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Report for Clinical Trial NCT02392871

Developed by Shray Alag, 2020.
SNP Clinical Trial Gene

An Open-label, Single-arm, Phase I/II, Multicentre Study to Evaluate the Safety and Efficacy of the Combination of Dabrafenib, Trametinib and Palliative Radiotherapy in Patients With Unresectable (Stage IIIc) and Metastatic (Stage IV) BRAF V600E/K Mutation-positive Cutaneous Melanoma

The purpose of this study is to investigate the side effects and safety, and effectiveness of combining dabrafenib and trametinib with radiotherapy. Previous and ongoing clinical trials have demonstrated the effectiveness and safety of combining both dabrafenib and trametinib compared with dabrafenib alone. This has led to the approval for the use of both drugs in combination in people with metastatic melanoma with the BRAF mutation. Melanoma that has spread to other parts of the body may also benefit from radiotherapy to help reduce symptoms from melanoma. Previous studies have shown that melanoma may be sensitive to radiotherapy and that it can help to improve quality of life. The intention of the CombiRT study is to establish if dabrafenib, trametinib and radiotherapy combined is a safe and effective treatment for metastatic melanoma.

NCT02392871 Metastatic Melan Metastatic Melanoma
MeSH:Melanoma
HPO:Cutaneous melanoma Melanoma

2 Interventions

Name: Palliative radiotherapy

Type: Radiation
Group Labels: 1

Radiotherapy

Name: Dabrafenib and trametinib (combination)

Description: Patients should be taking dabrafenib and trametinib for at least 2 weeks prior to enrolment into the study.
Type: Drug
Group Labels: 1

Radiotherapy


Primary Outcomes

Measure: Toxicity profile for patients receiving dabrafenib and trametinib in combination with RT, by measuring adverse events and radiotherapy associated toxicities.

Time: 0-12 months

Secondary Outcomes

Measure: Patients' pain using a visual analog scale (questionnaire)

Time: 0-12 months

Measure: Overall disease response by measuring progression free survival and overall survival.

Time: 0-12 months

Measure: Local treatment response in the irradiated index lesion(s).

Time: 0-12 months

Measure: Time to local progression in the irradiated index lesion(s).

Time: 0-12 months

Purpose: Treatment

Allocation: N/A

Single Group Assignment


There is one SNP

SNPs


1 V600E

An Open-label, Single-arm, Phase I/II, Multicentre Study to Evaluate the Safety and Efficacy of the Combination of Dabrafenib, Trametinib and Palliative Radiotherapy in Patients With Unresectable (Stage IIIc) and Metastatic (Stage IV) BRAF V600E/K Mutation-positive Cutaneous Melanoma. --- V600E ---

3. Histologically confirmed cutaneous melanoma that is either Stage IIIC (unresectable) or Stage IV (metastatic), and determined to be BRAF V600E/K mutation-positive as determined by a BRAF mutation assay. --- V600E ---



HPO Nodes


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