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Trial record 5 of 9 for:    erdheim chester

A Study of Lenalidomide for Adult Histiocyte Disorders

This study is currently recruiting participants.
See Contacts and Locations
Verified May 2017 by Eric Jacobsen, MD, Dana-Farber Cancer Institute
Sponsor:
Collaborator:
Celgene
Information provided by (Responsible Party):
Eric Jacobsen, MD, Dana-Farber Cancer Institute
ClinicalTrials.gov Identifier:
NCT02523040
First received: August 12, 2015
Last updated: May 31, 2017
Last verified: May 2017
  Purpose
This research study is studying a chemotherapy drug Lenalidomide as a possible treatment for one of three histiocyte disorders: Langerhans cell histiocytosis (LCH), Erdheim-Chester disease (ECD), or histiocytic sarcoma (HS).

Condition Intervention Phase
Langerhans Cell Histiocytosis (LCH) Histiocytoses Erdheim-chester Disease Histiocytic Sarcoma (HS) Drug: Lenalidomide Phase 2

Study Type: Interventional
Study Design: Intervention Model: Single Group Assignment
Masking: No masking
Primary Purpose: Treatment
Official Title: A Phase II Study of Lenalidomide for Adult Histiocyte Disorders

Resource links provided by NLM:


Further study details as provided by Eric Jacobsen, MD, Dana-Farber Cancer Institute:

Primary Outcome Measures:
  • Response Rate [ Time Frame: 12 Months ]

Secondary Outcome Measures:
  • Progression Free Survival (PFS) [ Time Frame: 12 Months ]
  • Overall Survival [ Time Frame: 12 Months ]
  • Number of Participating with Grade 3-4 toxicity [ Time Frame: 12 Months ]
  • Quantitative serial measurements of urine cell free DNA for BRAF mutation as a biomarker of response [ Time Frame: 12 Months ]
  • Quantitative serial measurements of serum TNF-alpha levels as a biomarker of response [ Time Frame: 12 Months ]
  • Quantitative serial measurements of plasma cell free DNA for BRAF mutation as a biomarker of response [ Time Frame: 12 months ]

Estimated Enrollment: 12
Study Start Date: August 2015
Estimated Study Completion Date: August 2022
Estimated Primary Completion Date: August 2018 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Lenalidomide

After the screening procedures confirm participation in the research study.

- Lenalidomide Oral, Daily for 21 days of each cycle

Drug: Lenalidomide
Other Name: Revlimid

Detailed Description:

This research study is a Phase II clinical trial. Phase II clinical trials test the safety and effectiveness of an investigational intervention to learn whether the intervention works in treating a specific disease. "Investigational" means that the intervention is being studied.

The FDA (the U.S. Food and Drug Administration) has not approved lenalidomide for your specific disease but it has been approved for other uses. Lenalidomide is a chemotherapy drug that belongs to a class of drugs called immunomodulatory drugs (IMiDs), which modify a participant's immune response in order to treat cancer. Lenalidomide alters the body's immune system and it may also interfere with the development of tiny blood vessels that help support tumor growth. Therefore, it may reduce or prevent the growth of cancer cells. Lenalidomide has been shown to restore the immune cells' ability to attack and kill tumor cells Lenalidomide is approved by the FDA to treat certain cancers including multiple myeloma and myelodysplastic syndrome.

  Eligibility

Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Patients must have histologically or cytologically confirmed LCH, ECD or HS. Confirmation of outside pathology at BWH will be performed but is not mandatory prior to study enrollment (see section 3).
  • Detectable disease by at least one of the following modalities: CT, PET, bone scan, or MRI.
  • Patients with LCH must require systemic therapy according to the Histiocyte Society LCH Evaluation and Treatment Guidelines (HS 2009)

    -- Or

  • Patients with HS requiring systemic treatment as defined by disease that cannot be surgically resected and/or encompassed in a single radiation field.
  • Age 18 years or older.
  • ECOG performance status ≤2 (Karnofsky ≥60%, see Appendix A)
  • Participants must have normal organ and marrow function as defined below:

    • absolute neutrophil count ≥1,000/mcL
    • platelets ≥100,000/mcL
    • total bilirubin within 1.5 times normal institutional limits
    • AST(SGOT)/ALT(SGPT) ≤3 × institutional upper limit of normal
    • creatinine within 2 times normal institutional limits

      --- OR

    • creatinine clearance ≥30 mL/min/1.73 m2. Note, dose adjustments are required for CrCl ≥30 mL/min but ≤60 ml/min.
  • Able to take aspirin 81 mg daily as prophylactic anticoagulation if not on warfarin, low molecular weight heparin or oral factor Xa inhibitor. Patients intolerant to ASA may use warfarin or low molecular weight heparin at doses designed to treat deep venous thrombosis.
  • All study participants must be registered into the mandatory Revlimid REMS® program, and be willing and able to comply with the requirements of the REMS® program.
  • Women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry and for the duration of study participation.
  • Ability to understand and the willingness to sign a written informed consent document.

Exclusion Criteria:

  • Prior chemotherapy or radiation within 2 weeks (6 weeks for nitrosoureas or mitomycin C) prior to entering the study or those who have not recovered from adverse events due to agents administered more than 2 weeks earlier.
  • Participants who are receiving any other investigational agents.
  • Prior treatment with lenalidomide. Patients previously treated with thalidomide who discontinued treatment for reasons aside from an adverse reaction to thalidomide are permitted.
  • History of another invasive malignancy unless treated with curative intent 5 years or more prior to study entry. Patients with localized carcinoma of the cervix, non-melanoma skin cancer, or early stage prostate cancer requiring observation only are eligible regardless of timing of diagnosis.
  • 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.
  • Pregnant women are excluded from this study because lenalidomide has known teratogenic effects. Because there is an unknown but potential risk for adverse events in nursing infants secondary to treatment of the mother with lenalidomide, breastfeeding should be discontinued if the mother is treated with lenalidomide.
  • Known active hepatitis B (HBV) or hepatitis C (HCV) infection. Patients who are positive only for HBV surface antibody as a result of prior vaccination are eligible. Patients with a positive HBV core antibody but undetectable HBV viral load are eligible.
  • HIV-positive participants on combination antiretroviral therapy are ineligible because of the potential for pharmacokinetic interactions with lenalidomide. In addition, these participants are at increased risk of lethal infections when treated with marrow-suppressive therapy. Appropriate studies will be undertaken in participants receiving combination antiretroviral therapy when indicated.
  • Concomitant corticosteroids unless patient has been on a stable dose of prednisone (or equivalent) of ≤10 mg daily for at least 2 weeks prior to first dose of study drug.
  • Inability to swallow pills.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT02523040

Contacts
Contact: Eric Jacobsen, MD 617-632-6633 edjacobsen@partners.org

Locations
United States, Massachusetts
Dana-Farber Cancer Institute Recruiting
Boston, Massachusetts, United States, 02115
Contact: Eric Jacobsen, MD    617-632-6633    eric_jacobsen@dfci.harvard.edu   
Contact: Ashley Newcomb    617-632-2328    AshleyN_Newcomb@dfci.harvard.edu   
Principal Investigator: Eric Jacobsen, MD         
Sponsors and Collaborators
Dana-Farber Cancer Institute
Celgene
Investigators
Principal Investigator: Eric Jacobsen, MD Dana-Farber Cancer Institute
  More Information

Responsible Party: Eric Jacobsen, MD, Principal Investigator, Dana-Farber Cancer Institute
ClinicalTrials.gov Identifier: NCT02523040     History of Changes
Other Study ID Numbers: 15-197
Study First Received: August 12, 2015
Last Updated: May 31, 2017

Keywords provided by Eric Jacobsen, MD, Dana-Farber Cancer Institute:
Langerhans cell histiocytosis (LCH)
Erdheim-Chester disease (ECD)
Histiocytic Sarcoma (HS)

Additional relevant MeSH terms:
Erdheim-Chester Disease
Sarcoma
Histiocytosis
Histiocytosis, Langerhans-Cell
Histiocytic Sarcoma
Neoplasms, Connective and Soft Tissue
Neoplasms by Histologic Type
Neoplasms
Lymphatic Diseases
Lung Diseases, Interstitial
Lung Diseases
Respiratory Tract Diseases
Histiocytosis, Non-Langerhans-Cell
Histiocytic Disorders, Malignant
Lenalidomide
Thalidomide
Immunologic Factors
Physiological Effects of Drugs
Angiogenesis Inhibitors
Angiogenesis Modulating Agents
Growth Substances
Growth Inhibitors
Antineoplastic Agents
Immunosuppressive Agents
Leprostatic Agents
Anti-Bacterial Agents
Anti-Infective Agents

ClinicalTrials.gov processed this record on July 25, 2017