Pomalidomide and Nivolumab in People With Virus-Associated Malignancies With or Without HIV

A Phase I Study of Pomalidomide and Nivolumab in Patients With Virus-Associated Malignancies With or Without HIV

Background:

Less toxic and more effective treatments are needed for cancers caused by viruses. These cancers include Hodgkin and non-Hodgkin lymphoma, hepatocellular carcinoma, head and neck cancer, nasopharyngeal carcinoma, gastric cancer, anal cancer, cervical cancer, vaginal cancer, vulvar cancer, penile cancer, Merkel cell carcinoma, Kaposi sarcoma, and leiomyosarcoma. Researchers want to see if a combination of drugs can help.

Objective:

To find a safe dose of pomalidomide plus nivolumab in people with cancers caused by viruses.

Eligibility:

Adults ages 18 or older who have cancers caused by Epstein Barr virus (EBV), human herpes virus 8/Kaposi sarcoma herpesvirus (HHV8/KSHV), human papilloma virus (HPV), hepatitis B or C virus (HBV/HCV), and Merkel cell polyomavirus (MCPyV) that have not responded to previous treatments or have relapsed, or in adults who do not want to have surgery because of disfigurement or other risks. Adults who have HIV with any CD4 T cell count are eligible.

Design:

Participants will be screened with blood and urine tests, scans, and heart tests. They will have a physical exam. Their ability to perform normal daily activities will be assessed. They may have a tumor biopsy.

Treatment will be given in 28-day cycles. Participants will take pomalidomide as a tablet by mouth for 21 days of each cycle, for up to 24 cycles. They will get nivolumab by intravenous infusion once each cycle. They will take an aspirin each day until 30 days after their last dose of the study drugs.

Participants will keep a pill diary. They will bring it to their study visit at the end of each cycle. At these visits, some screening tests will be repeated. Participants with Kaposi sarcoma will have pictures taken of their lesions.

Participants will give blood and saliva samples for research. They may have optional anal and/or cervical swabs. They may have optional biopsies.

Participants will have a follow-up visit 30 days after they stop taking the study drugs, then every month for 100 days. Some screening tests will be repeated. Then they may by contacted by phone every 3 months for 9 months, and then every 6 months thereafter....

Study Overview

• Status: Recruiting
• Conditions: Kaposi Sarcoma; Viral Associated Malignancies; EBV/KSHV-associated Lymphomas
• Intervention / Treatment: Drug: Pomalidomide; Drug: Nivolumab

Detailed Description

Background:

• There is an unmet need for less toxic and more effective treatments for virus-associated malignancies.
• Pomalidomide induces polyfunctional T cell, NK cell, and dendritic cell activation.
• Pomalidomide has shown promising activity in Kaposi sarcoma, likely due in part to immune modulation.
• Downregulation and/or deregulation of immune surface markers by viruses can thwart immunologic therapy, which may be prevented or reversed by pomalidomide.
• PD-L1 is expressed in virus-associated malignancies and modulation of PD-1 signaling is a promising approach to treatment of virus-associated malignancies.
• Checkpoint inhibitors used alone have been shown to have some activity in certain virus-induced tumors (e.g. Hodgkin and non-Hodgkin lymphomas, Merkel cell carcinoma, and HPV-associated nasopharyngeal cancer). It is thus rational to explore combination strategies that overcome viral-mediated immune evasion and provide potentially better immunologic anti-tumor activity.

Objectives:

-Assess the safety and tolerability of pomalidomide plus nivolumab (Pom/Nivo) in participants with virus-associated solid malignancies

Eligibility:

• Age greater than or equal to 18 years
• Histologically or cytologically proven selected virus-associated tumors that are systemic, metastatic or locally advanced and not amenable to curative treatment options or relapsed/refractory to first-line therapy
• For solid tumors or hematologic malignancies at least one measurable disease
• At least five measurable cutaneous KS lesions with no previous local radiation, surgical or intralesional cytotoxic therapy to these measurable lesions.
• ECOG Performance Status (PS) less than or equal to 2
• Participants must be willing to give informed consent.
• Participants can be HIV positive or negative.
• Antiretroviral therapy (ART) for HIV+ patients
• Participants receiving other investigational agents will not be eligible.

Design:

• This is a Phase I study assessing the safety and efficacy of a fixed dose of nivolumab combined with increasing doses of pomalidomide in participants with viral associated malignancies.
• Up to 6 participants treated in a 3+3 dose de-escalation schema for pomalidomide using one dose de-escalation and one dose escalation levels.
• Following identification of an optimal dose, an expansion phase will be initiated through a protocol amendment. Up to 30 participants will be enrolled. Of these 12 participants must have a KS diagnosis and 12 participants must have EBV and/or KSHV-associated lymphomas.
• Nivolumab will be administered IV at a dose of 480 mg at day one of each cycle, except for cycle one when it will be administered on day 8. One cycle equals 28 days.
• Pomalidomide will be administered as an oral planned starting dose of 3 mg daily. Pomalidomide will be given from day 1 to day 21 of each cycle.
• Participants will receive therapy up to 24 cycles or until unacceptable toxicity, clinical progression, the participant s request to discontinue therapy, or PI decision.

• Study Type: Interventional
• Enrollment (Estimated): 54
• Phase: Phase 1

Contacts and Locations

• Study Contact: Name: Kathryn A Lurain, M.D.; Phone Number: (301) 250-5156; Email: kathryn.lurain@nih.gov
• Study Contact Backup: Name: Irene Ekwede, R.N.; Phone Number: (240) 760-6126; Email: irene.ekwede@nih.gov

Study Locations

• United States
  • Maryland
    • Bethesda, Maryland, United States, 20892
      • Recruiting
      • National Institutes of Health Clinical Center
      • Contact: For more information at the NIH Clinical Center contact National Cancer Institute Referral Office; Phone Number: 888-624-1937

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No

Description

• INCLUSION CRITERIA:
• Histologically or cytologically proven selected virus-associated tumors that are systemic, metastatic or locally advanced and not amenable to curative treatment options or are relapsed/refractory to first-line therapy as appropriate for each tumor type as outlined below. Also, participants with eligible solid tumors, who after evaluation by an expert in the area are deemed to be potentially curable after extensive surgery, but refuse such surgical procedure due to associated disfigurement and/or morbidity, may be eligible for the study with the necessary informed consent. Pathology confirmation by NCI Laboratory of Pathology is needed for eligibility.

The following tumor types listed below are eligible, and require assessing of virus infection of the tumor cells with EBV EBER by in situ hybridization (ISH), KSHV LANA , p16, and Merkel cell polyomavirus large T antigen by immunohistochemistry (IHC) to document the respective viral infection (EBV, KSHV, HPV, MCPvY) (116-119); or detection of serum HBV surface antigen, anti-HBV core antibody, elevated HBV DNA viral load, positive HVC antibody or elevated HCV RNA viral load. The tumor types studied in the phase 1 trial will be as below. For tumors where >95% are known to be virus-associated, such as cervical cancer, confirmation of virus status is not required.

--EBV-positive Hodgkin lymphoma meeting the following criteria:

• Relapsed or refractory de novo classical Hodgkin lymphoma having failed standard first-line therapy; and
• Unresponsive or progressive disease after treatment with brentuximab vedotin or may be brentuximab vedotin na(SqrRoot) ve but is ineligible or unable to receive brentuximab vedotin; and
• Unresponsive or progressive disease after checkpoint inhibitor therapy;

and

• Unresponsive or progressive disease after or is ineligible for autologous stem cell transplant (auto-SCT)

  --EBV-positive aggressive non-Hodgkin lymphomas (except primary CNS lymphoma and Burkitt lymphoma) meeting the following criteria:

• Relapsed/refractory disease after standard first-line chemotherapy; and
• Relapsed disease after autologous stem cell transplant if indicated for histology (i.e diffuse large B-cell lymphoma) or autologous stem cell transplant is not feasible; and

• Relapsed after CAR-T cell therapy for HIV-negative participants only if indicated for histology (i.e diffuse large B-cell lymphoma) or CAR-T cell therapy is not feasible

  • EBV-positive nasopharyngeal cancer unresponsive or progressive disease on or after platinum-containing chemotherapy and/or radiotherapy
  • EBV-positive gastric cancer that is unresponsive or progressive disease on or after first-line chemotherapy
  • EBV-positive leiomyosarcomas that is unresponsive or progressive disease on or after 2 systemic regimens (CCRT/platinum-taxane)
  • Kaposi sarcoma impairing physical wellbeing (for example, tumor edema, pain, skin ulceration or breakdown, oral disease impairing function), no active KSHV- associated multicentric Castleman disease in past 12 months, and one or more of the following:
• Inadequate tumor response after 6 or more cycles of liposomal doxorubicin or paclitaxel or other active cytotoxic agents (i.e. etoposide, bleomycin, anthracyclines, vincristine, vinblastine); or
• Progressive disease while receiving liposomal doxorubicin or paclitaxel or other active cytotoxic agents (i.e. etoposide, bleomycin, anthracyclines, vincristine, vinblastine); or

• Intolerant of liposomal doxorubicin and paclitaxel

  • Primary effusion lymphoma unresponsive or progressive disease on or after first- line combination chemotherapy
  • HPV-positive head and neck cancer that is unresponsive or progressive on or after first-line combination chemotherapy +/- radiotherapy
  • HPV-positive cervical cancer that is unresponsive or progressive on at least one systemic regimen for recurrent (does not include initial CCRT) or metastatic disease. Tumor HPV testing will not be a requirement for study eligibility for cervical cancer.
  • HPV-positive anal cancer that is unresponsive or progressive on or after first-line combination chemotherapy +/- radiotherapy
  • HPV-positive vaginal cancer that is unresponsive or progressive on or after first- line chemotherapy
  • HPV-positive penile cancer that is unresponsive or progressive on or after surgery and first-line chemotherapy
  • HPV-positive vulvar cancer that is unresponsive or progressive on or after first- line combination chemotherapy
  • MCPyV-positive Merkel cell carcinomas that is relapsed or refractory after prior checkpoint inhibitor therapy

  • HBV- or HCV-associated hepatocellular carcinoma that is not amenable to local therapy or liver transplant and has progressed on first-line therapy with sorafenib or levatinib or atezolizumab+bevacizumab

    • For solid tumors, participants must have measurable disease, defined as at least one lesion that can be accurately measured in at least one dimension (longest diameter to be recorded for non-nodal lesions and short axis for nodal lesions) as greater than or equal to 20 mm (greater than or equal to 2 cm) by chest x-ray or as greater than or equal to 10 mm (greater than or equal to 1 cm) with CT scan, MRI, or calipers by clinical exam.
    • For hematologic malignancies, participants must have measurable disease, defined as at least one lesion that can be accurately measured in at least one dimension (lymph nodes must measure greater than or equal to 15 mm in the short axis and extranodal lesions must measure greater than or equal to 10 mm in the short axis with CT scan. For primary effusion lymphoma, body cavity effusions may be followed as measurable disease by CT scan.
    • For KS, participants must have measurable disease, defined as 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.
    • Prior immunomodulatory therapy and checkpoint inhibitor therapy is allowed if previously tolerated without severe toxicities. Participants may not have received chemotherapy, radiotherapy, monoclonal antibody therapy, or targeted therapy within 2 weeks.
    • Age greater than or equal to 18 years. Because no dosing or adverse event data are currently available on the use of pomalidomide in combination with nivolumab in participants <18 years of age, children are excluded from this study.
    • ECOG performance status less than or equal to 2 (Karnofsky greater than or equal to 60%.
    • Participants must have adequate organ and marrow function as defined below:
  • leukocytes no lower limit
  • absolute neutrophil count greater than or equal to 1,000/mcL

  • platelets greater than or equal to 75,000/mcL

    • total bilirubin less than or equal to institutional upper limit of normal (ULN), except for participants with Gilbert disease or in whom the elevated bilirubinemia is due to ART (must be grade less than or equal to 2)
    • AST(SGOT)/ALT(SGPT) less than or equal to 3x institutional ULN

  • glomerular filtration rate (GFR) >=30 mL/min/1.73 m2

    -Participants with any HIV status are eligible; for HIV-positive participants:

  • Must be on antiretroviral therapy (ART) > 4 weeks and with evidence of viral suppression defined as HIV viral load < 400 copies/mL
  • Must have no major (e.g. AIDS-defining) opportunistic infections within the last 6 months except for the following which will be allowed:
  • Esophageal candidiasis treated within last 6 months or currently improving with antifungal treatment

  • Oral and/or genital HSV treated within last 6 months or currently improving with antiviral treatment

    • Mycobacterium avium infection in last 6 months or that has been treated for at least 1 month
    • For participants with evidence of chronic hepatitis B virus (HBV) infection, participants must be on suppressive therapy.
    • Participantatients with a history of hepatitis C virus (HCV) infection must have been treated and cured. For participants with HCV infection who are currently on treatment, they are eligible if they have an undetectable HCV viral load.
    • Able to take aspirin 81mg daily or a substitute thromboprophylaxis such as low molecular weight heparin at a prophylactic dose.
    • Participants with treated brain metastases are eligible if follow-up brain imaging after central nervous system (CNS)-directed therapy shows no evidence of progression.
    • Participants with new or progressive brain metastases (active brain metastases) or leptomeningeal disease are eligible if the treating physician determines that immediate CNS specific treatment is not required and is unlikely to be required during the first cycle of therapy.
    • Participants with a prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy assessment of the investigational regimen are eligible for this trial, such as carcinoma in situ or low-grade prostate carcinoma.
    • Participants may not have cardiac or pulmonary abnormalities severe enough that they would pose a danger to receive treatment. To mitigate risks for cardiac AEs, screening EKG, echocardiogram, CPK, and troponin will be required and significant abnormalities as determined by the PI will need to be evaluated by Cardiology prior to enrollment. Participants with pulmonary symptoms will be required to undergo pulmonary function testing and Pulmonary evaluation at the discretion of the PI prior to enrollment.
    • Current or history of systemic autoimmune disease requiring systemic immunosuppressive therapy will not be allowed. Note: the following will not be exclusionary: 1) the presence of laboratory evidence of autoimmune disease (e.g. positive antinuclear antibody titer or lupus anticoagulant) without associated symptoms; 2) clinical evidence of vitiligo or other forms of depigmenting illness; 3) mild

autoimmunity not impacting the function of major organs (e.g. controlled Hashimoto thyroiditis, limited psoriasis)

• Persons of childbearing potential (PCBP, defined as a sexually mature person assigned female at birth who: 1) has not undergone a hysterectomy or bilateral oophorectomy; or 2) has not been naturally postmenopausal for at least 24 consecutive months, i.e., has had menses at any time in the preceding 24 consecutive months) must have a negative serum or urine pregnancy test with a sensitivity of at least 25 mIU/mL within 10-14 days prior to and again within 24 hours of starting pomalidomide and must either commit to continued abstinence from receptive vaginal 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. PCBP must also agree to ongoing pregnancy testing. Persons assigned male at birth must agree to use a latex condom during penetrative vaginal intercourse with a PCBP even if they have had a vasectomy. All participants must be counseled at a minimum of every 28 days about pregnancy precautions and risks of fetal exposure.
• Ability to understand and the willingness to sign a written informed consent document.

EXCLUSION CRITERIA:

• Participants who have had anticancer treatment within the last 2 weeks, unless the cancer treatment is for a malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy assessment of the investigational regimen are eligible for this trial, such as local treatment for carcinoma in situ or hormonal therapy for prostate or breast carcinoma.

• Participants who have not recovered from adverse events due to prior anti-cancer therapy (i.e., have residual toxicities > Grade 1) with the following exceptions:

  • Elevated triglyceride attributed to ART and/or HIV (must be less than or equal to Grade 2)
  • Laboratory or clinical abnormalities that are assessed as more likely to be from the underlying tumors, HIV disease, or other non-treatment causes will not be considered an exclusion criterion.
  • Alopecia, neuropathy and ototoxicity (i.e., AEs that are not expected to improve within the washout period)
  • Participants who are receiving any other investigational agents.
• Participants will be excluded if they are on systemic steroid therapy that cannot be discontinued, with the exception of the use of prednisone or equivalent <0.125mg/kg/day as replacement therapy. Inhaled or topical steroids are permitted.
• History of allergic reactions attributed to pomalidomide and/or nivolumab or compounds of similar chemical or biologic composition to pomalidomide and/or nivolumab.
• Participants who have received prior allogeneic stem cell or organ transplant.
• Participants with severe uncontrolled intercurrent illness.
• Cirrhosis with Child-Pugh score of B or C
• Participants with psychiatric illness/social situations that would limit compliance with study requirements.
• Pregnant and nursing persons are excluded from this study because pomalidomide is a thalidomide analog. Thalidomide is a known human teratogen that causes severe birth defects or embryo-fetal death. These potential risks may also apply to nivolumab based on its mechanism of action and data from animal studies. In animal reproduction studies, administration of nivolumab to cynomolgus monkeys from the onset of organogenesis through delivery resulted in increased abortion and premature infant death.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Non-Randomized
• Interventional Model: Sequential Assignment
• Masking: None (Open Label)

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: 1/Dose De-Escalation; Treatment with pomalidomide at de-escalating doses if necessary and nivolumab at a fixed dose	Drug: Pomalidomide; Pomalidomide will be administered as an oral planned starting dose of 3 mg daily. Pomalidomide will be given from day 1 to day 21 of each cycle; Drug: Nivolumab; Nivolumab will be administered IV at a dose of 480 mg at day one of each cycle, except for cycle one when it will be administered on day 8. One cycle equals 28 days
Experimental: 2/Dose Expansion; Nivolumab + pomalidomide (at optimal dose determined in dose escalation portion of the study) for up to 30 participants	Drug: Pomalidomide; Pomalidomide will be administered as an oral planned starting dose of 3 mg daily. Pomalidomide will be given from day 1 to day 21 of each cycle; Drug: Nivolumab; Nivolumab will be administered IV at a dose of 480 mg at day one of each cycle, except for cycle one when it will be administered on day 8. One cycle equals 28 days

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Safety and tolerability of pomalidomide with nivolumab	The fraction of patients with toxicity noted at each dose level will be reported by grade and type of toxicity identified. Maximum tolerated dose will also be reported.	24 months of treatment, until confirmed progression, unacceptable toxicity or trial withdrawal

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
anti-tumor activity and clinical benefits	To observe and record the anti-tumor activity (RECIST 1.1, Lugano criteria or other appropriate tumor associated response criteria including modified ACTG criteria for KS) and clinical benefit in participants with Kaposi sarcoma and other virus-associated malignancies treated with Pom/Nivo	Every month (+/-1week) for 100 days after stopping treatment; then every 3 months (+/-2 weeks) for 1 year following end-of-treatment; then every 6 months

Collaborators and Investigators

• Sponsor: National Cancer Institute (NCI)
• Investigators: Principal Investigator: Kathryn A Lurain, M.D., National Cancer Institute (NCI)

Publications and helpful links

Helpful Links

• NIH Clinical Center Detailed Web Page

Study record dates

Study Major Dates

• Study Start (Actual): December 10, 2021
• Primary Completion (Estimated): December 1, 2025
• Study Completion (Estimated): December 1, 2026

Study Registration Dates

• First Submitted: May 25, 2021
• First Submitted That Met QC Criteria: May 25, 2021
• First Posted (Actual): May 26, 2021

Study Record Updates

• Last Update Posted (Actual): March 26, 2024
• Last Update Submitted That Met QC Criteria: March 23, 2024
• Last Verified: March 22, 2024

More Information

Terms related to this study

• Keywords: AIDS; PD-L1; Immune Therapy; Small Molecule Inhibitor
• Additional Relevant MeSH Terms: Virus Diseases; Infections; Neoplasms, Connective and Soft Tissue; Neoplasms by Histologic Type; DNA Virus Infections; Herpesviridae Infections; Sarcoma; Neoplasms, Vascular Tissue; Neoplasms; Sarcoma, Kaposi; Physiological Effects of Drugs; Molecular Mechanisms of Pharmacological Action; Antineoplastic Agents; Immunologic Factors; Antineoplastic Agents, Immunological; Angiogenesis Inhibitors; Angiogenesis Modulating Agents; Growth Substances; Growth Inhibitors; Immune Checkpoint Inhibitors; Pomalidomide; Nivolumab
• Other Study ID Numbers: 210023; 21-C-0023

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: YES
• IPD Plan Description: .All IPD recorded in the medical record will be shared with intramural investigators upon request.
• IPD Sharing Time Frame: Clinical data available during the study and indefinitely.
• IPD Sharing Access Criteria: Clinical data will be made available via subscription to BTRIS and with the permission of the study PI. @@@@@@Requests for all collected IPD data from clinical trials, conducted under a binding collaborative agreement between NCI/DCTD and a pharmaceutical/biotechnology company, that are not under DSMB monitoring must be in compliance with the terms of the binding collaborative agreement and must be approved by NCI/DCTD and the Pharmaceutical Collaborator (i.e., the NCI ETCTN Director in conjunction with the NCI/DCTD Regulatory Affairs Branch)
• IPD Sharing Supporting Information Type: STUDY_PROTOCOL; SAP; ICF

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: Yes
• Studies a U.S. FDA-regulated device product: No