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Benefit of Gemcitabine/Nab-Paclitaxel Rescue of Patients With Borderline Resectable or Locally Advanced Pancreatic Adenocarcinoma After Early Failure of FOLFIRINOX

机译:吉西他滨/富紫外框的益处患者患者患者在FOLFIRINOX早期失败后濒临覆盖物可重演或局部晚期胰腺腺癌患者

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Objectives Neoadjuvant therapy (NT) is used for advanced pancreatic ductal adenocarcinoma (PDAC). No clear guidelines exist for switching therapies when patients do not respond to initial NT. We sought to characterize patients who underwent early switch from FOLFIRINOX to gemcitabine/nab-paclitaxel (GA) as NT for PDAC. Methods We identified patients at a single institution switched from FOLFIRINOX to GA within the first 4 months of NT for PDAC during 2012-2017. We compared clinicopathologic data and oncologic outcomes. Results Of 25 patients who met the criteria, 21 showed a serologic or radiographic response to GA; 11 (52%) reached resection. Responders had decreased carbohydrate antigen (CA) 19-9 levels from pretreatment to post-GA (P = 0.036). Resected responders had significantly decreased CA 19-9 comparing preswitch to post-GA (P = 0.048). The only predictor of GA response was prechemotherapy CA 19-9 of less than1000 U/mL (P = 0.021). Predictors of reaching resection were head/uncinate tumor (P = 0.010) and presenting stage lower than locally advanced (P = 0.041). Conclusions When patients do not respond to neoadjuvant FOLFIRINOX, early switch to GA should be considered. Future efforts should be directed toward identifying markers that will allow correct choice of initial therapy rather than attempting to rescue patients who respond poorly to first-line therapy.
机译:目的是Neoadjuvant治疗(NT)用于晚期胰腺导管腺癌(PDAC)。当患者没有响应初始NT时,不存在用于切换疗法的明确指南。我们试图将从Folfirinox接受早期切换到Gemcitabine / Nab-Paclitaxel(GA)作为PDAC的患者的患者。方法我们在2012-2017期间在NT的PDAC的第4个月内从Folfirinox转换为Ga的单个机构的患者。我们比较了临床病理数据和肿瘤学结果。结果25例符合标准的25名患者表明了对GA的血清学或射线照相反应; 11(52%)达到切除。响应者从预处理到后GA(P = 0.036)降低了碳水化合物抗原(CA)19-9水平。切除的响应者将PRESWITIT和POST-GA比较(P = 0.048)显着降低了CA 19-9。 GA响应的唯一预测因子​​是少于1000 u / ml的Ca 19-9(p = 0.021)。达到切除切除的预测因子是头部/ unnatinate肿瘤(p = 0.010),并且呈阶段低于局部晚期(p = 0.041)。结论当患者没有响应Neoadjuvant folfirinox时,应该考虑早期开关到Ga。未来的努力应该针对识别初始治疗的标记,而不是试图拯救对一线治疗不良的患者。

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