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临床试验/NCT01872416
NCT01872416Unknown2 期

A Clinical Study of Liposomal Doxorubicin Combined With Ifosfamide Second-line Treatment in Small Cell Lung Cancer: Single Center, Single-arm Study

The First Affiliated Hospital of Guangzhou Medical University1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2012年10月1日最近更新:
适应症

试验速览

阶段
2 期
发起方
入组人数
30
试验地点
1
主要终点
objective response rate

研究概览

简要总结

At present, there is no standard second-line treatment of refractory and relapsed SCLC, topotecan, gemcitabine, paclitaxel, irinotecan and drugs such as cyclophosphamide second-line treatment of small cell lung cancer currently being explored, Anthracycline antibiotics is a cell cycle non-specific anticancer drugs could inhibit the synthesis of DNA, DNA and dependent RNA, its wide antitumor spectrum, widely used in malignant hematologic diseases and lung cancer and other solid tumors. Jacot W, et al evaluated epirubicin combined with ifosfamide (EI) for treatment of refractory and recurrent SCLC in 70 cases, the objective response rate (ORR) reached 21.4%, including 1 cases of complete remission, 10% other patients obtained stable disease (SD), all the patients had a median survival of 3.9 months, most (71%) patients with neutropenia, platelet count and anemia are also common, showed that EI treatment of refractory and relapsed SCLC is effectively controlled, toxicity.

In view of epirubicin combined with ifosfamide (EI) scheme is effective and safety in the treatment of refractory and relapsed SCLC, the investigators will use liposomal doxorubicin plus ifosfamide second-line treatment of refractory and relapsed small cell lung cancer, may obtain better tumor remission rate, improve the prognosis of the patients.

详细描述

the investigators will evaluate the overall response rate (complete and partial responses) in first-line treatment failure or relapse after first-line therapy SCLC treated with Pegylated liposomal doxorubicin and ifosfamide We will evaluate the progression-free survival (PFS) and overall survival (OS) i in receiving first-line treatment failure or relapse after first-line therapy SCLC treated with Pegylated liposomal doxorubicin and ifosfamide

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Male or female patients >=18 years of age
  • the histological diagnosis of small cell lung cancer;
  • Patients who had first-line treatment failure or relapse after first-line therapy;
  • enough tumor tissue specimens for molecular marker analysis;
  • Measurable disease by RECIST criteria
  • ECOG performance status of <=
  • Life expectancy of at least 3 months.
  • Laboratory values as follows:: ANC ≥ 1.5 × 109/L; platelet count ≥ 100 × 109/L; HB ≥ 90g/L; serum bilirubin ≤ 1.5 upper limit of normal (N); ALT/AST≤ 2N (in patients with liver metastases :ALT/AST≤ 5N) creatinine≤1.25 N;and clearance rate of creatinine ≥ 60mLl/min; proteinuria < 2+, or were detected in 24 hour urine protein, protein content is ≤1g
  • Patient must be accessible for treatment and follow-up
  • All patients must be able to understand the nature of the study and give written informed consent prior to study entry

排除标准

  • mixed small cell lung cancer;
  • patients had a previous diagnosis of malignant tumor;
  • HIV infection;
  • A history of cardiac disease as defined by malignant hypertension, unstable angina, congestive heart failure of > grade 2 per New York Heart Association (NYHA) criteria, myocardial infarction within the previous 6 months, or symptomatic cardiac arrhythmias.
  • patients had the motor or sensory neurons lesions/symptoms of NCI - CTC AE > 1;
  • patients had serious active infections;
  • patients were allergic to ifosfamide or liposomal doxorubicin

结局指标

主要结局

objective response rate

时间窗: From date of randomization until the date of progression, assessed up to 5 months

participants will be followed for the duration of hospital stay, an expected average of 5 months

次要结局

  • progression free survival(PFS)(From date of randomization until the date of progression, assessed up to 5 months)

研究者

发起方
The First Affiliated Hospital of Guangzhou Medical University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Jianxing He

The First Affiliated Hospital of Guangzhou Medical University

The First Affiliated Hospital of Guangzhou Medical University

研究点 (1)

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