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基于RTOG 0413方案的MammoSite近距离放射治疗的临床和剂量学经验。

Clinical and dosimetric experience with MammoSite-based brachytherapy under the RTOG 0413 protocol.

作者信息

Wojcicka Jadwiga B, Lasher Donette E, Malcom Ronald, Fortier Gregory

机构信息

Department of Radiation Oncology, York Cancer Center, York, Pennsylvania, U.S.A.

出版信息

J Appl Clin Med Phys. 2007 Oct 24;8(4):176-184. doi: 10.1120/jacmp.v8i4.2654.

Abstract

MammoSite balloon brachytherapy is a relatively new technique for partial breast irradiation. The present paper focuses on the treatment planning, dosimetry, and quality assurance aspects of that treatment, based on the Radiation Therapy Oncology Group 0413 randomized prospective trial (RTOG 0413) protocol. We investigate the usefulness of evaluating implants for treatment appropriateness according to the full set of RTOG criteria as compared with the manufacturer's guidelines. We describe our methods to improve MammoSite balloon implants that would otherwise not comply with the protocol. The initially acquired computed tomography (CT) images are evaluated for tissue conformance, balloon surface-to-skin distance, and balloon symmetry. If the implant fails to meet the foregoing criteria, corrective action such as delay in the CT scan, balloon manipulation, or fluid volume adjustment is taken, and the patient is re-scanned. If the corrective action appears to be successful, three dimensional treatment planning and dose-volume histogram analysis is performed to evaluate the geometric and dosimetric parameters with regard to the RTOG 0413 protocol. The evaluated parameters include, volume ratio of the lumpectomy cavity to the ipsilateral breast, target volume coverage, tissue-balloon conformance, balloon symmetry, minimal balloon surface-to-skin distance, maximum skin dose, and normal breast tissue dose-volume parameters V150 and V200. Among our implants, 21.7% did not initially meet the RTOG 0413 acceptance criteria. Asymmetry and poor conformance values reduce the target volume coverage, and so an implant with moderate conformance and asymmetry can be within the manufacturer's guidelines, but still not meet the RTOG criteria. Our intervention corrected all but one of the implants that failed to meet the criteria. Manipulating the cavity and adjusting the balloon volume may salvage an implant and meet the strict geometric and dosimetric criteria imposed by the RTOG 0413 protocol.

摘要

MammoSite球囊近距离放射疗法是一种相对较新的部分乳腺照射技术。本文基于放射治疗肿瘤学组0413随机前瞻性试验(RTOG 0413)方案,重点关注该治疗的治疗计划、剂量测定和质量保证方面。我们研究了根据RTOG全套标准评估植入物是否适合治疗的有用性,并与制造商的指南进行比较。我们描述了改进MammoSite球囊植入物的方法,否则这些植入物将不符合该方案。对最初获取的计算机断层扫描(CT)图像进行组织贴合度、球囊表面到皮肤距离和球囊对称性评估。如果植入物不符合上述标准,则采取诸如延迟CT扫描、球囊操作或液体体积调整等纠正措施,并对患者进行重新扫描。如果纠正措施似乎成功,则进行三维治疗计划和剂量体积直方图分析,以根据RTOG 0413方案评估几何和剂量参数。评估的参数包括肿块切除腔与同侧乳腺的体积比、靶体积覆盖率、组织 - 球囊贴合度、球囊对称性、最小球囊表面到皮肤距离、最大皮肤剂量以及正常乳腺组织剂量体积参数V150和V200。在我们的植入物中,21.7%最初不符合RTOG 0413验收标准。不对称和贴合度不佳的值会降低靶体积覆盖率,因此,一个具有中等贴合度和不对称性的植入物可能符合制造商的指南,但仍不符合RTOG标准。我们的干预纠正了除一个之外所有不符合标准的植入物。操作腔隙和调整球囊体积可能挽救一个植入物,并符合RTOG 0413方案所规定的严格几何和剂量标准。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5d2/5722622/46840405515d/ACM2-8-176-g001.jpg

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