NEO- and Adjuvant Targeted Therapy in Braf-mutated Anaplastic Cancer of the Thyroid (NEO-ATACT Study)

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Anaplastic thyroid cancer (ATC) is an almost invariable lethal cancer in humans. Most patients present with a rapid progressive mass in the neck with progressive complaints like dyspnoea, dysphagia or pain. The risk of suffocation is the main reason for rapid surgical intervention, but we know from literature that an oncological resection with clear margins is seldomly achieved. Some patients deteriorate that fast after surgery that radiation therapy and/or chemotherapy is not feasible anymore. Patients with BRAF-mutated ATC already have shown to benefit from targeted BRAF/MEK inhibition. This study aims to increase the number of patients that undergo a successful R0 tumor resection after neo-adjuvant BRAF/MEK inhibitor treatment.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Informed consent.

• Age over 18 years old.

• World Health Organization (WHO) Performance Status 0 or I.

• Histologically confirmed ATC (centrally reviewed).

• Confirmed presence of BRAFV600E/K mutation in primary tumor tissue.

• No distant metastases (M0).

• Free or secured airway.

• Able to swallow pills.

• Patients must have undergone complete disease staging including: PET-CT scan and CT-neck/thorax/abdomen.

⁃ No prior anticancer systemic treatment (including chemotherapy, immunotherapy, oncolytic viral therapy, other systemic therapies).

⁃ No prior radiotherapy to site of interest.

⁃ Screening laboratory values must meet the following criteria: WBC ≥ 2.0x109/L, Neutrophils ≥ 1.0x109/L, Platelets ≥ 100 x109/L, Hemoglobin ≥ 6.5 mmol/L, AST ≤ 2.5 x ULN, ALT ≤ 2.5 x ULN, Total bilirubin ≤ 1.5 X ULN, INR and PTT in normal range, LDH \< 2xULN. Serum creatinine ≤ 1.5 × ULN; or calculated creatinine clearance ≥ 50 mL/min by Cockcroft-Gault formula; or estimated glomerular filtration rate \> 50 mL/min/1.73m2.

⁃ Absence of additional severe and/or uncontrolled concurrent disease.

Locations
Other Locations
Netherlands
Ellen Kapiteijn
RECRUITING
Leiden
Contact Information
Primary
Ellen Kapiteijn, MD, PhD
h.w.kapiteijn@lumc.nl
0031-71-5263486
Backup
Saskia Luelmo, MD
S.A.C.Luelmo@lumc.nl
0031-71-5263464
Time Frame
Start Date: 2023-01-01
Estimated Completion Date: 2028-01-01
Participants
Target number of participants: 20
Treatments
Experimental: neo-adjuvant and adjuvant braf/mek-inhibition
Participants will undergo neo-adjuvant treatment with dabrafenib/trametinib. After 6 weeks of BRAF/MEK inhibitors, participants will undergo an evaluation of resectability. If the tumor is resectable, patients undergo tumor resection. If not resectable, neo-adjuvant treatment continues for another 6 weeks followed by a new evaluation. All resected patients receive adjuvant dabrafenib/trametinib up to a total treatment duration of 52 weeks. If resection is not possible, patients will continue on dabrafenib/trametinib.
Sponsors
Leads: Leiden University Medical Center
Collaborators: Novartis

This content was sourced from clinicaltrials.gov