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Trial of SBRT With Concurrent Ipilimumab in Metastatic Melanoma

Phase 1
Completed
Conditions
Melanoma
Effects of Immunotherapy
Adverse Effect of Radiation Therapy
Interventions
Radiation: Stereotactic body radiotherapy (SBRT)
Registration Number
NCT02406183
Lead Sponsor
Radiotherapie
Brief Summary

The prognosis of advanced metastatic melanoma remains poor although a breakthrough has been achieved with the novel anti-CTLA-4 treatment (ipilimumab) for a subset of patients. Unfortunately, due to immune resistance, the majority of patients do not obtain long-lasting clinical benefit. Radiotherapy is able to interfere with immune resistance by inducing immunogenic cell death. Preclinical evidence indicates that combining radiotherapy with anti-CTLA-4 treatment increases response rates compared to single agent treatment. These data are supported by several spectacular clinical cases and one retrospective study. The investigators hypothesize that combining ipilimumab with radiotherapy will result in a higher response rate compared to ipilimumab or radiotherapy in monotherapy. Given the complexity of the interaction in anti-tumor immunity, the first goal of this project is to assess the safety of the combined treatment.

Detailed Description

The safety profiles of ipilimumab and SBRT are well studied separately 22-24, but prospective data on the combination of ipilimumab and high-dose SBRT are lacking. Consequently, the first goal of the proposed prospective phase I trial is to assess the safety (dose limiting toxicity, DLT) of the combination of high-dose SBRT and ipilimumab in patients with advanced melanoma.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
13
Inclusion Criteria
  • Signed informed consent and willingness to comply to the treatment and follow-up
  • Histological diagnosis of melanoma,
  • at least 3 extracranial measurable metastatic lesions per RECIST 1.1,
  • Karnofsky Performance score >60,
  • Age ≥18,
  • Life expectancy ≥ 16 weeks
  • Women of childbearing potential must have a negative serum pregnancy test within 14 days of first dose of study treatment. Men and women should agree to use effective contraception, during the study and for 1 month following the last dose of investigational product.
  • ≥ 28 days between last treatment with standard or experimental chemotherapy, surgery, radiotherapy, cytokine therapy or immunotherapy. Patient should be completely recuperated of any clinical toxicity developed during previous treatments.
  • Patients should have adequate organ function for ipilimumab treatment
Exclusion Criteria
  • Central nervous system (CNS) metastases at baseline, with the exception of those subjects who have previously-treated CNS metastases (surgery ± radiotherapy, radiosurgery, or gamma knife) and who meet both of the following criteria: a) are asymptomatic and b) have no requirement for steroids or enzyme-inducing anticonvulsants.
  • Prior malignancy: Subjects who have had another malignancy and have been disease-free for 5 years, or subjects with a history of completely resected non-melanomatous skin carcinoma or successfully treated in situ carcinoma are eligible
  • Prior radiotherapy preventing treatment with SBRT.
  • Disorder precluding understanding of trial information.
  • Autoimmune disease: Patients with a history of inflammatory bowel disease (including Crohn's disease and ulcerative colitis) and autoimmune disorders such as rheumatoid arthritis, systemic progressive sclerosis [scleroderma], Systemic Lupus Erythematosus or autoimmune vasculitis [e.g., Wegener's Granulomatosis] are excluded from this study.
  • Known Human Immunodeficiency Virus (HIV), Hepatitis B, or Hepatitis C.
  • Concomitant therapy with any of the following: IL-2, interferon or other non-study immunotherapy regimens; cytotoxic chemotherapy; immunosuppressive agents; other investigational therapies; or chronic use of systemic corticosteroids (used in the management of cancer or non-cancer-related illnesses).
  • Pregnant women
  • Breast feeding
  • History of or current immunodeficiency disease or prior treatment compromising immune function, prior allogeneic stem cell transplantation.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Treatment (SBRT, Ipilimumab)Stereotactic body radiotherapy (SBRT)Drug: Ipilimumab Dosage: Ipilimumab will be administered intravenously at 3 mg/kg every 3 weeks for 4 cycles, Radiation: Stereotactic Body Radiotherapy Radiation therapy 24 Grays in 8 Grays fractions, Radiation therapy 30 Grays in 10 Grays fractions, Radiation therapy 36 Grays in 12 Grays fractions
Treatment (SBRT, Ipilimumab)IpilimumabDrug: Ipilimumab Dosage: Ipilimumab will be administered intravenously at 3 mg/kg every 3 weeks for 4 cycles, Radiation: Stereotactic Body Radiotherapy Radiation therapy 24 Grays in 8 Grays fractions, Radiation therapy 30 Grays in 10 Grays fractions, Radiation therapy 36 Grays in 12 Grays fractions
Primary Outcome Measures
NameTimeMethod
Maximal tolerated dose (MDT) that is associated with dose-limiting toxicity (DLT) in 25% of patients.2 years
Secondary Outcome Measures
NameTimeMethod
Overall survival2 years
Progression-free survival2 years
Preliminary anti-tumor activity following escalating doses of radiation combined to ipilimumab using the immune related response criteria irRC2 years
Immunomonitoring (absolute lymphocyte count)2 years

absolute lymphocyte count

Immunomonitoring (frequencies of Foxp3+ Treg-cells)2 years

frequencies of Foxp3+ Treg-cells

Immunomonitoring (functional analysis looking at shifts in Th1/Th2/Th17)2 years

functional analysis looking at shifts in Th1/Th2/Th17

Immunomonitoring (plasmacytoid dendritic cells and myeloid derived suppressor cells and their IDO expression)2 years

plasmacytoid dendritic cells and myeloid derived suppressor cells and their IDO expression,

Trial Locations

Locations (1)

Dept. of Radiotherapy, Ghent University Hospital

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Ghent, Oost-Vlaanderen, Belgium

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