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Phase I/II Trial of Sorafenib Plus Ixabepilone in HER2-Negative Metastatic Breast Cancer

2014年12月16日 更新者:SCRI Development Innovations, LLC

Phase I/II Trial of Sorafenib Plus Ixabepilone in HER2-Negative Metastatic Breast Cancer (MBC)

In this study, patients with metastatic HER2-negative breast cancer will receive treatment with ixabepilone and sorafenib until disease progression or unacceptable toxicity occurs. The Phase I portion of this study will determine the maximum tolerated doses (MTDs) of sorafenib and ixabepilone that may be used in combination for first- or second-line treatment of MBC. The MTDs identified in the Phase I portion of the study will be used in the Phase II portion which will evaluate the efficacy and safety of the combination of sorafenib and ixabepilone in patients who have received at least one prior chemotherapy treatment in either the adjuvant or neoadjuvant setting or following one prior MBC chemotherapy in MBC patients who had not received prior adjuvant or neoadjuvant breast cancer chemotherapy. This will be one of the initial trials investigating the use of this treatment combination for MBC.

This trial will be conducted under the leadership of the Sarah Cannon Research Institute (SCRI) Oncology Research Consortium, a community-based, multi-center, clinical trial organization.

研究概览

研究类型

介入性

注册 (实际的)

83

阶段

  • 阶段2
  • 阶段1

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

    • Florida
      • Ft. Myers、Florida、美国、33916
        • Florida Cancer Specialists
    • Indiana
      • Terre Haute、Indiana、美国、47802
        • Providence Medical Group
      • Terre Haute、Indiana、美国、47802
        • RHHP/ Hope Cancer Center
    • Kentucky
      • Louisville、Kentucky、美国、40207
        • Baptist Hospital East
    • Louisiana
      • Baton Rouge、Louisiana、美国、70806
        • Hematology Oncology Clinic, LLP
    • Maine
      • Portland、Maine、美国、04101
        • Mercy Hospital
    • Maryland
      • Bethesda、Maryland、美国、20817
        • Center for Cancer and Blood Disorders
      • Bethesda、Maryland、美国、20817
        • National Capital Clinical Research Consortium
    • Missouri
      • Chesterfield、Missouri、美国、63044
        • St. Louis Cancer Care
    • New Hampshire
      • Portsmouth、New Hampshire、美国、03801
        • Portsmouth Regional Hospital
    • New Jersey
      • Morristown、New Jersey、美国、07962
        • Hematology-Oncology Associates of Northern NJ
    • Ohio
      • Cincinnati、Ohio、美国、45242
        • Oncology Hematology Care
    • South Carolina
      • Columbia、South Carolina、美国、29210
        • South Carolina Oncology Associates
      • Spartanburg、South Carolina、美国
        • Spartanburg Regional Medical Center
    • Tennessee
      • Nashville、Tennessee、美国、37023
        • Tennessee Oncology, PLLC

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

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  1. Age ≥ 18 years.
  2. Histologically or cytologically confirmed breast cancer diagnosis

with metastatic disease. Patients without pathologic or cytologic

confirmation of metastatic disease should have unequivocal

evidence of metastasis.

3. Measurable disease, as per RECIST criteria (Therasse et al.

2000). Measurable disease cannot be previously irradiated

unless progression was documented. Measurable disease is

defined as: at least one lesion that can be accurately measured in

at least one dimension [longest diameter to be recorded] as

>20 mm with conventional techniques, or as >10 mm with spiral

computed tomography (CT) scan. Disease must be measurable,

i.e., bone-only disease or evaluable-only disease is not eligible.

4. Patients with brain metastasis may participate if they:

• have undergone appropriate treatment,

  • are at least 1 month post-treatment,
  • have no neurologic symptoms,
  • are not on steroids,
  • have a follow-up magnetic resonance imaging (MRI) scan that

demonstrates no residual active lesions, and

  • have no new untreated lesions.

    5 The following prior therapies are allowed:

  • No prior chemotherapy in the metastatic setting. However,

patients must have received prior adjuvant or neo-adjuvant

chemotherapy.

  • Prior radiation therapy in either the metastatic or early-stage

setting, as long as <25% of the bone marrow has been

treated. Radiation therapy must be completed at least

14 days prior to study registration, and all radiation-related

toxicities must be resolved to ≤ grade 1 before the patient is

eligible for study inclusion.

  • Any number of hormonal therapies in the neo-adjuvant,

adjuvant, or metastatic setting is allowed. Patients must

discontinue hormonal therapy at least 1 week prior to starting

study treatment.

•Prior bevacizumab administered >4 weeks before initiation of

study treatment is allowed.

6 HER2-negative status. Documentation of HER2 results must be

available at the time of study enrollment. HER2-negative is

defined as:

  • Immunohistochemical (IHC) 0 or IHC 1+ OR
  • Fluorescence in situ hybridization (FISH) negative (defined by

FISH ratio <2.2) OR

  • Silver in-situ hybridization (SISH) negative (defined by SISH

ratio <2.2).

Patients with an IHC 2+ will need to be validated as HER2-negative

by FISH.

7 An Eastern Cooperative Oncology Group (ECOG) performance

status of < or = to 2.

8. Normal bone marrow function as defined by:

  • absolute neutrophil count (ANC) >1,500/μL;
  • platelets >100,000/μL;
  • hemoglobin >9 g/dL.

    9 Normal hepatic function as defined by:

  • total bilirubin within normal institutional limits;
  • aspartate aminotransferase (AST) and alanine

aminotransferase (ALT) <2.5 × the institutional upper limit of

normal (ULN) for patients without liver metastasis; <5.0 × ULN

for patients with liver metastasis.

10. Normal renal function as defined by creatinine <1.5 × ULN.

11. Left ventricular ejection fraction (LVEF) within institutional limits of

normal.

12. International normalized ratio (INR) <1.5 or a prothrombin

time/partial thromboplastin time (PT/PTT) within normal limits.

Patients receiving anti-coagulation treatment with an agent such

as warfarin or heparin may be allowed to participate. The INR

should be measured prior to initiation of sorafenib, and for

patients on warfarin, INR should be monitored at least weekly

following initiation of protocol treatment, until the INR is stable and

therapeutic.

13. Life expectancy of >6 months.

14. For women of childbearing potential, negative serum pregnancy

test within 7 days prior to starting treatment.

15. For women of childbearing potential and men, agreement to use a

method of contraception that is acceptable to their physician from

time of first signing the informed consent and for the study

duration. Men should use adequate birth control for at least three

months after the last administration of sorafenib. If a woman

becomes pregnant or suspects she is pregnant while participating

in this study, she must agree to inform her treating physician

immediately. As applicable, patients must agree to discontinue

breast-feeding until at least 3 weeks after their last dose of study

drug.

16. Recovery to < grade 1 toxicity due to prior therapy.

17. Ability to understand and willingness to sign a written informed

consent document.

Exclusion Criteria

  1. More than one (>1) prior chemotherapy regimen.
  2. Treatment with chemotherapy, biologic agents, or targeted agents

    within the previous 4 weeks.

  3. Previous treatment with sorafenib or ixabepilone.
  4. Women who are pregnant or breastfeeding.
  5. Neuropathy (motor or sensory) greater than grade 1.
  6. Uncontrolled intercurrent illness including (but not limited to)

    ongoing or active infection >grade 2.

  7. Known history of human immunodeficiency virus (HIV), Hepatitis

    B, or Hepatitis C infection.

  8. History of other non-breast cancer malignancy treated with

    curative intent within the 5 years preceding study enrollment with

    the exception of carcinoma in situ of the cervix, non-melanoma

    skin cancer, or follicular thyroid cancer.

  9. Concurrent hormonal therapy, chemotherapy other than

    ixabepilone, or radiation treatments while on study as well as

    treatment with other investigational agents while on study.

  10. Cardiac disease:

    •Congestive heart failure (CHF) greater than New York Heart Association

    (NYHA) Class II (see Appendix B).

    • Unstable angina (anginal symptoms at rest) or new onset angina

      (i.e., began within the last 3 months).

    • Myocardial infarction within the past 6 months.
    • Cardiac ventricular arrhythmias requiring anti-arrhythmic therapy.
  11. Uncontrolled hypertension (systolic blood pressure >150 mmHg

    or diastolic pressure >100 mmHg despite optimal medical

    management).

  12. Thrombolic or embolic events such as cerebrovascular accident,

    including transient ischemic attacks, within the past 6 months.

  13. Pulmonary hemorrhage or bleeding event ≥ grade 2 within

4 weeks of the first dose of study treatment, or any other

hemorrhage or bleeding event ≥ grade 3 within 4 weeks of the

first dose of study treatment.

14. Serious non-healing wound, ulcer, or bone fracture.

15. Evidence or history of bleeding diathesis or coagulopathy.

16. Major surgery, open biopsy or significant traumatic injury within

4 weeks of the first dose of study drugs or anticipation of the need

for major surgical procedure.

17. Chronic use of CYP3A4 inducers and use of the following strong

CYP3A4 inhibitors: ketoconazole, itraconazole, clarithromycin,

atazanavir, nefazodone, saquinavir, telithromycin, ritonavir,

amprenavir, indinavir, nelfinavir, delavirdine, and voriconazole.

Use of these agents should be discontinued at least 72 hours

prior to initiation of study treatment.

18. Use of St. John's Wort or rifampin (rifampicin).

19. Any condition that impairs patient's ability to swallow whole pills or

gastrointestinal (GI) tract disease that involves an inability to take

oral medication, malabsorption syndrome, a requirement for

intravenous (IV) alimentation, prior surgical procedures affecting

absorption, or uncontrolled inflammatory GI disease (e.g., Crohn's

disease or ulcerative colitis).

20. Psychiatric illness/social situations that would limit compliance

with study requirements.

21. Known or suspected allergy to sorafenib, Cremophor EL

(polyoxyethylated castor oil) or a drug formulated in

Cremophor EL such as paclitaxel or any other agent given in the

course of this trial.

Exclusion Criteria:

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:非随机化
  • 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:Dose Level 1
Sorafenib PO BID (200mg), Ixabepilone IV every 21 days (40mg/m^2)
Dose Level 1 - Sorafenib PO BID (200mg) Dose Level -1 - Sorafenib PO BID (200mg) Dose Level 1a - Sorafenib PO BID (400mg)
其他名称:
  • Nexavar (Sorafenib)
Dose Level 1 - Ixabepilone IV every 21 days (40mg/m^2) Dose Level -1 - Ixabepilone IV every 21 days (32mg/m^2) Dose Level 1a - Ixabepilone IV every 21 days (32mg/m^2)
其他名称:
  • Ixempra (Ixabepilone)
实验性的:Dose Level -1
Sorafenib PO BID (200mg), Ixabepilone IV every 21 days (32mg/m^2)
Dose Level 1 - Sorafenib PO BID (200mg) Dose Level -1 - Sorafenib PO BID (200mg) Dose Level 1a - Sorafenib PO BID (400mg)
其他名称:
  • Nexavar (Sorafenib)
Dose Level 1 - Ixabepilone IV every 21 days (40mg/m^2) Dose Level -1 - Ixabepilone IV every 21 days (32mg/m^2) Dose Level 1a - Ixabepilone IV every 21 days (32mg/m^2)
其他名称:
  • Ixempra (Ixabepilone)
实验性的:Dose Level 1a
Sorafenib PO BID (400mg), Ixabepilone IV every 21 days (32mg/m^2)
Dose Level 1 - Sorafenib PO BID (200mg) Dose Level -1 - Sorafenib PO BID (200mg) Dose Level 1a - Sorafenib PO BID (400mg)
其他名称:
  • Nexavar (Sorafenib)
Dose Level 1 - Ixabepilone IV every 21 days (40mg/m^2) Dose Level -1 - Ixabepilone IV every 21 days (32mg/m^2) Dose Level 1a - Ixabepilone IV every 21 days (32mg/m^2)
其他名称:
  • Ixempra (Ixabepilone)

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
Progression-Free Survival (PFS)
大体时间:every 9 weeks until treatment discontinuation or death on study
Measured from Day 1 of study drug administration to disease progression as defined by Response Evaluation Criteria in Solid Tumors (RECIST) - progression is defined as a 20% increase in the sum of the longest diameter of target lesions, or a measurable increase in a non-target lesion, or the appearance of new lesions
every 9 weeks until treatment discontinuation or death on study

次要结果测量

结果测量
措施说明
大体时间
6-month Progression-Free Survival
大体时间:every 9 weeks, up to 6 months
Measured from Day 1 of study drug administration to disease progression as defined by RECIST v1.1, or death on study. Progression is defined as a 20% increase in the sum of the longest diameter of target lesions, or a measurable increase in a non-target lesion, or the appearance of new lesions
every 9 weeks, up to 6 months
Objective Response Rate
大体时间:every 9 weeks until discontinuation of treatment
Objective Response will be evaluated in this study using the Response Evaluation Criteria in Solid Tumors (RECIST).
every 9 weeks until discontinuation of treatment
Overall Survival (OS)
大体时间:every 9 weeks until treatment discontinuation or death on study
Measured from Day 1 of study drug administration to date of death due to any cause.
every 9 weeks until treatment discontinuation or death on study
Number of Patients With Adverse Events as a Measure of of Safety and Tolerability
大体时间:every 9 weeks until treatment discontinuation or unacceptable toxicity
Assessments are made through analysis of reported incidence of treatment-emergent AEs and SAEs.
every 9 weeks until treatment discontinuation or unacceptable toxicity

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。

调查人员

  • 学习椅:Denise A. Yardley, M.D.、SCRI Development Innovations, LLC

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

2009年3月1日

初级完成 (实际的)

2013年6月1日

研究完成 (实际的)

2014年8月1日

研究注册日期

首次提交

2009年1月19日

首先提交符合 QC 标准的

2009年1月19日

首次发布 (估计)

2009年1月21日

研究记录更新

最后更新发布 (估计)

2014年12月22日

上次提交的符合 QC 标准的更新

2014年12月16日

最后验证

2014年12月1日

更多信息

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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