Evaluation of the efficacy of nilotinib in the treatment of patients with pigmented villo-nodular synovitis / tenosynovial giant cell tumour

Phase 2

• Conditions: Pigmented villo-nodular synovitis; Tenosynovial giant cell tumour; Cancer - Sarcoma (also see 'Bone') - soft tissue

• Registration Number: ACTRN12612000019808
• Lead Sponsor: Centre Leon Berard

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2012-01-05
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

1. Age >= 18 years
2. Histologically confirmed diagnosis of inoperable progressive or relapsing PVNS/TGCT
OR resectable tumour requesting mutilating surgery
3. Demonstrated progressive disease in the last 12 months
4. At least one measurable site of disease on MRI/CT scan according to RECIST criteria (RECIST version 1.1) based on investigator’s assessment
5. WHO Performance status of 0, 1 or 2
6. Adequate organ, electrolyte and marrow function, defined as the following: serum bilirubin <=1.5 x ULN; ALT and AST <=2.5 x ULN; serum creatinine <=1.5 x ULN or creatinine clearance >=50 mL/min; absolute neutrophil count (ANC) >=1.5x10^9/L; platelets >=100x10^9/L; serum lipase <=1.5 x ULN; magnesium = lower limit of normal (LLN) and potassium = LLN
7. Prior adequate physical examination including weight, height, ECOG PS and vital signs (systolic and
diastolic blood pressure, heart rate after at least 5 minutes in supine position)
8. Signed written informed consent form

Exclusion Criteria

1. Pregnant or lactating female or female of child-bearing potential not employing adequate contraception during the study and for up to three months following termination of the study
2. Known hypersensitivity to nilotinib or to any of the excipients, galactose intolerance, lactase deficiency or glucose-galactose malabsorbtion prior to enrolment
3. Acute or chronic uncontrolled liver disease, or severe renal disease
4. Impaired cardiac function, including:
- LVEF<50% or below the institutional lower limit of the normal range (whichever is higher) as determined by echocardiogram or MUGA scan
- History or signs of prior myocardial infarction
- History of unstable angina
- Congenital long QT prolongation
- Personal history of unexplained syncope
- QTc interval >= 450 msec on screening ECG
- Other clinically significant heart disease (e.g. bradycardia, congestive heart failure or uncontrolled hypertension)
5. Patient with family history of long QT syndrome, of unexplained syncope or of unexplained sudden
death
6. Patients with severe and/or uncontrolled concurrent medical disease that in the opinion of the investigator could cause unacceptable safety risks or compromise compliance with the protocol e.g. uncontrolled diabetes, active or uncontrolled infection, history of pancreatitis
7. History of non-compliance to medical regimens
8. Concomitant treatment with medicinal products that induce CYP3A4 (e.g. dexamethasone, phenytoin, carbamazepine, rifampicin, phenobarbital or St. John’s Wort), or that inhibit the CYP3A4 activity (e.g. ketoconazole, itraconazole, voriconazole, erythromycin, clarithromycin, telithromycin)
9. Concomitant treatment with warfarin
10. Concomitant treatment with anti-arrhythmic drug (e. g. amiodarone, sotalol, disopyramide, quinidine, procainamide) or medication that prolongs the QT interval (e.g. chloroquine, chlorpromazine, domperidone, droperidol, halofantrine, haloperidol, methadone, pentamidine, pimozide, thioridazine)
11. Prior treatment with imatinib except if no progression was demonstrated

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The non-progression rate after 12 weeks (3 months) of<br>treatment, based on the response evaluated by CT scan or MRI according to RECIST criteria (RECIST<br>version 1.1) and validated by a central review committee[12 weeks]