定义最佳剂量为3维符合加速部分乳房辐射:15年后期的剂量升级试验
Alphonse G Taghian1, George E Naoum2, Lior Z Braunstein3
1Radiation Oncology Department, Harvard Medical School, Boston, Massachusetts; Radiation Oncology Department, Massachusetts General Hospital, Boston, Massachusetts.
International journal of radiation oncology, biology, physics
|January 11, 2025
概括
对于加速部分乳房照射 (APBI),32 Gy,36 Gy和40 Gy显示出类似的局部瘤控制. 高剂量的APBI增加了纤维化和恶化的化品结果,这表明32 Gy是最佳的.
科学领域:
- 在瘤学瘤学.
- 辐射瘤学 辐射瘤学
- 乳腺癌治疗方法 乳腺癌治疗方法
背景情况:
- 加快部分乳房照射 (APBI) 是全乳房照射的替代方案.
- 对于瘤控制和毒性来说,最佳的APBI剂量尚未确立.
研究的目的:
- 在早期乳腺癌患者中评估升级剂量APBI的疗效和毒性.
- 确定APBI的最佳剂量,以最大限度地控制瘤并最大限度地减少不良影响.
主要方法:
- 一个连续剂量升级试验,涉及324名在位管道癌或I期侵袭性乳腺癌患者.
- 外部光束APBI每天两次以4Gy分数输送,总剂量为32Gy,36Gy和40Gy.
- 对局部衰竭,纤维化和化品结果的随访.
主要成果:
- 在32 Gy,36 Gy和40 Gy剂量队列中的15年局部失效率没有显著差异 (P = .21).
- 10年中度/重度纤维化发生率随着剂量增加而显著增加 (40%对58%对67%,P<.01).
- 10年化品结局 (患者和医生评估) 在较高的APBI剂量 (P < .01) 时明显恶化.
结论:
- 经过测试的APBI分成方案没有证明在超过32 Gy的剂量中,局部失效率有好处.
- 较高的APBI剂量 (36 Gy和40 Gy) 与纤维化率的增加和更差的化品效果有关.
- 在这种分成方案中,32 Gy似乎是最佳剂量,平衡有效性和毒性.
更多相关视频
08:34Proton Therapy Delivery and Its Clinical Application in Select Solid Tumor Malignancies
Published on: February 6, 2019
20.3K
07:57Positron Emission Tomography-based Dose Painting Radiation Therapy in a Glioblastoma Rat Model using the Small Animal Radiation Research Platform
Published on: March 24, 2022
2.7K
相关概念视频
Dosage Regimens: Designs and Approaches
600
Designing a dosage regimen, which refers to the manner of drug administration, is a complex process involving the selection of drug dose, route, and frequency. This process is underpinned by pharmacokinetic parameters derived from tests and population averages. These parameters are then tailored to patient-specific variables such as diagnosis, demographics, and allergy status. Once therapy commences, therapeutic response monitoring is critical and achieved through clinical and physical...
600
Determination of Multiple Dosing Parameters: Loading and Maintenance Doses
394
A loading dose is an essential pharmacological strategy to rapidly achieve the target plasma drug concentration necessary for an immediate therapeutic effect. This approach is especially critical for drugs characterized by slow absorption or extended half-lives, where delaying therapeutic plasma levels could compromise treatment outcomes. By administering a loading dose, clinicians ensure a prompt onset of drug action, even for agents with complex pharmacokinetic profiles.Achieving steady-state...
394
