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首页> 外文期刊>Cancer chemotherapy and pharmacology. >Ineligibility for the PACIFIC trial in unresectable stage III non-small cell lung cancer patients
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Ineligibility for the PACIFIC trial in unresectable stage III non-small cell lung cancer patients

机译:不可切除阶段III型非小细胞肺癌患者的太平洋试验的不可认识

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摘要

PurposeRecently, based on results of the PACIFIC trial, durvalumab after chemoradiotherapy (CRT) became the standard therapy for unresectable stage III non-small cell lung cancer (NSCLC). However, in the PACIFIC trial, patients were recruited and randomized after CRT, and certain patients were considered ineligible after CRT in the real world. No study has been conducted on the patients who were ineligible for the PACIFIC trial, and hence, we conducted a retrospective study on them.MethodsWe identified 82 patients with stage III NSCLC who received definitive platinum-based concurrent CRT and had World Health Organization performance status of 0-1. We investigated the proportion, clinical characteristics, and prognoses of patients who became ineligible for the PACIFIC trial after CRT.ResultsAfter CRT, 19 of 82 patients (23%) became ineligible for the PACIFIC trial. Comparison between eligible and ineligible patients revealed that old age (p=0.042), male gender (p=0.031), and radiation therapy with V20 >= 35% (p=0.032) were associated with ineligibility after CRT. Moreover, ineligible patients showed shorter PFS (6.6 vs. 15.7months, hazard ratio [HR] 2.61, 95% confidence interval [CI] 1.16-5.89, p=0.016) and shorter OS (18.6 vs. 44.3months, HR 3.03, 95% CI 1.29-7.10, p=0.007) than eligible patients.ConclusionsOur study revealed the clinical characteristics and prognoses of patients who became ineligible for the PACIFIC trial after CRT. Physicians should be careful while prescribing CRT for patients with characteristics such as old age, male gender, and radiation therapy with V20 >= 35%.
机译:在ChemorAdiotherapy(CRT)之后,基于太平洋试验的结果,基于太平洋试验的结果(CRT),成为INII III非小细胞肺癌(NSCLC)的标准治疗。然而,在太平洋审判中,CRT后招募和随机化,某些患者在现实世界的CRT之后被认为是没有资格的。没有关于不符合太平洋审判的患者进行的研究,从而对其进行了回顾性研究..甲基一德鉴定了82例阶段III NSCLC患者,他们接受了最终的铂族的并发CRT,并有世界卫生组织绩效状况0-1。我们调查了患者的比例,临床特征和预测,患者在CRT.Resultsafter CRT之后,82名患者(23%)中有19名患者(23%)的患者。符合条件和不合格患者之间的比较显示,老年龄(P = 0.042),男性性别(P = 0.031)和v20> = 35%(p = 0.032)的放射治疗与CRT后的损伤有关。此外,没有资格的患者显示较短的PFS(6.6与15.7months,危害比[HR] 2.61,95%置信区间[CI] 1.16-5.89,P = 0.016)和更短的OS(18.6与44.3个月,HR 3.03,95 %CI 1.29-7.10,P = 0.007)比符合条件的患者.Conclusoursour的研究表明,在CRT之后患者缺乏符合太平洋审判的患者的临床特征和预期。对于患有老年,男性性别和辐射治疗等特性,v20> = 35%的患者,医生应该小心。

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  • 作者单位

    Kobe City Med Ctr Gen Hosp Dept Resp Med Chuo Ku 2-1-1 Minatojima Minamimachi Kobe Hyogo;

    Kobe City Med Ctr Gen Hosp Dept Resp Med Chuo Ku 2-1-1 Minatojima Minamimachi Kobe Hyogo;

    Kobe City Med Ctr Gen Hosp Dept Resp Med Chuo Ku 2-1-1 Minatojima Minamimachi Kobe Hyogo;

    Kobe City Med Ctr Gen Hosp Dept Resp Med Chuo Ku 2-1-1 Minatojima Minamimachi Kobe Hyogo;

    Kobe City Med Ctr Gen Hosp Dept Resp Med Chuo Ku 2-1-1 Minatojima Minamimachi Kobe Hyogo;

    Kobe City Med Ctr Gen Hosp Dept Resp Med Chuo Ku 2-1-1 Minatojima Minamimachi Kobe Hyogo;

    Kobe City Med Ctr Gen Hosp Dept Resp Med Chuo Ku 2-1-1 Minatojima Minamimachi Kobe Hyogo;

    Kobe City Med Ctr Gen Hosp Dept Resp Med Chuo Ku 2-1-1 Minatojima Minamimachi Kobe Hyogo;

    Kobe City Med Ctr Gen Hosp Dept Radiat Oncol Chuo Ku 2-1-1 Minatojima Minamimachi Kobe Hyogo;

    Kobe City Med Ctr Gen Hosp Dept Radiat Oncol Chuo Ku 2-1-1 Minatojima Minamimachi Kobe Hyogo;

    Kobe City Med Ctr Gen Hosp Dept Resp Med Chuo Ku 2-1-1 Minatojima Minamimachi Kobe Hyogo;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 药理学;
  • 关键词

    Non-small cell lung cancer; Definitive chemoradiotherapy; Durvalumab; Eligibility criteria; Outcome;

    机译:非小细胞肺癌;明确的化学疗法;Durvalumab;资格标准;结果;

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