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Study of Cisplatin and Pemetrexed in Combination With Panobinostat in Solid Tumors

2018년 1월 5일 업데이트: University of California, Davis

Phase I Trial of Cisplatin and Pemetrexed in Combination With Panobinostat in Advanced Solid Tumors, With Emphasis on Non-Small Cell Lung Cancer

The purpose of this study is to find out if panobinostat taken with cisplatin and pemetrexed can be used safely without increasing side effects and that the combination will have a better effect than platinum-based doublet chemotherapy alone.

연구 개요

상세 설명

The purpose of this phase I study of oral panobinostat plus cisplatin and pemetrexed is to determine the maximum tolerated dose (MTD) and dose limiting toxicities (DLTs) in patients with advanced solid tumors, with an emphasis in non-small cell lung cancer. Another purpose of this study is to find out if oral panobinostat in combination with cisplatin and pemetrexed can be administered safely without significant increase in toxicity and that the combination will increase efficacy compared to platinum-based doublet chemotherapy alone.

연구 유형

중재적

등록 (실제)

23

단계

  • 1단계

연락처 및 위치

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

연구 장소

    • California
      • Sacramento, California, 미국, 95817
        • University of California Davis Cancer Center
    • Michigan
      • Detroit, Michigan, 미국, 48202
        • Henry Ford Health System

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

Inclusion Criteria:

  • Histological or cytological proven advanced solid tumors for which curative standard treatments are not available.
  • Must have measurable or evaluable disease.
  • Male or female patients aged ≥ 18 years old.
  • Any number of prior chemotherapy regimens.
  • ECOG Performance Status of ≤ 2 with a life expectancy greater than 3 months.
  • Clinically euthyroid (may be on thyroid hormone replacement)
  • Women of childbearing potential (WOCBP) must have a negative serum pregnancy test within 7 days of the first administration of study treatment.
  • Ability to provide written informed consent
  • Must meet the following laboratory criteria:

Hematology:

  • Neutrophil count of ≥ 1.5 x 109/L
  • Platelet count of ≥ 100 x 109/L
  • Hemoglobin ≥ 9 g/dL

Biochemistry:

  • AST/SGOT and ALT/SGPT ≤ 2.5 x upper limit of normal (ULN) or ≤ 5.0 x ULN if the transaminase elevation is due to disease involvement
  • Serum bilirubin ≤ 1.5 x ULN
  • Serum creatinine ≤ 1.5 x ULN or 24-hour creatinine clearance ≥ 50 ml/min
  • Total serum calcium (corrected for serum albumin) or ionized calcium ≥ LLN and ≤ ULN
  • Serum potassium ≥ LLN and ≤ ULN
  • Serum sodium ≥ LLN and ≤ ULN
  • Serum albumin ≥ LLN or 3g/dl
  • Serum magnesium ≥ LLN and ≤ ULN
  • Any elevated Alkaline Phosphatase due to bone metastasis can be enrolled

Exclusion Criteria:

  • Prior HDAC, DAC, HSP90 inhibitors or valproic acid for the treatment of cancer.
  • Patients who will need valproic acid for any medical condition during the study or within 5 days prior to first panobinostat treatment.
  • Patients who have received chemotherapy, any investigational drug or undergone major surgery < 4 weeks prior to starting study drug or who have not recovered from side effects of such therapy.
  • Impaired cardiac function
  • Other concurrent severe and/or uncontrolled medical conditions that could cause unacceptable safety risks or compromise compliance with the protocol
  • Concomitant use of drugs which are generally recognized to have a risk of causing torsades de pointes where such treatment cannot be discontinued or switched to a different medication prior to starting study drug
  • Patients with unresolved diarrhea ≥ CTCAE grade 2
  • Impairment of gastrointestinal (GI) function or GI disease that may significantly alter the absorption of oral panobinostat. Inability to swallow panobinostat capsules whole.
  • Concomitant use of any anti-cancer therapy or radiation therapy
  • Uncontrolled or symptomatic brain metastases.
  • Women who are pregnant or breast feeding or women of childbearing potential (WOCBP) not willing to use a double barrier method of contraception during the study and 3 months after the end of treatment. One of these methods of contraception must be a barrier method. WOCBP are defined as sexually mature women who have not undergone a hysterectomy or who have not been naturally postmenopausal for at least 12 consecutive months (i.e., who has had menses any time in the preceding 12 consecutive months).
  • Male patients whose sexual partners are WOCBP not using a double method of contraception during the study and 3 months after the end of treatment.
  • Known positivity for human immunodeficiency virus (HIV) or hepatitis C; baseline testing for HIV and hepatitis C is not required
  • Any significant history of non-compliance to medical regimens or with inability to grant a reliable informed consent

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: Phase I dose-escalation
Drug: panobinostat Drug: cisplatin Drug: pemetrexed Other: Biomarker studies

Drug: Panobinostat Oral (by mouth) once daily every Monday, Wednesday, and Friday for the first two weeks of each three week cycle (as per dose escalation schedule (dose levels 1 and 2: AUC 5; dose levels 3 and 4: AUC 6). Number of cycles: 6 maximum.

Drug: Cisplatin IV (in the vein) on day 1 of a 21-day cycle Number of cycles: 6 maximum. Drug: Pemetrexed IV (in the vein) on day 1 of a 21-day cycle Other: Correlative studies Biomarker Analysis: blood collected pre-study and Cycles 2-6, Day 1.

다른 이름들:
  • 플라티놀
  • 알미타
  • LBH-589

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Safety and feasibility of oral panobinostat in combination with cisplatin and pemetrexed
기간: Within ±3 days of the scheduled day of assessment except for adverse events that will be evaluated continuously through the study. The expected time frame for this outcome measure is 18 weeks (or six cycles)
Safety assessments will consist of monitoring and recording all adverse events and serious adverse events, the regular monitoring of hematology, blood chemistry and urine values, regular measurement of vital signs and the performance of physical examination. Safety and tolerability will be assessed according to the NCI CTCAE v4.
Within ±3 days of the scheduled day of assessment except for adverse events that will be evaluated continuously through the study. The expected time frame for this outcome measure is 18 weeks (or six cycles)

2차 결과 측정

결과 측정
측정값 설명
기간
Maximum-tolerated dose as assessed by NCI CTCAE, Version 4.0
기간: 3 week cycle; the expected time frame is 18 weeks (or 6 cycles)
Determination of maximum tolerated dose (MTD) will be based on cycle 1 toxicities
3 week cycle; the expected time frame is 18 weeks (or 6 cycles)
Dose-limiting toxicities and toxicity profile as assessed by NCI CTCAE, Version 4.0
기간: 3 week cycle; the expected time frame is 18 weeks (or 6 cycles)
Dose-limiting toxicity (DLT) will be based on cycle 1 toxicities.
3 week cycle; the expected time frame is 18 weeks (or 6 cycles)
Exploratory biomarker analysis
기간: Blood specimens will be collected prior to treatment, prior to Cycles 2-6. In addition, a blood specimen will be collected if the patient is removed from the study due to progression of disease. the expected time frame is 18 weeks (or 6 cycles)
Molecular markers predictive for response to panobinostat remain unknown. This trial offers the opportunity to retrospectively study biomarkers and their association with clinical outcomes.
Blood specimens will be collected prior to treatment, prior to Cycles 2-6. In addition, a blood specimen will be collected if the patient is removed from the study due to progression of disease. the expected time frame is 18 weeks (or 6 cycles)
Efficacy of oral panobinostat in combination with cisplatin/pemetrexed in an expanded cohort of patients with NSCLC
기간: CT scans will be performed at baseline and every two cycles; the expected time frame is 18 weeks (or 6 cycles)
Response rate will be assessed by CT scan. CT scans will be performed at baseline and every two cycles. The evaluation of response will be based on standard RECIST criteria.
CT scans will be performed at baseline and every two cycles; the expected time frame is 18 weeks (or 6 cycles)

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 수석 연구원: David Gandara, MD, University of California, Davis

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

2011년 4월 1일

기본 완료 (실제)

2017년 1월 1일

연구 완료 (실제)

2017년 6월 1일

연구 등록 날짜

최초 제출

2011년 4월 11일

QC 기준을 충족하는 최초 제출

2011년 4월 14일

처음 게시됨 (추정)

2011년 4월 18일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2018년 1월 9일

QC 기준을 충족하는 마지막 업데이트 제출

2018년 1월 5일

마지막으로 확인됨

2018년 1월 1일

추가 정보

이 연구와 관련된 용어

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예

미국 FDA 규제 기기 제품 연구

아니

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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