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Safety and Efficacy of Avapritinib in Chinese Patients With Gastrointestinal Stromal Tumor (GIST) in the Real World

Registration Number
NCT05381753
Lead Sponsor
CStone Pharmaceuticals
Brief Summary

This study is an observational, multicenter, Real-word study to evaluate the safety and clinical efficacy of avapritinib in Chinese subjects with GIST.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
61
Inclusion Criteria
  • Cohort 1 and 4: Participants must have a confirmed diagnosis of unresectable GIST with mutations in the PDGFRα gene exon 18.
  • Cohort 2: Participants must have a confirmed diagnosis of GIST with mutations in the PDGFRα gene exon 18 and was/will be administrated avapritinib in an neoadjuvant and/or adjuvant setting.
  • Cohort 3: Participants must have a confirmed diagnosis of unresectable GIST without mutations in the PDGFRα gene exon 18, KIT gene exon 13, and KIT gene exon 14.
Exclusion Criteria
  • Participants who have participated and may participate in any other interventional clinical trail in the future.
  • Participants with any comorbidities not suitable for avapritinib (other TKIs, Cohort 4) treatment assessed by researchers.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Ava-mGSIT-P18AvapritinibUnresectable or metastatic PDGFRA exon 18 GIST
Ava-PerioperativeAvapritinibPerioperative PDGFRA exon 18 GIST
Ava-mGIST-otherAvapritinibUnresectable or metastatic GIST without KIT exon 13,14,or PDGFRA exon 18 mutation
TKITyrosine kinase inhibitors other than avapritinib ( imatinib, sunitinib, et al )Unresectable or metastatic PDGFRA exon 18 GIST
Primary Outcome Measures
NameTimeMethod
Dose adjustment of avapritinib in cohort 1, 2, and 3From the start of study drug until 30 days after the last dose, up to 3 years.
Incidence and severity of adverse events(AE) and serious adverse events(SAE)in cohort 1, 2, and 3AEs were collected from the start of study drug until 30 days after the last dose, SAEs were collected from the date of the informed consent signature until 30 days after the last dose of study drug, up to 3 years.
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Beijing Cancer Hospital

🇨🇳

Beijing, Beijing, China

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