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Phase 2 N=148 Randomized Treatment

A Study of the Efficacy and Safety of Imatinib Mesylate in Patients With Unresectable or Metastatic Gastrointestinal Stromal Tumors Expressing C-kit Gene

Unresectable or Metastatic Malignant Gastrointestinal Stromal Tumor (GIST)

Enrolled (actual)
148
Serious AEs
58.5%
Results posted
Jul 2014
Primary outcome: Primary: Best Tumor Response (Core) — 0; 1; 49; 49 participants

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Imatinib mesylate (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Novartis Pharmaceuticals
Primary completion
Jun 2013

Outcome Measures

OutcomeResultp-value
PRIMARY
Best Tumor Response (Core)
0; 1; 49; 49; 10; 13
PRIMARY
Best Tumor Response (Core + Extension)
1; 2; 49; 48; 10; 13
SECONDARY
Overall Survival (Core)
NA; NA
SECONDARY
Overall Survival (Core + Extension)
55.9; 57.1
SECONDARY
Duration of Response (Core)
113; 123
SECONDARY
Duration of Response (Core + Extension)
27; 30
SECONDARY
Progression Free Survival (PFS) (Core + Extension)
19.3; 25.2
SECONDARY
Time to Treatment Failure (Core)
84; 84
SECONDARY
Time to Treatment Failure (Core + Extension)
19; 19
SECONDARY
Time to Onset of Response (Core)
13; 12
SECONDARY
Time to Onset of Response (Core + Extension)
3; 3
SECONDARY
Time to Progression (Core + Extension)
19.8; 25.5

Summary

In the core study, participants with unresectable or metastatic gastrointestinal stromal tumors expressing c-kit were treated with either 400 mg or 600 mg imatinib mesylate for 3 years. The 10 year extension study allowed participants, who successfully completed the core study, to continue study treatment with imatinib mesylate provided they still benefited from treatment and did not demonstrate safety concerns as per the investigator's opinion.

Eligibility Criteria

Inclusion Criteria

  • Men and non-pregnant women ≥18 years of age with the histopathologically documented diagnosis of malignant GIST that was unresectable and/or metastatic. Confirmation of KIT (CD117) expression via immunohistochemical analysis of tumor sample was also required
  • At least one measurable lesion, as defined by Southwestern Oncology Group (SWOG) Solid Tumor Response Criteria, which had not been previously embolized or irradiated
  • Performance status ≤3 as defined by the Eastern Cooperative Oncology Group (ECOG) criteria, as well as a life expectancy ≥6 months and adequate end organ function defined as follows: Total bilirubin 1.5 x 10^9/L, platelet count >100 x 10^9/L

Exclusion Criteria

  • Patients with fewer than five years of disease-free survival from any other (non-GIST) malignancy except if the other malignancy was not currently clinically significant and did not require active intervention or if the other malignancy was a basal cell skin cancer or a cervical carcinoma in situ
  • Patients with known brain metastases
  • Evidence of any of the following disorders: Grade III/IV cardiac failure as defined by the New York Heart Association Criteria, severe concomitant disease, acute or known chronic liver disease (i.e. chronic active hepatitis, cirrhosis) or HIV infection
  • Chemotherapy or other investigational therapy within four weeks prior to study entry (six weeks for nitrosourea or mitomycin-C) and/or radiotherapy to ≥25% of the bone marrow
  • Inability to cooperate
  • Major surgery within two weeks or exposure to other investigational agents within 28 days of entry into the study

Other protocol-defined inclusion / exclusion criteria may have applied.

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00237185). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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