Objective: To report clinical and dosimetric outcomes of a consecutive series of patients with anal cancer treated with volumetric-modulated arc therapy (VMAT) concomitant to chemotherapy (CT). Methods: A cohort of 39 patients underwent VMAT employing a schedule consisting of 50.4Gy/28 fractions to the gross tumour volume (GTV) and 42Gy/28 fractions to the elective nodal volumes for patients with cT2N0 disease. Patients with cT3–T4/N0–N3 tumours were prescribed 54Gy/30 fractions to the GTV and 50.4Gy/30 fractions to the gross nodal volumes if sized #3cm or 54Gy/30 fractions if . 3cm. Elective nodal regions were given 45Gy/30 fractions. CT was administered concurrently following Nigro’s regimen. The primary end point was acute toxicity. Secondary end points were colostomy-free survival (CFS), disease-free survival (DFS), cancer-specific survival (CSS) and overall survival (OS). Dosimetric data are also provided. Results: Median follow-up was 21 months. Maximum acute toxicities were: dermatologic—G3: 18%; gastrointestinal–G3: 5%; genitourinary–G3: 2%; anaemia—G2: 7%; leukopenia— G3: 28%; G4: 8%; neutropenia—G3: 13%; G4: 18%; thrombocytopenia—G3: 11%; and G4: 2%. The actuarial 2-year CFS was 77.9% [95% confidence interval (CI): 54–90.4%]. Actuarial 2-year OS and CSS were 85.2% (95% CI: 60.1–95.1%), while DFS was 75.1% (95% CI: 52.4.7–88.1%). Conclusion: Our clinical results support the use of VMAT as a safe and effective intensity-modulated radiotherapy (IMRT) option in the combined modality treatment of anal cancer, with consistent dosimetry, mild toxicity and promising sphincter preservation and survival rates. Advances in knowledge: IMRT is a standard of care for patients with anal cancer, and VMAT is a robust technical solution in this setting.

Volumetric modulated arc therapy (VMAT) in the combined modality treatment of anal cancer patients

FRANCO, Pierfrancesco
First
;
ARCADIPANE, FRANCESCA;RAGONA, Riccardo;MISTRANGELO, Massimiliano;CASSONI, Paola;MORINO, Mario;RICARDI, Umberto
Last
2016-01-01

Abstract

Objective: To report clinical and dosimetric outcomes of a consecutive series of patients with anal cancer treated with volumetric-modulated arc therapy (VMAT) concomitant to chemotherapy (CT). Methods: A cohort of 39 patients underwent VMAT employing a schedule consisting of 50.4Gy/28 fractions to the gross tumour volume (GTV) and 42Gy/28 fractions to the elective nodal volumes for patients with cT2N0 disease. Patients with cT3–T4/N0–N3 tumours were prescribed 54Gy/30 fractions to the GTV and 50.4Gy/30 fractions to the gross nodal volumes if sized #3cm or 54Gy/30 fractions if . 3cm. Elective nodal regions were given 45Gy/30 fractions. CT was administered concurrently following Nigro’s regimen. The primary end point was acute toxicity. Secondary end points were colostomy-free survival (CFS), disease-free survival (DFS), cancer-specific survival (CSS) and overall survival (OS). Dosimetric data are also provided. Results: Median follow-up was 21 months. Maximum acute toxicities were: dermatologic—G3: 18%; gastrointestinal–G3: 5%; genitourinary–G3: 2%; anaemia—G2: 7%; leukopenia— G3: 28%; G4: 8%; neutropenia—G3: 13%; G4: 18%; thrombocytopenia—G3: 11%; and G4: 2%. The actuarial 2-year CFS was 77.9% [95% confidence interval (CI): 54–90.4%]. Actuarial 2-year OS and CSS were 85.2% (95% CI: 60.1–95.1%), while DFS was 75.1% (95% CI: 52.4.7–88.1%). Conclusion: Our clinical results support the use of VMAT as a safe and effective intensity-modulated radiotherapy (IMRT) option in the combined modality treatment of anal cancer, with consistent dosimetry, mild toxicity and promising sphincter preservation and survival rates. Advances in knowledge: IMRT is a standard of care for patients with anal cancer, and VMAT is a robust technical solution in this setting.
2016
89
1060 - 20150832
1
8
Radiotherapy; Anal cancer; IMRT; VMAT
Franco, Pierfrancesco; Arcadipane, Francesca; Ragona, Riccardo; Mistrangelo, Massimiliano; Cassoni, Paola; Munoz, Fernando; Rondi, Nadia; Morino, Mario; Racca, Patrizia; Ricardi, Umberto
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/1558634
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