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首页> 外文期刊>Journal of Cancer Research and Clinical Oncology >Hypofractionated sequential radiotherapy boost: a promising strategy in inoperable locally advanced pancreatic cancer patients
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Hypofractionated sequential radiotherapy boost: a promising strategy in inoperable locally advanced pancreatic cancer patients

机译:低辐射顺序放射疗法提升:在局部晚期胰腺癌患者中有希望的策略

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Purpose To investigate the potential benefits of a hypofractionated radiotherapy boost (HRB) after chemotherapy (CT) and concomitant chemoradiotherapy (CRT) in locally advanced pancreatic cancer (LAPC) patients. Primary endpoints were early and late toxicity, local control (LC) and pain-free progression (PFP) assessment. Two-years overall survival (OS), metastasis-free survival (MFS) and disease-free survival (DFS) were secondary endpoints. Materials and methods Patients (pts) affected by unresectable non-metastatic LAPC, previously treated with CT and CRT in upfront or sandwich setting, were selected for sequential HRB. Total prescribed dose was 30 Gy in 5 fractions (fr) to pancreatic primary lesion. Dose de-escalation was allowed in case of failure in respecting organs at risk constraints. Early and late toxicity were assessed according to CTCAE v.4.0 classification. The Kersh-Hazra scale was used for pain assessment. Local Control, PFP, MFS and DFS were calculated from the date of HRB to the date of relapse or the date of the last follow-up. Results Thirty-one pts affected by unresectable, non-metastatic LAPC were consecutively enrolled from November 2004 to October 2019. All pts completed the planned HRB. Total delivered dose varied according to duodenal dose constraint: 20 Gy in 5 fr (N: 6; 19.4%), 20 Gy in 4 fr (N: 5; 16.2%), 25 Gy in 5 fr (N: 18; 58.0%) and 30 Gy in 6 fr (N: 2; 6.4%). Early and late toxicity were assessed in all pts: no Grade 3 or 4 acute gastrointestinal toxicity and no late gastrointestinal complications occurred. Median LC was 19 months (range 1-156) and 1- and 2-year PFP were 85% and 62.7%, respectively (median 28 months; range 2-139). According to the Kersh-Hazra scale, four pts had a Grade 3 and four pts had a Grade 1 abdominal pain before HRB. At the last follow-up only 3/31 pts had residual Grade 1 abdominal pain.Median MFS was 18 months (range 1-139). The 2-year OS after HRB was 57.4%, while 2-year OS from diagnosis was 77.3%. Conclusion Treatment intensification with hypofractionated radiotherapy boost is well tolerated in pts affected by unresectable LAPC previously treated with CT/CRT. Its rates of local and pain control are encouraging, supporting its introduction in clinical practice. Timing, schedule and dose of HRB need to be further investigated to personalize therapy and optimize clinical advantages.
机译:目的探讨局部晚期胰腺癌(LAPC)患者化疗(CT)和同步放化疗(CRT)后低分割放射治疗(HRB)的潜在益处。主要终点为早期和晚期毒性、局部控制(LC)和无疼痛进展(PFP)评估。次要终点为两年总生存率(OS)、无转移生存率(MFS)和无病生存率(DFS)。材料和方法选择受无法切除的非转移性LAPC影响的患者(pts)进行连续HRB,这些患者之前在前方或三明治环境下接受CT和CRT治疗。胰腺原发病变的总处方剂量为30 Gy,分5个部分(fr)。如果未能遵守存在风险约束的器官,则允许剂量降低。根据CTCAE v.4.0分类评估早期和晚期毒性。疼痛评估采用Kersh-Hazra量表。从HRB日期到复发日期或最后一次随访日期,计算局部对照、PFP、MFS和DFS。结果从2004年11月至2019年10月,31例受不可切除、非转移性LAPC影响的患者连续入选。所有临时秘书处都完成了计划的HRB。根据十二指肠的剂量限制,总给药剂量有所不同:5FR中的20Gy(N:6;19.4%)、4FR中的20Gy(N:5;16.2%)、5FR中的25Gy(N:18;58.0%)和6FR中的30Gy(N:2;6.4%)。对所有pts进行早期和晚期毒性评估:无3级或4级急性胃肠道毒性,无晚期胃肠道并发症发生。中位LC为19个月(范围1-156),1年和2年PFP分别为85%和62.7%(中位28个月;范围2-139)。根据Kersh-Hazra评分,4名患者在HRB前腹痛等级为3级,4名患者在HRB前腹痛等级为1级。在最后一次随访中,仅有3/31患者出现残余1级腹痛。中位MFS为18个月(范围1-139)。HRB后2年的OS为57.4%,而诊断后2年的OS为77.3%。结论CT/CRT不能切除LAPC的pts患者可以接受低分割放射治疗增强治疗。它的局部和疼痛控制率令人鼓舞,支持其在临床实践中的引入。HRB的时间、时间表和剂量需要进一步研究,以个性化治疗和优化临床优势。

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