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Ripretinib in Chinese Patients With Advanced GIST: a Real World Study

P

Peking University

Status

Active, not recruiting

Conditions

Gastrointestinal Stromal Tumors

Treatments

Drug: Ripretinib Oral Tablet

Study type

Observational

Funder types

Other

Identifiers

NCT05697107
GIST-R-RWD-001

Details and patient eligibility

About

to evaluate the clinical efficacy, safety and predictive factors of ripetinib in Chinese patients with advanced GIST in the real world

Full description

Ripretinib has become the standard ≥ 4L treatment in advanced GIST. Given the small sample size of patients in the China bridging study of INVICTUS as well as the short marketing time of ripretinib, further exploration on the long-term efficacy and safety of ripretinib, as well as the dominant gene mutation type of ripretinib in Chinese GIST patients is required. Hence, we plan to further explore the efficacy of ripretinib, predictors of efficacy, etc. by collecting and analyzing real-world data from Chinese patients with advanced GIST recieving ripretinib.

Enrollment

308 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

-≥18 years old

  • Histologically confirmed gastrointestinal stromal tumor (GIST)
  • At least one measurable lesion (mRECIST v1.1)
  • Received or receiving ripretinib treatment

Exclusion criteria

  • Patients who received <1 cycle of ripretinib treatment
  • Medical records are incomplete

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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