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首页> 外文期刊>Cancer chemotherapy and pharmacology. >Time to CA19-9 nadir: a clue for defining optimal treatment duration in patients with resectable pancreatic ductal adenocarcinoma
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Time to CA19-9 nadir: a clue for defining optimal treatment duration in patients with resectable pancreatic ductal adenocarcinoma

机译:Time To Ca19-9 Nadir:用于定义可重置胰腺导管腺癌患者的最佳治疗持续时间的线索

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Background Defining optimal treatment duration in patients with resectable pancreatic ductal adenocarcinoma (PDAC) receiving primary chemotherapy is an unmet need. The role of time to CA19-9 nadir and of nadir magnitude was explored in this study. Patients and methods The databases of our institution's prospective trials were queried to speculate on the time to maximum chemotherapy response. Patients with pathologically proven, metastatic (N = 356) or non-metastatic non-resected (N = 163) PDAC and elevated baseline (> 34 UI/mL) CA19-9 were analyzed. Survival curves were estimated using the Kaplan-Meier method and compared by means of the log-rank test for analyses including at least 45 patients. Multivariable Cox proportional hazards model was used to estimate clinical features for their association with OS. All probability values were from two-sided tests. Results Time to CA19-9 nadir was >= 4 months in 184 of 346 (53%) metastatic and 121 of 163 (74%) non-metastatic patients (p = 0.002). The likelihood of a later nadir was higher with taxane-based chemotherapy as compared to taxane-free combinations (73% versus 56%; p = 0.02). Both metastatic and non-metastatic patients had significantly longer survival when nadir occurred later. Patients with a larger CA19-9 nadir magnitude had significantly longer survival. Metastatic patients with CA19-9 reduced by 89% and had a median survival of 7.4, 9.8, and 14.7 months, respectively (p 89%; p = 0.14 for 50-89% versus > 89%). Multivariable analyses showed that time to CA19-9 nadir but not CA19-9 nadir magnitude was independently predictive of survival. Conclusion The present study suggests that a 4-6 months program might be a more suitable candidate for prospective assessment in comparison to shorter pre-defined period in patients who are candidates to surgery after primary chemotherapy.
机译:背景:确定接受一期化疗的可切除胰腺导管腺癌(PDAC)患者的最佳治疗时间是一个尚未满足的需求。本研究探讨了到达CA19-9最低点的时间和最低点大小的作用。患者和方法通过查询我院前瞻性试验数据库,推测达到最大化疗反应的时间。对经病理证实的转移性(N=356)或非转移性非切除性(N=163)PDAC和基线升高(>34 UI/mL)CA19-9的患者进行分析。使用Kaplan-Meier方法估计生存曲线,并通过对数秩检验对至少45名患者进行分析比较。多变量Cox比例风险模型用于评估与OS相关的临床特征。所有概率值均来自双边测试。结果在346例(53%)转移性患者中,184例(163例(74%)非转移性患者中,到达CA19-9最低点的时间>=4个月(p=0.002)。与不含紫杉烷的联合化疗相比,基于紫杉烷的化疗后出现低谷的可能性更高(73%对56%;p=0.02)。当最低点出现较晚时,转移性和非转移性患者的生存期都显著延长。CA19-9最低点较大的患者生存期显著延长。CA19-9转移患者减少了89%,中位生存期分别为7.4、9.8和14.7个月(p 89%;p=0.14,50-89%与>89%)。多变量分析显示,到达CA19-9最低点的时间(而非CA19-9最低点的幅度)独立预测生存率。结论本研究表明,对于初次化疗后手术的患者,与较短的预定时间相比,4-6个月的计划可能更适合进行前瞻性评估。

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