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Lapatinib Ditosylate and Capecitabine in Treating Patients With Metastatic Pancreatic Cancer

2014년 12월 30일 업데이트: Cancer Trials Ireland

A Phase II Study of Lapatinib and Capecitabine in the Treatment of Metastatic Pancreatic Cancer.

RATIONALE: Lapatinib ditosylate may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as capecitabine, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving lapatinib ditosylate together with capecitabine may kill more tumor cells.

PURPOSE: This phase II trial is studying how well giving lapatinib ditosylate together with capecitabine works in treating patients with metastatic pancreatic cancer.

연구 개요

상세 설명

OBJECTIVES:

Primary

  • To evaluate the efficacy of lapatinib ditosylate and capecitabine as first-line therapy, in terms of overall survival, in patients with metastatic pancreatic cancer.

Secondary

  • To evaluate the progression-free survival of patients treated with this regimen.
  • To evaluate the overall response rate (complete and partial responses) in patients treated with this regimen.
  • To evaluate the clinical benefit (complete response, partial response, or stable disease for ≥ 6 months) of this regimen in these patients.
  • To evaluate the qualitative and quantitative toxicity associated with this regimen in these patients.
  • To determine the intra-tumoral expression of ErbB1 (EGFR) and ErbB2 (HER2/neu) in these patients.
  • To seek pilot information on the intra-tumoral expression of markers of tumor resistance and sensitivity to treatment, including resistance drug pump expression and growth factor receptor expression.
  • To collect pre- and post-treatment serum samples from these patients for proteomic analyses to elucidate if any serum cancer marker profiles can be detected.

OUTLINE: This is a multicenter study.

Patients receive oral lapatinib ditosylate once daily on days 1-21 and oral capecitabine twice daily on days 1-14. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed up every 6-12 weeks.

연구 유형

중재적

등록 (실제)

9

단계

  • 2 단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

      • Cork, 아일랜드
        • Cork University Hospital
      • Cork, 아일랜드
        • Mercy University Hospital
      • Dublin, 아일랜드, 9
        • Beaumont Hospital
      • Dublin, 아일랜드, 7
        • Mater Misericordiae University Hospital
      • Dublin, 아일랜드, 4
        • St. Vincent'S University Hospital
      • Dublin, 아일랜드, 7
        • Mater Private Hospital
      • Dublin, 아일랜드, 24
        • Adelaide and Meath Hospital, Dublin Incorporating the National Children's Hospital
      • Dublin, 아일랜드, 8
        • St. James's Hospital
      • Galway, 아일랜드
        • University College Hospital

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

18년 이상 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

설명

DISEASE CHARACTERISTICS:

  • Histologically or cytologically confirmed metastatic adenocarcinoma of the pancreas
  • Measurable or non-measurable disease

    • Measurable disease is defined as ≥ 1 lesion that can be accurately measured in ≥ 1 dimension (longest diameter to be recorded) as ≥ 20 mm with conventional techniques or as ≥ 10 mm with spiral CT scan
  • No known brain metastases or leptomeningeal disease

PATIENT CHARACTERISTICS:

  • ECOG performance status 0-1
  • Life expectancy > 12 weeks
  • ANC ≥ 1,500/mm^3
  • Platelet count ≥ 100,000/mm^3
  • Hemoglobin ≥ 9 g/dL
  • Albumin ≥ 2.5 g/dL
  • Serum bilirubin ≤ 1.5 times upper limit of normal (ULN) (2.5 times ULN if Gilbert's syndrome is present)
  • AST and ALT ≤ 3 times ULN (5 times ULN if documented liver metastases are present)
  • Creatinine < 1.5 times ULN
  • Cardiac ejection fraction normal by ECHO or MUGA scan
  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective contraception
  • Able to swallow and retain oral medication
  • No gastrointestinal (GI) tract disease resulting in an inability to take oral medication, malabsorption syndrome, requirement for IV alimentation, or uncontrolled inflammatory GI disease (e.g., Crohn's disease or ulcerative colitis)
  • No active hepatic or biliary disease, except for Gilbert's syndrome, asymptomatic gallstones, liver metastases, or stable chronic liver disease per investigator assessment
  • No active cardiac disease within the past 6 months, including any of the following:

    • Uncontrolled angina
    • Clinically significant arrhythmia, except for asymptomatic atrial fibrillation requiring anticoagulation
    • Myocardial infarction
    • Uncontrolled or symptomatic congestive heart failure
    • Any other cardiac condition that, in the opinion of the treating physician, would make this study unreasonably hazardous for the patient
  • No concurrent uncontrolled illness including, but not limited to, ongoing or active infection or psychiatric illness/social situation that would limit compliance with study requirements
  • No known immediate or delayed hypersensitivity reaction or idiosyncrasy to drugs chemically related to lapatinib ditosylate or any of its excipients, capecitabine, or fluorouracil
  • No known dihydropyrimidine dehydrogenase (DPD) deficiency
  • No other malignancy within the past 5 years except for completely resected nonmelanoma skin cancer or successfully treated in situ carcinoma

PRIOR CONCURRENT THERAPY:

  • Recovered from prior radiotherapy or surgery
  • No prior surgical procedures affecting absorption
  • No prior EGFR- or ErbB2-targeting therapies
  • No prior capecitabine
  • No prior chemotherapy for locally advanced or metastatic pancreatic cancer
  • At least 3 months since prior adjuvant chemotherapy

    • Prior fluorouracil allowed as a radiosensitizer only
  • More than 30 days (or 5 half-lives) since prior investigational drugs
  • No concurrent radiotherapy or surgery for metastatic cancer
  • No concurrent combination antiretroviral therapy for HIV-positive patients
  • No concurrent CYP3A4 inducers or inhibitors
  • No other concurrent investigational agents or anticancer therapy (e.g., cytotoxic or biologic therapy)
  • No concurrent herbal (alternative) medicines

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 해당 없음
  • 중재 모델: 단일 그룹 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: Capecitabine and Lapatinib

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
기간
6-month survival rate
기간: 6 months
6 months

2차 결과 측정

결과 측정
측정값 설명
기간
Progression-free survival
기간: 6 months
Progression-free survival (PFS) will be measured as the number of days between patient's enrolment and his or her date of progression of disease. Patients who are still living six months after the last patient has been enrolled will be censored for the analyses, using the number of days between enrolment and the date of last follow-up. Disease progression will be determined according to definitions established in the modified response evaluation criteria in solid tumours (RECIST) (refer to Appendix G). For patients with non-measureable tumours disease progression will be determined by the treating physician in consultation with the Chief investigator for the study.
6 months
Overall response rate
기간: up to 6 months
The overall response rate will be an aggregation of the complete responses and partial responses. For patients to be given the status of complete response or partial response a confirmatory disease assessment should be performed no less than four weeks after the criteria for response are first met.
up to 6 months
Clinical benefit
기간: 6 months
A patient will be regarded as' having experienced clinical benefit if they have shown a complete response, a partial response, or stable disease for at least six months.
6 months
Safety and tolerability
기간: Throughout course of study
Throughout course of study
Tumour biomarker analysis
기간: Currently ongoing
Characterising the patient population by determination of intra-tumoural expression of ErbB1 (EGFR) and ErbB2 (Her2/neu).Seeking pilot information as to the intra-tumoural expression of markers of tumour resistance and sensitivity to treatment. Proteomic analysis of serum samples for potential markers.
Currently ongoing

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 수석 연구원: Ray McDermott, MD, Adelaide and Meath Hospital, Dublin Incorporating the National Children's Hospital

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작

2009년 1월 1일

기본 완료 (실제)

2010년 12월 1일

연구 등록 날짜

최초 제출

2009년 8월 19일

QC 기준을 충족하는 최초 제출

2009년 8월 19일

처음 게시됨 (추정)

2009년 8월 20일

연구 기록 업데이트

마지막 업데이트 게시됨 (추정)

2014년 12월 31일

QC 기준을 충족하는 마지막 업데이트 제출

2014년 12월 30일

마지막으로 확인됨

2012년 10월 1일

추가 정보

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

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