito Tiziana1,Bertuzzi Alexia2,Marrari Andrea2,Colombo Piergiuseppe3,Quagliuolo Vittorio45,Santoro Armando25,Scorsetti Marta15

Affiliation:

1. Radiotherapy and Radiosurgery Department, Humanitas Clinical and Research Center – IRCCS, Rozzano - Milano – Italy,

2. Medical Oncology Department, Humanitas Clinical and Research Center – IRCCS, Rozzano - Milano – Italy,

3. Pahtology Department, Humanitas Clinical and Research Center – IRCCS-, Rozzano - Milano – Italy,

4. Surgical Oncology Unit, Humanitas Clinical and Research Center – IRCCS, Rozzano - Milano – Italy,

5. Department of Biomedical Sciences, Humanitas University, Rozzano-Milano, Italy

Abstract

Objective: To assess the impact of adjuvant volumetric modulated arc therapy (VMAT) compared with three-dimensional conformal radiation therapy (3DCRT) in terms of toxicity and local control (LC) in patients with soft tissue sarcoma of the extremities. Methods: From 2004 to 2016, 109 patients were treated, initially using 3DCRT and subsequently with VMAT. Clinical outcome was evaluated by contrast-enhanced MRI, thoracic and abdominal CT 3 months after treatments and then every 6 months. Toxicity was evaluated with Common Terminology Criteria for Adverse Events scale v. 4.3. Results: Patients presented Stage III soft tissue sarcoma disease (77%), localized tumor (95%) at the lower extremity (87%), adipocytic histotype (46%). Surgical resection was performed in all patients, followed by adjuvant 3DCRT in 38, and VMAT in 71. The median total dose was 66 Gy/33 fractions (range 60–70 Gy;25–35 fractions). More successful bone sparing was recorded using VMAT (p < 0.001). Median follow-up was 61 months, 93 and 58 months for 3DCRT and VMAT group, respectively. The 2- and 5 year LC were 95.3±2.1%, and 87.4±3.4% for the whole cohort, 92.0±4.5%, 82.9±6.4% for 3DCRT, 97.1±2.0%, 89.6±4.1% for VMAT (p = 0.150). On univariate and multivariate analysis the factors recorded as conditioning LC were the status of the surgical resection margins (p = 0.028) and the total dose delivered (p = 0.013). Conclusion: The availability of modern radiotherapy technique permit a better conformity on the target with maximum sparing of normal tissue and acceptable side-effects. VMAT is a safe and feasible treatment with limited rate of toxicity, compared to 3DCRT. Results on LC of VMAT are encouraging. Advances in knowledge: Soft tissue sarcoma of the extremities can benefit from the use of VMAT, with a reduction of the high dose to bones to avoid radiation osteonecrosis. An adequate total dose of at least 66 Gy and a radical surgical margin allow a good local control.

Publisher

British Institute of Radiology

Subject

Radiology, Nuclear Medicine and imaging,General Medicine

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