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Study on treatment after complete resection of high risk gastrointestinal stromal tumor (GIST)

Study on treatment after complete resection of high risk gastrointestinal stromal tumor (GIST) - STAR ReGISTry

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000009531
Enrollment
500
Registered
2012-12-13
Start date
2012-12-25
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Gastrointestinal stromal tumor

Interventions

None listed

Sponsors

The Research Group for Rare Neoplasms of Japan
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) The diagnosis of GIST is confirmed by KIT-positive of resected specimen or acquiring of genetic mutations with c-kit and PDGFRA 2) The subject is classified as high risk based on the modified-Fletcher Classification (Joensuu) 3) In initial GIST, a complete gross resection had been conducted and the resection is within 3 years prior to registration (if recurrence is found at the time, the registration shall be permitted when above condition is met.) 4) Over 20 years old 5) Patients are able to provide written informed consent, if the patient died at the time of registration, a consent must be obtained from the legal representative of the person (Unless it has been six months or more after the surgery) 6) After the surgery, a periodic imaging test (every 6 months) has been conducted to examine possibility of recurrence

Exclusion criteria

Exclusion criteria: 1) In case the patient has other serious illnesses other than GIST (other cancer, cardiovascular disease, brain disease, and hepatorenal diseases etc). 2) Resection of metastases/ disseminated lesion was concluded in initial GIST, a complete gross resection 3) In case the physician determines that participation in the study is not appropriate.

Design outcomes

Primary

MeasureTime frame
Recurrence-free survival

Secondary

MeasureTime frame
-Overall survival -Occurrence and severity of adverse events -Completion of treatment

Countries

Japan

Contacts

Public ContactSatoshi Nakagawa

Translational Research Center for Medical Innovation None

s-nakagawa@tri-kobe.org078-303-9093

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026