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A real-world study of Avapritinib in the treatment of D842V-mutated gastrointestinal stromal tumors

Effect of adjuvant Avapritinib therapy on prognosis of patients with PDGFRa D842V-mutated gastrointestinal stromal tumor resected by R0 surgery

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200062170
Enrollment
Unknown
Registered
2022-07-27
Start date
2022-08-01
Completion date
Unknown
Last updated
2023-04-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gastrointestinal stromal tumor

Interventions

Avapritinib group:Nil
no Avapritinib group:Nil

Sponsors

Fujian Medical University Union Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1.Age 18-75 years old, male or female; 2.GIST tumor is primary, no distant metastasis was found in preoperative examination and intraoperative exploration; 3.No targeted drug neoadjuvant therapy before operation; 4.Accepted Radical R0 surgical resection; 5.Postoperative pathologically confirmed soft tissue tumor, in line with GIST; 6.Genetic testing (first- or second-generation sequencing) confirmed PDGFRa Exon18 D842V mutation, and the remaining sites were detected c-kit (Exon-9, Exon-11, Exon-13, Exon-17) and PDGFRa (Exon-12) have no mutation; 7.Have understood and signed the informed consent.

Exclusion criteria

Exclusion criteria: 1.Combined with other malignant tumors; 2.The patient has cognitive or communication impairment, or severe mental illness; 3.Severe systemic diseases, including cardiac function = grade II, respiratory insufficiency, liver and kidney insufficiency, severe hematological disorders; 4.Severe uncontrolled recurrent infection, or other uncontrolled concomitant diseases; 5.The patient joins other clinical studies, and the intervention measures may affect the evaluation of this study; 6.Can not cooperate well with follow-up; 7.Data Missing leads to unanalyzable persons.

Design outcomes

Primary

MeasureTime frame
3-year disease free survival rate;

Secondary

MeasureTime frame
3-year overall survival rate;

Countries

China

Contacts

Public ContactYong-Jian Zhou

Fujian Medical University Union Hospital

yong_jian_zhou@163.com13015772221

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026