Sorafenib and Radioembolization With Sir-Spheres® for the Treatment of Metastatic Ocular Melanoma

Ocular Melanoma Clinical Trial

Official title:

Sorafenib and Radioembolization With Sir-Spheres® for the Treatment of Metastatic Ocular Melanoma

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01893099
• Other study ID #: CHUV-CePO-code 16295
• Status: Completed
• Phase: Phase 1
• First received: July 2, 2013
• Last updated: April 19, 2018
• Start date: June 2013
• Est. completion date: November 28, 2017

Study information

• Verified date: April 2018
• Source: Centre Hospitalier Universitaire Vaudois
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The best way to combine a loco-regional procedure such as chemoembolisation or radioembolization combined with an anti-angiogenic drug is not clear. This phase I trial aims to establish, first, the tolerability of the combination of liver radioembolization with SirSpheres® and sorafenib in uveal melanoma patients with liver metastasis studying different schedules of administration of sorafenib after and before radioembolization. Secondly, we aim to evaluate angiogenic markers modifications during these different schedules, either in the serum or radiologicaly. Dose of Sorafenib will be 400 mg BID and the timing of introduction will differ for one cohort to the other, given after the radioembolization for initials cohorts and finally, before and concomitantly to radioembolization for the last cohort.

Description:

Primary objective:

To evaluate the safety and tolerability of sorafenib in combination with SIR-Spheres® radioembolization in uveal melanoma patients metastatic to the liver.

Secondary objectives:

• Translational research on biomarkers (blood and liver biopsies) as well as on radiological exam by using microbubble contrast enhanced ultrasound. Angiogenic markers such as VEGF, IGF-2, TFG Angiopoietin-2 and IL-8 will be monitored. Correlations will be investigated between the angiogenic markers (blood & tumor tissue), angiogenic radiological exam and the response to the treatment.

• To evaluate the response, clinical benefit, PFS and survival of the patients.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 11
• Est. completion date: November 28, 2017
• Est. primary completion date: November 28, 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Metastatic uveal melanoma with proven histology (stage IV)

• Presence of liver metastases

• Concomitant non life-threatening metastases outside the liver are allowed

• Palliative radiotherapy will be allowed outside the liver

• Previous chemotherapy or immunotherapy at least 4 weeks before study treatment is allowed

• Age = 18 years

• ECOG Performance Status of 0 or 1

• Life expectancy of at least 12 weeks

• Subjects with at least one uni-dimensional (by RECIST) measurable lesion. Lesions must be measured by CT-scan or MRI

• Adequate bone marrow, liver and renal function as assessed by the following laboratory requirements to be conducted within 7 days prior to study treatment

• Hemoglobin = 9.0 g/dl

• Absolute neutrophil count (ANC) = 1,500/mm3

• Platelet count = 100,000/ul

• Total bilirubin = 1.5 times the upper limit of normal (ULN)

• ALT and AST = 5 x ULN

• Alkaline phosphatase < 4 x ULN

• PT-INR/PTT < 1.5 x ULN

• Serum creatinine = 1.5 x ULN

• Signed and dated informed consent before the start of specific protocol procedures

Exclusion Criteria:

• History of cardiac disease: congestive heart failure >NYHA class 2; active coronary artery disease (myocardial infarction more than 6 months prior to study entry is allowed); cardiac arrhythmias requiring anti-arrhythmic therapy (beta blockers or digoxin are permitted) or uncontrolled hypertension.

• History of HIV infection or chronic hepatitis B or C.

• Active clinically serious infections (> grade 2 NCI-CTC version 4.0).

• Symptomatic metastatic brain or meningeal tumors (unless the patient is > 6 months from definitive therapy, has a negative imaging study within 4 weeks before treatment start and is clinically stable with respect to the tumor at the time of study treatment).

• Patients with seizure disorder requiring medication (such as steroids or anti-epileptics).

• History of organ allograft.

• Patients with evidence or history of bleeding diasthesis.

• Patients undergoing renal dialysis.

• Previous or concurrent cancer that is distinct in primary site or histology from the cancer being evaluated in this study except cervical carcinoma in situ, treated basal cell carcinoma, superficial bladder tumor (Ta, Tis and T1) or any cancer curatively treated > 3 years prior to study treatment.

• Pregnant or breast-feeding patients. Women of childbearing potential must have a negative pregnancy test 72h before all investigations related to the protocol. Both men and women enrolled in this trial must use adequate barrier birth control measures during the course of the trial and two weeks after the completion of trial (and men for at least 3 months after last administration of study medication).

• Any condition that is unstable or could jeopardize the safety of the patient and their compliance in the study.

• Patients unable to swallow oral medications.

• Pre-treatment with any antiangiogenic agents (Bevacizumab, Sunitinib, or other TKI inhibitors affecting the vessels)

• Radiotherapy on the liver

• Major surgery within 4 weeks of start of treatment

• Autologous bone marrow transplant or stem cell rescue within 4 months of study treatment.

• Use of biologic response modifiers, such as G-CSF, within 3 weeks of study treatment.

• Investigational drug therapy outside of this trial during or within 4 weeks of study treatment

• Prior exposure to the study drug

• Substance abuse, medical, psychological or social conditions that may interfere with the patient's participation in the study or evaluation of the study results

Related Conditions & MeSH terms

• Melanoma
• Ocular Melanoma

Intervention

Drug:
• Sorafenib
Sorafenib will be given at the dosage of 400 mg BID. Initiation of the drug will vary dependently of the cohort and will be continued until progressive disease or intolerance.

Device:
• Radioembolization with SIR-Spheres® (Yttrium Microspheres)

Locations

Country	Name	City	State
Switzerland	Centre Hospitalier Universitaire Vaudois	Lausanne

Sponsors (1)

Lead Sponsor	Collaborator
Centre Hospitalier Universitaire Vaudois

Country where clinical trial is conducted

Switzerland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Toxicity	Toxicities will be assessed according to the NCI-CTCAE (version 4.0).	30 days of treatment of sorafenib
Secondary	Translational research on biomarkers	Measurement of angiogenic factors and evaluation of angiogenesis with dynamic micro-bubble contrast-enhanced US	2 years
Secondary	Clinical benefit	Clinical benefit (CR, PR and NC) evaluated with 18F-FDG-PET CT scan and CT scan by using respectively PERCIST criteria and RECIST criteria	2 years
Secondary	Progression-free survival (PFS)		2 years
Secondary	Overall survival (OS)		2 years