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CT引导下在线自适应立体定向体部放射治疗胰腺导管腺癌:剂量学及初步临床经验

CT-guided online adaptive stereotactic body radiotherapy for pancreas ductal adenocarcinoma: Dosimetric and initial clinical experience.

作者信息

Lee Albert, Pasetsky Jared, Lavrova Elizaveta, Wang Yi-Fang, Sedor Geoffrey, Li Feng L, Gallitto Matthew, Garrett Matthew, Elliston Carl, Price Michael, Kachnic Lisa A, Horowitz David P

机构信息

Department of Radiation Oncology, Columbia University Irving Medical Center, New York, NY, United States.

Herbert Irving Comprehensive Cancer Center Minority Underserved NCORP, New York, NY, United States.

出版信息

Clin Transl Radiat Oncol. 2024 Jul 7;48:100813. doi: 10.1016/j.ctro.2024.100813. eCollection 2024 Sep.

Abstract

PURPOSE/OBJECTIVES: Retrospective analysis suggests that dose escalation to a biologically effective dose of more than 70 Gy may improve overall survival in patients with pancreatic ductal adenocarcinoma (PDAC), but such treatments in practice are limited by proximity of organs at risk (OARs). We hypothesized that CT-guided online adaptive radiotherapy (OART) can account for interfraction movement of OARs and allow for safe delivery of ablative doses.

MATERIALS/METHODS: This is a single institution retrospective analysis of patients with PDAC treated with OART on the Ethos platform (Varian Medical Systems, a Siemens Healthineers Company, Palo Alto). All patients were treated to 40 Gy in 5 fractions. PTV overlapping with a 5 mm planning risk volume expansion on the stomach, duodenum and bowel received 25 Gy. Initial treatment plans were created conventionally. For each fraction, PTV and OAR volumes were recontoured with AI assistance after initial cone beam CT (CBCT). The adapted plan was calculated, underwent QA, and then compared to the scheduled plan. A second CBCT was obtained prior to delivery of the selected plan. Total treatment time (first CBCT to end of radiation delivery) and active physician time (first to second CBCT) were recorded. PTV_4000 V95 %, PTV_2500 V9 5%, and D0.03 cc to stomach, duodenum and bowel were reported for scheduled (S) and adapted (A) plans. CTCAEv5.0 toxicities were recorded. Statistical analysis was performed using a two-sided T test and α of 0.05.

RESULTS

21 patients with unresectable or locally-recurrent PDAC were analyzed, with a total of 105 fractions. Average total time was 29 min and 16 s (16:36-49:40) and average active physician time was 19:41 min (9:25-39:34). All fractions were treated with adapted plans. 97 % of adapted plans met PTV_4000 V95.0 % >95.0 % coverage goal and 100 % of adapted plans met OAR dose constraints. Median follow up was 6.6 months. Only 1 patient experienced acute grade 3+ toxicity directly attributable to radiation. Only 1 patient experienced late grade 3+ toxicity directly attributable to radiation.

CONCLUSIONS

Daily CT-based OART was associated with significantly reduced dose OARs while achieving superior PTV coverage. Given the relatively quick total treatment time, radiation delivery was generally well tolerated and easily incorporated into the clinic workflow. Our initial clinical experience demonstrates OART allows for safe dose escalation in the treatment of PDAC.

摘要

目的/目标:回顾性分析表明,将剂量提升至生物等效剂量超过70 Gy可能会改善胰腺导管腺癌(PDAC)患者的总生存期,但在实际应用中,此类治疗受到危及器官(OARs)位置的限制。我们假设CT引导下的在线自适应放疗(OART)可以考虑到OARs的分次间移动,并允许安全地给予消融剂量。

材料/方法:这是一项在Ethos平台(瓦里安医疗系统公司,西门子医疗公司旗下,帕洛阿尔托)对接受OART治疗的PDAC患者进行的单机构回顾性分析。所有患者均接受5次分割,每次分割剂量为40 Gy。与胃、十二指肠和肠道的5 mm计划风险体积扩展重叠的计划靶体积(PTV)接受25 Gy照射。初始治疗计划按常规制定。对于每个分割,在初始锥形束CT(CBCT)后,借助人工智能重新勾勒PTV和OARs的体积。计算调整后的计划,进行质量保证,然后与预定计划进行比较。在实施选定计划之前获取第二次CBCT。记录总治疗时间(从第一次CBCT到放疗结束)和医生实际操作时间(从第一次到第二次CBCT)。报告预定(S)计划和调整(A)计划的PTV_4000 V95%、PTV_2500 V95%以及胃、十二指肠和肠道的D0.03 cc剂量。记录CTCAEv5.0毒性反应。采用双侧T检验进行统计分析,α值为0.05。

结果

分析了21例不可切除或局部复发的PDAC患者,共105次分割。平均总时间为29分16秒(16:36 - 49:40),平均医生实际操作时间为19分41秒(9:25 - 39:34)。所有分割均采用调整后的计划进行治疗。97%的调整后计划达到PTV_4000 V95.0% > 95.0%的覆盖目标,100%的调整后计划符合OAR剂量限制。中位随访时间为6.6个月。只有1例患者经历了直接归因于放疗的3级及以上急性毒性反应。只有1例患者经历了直接归因于放疗的3级及以上晚期毒性反应。

结论

基于每日CT的OART在实现PTV良好覆盖的同时,显著降低了OARs的剂量。鉴于总治疗时间相对较短,放疗耐受性总体良好,且易于纳入临床工作流程。我们的初步临床经验表明,OART允许在PDAC治疗中安全地增加剂量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92be/11324999/b635565caf25/gr1.jpg

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