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Effectiveness and feasibility of concurrent chemoradiotherapy using simultaneous integrated boost-intensity modulated radiotherapy with and without induction chemotherapy for locally advanced pancreatic cancer

机译:联合放化疗联合或不联合诱导化疗对局部晚期胰腺癌同步放化疗的有效性和可行性

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Purpose To evaluate the effectiveness and feasibility of chemoradiotherapy (CRT) using simultaneous integrated boost-intensity modulated radiotherapy (SIB-IMRT) in locally advanced pancreatic cancer (LAPC) patients. Materials and Methods Between January 2011 and May 2015, 47 LAPC patients received CRT using SIB-IMRT. Prior to SIB-IMRT, 37 patients (78.7%) received induction chemotherapy (IC-CRT group) and remaining 10 patients (21.3%) did not received induction chemotherapy (CRT group). During SIB-IMRT, all patients received concomitant chemotherapy, with gemcitabine (n = 37) and capecitabine (n = 10). Results At the time of analysis, 45 patients had died and 2 patients remained alive and the median follow-up time was 14.2 months (range, 3.3 to 51.4 months). For all patients, the median times of local progression-free survival (LPFS), progression-free survival (PFS), and overall survival (OS) were 18.1, 10.3, and 14.2 months, respectively. The median time of LPFS between IC-CRT and CRT groups was similar (18.1 months vs. 18.3 months, p = 0.711). IC-CRT group had a higher trend in PFS (10.9 months vs. 4.1 months, p = 0.054) and had significantly higher OS (15.4 months vs. 9.5 months, p = 0.007) than CRT group. In multivariate analysis, the use of induction chemotherapy and tumor response were significant factors associated with OS (p 0.05, each). During SIBIMRT, toxicity of grade ≥3 was observed in 7 patients (14.9%) in all patients. Conclusions CRT using SIB-IMRT is feasible and promising in LAPC patients.
机译:目的评估在局部晚期胰腺癌(LAPC)患者中使用同步综合增强强度调制放疗(SIB-IMRT)进行放化疗的有效性和可行性。材料和方法2011年1月至2015年5月之间,有47位LAPC患者通过SIB-IMRT接受了CRT。在SIB-IMRT之前,有37例患者(78.7%)接受了诱导化疗(IC-CRT组),其余10例患者(21.3%)没有接受诱导化疗(CRT组)。在SIB-IMRT期间,所有患者均接受了吉西他滨(n = 37)和卡培他滨(n = 10)的化疗。结果分析时,有45例患者死亡,2例患者还活着,中位随访时间为14.2个月(范围3.3至51.4个月)。对于所有患者,局部无进展生存期(LPFS),无进展生存期(PFS)和总生存期(OS)的中位数时间分别为18.1、10.3和14.2个月。 IC-CRT和CRT组之间LPFS的中位时间相似(18.1个月vs. 18.3个月,p = 0.711)。与CRT组相比,IC-CRT组的PFS趋势更高(10.9个月vs.4.1个月,p = 0.054),OS显着更高(15.4个月vs. 9.5个月,p = 0.007)。在多变量分析中,诱导化疗的使用和肿瘤反应是与OS相关的重要因素(p均<0.05)。在SIBIMRT期间,所有患者中有7例(14.9%)观察到≥3级毒性。结论SIB-IMRT CRT在LAPC患者中是可行且有希望的。

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