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Association details:
Evidence:
Evidence Level:
Sensitive: A2 - Guideline
Source:
Published date:
03/13/2023
Excerpt:
Gastrointestinal Stromal Tumor….Systemic Therapy Agents and Regimens for GIST...Preferred regimens: Imatinib for KIT or PDGFRA mutations (excluding PDGFRA exon 18 mutations that are insensitive to imatinib, including D842V).
Evidence Level:
Sensitive: C2 – Inclusion Criteria
New
Title:

Role of surgery in patients with resectable liver metastases from GISTs: a prospective, single-center, real-world study

Excerpt:
...Mutations are detected in c-kit or PDGFRα (not exon 18 D842V) using samples from biopsy or surgical specimens; 5. ...
Evidence Level:
Sensitive: C2 – Inclusion Criteria
New
Title:

Rechallenge of Imatinib in GIST Having no Effective Treatment: RIGHT

Excerpt:
...- Patients with metastatic or unresectable malignant gastrointestinal stromal tumour which has been histologically confirmed by the detection of CD117 on immunohistochemical staining or genetically confirmed by the detection of mutation in KIT or PDGFRα genes on direct sequencing of tumor DNA....
Trial ID:
More C2 evidence
Evidence Level:
Sensitive: C2 – Inclusion Criteria
New
Title:

Adjunction of cilostazol to imatinib for patients with an unresectable or metastatic GIST (Gatsrointestinal stromal tumor) already treated by imatinib or who will start a treatment with imatinib Association du cilostazol à l'imatinib pour le traitement des GIST (GastroIntestinal Stromal Tumor) non résécables et ou métastatiques nécessitant un traitement par imatinib ou déjà traités par imatinib

Excerpt:
...Inclusion Criteria: -histologically proven metastatic or locally advanced histologically proven non resectable GIST ( any primary tumor site) already treated by Glivec® (at any dose) for at least 12 months in first line therapy, or patients who will start Glivec® (at any dose) in first line therapy or after failure of all TKIs -exon 11, exon 9 or other kit mutations -written signed informed consent -ability to take oral medication -metabolic positivity of the tumor at the first PET-CT (positivity is defined as High 18F-FDG uptake by a lesion more than the surrounding tissue) -at least one measurable lesion by CT scanner -no contraindication to cilostazol -ECOG performance status 0 /1 at study entry -effective contraception for both male and female patients must be used for at least 8 weeks after the last study drug administration if the risk of conception exists -age > 18 years old -life expectancy at least 12 weeks - Adequate bone marrow, liver and renal function as assessed by the following laboratory requirements conducted within 7 days of starting to study treatment: o Serum creatinine <1.5x upper reference range o Total bilirubin <1.5x ULN o Alanine transaminase (ALT) and aspartate aminotransferase (AST) < 2.5x ULN (<5x ULN for patients with liver involvement of their cancer). ...
Evidence Level:
Sensitive: C2 – Inclusion Criteria
New
Title:

Imatinib TDM in GIST

Excerpt:
...- Histologically or cytologically confirmed GIST with KIT mutation or PDGFRA mutation (non-D842V)...
Trial ID:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
New
Title:

Ipilimumab and Imatinib Mesylate in Advanced Cancer

Excerpt:
...For expansion cohorts, patients must have metastatic or unresectable gastrointestinal stromal tumor (GIST), melanoma, or uncategorized tumors with tumor biopsies that are positive for c-KIT mutations by polymerase chain reaction (PCR) or immunohistochemistry (IHC)....
Trial ID:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
New
Title:

Imatinib Dose Escalation to 800 mg/Day in Korean Patients With Metastatic or Unresectable GIST Harboring KIT Exon 9 Mutation: KENEDI

Excerpt:
...- Histologically confirmed metastatic or unresectable GIST with CD117(+), DOG-1 (+), or KIT mutation...
Trial ID:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
New
Title:

Preoperative Imatinib Mesylate Combined With Rectal-sparing Surgery in Patients With c-KIT Gene-mutant Rectal GIST

Excerpt:
...C-KIT gene mutation....
Trial ID:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
New
Title:

5 Years of Adjuvant Imatinib in Patients With Gastrointestinal Stromal Tumor With a High Risk

Excerpt:
...Histologically confirmed GIST with CD117(+), DOG-1(+), or mutation in KIT or PDGFRα gene 3....
Trial ID:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
New
Title:

A Study of Intermittent Dosing Schedule of Imatinib in Patients With Tyrosine Kinase Inhibitor Refractory GISTs

Excerpt:
...- Patients with metastatic or unresectable GIST which has been histologically confirmed by the detection of CD117 on immunohistochemical staining or genetically confirmed by the detection of mutation in KIT or PDGFRα genes on direct sequencing of tumor DNA....
Trial ID:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
New
Title:

Prospective Multicenter Clinical Study of Neoadjuvant Imatinib Mesylate for Gastrointestinal Stromal Tumors

Excerpt:
...- Gene mutation test report including c-kit exons 9,11,13 and 17 and platelet-derived growth factor receptor alpha (PDGFRA) exons 12 and 18...
Trial ID:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
New
Title:

Dovitinib for Imatinib/Sumitinib-failed Gastrointestinal Stromal Tumors (GIST): TKI258

Excerpt:
...- Histologically confirmed metastatic and/or advanced GIST with CD117(+), DOG-1(+), or mutation in KIT or PDGFRα gene...
Trial ID:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
New
Title:

Adjuvant Imatinib in High-risk Gastrointestinal Stromal Tumor (GIST) With C-kit Mutation

Excerpt:
...- Presence of mutation in exon 11 of c-kit gene....
Trial ID:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
New
Title:

Management of Imatinib-associated Severe Skin Rash in Patients With Gastrointestinal Stromal Tumor

Excerpt:
...- Histologically confirmed metastatic and/or advanced (unresectable or recurrent) GIST with CD117(+), DOG-1(+), or mutation in KIT or PDGFRα gene...
Trial ID:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
New
Title:

Jejunoileal vs Gastric GIST in the Era of Imatinib.

Excerpt:
...Number of patients with a molecular analysis positive for KIT mutation`KIT Gene mutation`Number of patients with a molecular analysis positive for PDGFRA mutation`PDGFRA Gene mutation`Number of patients with immunohistochemical expression of CD117`Expression of CD117`Number of patients with immunohistochemical expression of DOG1`Expression of DOG1`Number of patients with recurrence after treatment with tyrosinkin inhibitors.`...
Trial ID:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
New
Title:

Pazopanib in Advanced Gastrointestinal Stromal Tumors Refractory to Imatinib and Sunitinib

Excerpt:
...- Metastatic and/or locally advanced GIST, with diagnosis based on histology with positive c-kit and/or DOG-1, or with a GIST-typical mutation in KIT or PDGFR...
Trial ID:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
New
Title:

A Study of AUY922 for GIST(Gastrointestinal Stromal Tumor) Patients

Excerpt:
...Patients with histologically proven CD117-positive and/or c-kit or PDGFR mutation gastrointestinal stromal tumor (GIST), which is metastatic or unresectable, locally advanced, and have failed to or intolerance of prior imatinib and sunitinib treatment 2....
Trial ID:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
New
Title:

Imatinib Mesylate With or Without Surgery in Treating Patients With Metastatic Gastrointestinal Stromal Tumor That is Responding to Imatinib Mesylate

Excerpt:
...- Histologically confirmed gastrointestinal stromal tumor expressing CD117+ or with documented mutation of the KIT or PDGFRA gene...
Trial ID:
Less C2 evidence
Evidence Level:
Sensitive: C3 – Early Trials
Title:

The analysis of 3-year adjuvant therapy with imatinib in patients with high-risk molecular profiled gastrointestinal stromal tumors (GIST) treated in routine practice

Published date:
08/16/2020
Excerpt:
The majority of GIST cases harboured exon 11 KIT mutations (88 cases, 82%), 11 cases had exon 9 KIT mutations (10%), 8 had other KIT/PDGFRA mutations potentially sensitive to imatinib. The disease relapse was detected in 19 patients, of them in 5 cases in exon 9 KIT mutants (45%), and 14 cases in patients with exon 11 KIT mutations (11%) [p < 0.01].
DOI:
10.1016/j.ejso.2020.08.004