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Nilotinib in Patients With Relapsed or Metastatic Pigmented Villonodular Synovitis/Tenosynovial Giant Cell Tumor/Diffuse-Type Giant Cell Tumor

This study is currently recruiting participants. (see Contacts and Locations)
Verified October 2014 by Dana-Farber Cancer Institute
Sponsor:
Collaborators:
Brigham and Women's Hospital
Massachusetts General Hospital
Novartis
Information provided by (Responsible Party):
Andrew J. Wagner, MD, PhD, Dana-Farber Cancer Institute
ClinicalTrials.gov Identifier:
NCT01207492
First received: September 21, 2010
Last updated: October 6, 2014
Last verified: October 2014

September 21, 2010
October 6, 2014
September 2010
December 2014   (final data collection date for primary outcome measure)
Progression free survival [ Time Frame: 2 years ] [ Designated as safety issue: No ]
To estimate progression free survival at 6 months in participants with recurrent PVNS treated with nilotinib.
Same as current
Complete list of historical versions of study NCT01207492 on ClinicalTrials.gov Archive Site
  • Overall tumor response rate [ Time Frame: 2 years ] [ Designated as safety issue: No ]
    To determine overall tumor response rate [% complete response + % partial response by RECIST 1.1]
  • Clinical Benefit Rate [ Time Frame: 2 years ] [ Designated as safety issue: No ]
    To determine the clinical benefit rate [% CR + % PR + % stable disease by RECIST 1.1] at 6 months
Same as current
Not Provided
Not Provided
 
Nilotinib in Patients With Relapsed or Metastatic Pigmented Villonodular Synovitis/Tenosynovial Giant Cell Tumor/Diffuse-Type Giant Cell Tumor
A Multi-Center Single Agent Phase II Study of the Efficacy of Nilotinib in Patients With Relapsed or Metastatic Pigmented Villonodular Synovitis/Tenosynovial Giant Cell Tumor/Diffuse-Type Giant Cell Tumor

Nilotinib is a drug that is used to treat a form of a blood cancer called leukemia. Nilotinib works by blocking the action of a protein that might be important for the growth of pigmented villonodular synovitis (PVNS). In this research study the investigators are testing whether nilotinib can stop the growth of PVNS or improve the symptoms experienced from PVNS.

  • In this research study, each cycle of study drug dosing will last 4 weeks (28 days). During each cycle, participants will take nilotinib by mouth twice daily. During the first cycle, participants will come to the clinic on Days 1 and 8. For Cycles 2-4 and every 3 cycles thereafter, they will come to the clinic on Day 1.
  • The following tests and procedures will be performed at specific time points during study treatment: MRI or CT scans; physical examinations; vital signs; blood work; questionnaires and EKG.
  • Participants may continue in this research study for as long as they do not have serious side effects or their disease does not get worse.
Interventional
Phase 2
Allocation: Non-Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
  • Pigmented Villonodular Synovitis
  • Diffuse-type Giant Cell Tumor
  • Tenosynovial Giant Cell Tumor
Drug: nilotinib
Taken orally twice daily
Experimental: Nilotinib
Nilotinib 200 mg taken as 400 mg twice daily, continuously
Intervention: Drug: nilotinib
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
25
Not Provided
December 2014   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Histologically confirmed diagnosis of recurrent PVNS ( or diffuse-type giant cell tumor or tenosynovial giant cell tumor) that is unresectable, metastatic, or for which the patient refuses surgical intervention
  • Progressive disease in the last 12 months, as demonstrated by imaging or clinical appearance of new tumors, in the opinion of the treating investigator
  • At least one site of measurable disease according to RECIST 1.1 on MRI (or CT scan for metastatic disease)
  • Any number or type of prior systemic therapies, with the exception of known or suspected CSF1 receptor inhibitors as outlined in exclusion criteria below
  • 18 years of age or older
  • Life expectancy greater than 6 months
  • ECOG Performance Status of 0, 1 or 2
  • Normal organ and marrow function as defined in the protocol
  • QTc less than or equal to 450 ms on 12-lead ECG
  • Negative urine or serum pregnancy test within days of start of study drug administration for women of childbearing potential.
  • Women of childbearing potential and men must agree to use adequate contraception prior to study entry, for the duration of study participation, and for 3 months following study drug discontinuation

Exclusion Criteria:

  • Prior treatment with known or suspected CSF1 receptor inhibitor, including nilotinib, imatinib, sunitinib, or sorafenib, or other approved or investigational tyrosine kinase inhibitors used for treatment of diffuse-type giant cell tumor
  • Concurrent treatment with other investigational agents
  • Inability to tolerate or contraindication to MRI scanning for participants with localized disease
  • Impaired cardiac function
  • Current treatment with strong CYP3A4 inhibitors that cannot either be discontinued or switched to a different medication prior to starting study drug
  • Current treatment with any medications that have the potential to prolong the QT interval and that cannot either be discontinued or switched to a different medication prior to starting study drug
  • Impaired gastrointestinal (GI) function or GI disease that may significantly alter the absorption of study drug
  • Acute or chronic pancreatic disease
  • Acute or chronic liver disease
  • Another primary malignant disease requiring systemic treatment or radiation
  • History of significant congenital or acquired bleeding disorder unrelated to cancer
  • Major surgery within 28 days prior to Day 1 of the study
  • Treatment with other investigational agents within 28 days of day 1
  • History of non-compliance to medical regimens or inability to grant consent
  • Women who are pregnant or breastfeeding
  • Other comorbidities that would interfere with study participation or safety in the opinion of the investigator
Both
18 Years and older
No
Contact: Andrew J. Wagner, MD, PhD 617-632-5204 anderw_wagner@dfci.harvard.edu
United States
 
NCT01207492
10-179, YUS23T
Yes
Andrew J. Wagner, MD, PhD, Dana-Farber Cancer Institute
Andrew J. Wagner, MD, PhD
  • Brigham and Women's Hospital
  • Massachusetts General Hospital
  • Novartis
Principal Investigator: Andrew J. Wagner, MD, PhD Dana-Farber Cancer Institute
Dana-Farber Cancer Institute
October 2014

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP