Status:
UNKNOWN
CAcTUS - Circulating Tumour DNA Guided Switch
Lead Sponsor:
The Christie NHS Foundation Trust
Collaborating Sponsors:
Bristol-Myers Squibb
University of Manchester
Conditions:
Melanoma
Eligibility:
All Genders
16+ years
Phase:
PHASE2
Brief Summary
The stay aims to determine whether switching from targeted therapy to immunotherapy based on a decrease in levels of circulating tumour DNA in the blood, will improve the outcome in melanoma patients.
Detailed Description
The optimal scheduling of targeted and immune therapies in metastatic melanoma is unknown. At present, patients are treated with targeted therapy until acquired resistance develops, and then switched ...
Eligibility Criteria
Inclusion
- Patient capable of giving written informed consent
- Patients must be willing and able to comply with scheduled visits, treatment schedule, laboratory tests and other requirements of the study.
- Histological confirmation of cutaneous melanoma
- ≥ 16 years
- Stage III un-resectable/ IV disease
- BRAF p.V600E/K/R mutation confirmed (exact point mutation must be provided to the investigators)
- At least one target lesion measurable by CT or MRI as per RECIST 1.1
- Baseline ctDNA (as defined by the mutant BRAF VAF in plasma) ≥1.5%
- Adequate organ function
- ECOG performance status 0/1
- Prior radiotherapy or radiosurgery must have been completed at least 2 weeks prior to the first dose of study drug
- Women of childbearing potential (WOCBP) must have a negative serum or urine pregnancy test (minimum sensitivity 25 IU/L or equivalent units of HCG) within 24 hours prior to the start of study drug.
- WOCBP must agree to follow instructions for method(s) of contraception for the duration of treatment with study drugs plus 5 half-lives of the drugs they are taking at treatment completion (5 times the half-life = 125 days \[nivolumab\]; 5 times the half-life = 90 days \[ipilimumab\]; 5 times the half life = 40 hours \[dabrafenib\]; 5 times the half life = 50 days \[trametinib\]) plus 30 days (duration of ovulatory cycle).
- Males who are sexually active with WOCBP must agree to follow instructions for method(s) of contraception for the duration of treatment plus 5 half-lives of the study drug as above plus 90 days (duration of sperm turnover).
- Azoospermic males and WOCBP who are continuously not heterosexually active are exempt from contraceptive requirements
Exclusion
- Prior systemic anti-cancer treatment (immune therapy, targeted therapy, vaccine therapy, or investigational treatment) for unresectable Stage III or Stage IV melanoma.
- Prior adjuvant therapy with BRAF +/- MEK inhibitor or adjuvant therapy with combination PD-1 inhibitor plus CTLA-4 inhibitor. Prior adjuvant therapy with PD-1 inhibitor is allowed so long as relapse occurred \> 6 months from discontinuation of treatment and treatment not stopped due to grade 3 or 4 toxicity.
- Current use of a prohibited medication
- History of another malignancy. Exception: patients who have been disease-free for 3 years, (i.e. patients with second malignancies that are indolent or definitively treated at least 3 years ago) or patients with a history of completely resected non-melanoma skin cancer. No additional therapy should be required whilst the patient is on study.
- Any serious or unstable pre-existing medical conditions (aside from malignancy exceptions specified above), psychiatric disorders, or other conditions that could interfere with the patients safety, obtaining informed consent, or compliance with study procedures.
- Known Human Immunodeficiency Virus (HIV), Hepatitis B Virus (HBV), or Hepatitis C Virus (HCV) infection (patients with laboratory evidence of cleared or chronic (not active) HBV and HCV infection will be permitted).
- A history of glucose-6-phosphate dehydrogenase (G6PD) deficiency.
- Patients with active, known or suspected autoimmune disease. Patients with type 1 diabetes mellitus, hypothyroidism only requiring hormone replacement, skin disorders (such as vitiligo, psoriasis or alopecia) not requiring systemic treatment, or conditions not expected to recur in the absence of an external trigger will be permitted to enrol.
- Patients with a condition requiring systemic treatment with either corticosteroids (\>10 mg daily prednisone equivalent) or other immunosuppressive medications within 14 days of study drug administration. Inhaled or topical steroids and adrenal replacement steroid doses \> 10 mg daily prednisone equivalent are permitted in the absence of active autoimmune disease.
- Patients with interstitial lung disease that is symptomatic or may interfere with the detection or management of suspected drug-related pulmonary toxicity.
- Brain metastases and leptomeningeal metastases are excluded unless:
- Asymptomatic and untreated at presentation, OR
- Symptomatic lesions have been definitively treated with surgery or stereotactic surgery (whole-brain radiation may be given as adjuvant treatment), and do not require steroids for control of symptoms
- Symptomatic metastases, treated or untreated, or metastases requiring steroids to control symptoms, are excluded
- No enzyme inducing anticonvulsants for ≥ 4 weeks prior to randomisation
- Coronary syndromes (including myocardial infarction within 6 months or unstable angina)
- A history or evidence of current ≥ Class II congestive heart failure as defined by the New York Heart Association (NYHA) guidelines with an ejection fraction of \<50%
- Treatment refractory hypertension defined as a blood pressure of systolic\> 150 mmHg and/or diastolic \> 95 mm Hg on \>3 occasions which cannot be controlled by anti-hypertensive therapy;
- Known cardiac metastases;
- Uncorrectable electrolyte abnormalities (e.g. hypokalaemia, hypomagnesaemia, hypocalcaemia), long QT syndrome or taking medicinal products known to prolong the QT interval.
- A history or current evidence/risk of retinal vein occlusion (RVO) or central serous retinopathy (CSR) including presence of predisposing factors to RVO or CSR (e.g., uncontrolled glaucoma or ocular hypertension, uncontrolled hypertension, uncontrolled diabetes mellitus, or a history of hyperviscosity or hypercoagulability syndromes)
- Known immediate or delayed hypersensitivity reaction or idiosyncrasy to drugs chemically related to the study treatments including monoclonal antibodies, their excipients, and/or dimethyl sulfoxide (DMSO) and/or Polysorbate-80-containing infusions.
- Females who are breast-feeding.
- Prisoners or patients who are involuntarily incarcerated.
- Patients who are compulsorily detained for treatment of either a psychiatric or physical (e.g., infectious disease) illness.
Key Trial Info
Start Date :
May 2 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
May 2 2024
Estimated Enrollment :
21 Patients enrolled
Trial Details
Trial ID
NCT03808441
Start Date
May 2 2019
End Date
May 2 2024
Last Update
August 25 2023
Active Locations (1)
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1
The Christie NHS Foundation Trust
Manchester, United Kingdom, M20 4BX