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Local Therapies for Oligometastatic Non-Small Cell Lung Cancer Harboring Sensitizing EGFR Mutations

2018年4月20日 更新者:Memorial Sloan Kettering Cancer Center

Pilot Study of Local Therapies for Oligometastatic Non-Small Cell Lung Cancer Harboring Sensitizing EGFR Mutations

This study will test if local therapies in addition to erlotinib can improve responses and delay the time until new treatment is required. This study will also collect blood samples for research blood tests.

研究概览

研究类型

介入性

注册 (实际的)

4

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • New Jersey
      • Basking Ridge、New Jersey、美国
        • Memoral Sloan Kettering Cancer Center
      • Middletown、New Jersey、美国、07748
        • Memorial Sloan Kettering Monmouth
    • New York
      • Commack、New York、美国、11725
        • Memorial Sloan Kettering Cancer Center @ Suffolk
      • Harrison、New York、美国、10604
        • Memorial Sloan Kettering Westchester
      • New York、New York、美国、10065
        • Memorial Sloan Kettering Cancer Center
      • Rockville Centre、New York、美国
        • Memorial Sloan Kettering at Mercy Medical Center
      • Sleepy Hollow、New York、美国、10591
        • Memoral Sloan Kettering Cancer Center at Phelps

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Newly diagnosed metastatic lung adenocarcinoma (recurrent or de novo) harboring sensitizing EGFR mutations (L858R, exon 19 deletion, G719A, L861Q, S768I, exon 19 insertions) with oligometastatic disease (≤5 discrete lesions of disease irrespective of location, inclusive of the primary lesion):
  • all sites of disease must be amenable to definitive treatment with a local therapy (surgical resection, stereotactic radiosurgery, ablation and conventional radiation therapy) as determined by surgery, interventional radiology and radiation oncology
  • all intrathoracic lymph nodes (including hilar, mediastinal, and supraclavicular nodal disease) are considered 1 discrete lesion.
  • Each brain metastasis is included as a distinct lesion.
  • Patients already started on erlotinib are eligible as long as their sites of disease are determined to be eligible for definitive local therapy by consensus of the principal investigators within 12 weeks of the patient first taking erlotinib.
  • Lung adenocarcinoma histology confirmed at MSKCC.
  • Available archived tissue to perform molecular analysis
  • Patients without available archived tissue can have repeat biopsies to determine EGFR status as per standard clinical care guidelines
  • Age 18 years or older
  • Karnofsky Performance Status ≥ 70%
  • Adequate bone marrow, liver and renal function, as specified below:
  • Absolute Neutrophil Count (ANC) ≥ 1.5 x 109/L
  • Hemoglobin ≥ 8 g/dL
  • Platelets ≥ 100 x 109/L
  • Serum total bilirubin ≤ 1.5 x upper limit of normal (ULN) (except for patients with documented Gilbert's Syndrome)
  • AST and ALT ≤ 2.5 x ULN or ≤ 5 x ULN if liver metastases are present
  • Serum creatinine ≤ 1.5 x upper limit of normal or creatinine clearance ≥ 60ml/min for patients with creatinine levels above institutional normal.
  • For women of child-bearing potential, negative pregnancy test within 14 days prior to starting treatment
  • Men and women of childbearing age must be willing to use effective contraception while on treatment and for at least 3 months thereafter

Exclusion Criteria:

  • Treatment with erlotinib prior to developing metastatic disease
  • Patients with activating but not sensitizing mutations (exon 20 insertions, EGFR T790M)
  • Malignant pleural effusion or pleural disease
  • Leptomeningeal disease
  • Any site of disease that is not amenable to definitively local therapy including surgery or radiation therapy
  • Women who are breastfeeding or pregnant
  • Concurrent malignancies other than non-melanoma skin cancer that require active ongoing treatment.
  • Any medical co-morbidities that would preclude surgery or radiation therapy

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:不适用
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Oligometastatic Non-Small Cell Lung Cancer
Patients will be placed on EGFR-TKI for their metastatic EGFR-mutant stage IV oligometastatic disease. All patients will undergo induction TKI for 12 weeks. At the conclusion of 12 weeks on erlotinib, patients without disease progression [partial response (PR) or stable disease (SD)] will undergo definitive local treatment to all remaining sites of disease. After local therapy, erlotinib will be resumed until progression of disease (POD) by RECIST criteria. All assessments completed during the 12 week TKI induction phase are to be performed per protocol with a ± 7 day window.
Definitive local therapies include surgical resection, stereotactic radiosurgery, ablation and conventional radiation therapy

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Feasibility as Measured by at Least Five Patients Will Need to Complete Local Therapy.
大体时间:2 years
At least five patients will need to complete local therapy within 2 years of the study being open to accrual for the primary endpoint to be met.
2 years

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2015年5月14日

初级完成 (实际的)

2017年12月11日

研究完成 (实际的)

2017年12月11日

研究注册日期

首次提交

2015年5月14日

首先提交符合 QC 标准的

2015年5月18日

首次发布 (估计)

2015年5月21日

研究记录更新

最后更新发布 (实际的)

2018年5月21日

上次提交的符合 QC 标准的更新

2018年4月20日

最后验证

2017年12月1日

更多信息

与本研究相关的术语

药物和器械信息、研究文件

研究美国 FDA 监管的药品

研究美国 FDA 监管的设备产品

在美国制造并从美国出口的产品

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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