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Single-arm Trial of BIBW 2992 (Afatinib) in Demographically and Genotypically Selected NSCLC Patients

2014年2月24日 更新者:Boehringer Ingelheim

A Phase II Single-arm Trial of BIBW 2992 in Demographically and Genotypically Selected NSCLC

The primary objective of this open-label, single arm Phase II trial is to explore the efficacy of BIBW 2992 defined by the objective response rate (CR, PR) as determined by the RECIST criteria, in patients with advanced NSCLC Stage IIIB or IV whose tumours harbour activating mutations within exon 18 to exon 21 of the EGFR receptor, in patients with mutations in the HER2/neu receptor and in patients with EGFR FISH positive tumours with no EGFR mutations.

調査の概要

研究の種類

介入

入学 (実際)

41

段階

  • フェーズ2

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

      • Badalona (Barcelona)、スペイン
        • 1200.41.34001 Boehringer Ingelheim Investigational Site
      • Antwerpen、ベルギー
        • 1200.41.32003 Boehringer Ingelheim Investigational Site
      • Charleroi、ベルギー
        • 1200.41.32007 Boehringer Ingelheim Investigational Site
      • Jette、ベルギー
        • 1200.41.32001 Boehringer Ingelheim Investigational Site
      • Leuven、ベルギー
        • 1200.41.32011 Boehringer Ingelheim Investigational Site
      • Liège、ベルギー
        • 1200.41.32008 Boehringer Ingelheim Investigational Site
      • Namur、ベルギー
        • 1200.41.32006 Boehringer Ingelheim Investigational Site

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年歳以上 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

説明

Inclusion criteria:

  1. patients with pathologically confirmed diagnosis of NSCLC stage IIIB/IV adeno- or bronchoalveolar carcinoma (BAC)
  2. non smokers patients or patients having smoked less than 15 pack years and who stopped smoking for at least one year before diagnosis (except for patients with her2-neu mutation)
  3. presence of activating mutation(s) in exon 18 to exon 21 of the EGFR or HER2-neu-receptor confirmed by direct DNA sequencing of NSCLC tumor tissue or increased copy number of the EGFR gene as determined by FISH analysis
  4. prior treatment up to 3 lines of chemotherapy except for HER2-neu patients (no restrictions) no prior EGFR TKI therapy for EGFR mutation negative and FISCH positive patients
  5. patients with at least one tumor lesion that can accurately be measured by CTscan or MRI in at least one dimension with long diameter to be recorded as > or equal to 20 mm using conventional techniques or > or equal to 10 mm with spiral CT scan
  6. male or female patient aged above or equal to 18 years
  7. life expectancy of at least 3 months
  8. written informed consents that is consistent with ICH-GCP guidelines
  9. ECOG performance score 0, 1 or 2

Exclusion criteria:

  1. more than 3 prior cytotoxic chemotherapy treatment regimen for relapsed or metastatic NSCLC, except for patients with HER2-neu mutations who may have received any prior therapy
  2. Any chemo-, hormone- or immunotherapy within the past 4 weeks or within less than 4 half-lives of the previous drug prior to treatment with the trial drug and/or persistence of toxicities of prior anticancer therapies which are deemed to be clinically relevant
  3. brain metastases which are symptomatic; patients with treated asymptomatic brain metastases are eligible with stable brain disease for at least 4 weeks without requirement for steroids or anti-epileptic therapy
  4. significant or recent acute gastrointestinal disorders with diarrhea as a major symptom e.g. Crohn's disease, malabsorption or CTCAE Grade > 2 diarrhea of any etiology at baseline
  5. patients who have any other life-threatening illness or organ system dysfunction, which in the opinion of the investigator, would either compromise patient safety or interfere with the evaluation of the safety of the test drug
  6. other malignancies diagnosed within the past 5 years (other than non melanomatous skin cancer and in situ cervical cancer)
  7. radiotherapy within the past 2 weeks prior to treatment with the trial drug
  8. patients with any serious active infection (i.e., requiring an IV antibiotic, antifungal, or antiviral agents)
  9. patients with known HIV, active hepatitis B or active hepatitis C
  10. known or suspected active drug or alcohol abuse
  11. women of childbearing potential or men who are able to father a child unwilling to use a medically acceptable method of contraception during the trial
  12. pregnancy or breast feeding
  13. patient unable to comply with the protocol
  14. history of clinically significant or uncontrolled cardiac disease, including congestive heart failure, angina, myocardial infarction, arrhythmia, including New York Heart Association (NYHA) functional classification of 3
  15. Cardiac left ventricular function with resting ejection fraction of less than 50% measured by multigated blood pool imaging of the heart (MUGA scan) or Echocardiogram.
  16. Absolute neutrophil count (ANC) less than 1500/mm³.
  17. Platelet count less than 100 000 / mm³.
  18. Bilirubin greater than 1.5 mg / dl (>26 µmol / L, SI unit equivalent).
  19. Aspartate amino transferase (AST) or alanine amino transferase (ALT) greater than three times the upper limit of normal (if related to liver metastases greater than five times the upper limit of normal).
  20. Serum creatinine greater than 1.5 times of the upper normal limit

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:非ランダム化
  • 介入モデル:単一グループの割り当て
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的:BIBW 2992
patient to receive tablets of BIBW 2992 once a day, starting at high dose until progression of the disease
tablet BIBW high dose
実験的:BIBW 2992 + paclitaxel
patient whose disease progressed on treatment with BIBW 2992 monotherapy to receive tablet of BIBW 2992 once a day in combination with i.v. paclitaxel 3 weekly
tablet BIBW 2992 in combination with i.v. paclitaxel 3 weekly

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Percentage of Participants With Best Objective Response
時間枠:Tumour assessments were performed at baseline (tumour assessment obtained within 4 weeks prior to beginning of treatment), week 8, and every 8 weeks thereafter.
Percentage of participants with best objective response: confirmed complete response (CR) or confirmed partial response (PR) according to RECIST version 1.0.
Tumour assessments were performed at baseline (tumour assessment obtained within 4 weeks prior to beginning of treatment), week 8, and every 8 weeks thereafter.

二次結果の測定

結果測定
メジャーの説明
時間枠
Percentage of Participants With Disease Control (DC)
時間枠:Tumour assessments were performed at baseline (tumour assessment obtained within 4 weeks prior to beginning of treatment), week 8, and every 8 weeks thereafter.
Percentage of participants with OR or stable disease (SD) as determined by RECIST version 1.0.
Tumour assessments were performed at baseline (tumour assessment obtained within 4 weeks prior to beginning of treatment), week 8, and every 8 weeks thereafter.
Progression Free Survival (PFS) Time
時間枠:Tumour assessments were performed at baseline (tumour assessment obtained within 4 weeks prior to beginning of treatment), week 8, and every 8 weeks thereafter.
PFS time defined as time from the start of treatment to the earliest of progression (RECIST), clinical progression (investigator), start of new anti-cancer treatment or death.
Tumour assessments were performed at baseline (tumour assessment obtained within 4 weeks prior to beginning of treatment), week 8, and every 8 weeks thereafter.
Summary of Pre-dose Concentrations of Afatnib in Plasma
時間枠:Day 15, 29 and 57
Pre-dose Concentrations of Afatinib in Plasma at Steady State on Days 15, 29 and 57 (Cpre,ss,15, Cpre,ss,29 and Cpre,ss,57)
Day 15, 29 and 57

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

出版物と役立つリンク

研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。

便利なリンク

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始

2008年6月1日

一次修了 (実際)

2012年1月1日

試験登録日

最初に提出

2008年6月30日

QC基準を満たした最初の提出物

2008年8月7日

最初の投稿 (見積もり)

2008年8月8日

学習記録の更新

投稿された最後の更新 (見積もり)

2014年3月26日

QC基準を満たした最後の更新が送信されました

2014年2月24日

最終確認日

2014年2月1日

詳しくは

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

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