Immunostimulating Interstitial Laser Thermotherapy in Malignant Melanoma

Melanoma Clinical Trial

Official title:

Exploratory Study on Immunostimulating Interstitial Laser Thermotherapy in Malignant Melanoma

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT02650492
• Other study ID #: CTP-2015-004
• Status: Terminated
• Phase: N/A
• Start date: October 2015
• Est. completion date: May 1, 2019

Study information

• Verified date: July 2021
• Source: Clinical Laserthermia Systems AB
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Thermotherapy is a technology aiming at destroying tissue, for example tumor tissue. Immunostimulating Interstitial Laser Thermotherpy (imILT) is a specific form of thermotherapy, which, in addition to destroying tumor tissue, has been optimized to cause a tumor specific immunologic response. In laboratory animals the imILT method has also been shown to induce a so called abscopal effect. This means that when one tumor is treated with imILT other, untreated, tumors also decrease in size. The immunologic response has previously been characterized in breast cancer patients after receiving imILT treatment , and presumed abscopal effects induced by imILT have also been described in a malignant melanoma patient. The purpose of this trial is to investigate the functionality and safety of the imILT treatment method in patients diagnosed with malignant melanoma. The inflammatory process, following on the treatment, will also be described in order to provide a more in depth knowledge of the treatment for this indication. The purpose is also to evaluate efficiency when it comes to local tumor destruction as well as understanding of the subsequent immunological effects. Since immunologically based treatment of malignant melanoma is under intense review with so called "immune checkpoint inhibitors" this trial will also provide valuable information on how imILT, in the future, could be combined with these new and, for some patients, very effective treatment regimens. The treatment method has successfully been used for treatment of patients with breast cancer and malignant melanoma . Treatment of breast cancer patients caused an increase of cytotoxic T lymphocytes in the treated tumor, as well as activated dendritic cells at the tumor border. Regulatory T lymphocytes decreased in the regional lymph nodes. This trial is explorative, prospective, open and non-randomized. Five malignant melanoma patients stage III - IV will be treated in this trial, which is estimated to be carried out during a time period of 12 months.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 2
• Est. completion date: May 1, 2019
• Est. primary completion date: November 1, 2016
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• >18 years of age
• histologically confirmed malignant melanoma
• advanced melanoma disease (Stage III inoperable or Stage IV) that has progressed on standard first line treatment such as kinase inhibitor(s) and/or immunoregulatory monoclonal antibodies. Previously untreated patients with a dominant tumour lesion deemed suitable for local and highly tumour-destructive ablation may also be included
• time interval between previous systemic treatment and imILT of at least one month
• at least one lesion located in such a way (typically subcutaneously) that it can be treated without risk of skin necrosis or serious damage to other adjacent vital and healthy tissue
• verbal and written informed consent to participate
• adequate haematologic, renal and hepatic functions
• have an ECOG performance status = 2 (Karnofsky = 60%)

Exclusion Criteria:

• known HIV infection
• autoimmune disease which is judged to reduce an anti-tumour immune response
• systemic corticosteroid medication
• bleeding diathesis
• pregnancy or breast-feeding

Related Conditions & MeSH terms

• Malignant Melanoma
• Melanoma

Intervention

Device:
• Immunostimulating Interstitial Laser Thermotherapy
Immunostimulating Interstitial Laser Thermotherpy (imILT) is a specific form of thermotherapy, which, in addition to destroying tumor tissue, has been optimized to cause a tumor specific immunologic response.

Locations

Country	Name	City	State
Sweden	Karolinska University Hospital Solna	Stockholm

Sponsors (1)

Lead Sponsor	Collaborator
Clinical Laserthermia Systems AB

Country where clinical trial is conducted

Sweden, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Safety (adverse events)	Evaluation of adverse events.	18 months
Primary	Usability of the device as evaluated by treatment logs	Evaluation of the laser system by analysis of treatment logs of the device.	18 months
Primary	Usability of the device as evaluated by user questionnaire	Evaluation of the laser system by analysis of user questionnaire.	18 months
Secondary	Treatment effect (Measurement of tumor burden by irRC criteria)	Measurement of tumor burden by irRC criteria.	18 months
Secondary	Inflammatory response in tumor and circulation measured by quantification of inflammatory cell populations	Quantification of cellular infiltrate and activation markers by immunohistochemistry and flow cytometry.	18 months