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Pomalidomide in Combination With Liposomal Doxorubicin in People With Advanced or Refractory Kaposi Sarcoma

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Descriptive Information
Brief Title † Pomalidomide in Combination With Liposomal Doxorubicin in People With Advanced or Refractory Kaposi Sarcoma
Official Title † A Phase 1 Trial of Pomalidomide in Combination With Liposomal Doxorubicin in Patients With Advanced or Refractory Kaposi Sarcoma
Brief Summary Background: Kaposi sarcoma (KS) is a cancer most often seen in people with HIV. It causes lesions. These are usually on the skin but sometimes in the lymph nodes, lungs, and gastrointestinal tract. Researchers think a combination of drugs may help treat KS. Objective: To test a combination of the anti-cancer drugs pomalidomide (CC-4047) and liposomal doxorubicin (Doxil) in people with KS. Eligibility: People ages 18 and over with KS Design: Participants will be screened with: Medical history Questionnaires Physical exam Blood, urine, and heart tests Chest X-ray Biopsy: A small sample of tissue is taken from a KS lesion. Possible CT scan Possible exam of lungs or gastrointestinal tract with an endoscope: A flexible instrument examines inside the organ. Participants will take the drugs in 4-week cycles. They will take Doxil through an IV on Day 1 of each cycle. They will take CC-4047 tablets by mouth each day for the first 3 weeks of each cycle. Participants will have many visits: Before starting treatment To start each cycle Day 15 of first 2 cycles Visits include repeats of screening tests and: Multiple blood draws Photographs of lesions Participants will keep a drug diary. Participants will take aspirin or other drugs to prevent blood clots. Participants with HIV will have combination antiretroviral therapy. Some participants will have a PET scan. Participants will continue treatment as long as they tolerate it and their KS improves. After treatment, they will have several follow-up visits for up to 5 years
Detailed Description Background: - Kaposi Sarcoma (KS) is a multicentric angioproliferative tumor that most frequently involves skin, but can also involve lymph nodes, lungs and gastrointestinal tract. It is most common in people with HIV or other forms of immune compromise. Patients with AIDS-associated KS have worse survival than HIV-infected patients without KS. - Patients may present with advanced disease KS and/or concurrent KSHV-associated multicentric Castleman disease (MCD) or an IL-6 related KSHV-associated cytokine syndrome (KICS). Patients with the latter conditions have poor outcomes when treated with FDA-approved cytotoxic therapies used for KS, and novel approaches are needed. - A Phase I/II Study demonstrated that pomalidomide 5 mg daily on days 1- 21 of a 28 Day Cycle was safe and tolerable in patients with KS with or without HIV. Increased CD4+ and CD8+ T-cell counts and KS regression were observed. - Combination of pomalidomide with liposomal doxorubicin may offer a new approach for patients with advanced KS or KS and concurrent KSHV-associated MCD or KICS Objectives: - Evaluate the safety and tolerability of various dose combinations of pomalidomide and liposomal doxorubicin in two groups of patients: Group I) KS requiring systemic therapy; Group II) KS with concurrent KSHV-associated MCD or KICS - To assess the pharmacokinetics (PK) of pomalidomide in combination with liposomal doxorubicin; and for patients with HIV in combination with antiretroviral therapy Eligibility: - Patients with biopsy proven (confirmed in the Laboratory of Pathology, CCR) Kaposi sarcoma (KS) - Group I: KS requiring systemic therapy (no prior therapy required) - T1 KS, KS on skin sufficiently widespread that it is not amenable to local therapy, or KS affecting quality of life due to local symptoms or psychological distress OR --KS patients with an inadequate response to pomalidomide (either progressive disease or stable disease after 4 months) OR - KS patients with an inadequate response to liposomal doxorubicin, paclitaxel, or other systemic chemotherapy (either progressive disease or stable disease after 6 cycles) - Group I will exclude patients eligible for Group II (below). - A wash out period off treatment of 3 weeks will be required, except in the case of patients with progressive, severe disease in which delay of treatment cannot be justified (i.e. symptomatic pulmonary KS) -Group II: KS in one of the following high-risk groups (no prior therapy required): - Concurrent KSHV-associated multicentric Castleman disease (MCD) - KSHV Inflammatory Cytokine Syndrome (KICS), including those also meeting clinical criteriafor KS immune reconstitution syndrome (KS IRIS) o Patients with primary effusion lymphoma or a large cell lymphoma arising in KSHV-associated MCD are excluded. - At least five measurable cutaneous KS lesions with no previous local radiation, surgical or intralesional cytotoxic therapy that would prevent response assessment for that lesion; or other evaluable disease. - ECOG Performance Status (PS): Group I: less than or equal to 2, Group II: less than or equal to 3, ECOG PS of 4 (with Karnofsky 20%) will be allowed in Group II only if symptoms due to pulmonary KS. - Measurable disease by the criteria proposed by the AIDS Clinical Trials Group Oncology Committee (for KS). - Patient or legal guardian must be willing to give informed consent. - Patients can be HIV positive or negative. - HAART for HIV+ patients. Design: - This is a Phase I study evaluating 2 groups of patients with KS. Patients will receive pomalidomide once a day, days 1-21 of a 28-day cycle, at the various dose levels combined with liposomal doxorubicin IV day 1 of a 28-day cycle until optimal tumor response, unacceptable toxicity, or patient request to discontinue - Patients with HIV will be prescribed HAART. - All patients will receive thromboprophylaxis, generally with aspirin 81 mg tablet daily. - This study will also evaluate the characteristics of 18fluoro-thymidine (FLT) positron emission tomography (PET) in patients with KS and concurrent KSHV-associated MCD or KICS, and correlate with markers of KSHV-lytic activation
Study Phase Phase 1
Study Type † Interventional
Study Design †
Primary Outcome Measure † safety/tolerability of dose combinations
Secondary Outcome Measure †
Condition † Kaposi Sarcoma
Intervention † Drugliposomal doxorubicin
Study Arms / Comparison Groups Group 1 pomalidomide and liposomal doxorubicin in patients with KS requiring systemic therapy Group 2 pomalidomide with liposomal doxorubicin in patients with advanced KS or KS and concurrent KSHV associated MCD or KICS
Publications *

* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.

Recruitment Information
Recruitment Status † Drug
Estimated Enrollment † 54
Start Date † January 4, 2016
Completion Date November 30, 2021
Primary Completion Date November 1, 2021
Eligibility Criteria † - INCLUSION CRITERIA: - Patients must have histologically confirmed Kaposi sarcoma (KS) confirmed by the Laboratory of Pathology, NCI. - All patients should have either five measurable cutaneous KS lesions with no previous local radiation, surgical or intralesional cytotoxic therapy that would prevent response assessment for that lesion; or other assessable disease - Group I: KS requiring systemic therapy (no prior therapy required) and: - Group I patients should have one or more of the following: - T1 KS, KS on skin sufficiently widespread that it is not amenable to local therapy, or KS affecting quality of life due to local symptoms or psychological distress - KS patients with an inadequate response to pomalidomide (either progressive disease or stable disease requiring additional therapy after 4 months) - KS patients with an inadequate response to liposomal doxorubicin, paclitaxel, or other systemic chemotherapy (either progressive disease or stable disease requiring additional therapy after 6 cycles) - Group I will exclude patients eligible for Group II (below). - A wash out period off treatment of 3 weeks will be required, except in the case of patients with progressive, severe disease in which delay of treatment cannot be justified (i.e. symptomatic pulmonary KS) - Group II: KS (no prior therapy required): - Concurrent KSHV-associated multicentric Castleman disease (MCD) - KSHV Inflammatory Cytokine Syndrome (KICS), including those also meeting clinical criteria for KS immune reconstitution syndrome (KS IRIS) - At least five measurable cutaneous KS lesions with no previous local radiation, surgical or intralesional cytotoxic therapy that would prevent response assessment for that lesion; or other assessable disease - ECOG Performance Status (PS): - Group I: less than or equal to 2 - Group II: less than or equal to 3 - ECOG PS of 4 will be allowed in Group II only if symptoms due to pulmonary KS. (with Karnofsky = 20%). - Measurable disease by the criteria proposed by the AIDS Clinical Trials Group Oncology Committee (for KS). - Patients can be HIV positive or negative. - HAART for HIV+ patients: - All HIV+ patients must be willing to be compliant with HAART - Group I-on HAART for 1 month with stable disease; however, no minimum time restriction for patients with progressive and/or end-organ threatening disease - Group II-no minimum time restriction on prior HAART, patients may be HAART naive. - Age greater than or equal to18 years. --Because no dosing or adverse event data are currently available on the use of pomalidomide in combination with liposomal doxorubicin in patients 75,000/mcL - Hemoglobin - Group I: greater than or equal to 8 gm/dL; - Group II: if anemia attributed to KS, KSHV-MCD, or KICS greater than or equal to 7gm/dL, otherwise greater than or equal to 8 gm/dL - Total bilirubin less than or equal to1.5 upper limit of normal unless the patient is receiving a protease inhibitor known to be associated with increased bilirubin (e.g. atazanavir), in which case total bilirubin less than or equal to 7.5 mg/dL with direct fraction less than or equal to 0.7 - AST(SGOT)/ALT(SGPT) less than or equal to 2.5 X institutional upper limit of normal - Creatinine within normal institutional limits OR Creatinine clearance >60 mL/min/1.73 m(2) as estimated by either Cockroft-Gault or 24-hour urine collection for patients with creatinine levels above institutional normal - Cardiac ejection fraction greater than or equal to 50% by echocardiogram - Patients with a cumulative lifetime history of anthracycline greater than 430 mg/m(2) are eligible, after consultation with a cardiologist, if there are none of the following cardiac risk factors: - Diabetes mellitus - History of acute coronary syndrome - Hypertension; defined as a sustained systolic blood pressure greater than 140 mmHg and/or diastolic blood pressure greater than 90 mmHg OR use of an antihypertensive medication for the indication of hypertension. - All study participants must agree to be registered into the mandatory POMALYST REMS program, and be willing and able to comply with the requirements of the POMALYST REMS program - Females of reproductive potential must adhere to the scheduled pregnancy testing as required in the POMALYST REMSTM program - Able to take aspirin 81mg daily or if intolerant of aspirin, able to take a substitute thromboprophylaxis such as low molecular weight heparin at a thromboprophylactic dose (such as enoxaparin 0.5mg/kg once daily) - Because pomalidomide is an agent with the potential for teratogenic or abortifacient effects, females of childbearing potential (FCBP) must have a negative serum or urine pregnancy test with a sensitivity of at least 25 mIU/mL within 14 days prior to and again within 24 hours before starting pomalidomide and must either commit to continued abstinence from heterosexual intercourse or begin TWO acceptable methods of birth control, one highly effective method and one additional effective method AT THE SAME TIME, at least 28 days before she starts taking pomalidomide. FCBP must also agree to ongoing pregnancy testing. Men must agree to use a latex condom during sexual contact with a FCBP even if they have had a vasectomy. All subjects must be counseled at a minimum of every 28 days about pregnancy precautions and risks of fetal exposure. - Ability of subject to understand and the willingness to sign a written informed consent document. EXCLUSION CRITERIA: - Patients who are receiving any other investigational agents. - Patients with primary effusion lymphoma or other concurrent malignancy, except for basal cell carcinoma or squamous carcinoma of the skin or in situ cervical or anal dysplasia - History of malignant tumors other than KS or KSHV-MCD, unless: - In complete remission for greater than or equal to 1 year for the time complete remission was first documented - Resected basal cell or squamous cell carcinoma of the skin - In situ cervical or anal dysplasia - Uncontrolled intercurrent illness including, but not limited to, uncontrolled active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements - History of allergic reactions attributed to thalidomide, lenalidomide, or other compounds of similar chemical or biologic composition to pomalidomide or other agents used in study - Because there is an unknown but potential risk for adverse events in nursing infants secondary to treatment of the mother with pomalidomide, breastfeeding should be discontinued if the mother is treated with pomalidomide. These potential risks may also apply to other agents used in this study.
Gender All
Ages 18 Years - 99 Years
Accepts Healthy Volunteers No
Contacts †† Anaida Widell, (301) 451-3694, awidell@cc.nih.gov
Location Countries † United States
Administrative Information
NCT ID † NCT02659930
Organization ID 160047
Secondary IDs †† 16-C-0047
Responsible Party Sponsor
Study Sponsor † National Cancer Institute (NCI)
Collaborators ††
Investigators † Principal Investigator: Thomas S Uldrick, M.D., National Cancer Institute (NCI)
Information Provided By
Verification Date April 11, 2017
First Received Date † January 20, 2016
Last Updated Date May 31, 2017
† Required WHO trial registration data element.
†† WHO trial registration data element that is required only if it exists.
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