RECRUITING

A Pilot of a Microdevice For In Situ Candidate Drug Screening in Cutaneous Lesions of T-Cell Lymphoma

Conditions

Cutaneous T Cell Lymphoma Peripheral T Cell Lymphoma

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This research is being done to study the safety of implanting and retrieving a microdevice that releases up to 19 drugs directly within a cancerous lesion as a possible tool to evaluate the effectiveness of several approved cancer drugs against cutaneous T cell lymphoma and peripheral T cell lymphoma

Official Title

A Pilot of a Microdevice For In Situ Candidate Drug Screening in Cutaneous Lesions of T-Cell Lymphoma

Quick Facts

Study Start:2019-12-11

Study Completion:2027-01-01

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT04045470

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:No

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
* Participants must have clinical diagnosis of cutaneous T-cell lymphoma or peripheral T-cell lymphoma with cutaneous involvement supported by histological evaluation of skin lesions. * Participants must have measurable cutaneous disease, based on the modified Severity Weighted Assessment Tool (mSWAT; definition provided in appendix E). Skin lesions situated in a previously irradiated area are considered measurable if progression has been demonstrated in such lesions. * Two lesions are amenable to placement of multiple devices in terms of lesion size and location, as assessed by dermatologist (minimum diameter of 1.5 cm). * Patient must have the following minimum washout period from previous treatments and cannot be on any systemic therapy at the time of implantation. * 2 week from topical therapies of lesional skin selected for implantation * 2 weeks from retinoids, interferons, vorinostat, romidepsin, therapeutic doses of oral corticosteroids (physiologic replacement doses of oral corticosteoids are allowed) * 4 weeks from phototherapy * 5 half-lives for systemic cytotoxic anticancer agents, monoclonal antibodies, and investigational therapy * 12 weeks from local radiation therapy of lesional skin selected for implantation * 15 weeks from systemic immunotherapy targeting PD-1/PD-L1 * Age minimum of age 18. * ECOG performance status ≤2 (Karnofsky ≥60%, see Appendix A). * Participants will undergo laboratory testing within 28 days prior to the procedure. Participants must have marrow function as defined below: * absolute neutrophil count ≥500/mcL * platelets ≥50,000/mcL * Participants must be evaluated by a dermatologist or medical oncologist who will determine the clinically appropriate treatment strategy based on clinical history and extent of disease. Systemic therapy will be mandatory for cohort 2/expansion cohort, not for cohort 1. Systemic therapy may be initiated anytime within 4 weeks of MD removal. * Patients must be deemed medically stable to undergo percutaneous procedures by their treating cutaneous oncologist. * Ability to understand and the willingness to sign a written informed consent document. * Patients must be willing to undergo research-related genetic and transcriptomic sequencing (somatic and germline) and data management, including the deposition of de-identified genetic sequencing data in NIH central data repositories. * Patient is considered to have capacity to properly follow instructions at home for the care of device(s) that will each have an attached thin guidewire protruding through the skin and fixed in place (see Appendix B).	* Positive serum pregnancy test at screening visit. * Uncorrectable bleeding or coagulation disorder known to cause increased risk with surgical or biopsy procedures * History of allergic reactions attributed to compounds of similar chemical or biologic composition to agents used in this study. * Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements. * Patients who will receive standard of care systemic therapy are not allowed to start any new skin directed therapy (e.g. topical steroids, radiation, phototherapy) concurrent with first systemic therapy initiated after device implantation and retrieval. Should a patient clinically progress on first systemic therapy and require a change in treatment, skin directed therapies may be introduced. * Patients unable to undergo treatment wash-out period due to rapidly progressive disease requiring immediate systemic therapy

Inclusion Criteria

Exclusion Criteria

* Participants must have clinical diagnosis of cutaneous T-cell lymphoma or peripheral T-cell lymphoma with cutaneous involvement supported by histological evaluation of skin lesions.
* Participants must have measurable cutaneous disease, based on the modified Severity Weighted Assessment Tool (mSWAT; definition provided in appendix E). Skin lesions situated in a previously irradiated area are considered measurable if progression has been demonstrated in such lesions.
* Two lesions are amenable to placement of multiple devices in terms of lesion size and location, as assessed by dermatologist (minimum diameter of 1.5 cm).
* Patient must have the following minimum washout period from previous treatments and cannot be on any systemic therapy at the time of implantation.
* 2 week from topical therapies of lesional skin selected for implantation
* 2 weeks from retinoids, interferons, vorinostat, romidepsin, therapeutic doses of oral corticosteroids (physiologic replacement doses of oral corticosteoids are allowed)
* 4 weeks from phototherapy
* 5 half-lives for systemic cytotoxic anticancer agents, monoclonal antibodies, and investigational therapy
* 12 weeks from local radiation therapy of lesional skin selected for implantation
* 15 weeks from systemic immunotherapy targeting PD-1/PD-L1
* Age minimum of age 18.
* ECOG performance status ≤2 (Karnofsky ≥60%, see Appendix A).
* Participants will undergo laboratory testing within 28 days prior to the procedure. Participants must have marrow function as defined below:
* absolute neutrophil count ≥500/mcL
* platelets ≥50,000/mcL
* Participants must be evaluated by a dermatologist or medical oncologist who will determine the clinically appropriate treatment strategy based on clinical history and extent of disease. Systemic therapy will be mandatory for cohort 2/expansion cohort, not for cohort 1. Systemic therapy may be initiated anytime within 4 weeks of MD removal.
* Patients must be deemed medically stable to undergo percutaneous procedures by their treating cutaneous oncologist.
* Ability to understand and the willingness to sign a written informed consent document.
* Patients must be willing to undergo research-related genetic and transcriptomic sequencing (somatic and germline) and data management, including the deposition of de-identified genetic sequencing data in NIH central data repositories.
* Patient is considered to have capacity to properly follow instructions at home for the care of device(s) that will each have an attached thin guidewire protruding through the skin and fixed in place (see Appendix B).

* Positive serum pregnancy test at screening visit.
* Uncorrectable bleeding or coagulation disorder known to cause increased risk with surgical or biopsy procedures
* History of allergic reactions attributed to compounds of similar chemical or biologic composition to agents used in this study.
* Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
* Patients who will receive standard of care systemic therapy are not allowed to start any new skin directed therapy (e.g. topical steroids, radiation, phototherapy) concurrent with first systemic therapy initiated after device implantation and retrieval. Should a patient clinically progress on first systemic therapy and require a change in treatment, skin directed therapies may be introduced.
* Patients unable to undergo treatment wash-out period due to rapidly progressive disease requiring immediate systemic therapy

Contacts and Locations

Study Contact

Cecilia Larocca, MD

CONTACT

617-632-6571

clarocca@partners.org

Principal Investigator

Cecilia Larocca, MD

PRINCIPAL_INVESTIGATOR

Dana-Farber Cancer Institute

Study Locations (Sites)

Dana Farber Cancer Institute

Boston, Massachusetts, 02115

United States

Collaborators and Investigators

Sponsor: Dana-Farber Cancer Institute

Cecilia Larocca, MD, PRINCIPAL_INVESTIGATOR, Dana-Farber Cancer Institute

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2019-12-11

Study Completion Date2027-01-01

Study Record Updates

Study Start Date2019-12-11

Study Completion Date2027-01-01

Terms related to this study

Keywords Provided by Researchers

Cutaneous T Cell Lymphoma
Peripheral T Cell Lymphoma

Additional Relevant MeSH Terms

Cutaneous T Cell Lymphoma
Peripheral T Cell Lymphoma