Treatment of BRAF ( B-Rapidly Accelerated Fibrosarcoma) Mutated Papillary Craniopharyngioma

Craniopharyngioma Clinical Trial

— Swecranio  

Official title:

Neoadjuvant and Postoperative Treatment With Dabrafenib and Trametinib in BRAF Mutated Papillary Craniopharyngioma

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05525273
• Other study ID #: ver 1-21
• Status: Recruiting
• Phase: Phase 2
• Start date: September 1, 2023
• Est. completion date: April 10, 2028

Study information

• Verified date: February 2024
• Source: Skane University Hospital
• Contact: Eva Marie Erfurth, MD. PhD.
• Phone: +4646172363
• Email: eva_marie.erfurth[@]med.lu.se
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Subjects with papillary craniopharyngioma harboring a BRAF mutation will be treated with a BRAF + MEK inhibitor (dabrafenib + trametinib) after informed consent. Study participants will be administered oral dabrafenib and trametinib until maximal tumor volume reduction assessed by MRI. Progression free survival, cognition, ophthalmologic status, hypothalamic status and quality of life will be assessed 1 year after initiation of study treatment

Description:

Background. Papillary craniopharyngioma harbours a BRAF mutation in 90% of cases. Treatment with BRAF + MEK (mitogen activated protein kinase ) inhibitors (dabrafenib + trametinib) may prevent patients from undergoing surgery with a high risk of serious side effects, or provide an additional treatment option when further surgery is not advised. Study intervention Subjects with newly diagnosed craniopharyngioma where radical surgery is not considered adequate or patients with recurrence of craniopharyngioma where further surgery is not considered possible without serious sequelae will be asked for informed consent Study participants are treated continuously with dabrafenib and trametinib orally, until maximal tumor shrinkage. Evaluation is done by MRI to measure tumor volume, as well as assessment of performance status, quality of life, cognition, ophthalmologic status, performance status and hypothalamic status. Study type The study is a Phase II, single armed, open label and multicenter study Study drugs are Dabrafenib (Tafinlar) and trametinib (Mekinist) Primary outcome To evaluate tumor response in the form of reduced tumor volume on MRI in patients with papillary craniopharyngioma during treatment with dabrafenib and trametinib. Secondary outcomes To evaluate dabrafenib and trametinib treatment for the following aspects: - response according to RECIST Duration of response for patients treated without subsequent surgery - how many patients become operable after neoadjuvant treatment - progression-free survival after 1 and 2 years - quality of life during and after treatment The effect of treatment on vision, cognition and hypothalamic effects Exploratory outcomes Levels of circulating BRAF Trial population 25 patients Trial duration Participants are treated with the study treatment for at least one year if the treatment is well tolerated, to maximum tumor reduction, or longer according to the investigators´s assessment. Treatment is discontinued in case of progression, unacceptable toxicity or at the request of the patient.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 25
• Est. completion date: April 10, 2028
• Est. primary completion date: September 10, 2027
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Histologically verified papillary craniopharyngioma.

2. BRAF mutated V600E (valine 600 glutamine), verified immunohistochemically and by molecular genetic analysis

3. Newly diagnosed tumor, or recurrence after previous surgery, where surgery is not considered to be able to be performed radically without the risk of serious or permanent sequelae.

4. Age over 18 years

5. Functional status according to ECOG (Eastern Cooperative Oncology Group performance status) 0-2

6. Adequate organ function:

neutrophils> 1.5 x 109 platelets> 100 x 109 creatinine <1.5 x ULN (upper limit of normal) or creatinine clearance <45 ml / min bilirubin <1.5 x ULN ASAT (aspartate aminotransferase) / ALAT (alanine aminotransferase) <2.5 x ULN

7. Ability to understand and give informed consent.

8. Previous cancer, which does not require current treatment is allowed.

9. The patient agrees to use an adequate method to avoid pregnancy.

Exclusion Criteria:

1. Ongoing treatment in another drug study or other experimental treatment.

2. Previous treatment with BRAF or MEK inhibitors.

3. Hypersensitivity to study drugs.

4. Ongoing treatment with non-authorized drugs, (strong inducers of CYP2C8 or CYP3A4). If the patient is on unauthorized drugs, they must be discontinued at least 14 days before inclusion.

5. Known cardiovascular disease where treatment with MEK inhibitors is considered inappropriate, eg severe heart failure, prolongation of QT time, uncontrolled arrhythmia, recent (<6 months) cardiac infarction, uncontrolled hypertension.

6. Active bleeding; intracranial hemorrhage last 4 weeks before inclusion.

7. Thromboembolic disease last 6 months and unstable anticoagulant treatment less than 4 weeks before inclusion.

8. Women who are pregnant or breastfeeding.

9. Previous central serous retinopathy or retinal vein occlusion.

10. Previous uveitis or iritis last 4 weeks before inclusion.

11. Surgery within the last 3 weeks.

12. For postoperative patients; radiation therapy within the last 3 months.

Related Conditions & MeSH terms

• Craniopharyngioma

Intervention

Drug:
• Oral dabrafenib and trametinib
Neoadjuvant or postoperative treatment of patients with verified BRAF mutated papillary craniopharyngioma

Locations

Country	Name	City	State
Sweden	Department of Endocrinology	Lund

Sponsors (2)

Lead Sponsor	Collaborator
Eva Marie Erfurth, MD, PhD	Novartis

Country where clinical trial is conducted

Sweden, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Levels of circulating mutated BRAF	BRAF assessed by plasma analysis and compared to baseline levels	1 week after initiation of trial treatment
Other	Levels of circulating mutated BRAF	BRAF assessed by plasma analysis and compared to baseline levels	2 weeks after initiation of trial treatment
Other	Levels of circulating mutated BRAF	BRAF assessed by plasma analysis and compared to baseline levels	6 months after initiation trial treatment
Other	Levels of circulating mutated BRAF	BRAF assessed by plasma analysis and compared to baseline levels	12 months after initiation trial treatment
Other	Levels of circulating of mutated BRAF	BRAF assessed by plasma analysis and compared to baseline levels	3 months after end of trial treatment
Primary	Tumor response	To evaluate tumor response measured as maximally reduced tumor volume on MRI during treatment with dabrafenib and trametinib. Maximally reduced volume is defined as the time point where no further reduction of tumor volume can be observed	1 month to 5 years (sliding timepoints)
Secondary	Response ratio	Response ratio according to RECIST	1 year after initiation of study treatment
Secondary	Response duration	Duration of response for patients treated without subsequent surgery	From time of study drug discontinuation to time of observed increased tumor volume assessed up to 1 year
Secondary	Operability after neoadjuvant trial treatment	Number of patients which become operable after neoadjuvant treatment	1 year after initiation of study treatment
Secondary	Progression-free survival 1 year	Defined as unchanged or diminished tumor volume	1 year
Secondary	Progression-free survival 2 years	Defined as unchanged or diminished tumor volume	2 years
Secondary	QOL after treatment	Quality of life assessed by EQ5D5L (EuroQual 5 dimensions 5 levels) at 1 year after start of study treatment and compared to baseline	1 year
Secondary	QOL after treatment	Quality of life assessed by EORTC QLQ30 (European Organisation for Research and Treatment of Cancer-Quality of Life Questionnaire 30) at 1 year after start of study treatment and compared to baseline	1 year
Secondary	Cognitive status after treatment	Cognitive status assessed by CNS (central nervous system) Vital Signs 1 year after initiation of treatment and compared to baseline	1 year
Secondary	Opthalmologic status after treatment	Opthalmologic status assessed as compound measure of visual acuity and visual field defects 1 year after initiation of treatment and compared to baseline	1 year
Secondary	Hypothalamic status after treatment	Hypothalamic status assessed as compound measure of pituitary and hypothalamic status 1 year after initiation of treatment and compared to baseline	1 year