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

16 december 2014 uppdaterad av: 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.

Studieöversikt

Status

Avslutad

Studietyp

Interventionell

Inskrivning (Faktisk)

83

Fas

  • Fas 2
  • Fas 1

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

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

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

18 år och äldre (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Allt

Beskrivning

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:

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Behandling
  • Tilldelning: Icke-randomiserad
  • Interventionsmodell: Enskild gruppuppgift
  • Maskning: Ingen (Open Label)

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: 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)
Andra namn:
  • 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)
Andra namn:
  • Ixempra (Ixabepilone)
Experimentell: 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)
Andra namn:
  • 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)
Andra namn:
  • Ixempra (Ixabepilone)
Experimentell: 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)
Andra namn:
  • 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)
Andra namn:
  • Ixempra (Ixabepilone)

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Progression-Free Survival (PFS)
Tidsram: 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

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
6-month Progression-Free Survival
Tidsram: 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
Tidsram: 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)
Tidsram: 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
Tidsram: 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

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Samarbetspartners

Utredare

  • Studiestol: Denise A. Yardley, M.D., SCRI Development Innovations, LLC

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart

1 mars 2009

Primärt slutförande (Faktisk)

1 juni 2013

Avslutad studie (Faktisk)

1 augusti 2014

Studieregistreringsdatum

Först inskickad

19 januari 2009

Först inskickad som uppfyllde QC-kriterierna

19 januari 2009

Första postat (Uppskatta)

21 januari 2009

Uppdateringar av studier

Senaste uppdatering publicerad (Uppskatta)

22 december 2014

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

16 december 2014

Senast verifierad

1 december 2014

Mer information

Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .

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