Trial record 5 of 27 for:    "chordoma"

Nilotinib With Radiation for High Risk Chordoma

This study is currently recruiting participants. (see Contacts and Locations)
Verified March 2014 by Massachusetts General Hospital
Sponsor:
Information provided by (Responsible Party):
Edwin Choy, MD, Massachusetts General Hospital
ClinicalTrials.gov Identifier:
NCT01407198
First received: July 28, 2011
Last updated: March 26, 2014
Last verified: March 2014
  Purpose

The study drug, Nilotinib, is believed to slow down tumor growth by regulating a gene involved in cellular growth of chordoma cells. During this research study, subjects will also receive radiation therapy which is considered a standard treatment for advanced chordomas. It is hoped by adding nilotinib, the benefits of radiation therapy can be enhanced without adding significant toxicities.

The purpose of this research study is to determine the safety of nilotinib when used in combination with radiation therapy, and the highest dose of nilotinib that can be given safely with radiation therapy.


Condition Intervention Phase
Chordoma
Drug: Nilotinib
Radiation: Radiation therapy
Phase 1

Study Type: Interventional
Study Design: Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Phase I Study of Nilotinib Given With Radiation For Patients With High Risk Chordoma

Resource links provided by NLM:


Further study details as provided by Massachusetts General Hospital:

Primary Outcome Measures:
  • To determine the dose limiting toxicities (DLTs) for participants when treated above the maximum tolerated dose (MTD). [ Time Frame: 2 years ] [ Designated as safety issue: Yes ]

    A DLT will be defined as any of the following events occurring during days 1-56 of study according to CTCAE version 4.0. MTD is then determined by identifying a dose cohort demonstrating > or = 30% rate of DLTs, which are defined as:

    • Any Grade ≥ 3 nonhematologic toxicity except alopecia, nausea, or vomiting not otherwise controlled by maximual supportive care.
    • Grade 4 neutropenia (ANC < 500/µL) lasting > 5 days, Grade 3 thrombocytopenia lasting > 7 days, or Grade 4 thrombocytopenia
    • Failure to resume treatment delays within a defined period of time.


Secondary Outcome Measures:
  • Number of Participants with Adverse Events [ Time Frame: 2 years ] [ Designated as safety issue: Yes ]

    Adverse event profile, as determined by CTC AE version 4.0, will be determined for patients treated with nilotinib and radiation therapy.

    Adverse events analyses will include:

    • Detailed examination of adverse events
    • Laboratory test results
    • Vital signs or other physical findings
    • Frequency and extent of dose modification

    The assessment of adverse events will be based mainly on the frequency of adverse events, particularly adverse events leading to discontinuation of treatment and on the number of significant laboratory abnormalities.


  • Survival [ Time Frame: 2 years ] [ Designated as safety issue: No ]
    To obtain preliminary data regarding local control, distant control, disease-free survival, and overall survival with this regimen

  • PDGFR signaling [ Time Frame: 2 years ] [ Designated as safety issue: No ]
    To determine if nilotinib decreases PDGFR signaling in chordoma tumor samples in treated patients


Estimated Enrollment: 29
Study Start Date: August 2011
Estimated Study Completion Date: August 2016
Estimated Primary Completion Date: August 2015 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Nilotinib/XRT
Nilotinib is administered 400mg PO BID for 2 weeks and then administered concurrently with daily XRT until completion of XRT. Participants can then undergo surgery if clinically possible. After either surgery or definitive radiation, participants have the option to continue on nilotinib therapy.
Drug: Nilotinib
Orally, daily 200 - 400 mg BID
Other Names:
  • AMN 107
  • Tasigna
Radiation: Radiation therapy
External beam radiation will be delivered at 1.8 Gy per day, 5 days per week (excluding holidays)for a total of 28 fractions over a 6 weeks period.
Other Name: External beam radiation

Detailed Description:

Nilotinib will be taken orally daily in two cycles of 28 days each. Two weeks after taking nilotinib, subjects will begin radiation therapy. Radiation therapy will continue every weekday until Day 56 of the study. If it is determined that the subject's tumor cannot be removed by surgery, an additional 3 weeks of radiation therapy will be applied after Day 56 of the study.

During study visits subjects will have physical exams, routine blood tests, urine and blood clotting tests, and EKGs. Subjects will also have tumor assessment by chest CT and MRI or CT of the tumor at screening, on approximately Day 56 of the study, then every 6 months for one year and then annually thereafter if ther is no disease progression.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Histologically confirmed chordoma
  • Considered to have high risk disease
  • Measurable disease
  • Life expectancy > 3 months
  • Adequate organ function
  • Able to swallow oral capsules

Exclusion Criteria:

  • Previous treatment with any other tyrosine kinase inhibitor
  • Previous treatment with radiotherapy to the primary or recurrent chordomas
  • Impaired cardiac function
  • Currently receiving treatment with strong CYP3A4 inhibitors
  • Requires anticoagulation with coumadin
  • Impaired GI function or GI disease that may significantly alter the absorption of study drug
  • Acute or chronic pancreatic disease
  • Known cytopathologically confirmed CNS infiltration
  • Another primary malignant disease which requires systemic treatment
  • Acute or chronic liver disease or severe renal disease considered unrelated to the cancer
  • History of significant congenital or acquired bleeding disorder unrelated to cancer
  • Major surgery within 4 weeks prior to Day 1 of the study or who have not recovered from prior surgery
  • Treatment with other investigational agents within 30 days of Day 1
  • History of non-compliance to medical regimens
  • Pregnant or breast-feeding
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01407198

Contacts
Contact: Edwin Choy, MD, PhD 617-643-0230 echoy@partners.org

Locations
United States, Massachusetts
Massachusetts General Hospital Recruiting
Boston, Massachusetts, United States, 02114
Contact: Barbara Anderson, RN    617-724-4000    BANDERSON15@PARTNERS.ORG   
Contact: Natasha McDowall    617-724-4000    nmcdowall@partners.org   
Principal Investigator: Edwin Choy, MD, PhD         
Sponsors and Collaborators
Massachusetts General Hospital
Investigators
Principal Investigator: Edwin Choy, MD, PhD Massachusetts General Hospital
  More Information

No publications provided

Responsible Party: Edwin Choy, MD, Instructor, Massachusetts General Hospital
ClinicalTrials.gov Identifier: NCT01407198     History of Changes
Other Study ID Numbers: 11-072
Study First Received: July 28, 2011
Last Updated: March 26, 2014
Health Authority: United States: Food and Drug Administration

Keywords provided by Massachusetts General Hospital:
High Risk Chordoma

Additional relevant MeSH terms:
Chordoma
Neoplasms, Germ Cell and Embryonal
Neoplasms by Histologic Type
Neoplasms

ClinicalTrials.gov processed this record on July 20, 2014