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Pazopanib in Advanced Gastrointestinal Stromal Tumors Refractory to Imatinib and Sunitinib (PAGIST)

The recruitment status of this study is unknown because the information has not been verified recently.
Verified January 2012 by Scandinavian Sarcoma Group.
Recruitment status was  Recruiting
Sponsor:
Collaborator:
GlaxoSmithKline
Information provided by (Responsible Party):
Scandinavian Sarcoma Group
ClinicalTrials.gov Identifier:
NCT01524848
First received: January 24, 2012
Last updated: February 1, 2012
Last verified: January 2012
  Purpose

Patients with metastatic or locally advanced gastrointestinal stromal tumors (GIST) who develop resistance against the two hitherto approved drugs for this disease, the tyrosin kinase inhibitors (TKIs) imatinib and sunitinib, have a poor prognosis. Sometimes a further response may be achieved by other drugs, mainly other TKIs, which have been explored in different studies but not yet have been approved for clinical use. Pazopanib is a TKI inhibiting the tyrosin kinases KIT, PDGFRA, and VEGF 1-3, all of which have important roles in the pathogenesis of GIST. Theoretically, it may function in GIST, and it deserves investigational trials. The drug is approved for metastatic renal cancer and is relatively well tolerated. In this trial (SSG XXI), the disease control rate (DCR) = (CR+PR+SD) after 12 weeks of treatment will be assessed as the primary endpoint, and at the same time trough levels will be measured. Secondary endpoints include ORR, PFS, toxicity, and disease control rate in relation to trough level week 12 and in relation to the primary mutation of the tumor (if known). The goal is to include 72 patients in the trial, which is open and single arm.


Condition Intervention Phase
Gastrointestinal Stromal Tumors
Drug: Pazopanib
Phase 2

Study Type: Interventional
Study Design: Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Pazopanib in Advanced GISTs Refractory to Imatinib and Sunitinib - A Non-comparative Phase II Multicenter Study by the Scandinavian Sarcoma Group

Resource links provided by NLM:


Further study details as provided by Scandinavian Sarcoma Group:

Primary Outcome Measures:
  • Disease control rate [ Time Frame: Week 12 ] [ Designated as safety issue: No ]
    The ratio of patients with CR (complete remission) + PR (partial remission) + SD (stable disease) at week 12 after start of treatment


Secondary Outcome Measures:
  • Progression free survival (PFS) [ Time Frame: The patients will be followed for the duration of the trial treatment, an expected average of 6 months ] [ Designated as safety issue: No ]
    Progression free survival (KM analysis) for all patients administered the study drug

  • DCR in relation to mutation [ Time Frame: Week 12 ] [ Designated as safety issue: No ]
    Disease control rate as described above in relation to the type of mutation of the primary tumor if this is available (not mandatory)

  • DCR in relation to plasma concentration [ Time Frame: Week 12 ] [ Designated as safety issue: No ]
    Disease control rate as defined above in relation to the trough level (plasma concentration) of the study drug at week 12

  • Toxicity [ Time Frame: The patients will be followed for the duration of the trial treatment + 1 month, an expected average of 7 months ] [ Designated as safety issue: Yes ]
    Recording of adverse events including SAE/SAR for all patients administered the study drug

  • Overall response rate [ Time Frame: The patients will be followed for the duration of the trial treatment, an expected average of 6 months ] [ Designated as safety issue: No ]
    ORR = CR+PR at the time of best response during the study period


Estimated Enrollment: 72
Study Start Date: February 2012
Estimated Primary Completion Date: January 2014 (Final data collection date for primary outcome measure)
Intervention Details:
    Drug: Pazopanib
    Two (2) tablets of 400 mg given once daily continuously
    Other Name: Votrient
  Eligibility

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

Eligibility Criteria:

  • Metastatic and/or locally advanced GIST, with diagnosis based on histology with positive c-kit and/or DOG-1, or with a GIST-typical mutation in KIT or PDGFR
  • Measurable disease on CT (computed tomography) as defined by RECIST criteria; at least one measurable lesion not given radiotherapy
  • History of progressive disease on CT according to RECIST criteria after both imatinib and sunitinib treatment, and also after nilotinib if this drug has been given
  • No other TKIs given than imatinib, sunitinib and nilotinib
  • Age at least 18 years at the time of diagnosis of GIST
  • WHO performance status 0-2
  • Resolution of all toxic side effects from earlier TKI treatment and any other potential non-TKI treatment to grade 1 or below
  • Sufficient organ functions as defined in the protocol
  • Absence of earlier or present certain other conditions as defined in the protocol
  • No pregnancy or lactation
  • Women with childbearing potential must accept the use of adequate contraception throughout the study period
  • Written informed consent
  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: NCT01524848

Contacts
Contact: Mikael H Eriksson, MD, PhD +46 46 171000 ext 77507 mikael.eriksson@med.lu.se

Locations
Norway
Dept of Oncology, Haukeland University Hospital Recruiting
Bergen, Norway, N-5021
Contact: Dorota Goplen, MD    +47 55979696    dgop@helse-bergen.no   
Principal Investigator: Dorota Goplen, MD         
Norwegian Radium Hospital Recruiting
Oslo, Norway, N-0310
Contact: Kirsten Sundby Hall, MD    +47 22 934000    k.s.hall@klinmed.uio.no   
Principal Investigator: Kirsten Sundby Hall, MD         
Dept of Oncology, Tromsö University Hospital Recruiting
Tromsö, Norway, N-9038
Contact: Eivind Smeland, MD    +47 77626788    eivind.smeland@unn.no   
Principal Investigator: Eivind Smeland, MD         
Dept of Oncology, St Olav Hospital Recruiting
Trondheim, Norway, N-7006
Contact: Heidi Knobel, MD    +47 73867830    heidi.knobel@stolav.no   
Principal Investigator: Heidi Knobel, MD         
Sweden
Dept of Oncology, Sahlgrenska University Hospital Recruiting
Gothenburg, Sweden, SE-413 45
Contact: Katarina Engström, MD    046 31 3421000    katarina.engstrom@vgregion.se   
Principal Investigator: Katarina Engstrom, MD         
Dept of Oncology, Linköping University Hospital Recruiting
Linköping, Sweden, SE-581 85
Contact: Najme Wall, MD    +46 13 222000    najme.wall@lio.se   
Principal Investigator: Najme Wall, MD         
Dept of Oncology, Skane University Hospital Recruiting
Lund, Sweden, SE-221 85
Contact: Mikael Eriksson, MD, PhD    +46 46 177507    mikael.eriksson@med.lu.se   
Principal Investigator: Mikael H Eriksson, MD, PhD         
Sub-Investigator: Marie Ahlström, MD         
Radiumhemmet, Karolinska University Hospital Recruiting
Stockholm, Sweden, SE-171 76
Contact: Christina Linder Stragliotto, MD    +46 8 517 70000    christina.linder-stragliotto@karolinska.se   
Principal Investigator: Christina Linder-Stragliotto, MD         
Dept of Oncology, Norrland University Hospital Recruiting
Umeå, Sweden, SE-901 85
Contact: Karin Papworth, MD    +46 90 7851000    karin.papworth@vll.se   
Principal Investigator: Karin Papworth, MD         
Dept of Oncology, Academic Hospital Recruiting
Uppsala, Sweden, SE-751 85
Contact: Hans Hagberg, MD    +46 46 6110000    hans.hagberg@akademiska.se   
Principal Investigator: Hans Hagberg, MD         
Sponsors and Collaborators
Scandinavian Sarcoma Group
GlaxoSmithKline
  More Information

No publications provided

Responsible Party: Scandinavian Sarcoma Group
ClinicalTrials.gov Identifier: NCT01524848     History of Changes
Other Study ID Numbers: SSG XXI
Study First Received: January 24, 2012
Last Updated: February 1, 2012
Health Authority: Sweden: Medical Products Agency
Norway: Norwegian Medicines Agency
Denmark: Danish Medicines Agency
Finland: Finnish Medicines Agency
Iceland: Icelandic Medicines Control Agency

Keywords provided by Scandinavian Sarcoma Group:
Clinical trial
Investigational drugs
Gastrointestinal stromal tumors
Pazopanib

Additional relevant MeSH terms:
Gastrointestinal Stromal Tumors
Neoplasms, Connective Tissue
Neoplasms, Connective and Soft Tissue
Neoplasms by Histologic Type
Neoplasms
Gastrointestinal Neoplasms
Digestive System Neoplasms
Digestive System Diseases
Gastrointestinal Diseases

ClinicalTrials.gov processed this record on September 18, 2014