A Randomised Trial of Imatinib Alternating With Regorafenib Compared to Imatinib Alone for the First Line Treatment of Advanced Gastrointestinal Stromal Tumour (GIST)

Launched by AUSTRALASIAN GASTRO-INTESTINAL TRIALS GROUP · Feb 11, 2015

Keywords

ClinConnect Summary

This clinical trial is studying the effects of two medications, imatinib and regorafenib, for treating advanced gastrointestinal stromal tumors (GIST) in adults. The goal is to see if alternating between these two drugs works better than taking imatinib alone as the first treatment for patients with this type of cancer that has spread and cannot be surgically removed.

To be eligible for the trial, participants must be adults over 18 with confirmed GIST that has spread, and they should not have received any previous treatments for metastatic disease, except for a short course of imatinib. They should also have measurable tumors and meet specific health criteria. Participants will receive the assigned treatments and will be monitored for their safety and response to the drugs. It's important to know that the study is currently active but not recruiting new participants. If you or a loved one are considering joining such a study, it’s essential to discuss it with your healthcare provider to understand the potential benefits and risks.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • Adults (over 18 yrs) with histologically confirmed GIST. In CD-117-negative cases DOG-1 must be positive or a KIT/PDGFRA mutation must be present.
• • Unresectable, metastatic disease.
• • No prior TKI for metastatic disease, with the exception of those patients who have had up to 21 days of uninterrupted treatment on 400mg daily of imatinib.
• • Imatinib therapy given as an adjuvant treatment and completed at least 3 months prior to entry into this trial is permitted. Patients who have progression of GIST while on adjuvant therapy are not eligible for this trial.
• • ECOG performance status 0-2
• • Measurable disease by RECIST version 1.1. (Note: Participants with only peritoneal disease will be eligible only if they have lesions measurable in two dimensions and have at least 1 lesion which is ≥ 2 cm in size).
• • Adequate bone marrow function (Haemoglobin ≥ 9.0g/dL, platelet count ≥ 100 x 109/L, and absolute neutrophil count ≥ 1.5 x 109/L).
• • Adequate liver function (Serum total bilirubin ≤1.5 x ULN, INR ≤ 1.5, and ALT, AST, ALP ≤2.5 x ULN (≤ 5 x ULN for participants with liver metastases). Lipase level must be ≤ 1.5 x ULN.
• • Adequate renal function (Creatinine clearance \> 50ml/min) based on either the Cockcroft Gault formula, 24 hour urine or Glomerular Filtration Rate (GFR scan); and serum creatinine ≤ 1.5 x ULN.
• • Tumour tissue available for central review.
• • Willing and able to comply with all study requirements, including treatment timing and/or nature of required assessments.
• • Study treatment both planned and able to start within 14 days of randomisation.
• • Signed, written informed consent.
• Exclusion Criteria:
• • Concurrent GI illness which may prevent absorption of imatinib or regorafenib - please note that prior gastrectomy or bowel resection does not exclude patients from this study.
• • Use of other investigational drugs within 4 weeks prior to enrolment.
• • Known sensitivity to any of the study drugs, study drug classes, or excipients in the formulation.
• • Participants receiving therapeutic doses of warfarin.
• • Presence of brain metastases.
• • The presence of PDGFR D842V mutation or other mutation known to cause imatinib resistance.
• • Inability to swallow tablets.
• • Arterial thrombotic or ischaemic events, such as cerebrovascular accident or pulmonary embolism within 6 months prior to randomisation; or major venous thrombotic events requiring use of an anticoagulant such as warfarin within 6 months prior to randomisation.
• • Poorly controlled hypertension (systolic blood pressure \> 140 mmHg or diastolic pressure \> 90 mmHg despite optimal medical management).
• • Major surgical procedure, open biopsy, or significant traumatic injury within 28 days prior to randomisation, or non healing wound, ulcer or fracture.
• • Congestive cardiac failure (NYHA ≥ grade 2), unstable angina or new onset angina within the previous 3 months, or AMI within the previous 6 months. Cardiac arrhythmias requiring anti-arrhythmic therapy (beta blockers or digoxin are permitted).
• • Haemorrhage or bleeding event ≥ Grade 3 according to CTCAE v4.0 within 4 weeks prior to randomisation.
• • Ongoing infection of \> Grade 2 according to CTCAE v4.0.
• • Active hepatitis B or C or HIV, or chronic hepatitis B or C requiring treatment with antiviral therapy. Testing for these is not mandatory unless clinically indicated.
• • Interstitial lung disease with ongoing signs and symptoms.
• • Persistent proteinuria of ≥ Grade 3 (\>3.5g/24 hours) according to CTCAE v4.0
• • Other significant medical or psychiatric condition judged by the investigator to interfere with protocol requirements.
• • Use of biological response modifiers such as granulocyte colony stimulating factor (G-CSF), within 3 weeks prior to randomisation.
• • Patients taking strong cytochrome P (CYP) CYP3A4 inhibitors (eg clarithromycin, indinavir, itraconazole, ketoconazole, nefazodone, nelfinavir, posaconazole, ritonavir, saquinovir, telithromycin, voriconazole) or strong CYP3A4 inducers (eg carbamazepine, phenobarbitol, phenytoin, rifampicin, St John's wort).
• • History of another malignancy within 5 years prior to registration. Patients with a past history of adequately treated carcinoma-in-situ, basal cell carcinoma of the skin, squamous cell carcinoma of the skin, or superficial transitional cell carcinoma of the bladder are eligible. Patients with a history of other malignancies are eligible if they have been continuously disease free for at least 5 years after definitive primary treatment.
• • Pregnancy, lactation, or inadequate contraception. Women must be post menopausal, infertile, or use a reliable means of contraception. Women of childbearing potential must have a negative pregnancy test done within 7 days prior to registration. Women of childbearing potential and men must agree to use adequate contraception before entering the trial until at least 8 weeks after the last study drug administration.

Trial Officials