PMID- 23246253 OWN - NLM STAT- MEDLINE DCOM- 20131204 LR - 20130430 IS - 1873-4022 (Electronic) IS - 1873-4022 (Linking) VI - 38 IP - 2 DP - 2013 Summer TI - Clinical experience transitioning from IMRT to VMAT for head and neck cancer. PG - 171-5 LID - S0958-3947(12)00189-6 [pii] LID - 10.1016/j.meddos.2012.10.009 [doi] AB - To quantify clinical differences for volumetric modulated arc therapy (VMAT) versus intensity modulated radiation therapy (IMRT) in terms of dosimetric endpoints and planning and delivery time, twenty head and neck cancer patients have been considered for VMAT using Nucletron Oncentra MasterPlan delivered via an Elekta linear accelerator. Differences in planning time between IMRT and VMAT were estimated accounting for both optimization and calculation. The average delivery time per patient was obtained retrospectively using the record and verify software. For the dosimetric comparison, all contoured organs at risk (OARs) and planning target volumes (PTVs) were evaluated. Of the 20 cases considered, 14 had VMAT plans approved. Six VMAT plans were rejected due to unacceptable dose to OARs. In terms of optimization time, there was minimal difference between the two modalities. The dose calculation time was significantly longer for VMAT, 4 minutes per 358 degree arc versus 2 minutes for an entire IMRT plan. The overall delivery time was reduced by 9.2 +/- 3.9 minutes for VMAT (51.4 +/- 15.6%). For the dosimetric comparison of the 14 clinically acceptable plans, there was almost no statistical difference between the VMAT and IMRT. There was also a reduction in monitor units of approximately 32% from IMRT to VMAT with both modalities demonstrating comparable quality assurance results. VMAT provides comparable coverage of target volumes while sparing OARs for the majority of head and neck cases. In cases where high dose modulation was required for OARs, a clinically acceptable plan was only achievable with IMRT. Due to the long calculation times, VMAT plans can cause delays during planning but marked improvements in delivery time reduce patient treatment times and the risk of intra-fraction motion. CI - Copyright (c) 2013 American Association of Medical Dosimetrists. Published by Elsevier Inc. All rights reserved. FAU - Studenski, Matthew T AU - Studenski MT AD - Department of Radiation Oncology, Jefferson Medical College of Thomas Jefferson University, Philadelphia, PA 19107, USA. matthew.studenski@jeffersonhospital.org FAU - Bar-Ad, Voichita AU - Bar-Ad V FAU - Siglin, Joshua AU - Siglin J FAU - Cognetti, David AU - Cognetti D FAU - Curry, Joseph AU - Curry J FAU - Tuluc, Madalina AU - Tuluc M FAU - Harrison, Amy S AU - Harrison AS LA - eng PT - Comparative Study PT - Controlled Clinical Trial PT - Journal Article DEP - 20121214 PL - United States TA - Med Dosim JT - Medical dosimetry : official journal of the American Association of Medical Dosimetrists JID - 8908862 SB - IM MH - Head and Neck Neoplasms/*radiotherapy MH - Humans MH - Radiometry/*methods MH - *Radiotherapy Dosage MH - Radiotherapy Planning, Computer-Assisted/*methods MH - Radiotherapy, Intensity-Modulated/*methods MH - Reproducibility of Results MH - Sensitivity and Specificity MH - Treatment Outcome EDAT- 2012/12/19 06:00 MHDA- 2013/12/16 06:00 CRDT- 2012/12/19 06:00 PHST- 2012/05/31 00:00 [received] PHST- 2012/10/31 00:00 [revised] PHST- 2012/10/31 00:00 [accepted] PHST- 2012/12/19 06:00 [entrez] PHST- 2012/12/19 06:00 [pubmed] PHST- 2013/12/16 06:00 [medline] AID - S0958-3947(12)00189-6 [pii] AID - 10.1016/j.meddos.2012.10.009 [doi] PST - ppublish SO - Med Dosim. 2013 Summer;38(2):171-5. doi: 10.1016/j.meddos.2012.10.009. Epub 2012 Dec 14.