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

Anaplastic Thyroid Cancer Clinical Trial

— NEO-ATACT  

Official title:

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

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06079333
• Other study ID #: NEOAC
• Status: Recruiting
• Phase: Phase 2
• Start date: January 1, 2023
• Est. completion date: January 1, 2028

Study information

• Verified date: October 2023
• Source: Leiden University Medical Center
• Contact: Ellen Kapiteijn, MD, PhD
• Phone: 0031-71-5263486
• Email: h.w.kapiteijn[@]lumc.nl
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

Description:

Unmet need ATC is a very serious condition and is, apart from a few exclusive cases, always lethal. Many patients suffer uncontrollable loco-regional disease with even so uncontrollable complaints of airway obstruction, oesophagus obstruction, pain and neck movement impairment. One of the only shown beneficial treatment is complete surgical resection with clear surgical margins combined with radiotherapy and systemic treatment. However, in less than 10-15% of the patients the pathologist reports clear surgical margins. Thereby it is noticeable that surgery often results in serious morbidity, due to an esophagectomy, laryngectomy or trachea resection all accompanied by an extensive reconstruction. All of these come with serious morbidity and seldomly lead to clear margins and better outcome. Proposed solution A single center, phase II study for the evaluation of safety and efficacy of neo-adjuvant and adjuvant dabrafenib/trametinib treatment in BRAF mutated ATC patients. By introducing neo-adjuvant treatment the hypothesis is that better selection is done for patients who are eligible for complete surgery and that surgery results more often in clear surgical margins after neo-adjuvant treatment. Second benefit of treating patients with combined loco-regional and systemic agents before surgery is that micro/macrometastases (being there in at least 30% of the patients at diagnosis) are already being treated directly after diagnosis. Lastly, adjuvant treatment with dabrafenib/trametinib will hopefully result in reduction of local and distant recurrences after surgery.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 20
• Est. completion date: January 1, 2028
• Est. primary completion date: January 1, 2027
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Informed consent.

2. Age over 18 years old.

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

4. Histologically confirmed ATC (centrally reviewed).

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

6. No distant metastases (M0).

7. Free or secured airway.

8. Able to swallow pills.

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

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

11. No prior radiotherapy to site of interest.

12. 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.

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

Exclusion Criteria:

1. No informed consent.

2. History of cancer within 2 years from diagnosis of ATC (exception: basal cell skin cancer, in situ carcinoma).

3. Poorly differentiated transformation of previous differentiated thyroid cancer.

4. Presence of distant metastases.

5. Underlying medical conditions that, in the Investigator's opinion, will make the administration of study treatment hazardous or obscure the interpretation of toxicity determination or adverse events

6. History of congestive heart failure, active cardiac conditions, including unstable coronary syndromes, significant arrhythmias and severe valvular disease must be evaluated for risks of undergoing general anesthesia.

7. Pregnancy or nursing.

Related Conditions & MeSH terms

• Anaplastic Thyroid Cancer
• Thyroid Carcinoma, Anaplastic
• Thyroid Diseases
• Thyroid Neoplasms

Intervention

Drug:
• dabrafenib/trametinib
braf/mek-inhibition

Locations

Country	Name	City	State
Netherlands	Ellen Kapiteijn	Leiden	Zuid-Holland

Sponsors (2)

Lead Sponsor	Collaborator
Leiden University Medical Center	Novartis

Country where clinical trial is conducted

Netherlands, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	primary endpoint of the study will be R0 resection rate (efficacy).	primary endpoint of the study will be R0 resection rate (efficacy).	after 6-12 weeks braf/mek-inhibition
Secondary	Neo-adjuvant and adjuvant treatment related toxicity of dabrafenib/trametinib (according to CTCAE v. 5.0)	Neo-adjuvant and adjuvant treatment related toxicity of dabrafenib/trametinib (according to CTCAE v. 5.0) during 1 year of treatment with braf/mek-inhibition	during 1 year of treatment with braf/mek-inhibition
Secondary	30-day postoperative surgical complications	30-day postoperative surgical complications (within 30 days after surgery)	within 30 days after surgery
Secondary	Histopathological response after neo-adjuvant treatment	Histopathological response after neo-adjuvant treatment: complete response (<10% tumor cells), partial response (between more than 10% and up to 50% tumor cells), or no response (still more than 50% tumor cells)	6-12 weeks neo-adjuvant braf/mek-inhibition
Secondary	Locoregional-free survival	Locoregional-free survival	at 2 years
Secondary	Distant metastasis-free survival	Distant metastasis-free survival	at 2 years
Secondary	Overall survival	Overall survival	at 2 years