Poly-ICLC (Hiltonol®) Vaccine In Malignant Pleural Mesothelioma
NCT ID: NCT04525859
Last Updated: 2025-06-24
Study Results
Results pending
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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Recruitment Status
COMPLETED
Clinical Phase
PHASE1
Total Enrollment
19 participants
Study Classification
INTERVENTIONAL
Study Start Date
2020-08-19
Study Completion Date
2025-06-18
Brief Summary
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This study will examine the safety and potential effectiveness of poly-ICLC directly injected into malignant pleural mesothelioma at the time of biopsy up to 21 days prior to the cancer being removed by the surgeon
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Detailed Description
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* To evaluate the safety and toxicity of IT Poly-ICLC, Hiltonol® prior to surgical resection for patients with MPM.
* To determine objective response rate by RECIST 1.1 using CT imaging.
* To determine recurrence free survival of subjects treated with IT Poly-ICLC followed by surgical resection defined as the time of injection until the first date that recurrent disease is confirmed or date of documented death.
* To evaluate IT Poly-ICLC induced immune changes in the tumor microenvironment by comparing pre-injection biopsy to surgically resected tissue for immune cell infiltration and T cell receptor (TCR) diversity.
* To characterize additional immune parameters in IT Poly-ICLC injected tumors including in-depth phenotypic and functional characterization of immune infiltrating cells.
* To evaluate IT Poly-ICLC induced serological changes and changes of circulating immune cells, including regulatory T cells and NK cells, by comparing pre-injection to post-surgical resection blood samples.
* To determine objective response rate by RECIST 1.1 using CT imaging.
* To determine recurrence free survival of subjects treated with IT Poly-ICLC followed by surgical resection defined as the time of injection until the first date that recurrent disease is confirmed or date of documented death.
* To evaluate IT Poly-ICLC induced immune changes in the tumor microenvironment by comparing pre-injection biopsy to surgically resected tissue for immune cell infiltration and T cell receptor (TCR) diversity.
* To characterize additional immune parameters in IT Poly-ICLC injected tumors including in-depth phenotypic and functional characterization of immune infiltrating cells.
* To evaluate IT Poly-ICLC induced serological changes and changes of circulating immune cells, including regulatory T cells and NK cells, by comparing pre-injection to post-surgical resection blood samples.
Conditions
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Malignant Pleural Mesothelioma
Study Design
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Allocation Method
NON_RANDOMIZED
Intervention Model
PARALLEL
Study Subjects will receive poly-ICLC once within the pleural mesothelioma. Up to twenty one days later he/she will undergo surgery per the standard of care by the thoracic surgeon. The type of surgery will be decided upon by the treating thoracic surgeon. Follows up visits are scheduled every three months for the first year and then every 6 months thereafter. CT scans or surveillance scans to look for recurrences will be ordered by the treating surgeon and/or medical oncologist per the standard of care. If there is a need for adjuvant (after surgery) therapy, such as chemotherapy or radiation, this will be discussed with the study subject per the standard of care by the surgeon and/or a medical oncologist or radiation oncologist.
Primary Study Purpose
TREATMENT
Blinding Strategy
NONE
Study Groups
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Safety
Six patients will be enrolled in the Phase 1 safety cohort. Patients will have an IR guided biopsy and FNA. Up to four core biopsies and FNAs at one site will be performed prior to intratumoral (IT) administration of Poly-ICLC. Pleural fluid will be collected for research analysis if available. Poly-ICLC will be injected in 2 locations within the pleura. Patients will undergo surgery 21±7 days after the biopsy and Poly-ICLC intratumoral (IT) injection. The type of surgery that will be performed is at the discretion of the thoracic surgeon and per the standard of care. This includes pleurectomy/decortication or extrapleural pneumonectomy. Patients will be evaluated per the standard of care post-operatively. On day 7±4 days a final toxicity assessment, physical exam and research blood will be collected. All post-operative care and monitoring thereafter is as per standard of care.
Group Type
EXPERIMENTAL
Safety
Intervention Type
BIOLOGICAL
See previous Safety group description
Expansion Cohort
If at most one (1) patient in the Phase 1 safety cohort experiences a DLT then a total of thirteen (13) additional patients will be enrolled into the Phase 1b Expansion Cohort. Patients in the Expansion Cohort will receive the same dose and schedule of Poly-ICLC as in the Phase 1 safety cohort. Patients will be followed for safety and tolerability, as well as efficacy. If a total of 4 or more patients experience DLTs then the study will be closed due to excessive toxicity.
Group Type
EXPERIMENTAL
Expansion Cohort
Intervention Type
BIOLOGICAL
See previous Expansion Cohort
Interventions
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Safety
See previous Safety group description
Intervention Type
BIOLOGICAL
Expansion Cohort
See previous Expansion Cohort
Intervention Type
BIOLOGICAL
Eligibility Criteria
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Inclusion Criteria
1. Biopsy proven MPM
a. If biopsied at an outside institution, must have a tissue block sample available
2. Deemed to be surgically resectable by a dedicated thoracic surgeon.
3. Acceptable hematologic, renal and liver function as follows:
* Absolute neutrophil count \> 1000/mm3
* Platelets \> 50,000/mm3,
* Creatinine ≤ 2.5 mg/dl,
* Total bilirubin ≤ 1.5 mg/dl, unless patient has known Gilberts syndrome
* Transaminases ≤ 2 times above the upper limits of the institutional normal.
* INR\<1.6 if off of anticoagulation. Patients on anticoagulation therapy with an INR\>1.6 may be enrolled at the discretion of the investigator if they have not had any episodes of severe hemorrhage and if the site to be injected is fully surrounded by pleura where achieving homeostasis would be complicated.
4. Patient must be able to provide informed consent
5. Subject is willing to adhere to the study visit schedule and other protocol requirements.
a. If biopsied at an outside institution, must have a tissue block sample available
2. Deemed to be surgically resectable by a dedicated thoracic surgeon.
3. Acceptable hematologic, renal and liver function as follows:
* Absolute neutrophil count \> 1000/mm3
* Platelets \> 50,000/mm3,
* Creatinine ≤ 2.5 mg/dl,
* Total bilirubin ≤ 1.5 mg/dl, unless patient has known Gilberts syndrome
* Transaminases ≤ 2 times above the upper limits of the institutional normal.
* INR\<1.6 if off of anticoagulation. Patients on anticoagulation therapy with an INR\>1.6 may be enrolled at the discretion of the investigator if they have not had any episodes of severe hemorrhage and if the site to be injected is fully surrounded by pleura where achieving homeostasis would be complicated.
4. Patient must be able to provide informed consent
5. Subject is willing to adhere to the study visit schedule and other protocol requirements.
Exclusion Criteria
1. Serious concurrent infection or medical illness, which would jeopardize the ability of the patient to receive Poly-ICLC with reasonable safety.
2. History of any pulmonary process that precludes a biopsy to be done safely.
3. Known severe pulmonary hypertension; having a history of pulmonary hypertension or an estimated PA systolic pressure of \>60mmHg as measured by tricuspid regurgitation on preoperative echocardiogram.
4. Subject unable to cooperate in terms of maintaining position during the biopsy procedure.
5. AIDS defined as a CD4 count less than 200 in the context of HIV seropositivity or chronically is taking immunosuppressive medication such as steroids or transplant related medications.
6. Persistent toxicity from recent therapy that has not sufficiently resolved in the judgment of the study physician.
7. Subject has an active infection requiring therapy.
8. Subject has had an allogeneic tissue/solid organ transplant.
9. Subject has active autoimmune disease that has required systemic treatment within the past 2 years (eg, with use of disease modifying agents, corticosteroids or immunosuppressive drugs). Replacement therapy (eg, thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a form of systemic treatment.
10. Subject has known active Hepatitis B, Hepatitis C or tuberculosis. Active Hepatitis B is defined as a known positive HBsAg result. Active Hepatitis C is defined by a known positive Hep C Ab result and known quantitative HCV ribonucleic acid (RNA) results greater than the lower limits of detection of the assay.
11. Concomitant comorbidities that are uncontrolled that would preclude the patient from being a surgical candidate including uncontrolled CHF, diabetes or heart disease
12. Women with a positive serum or urine pregnancy test at baseline, or are pregnant or breastfeeding.
\-
2. History of any pulmonary process that precludes a biopsy to be done safely.
3. Known severe pulmonary hypertension; having a history of pulmonary hypertension or an estimated PA systolic pressure of \>60mmHg as measured by tricuspid regurgitation on preoperative echocardiogram.
4. Subject unable to cooperate in terms of maintaining position during the biopsy procedure.
5. AIDS defined as a CD4 count less than 200 in the context of HIV seropositivity or chronically is taking immunosuppressive medication such as steroids or transplant related medications.
6. Persistent toxicity from recent therapy that has not sufficiently resolved in the judgment of the study physician.
7. Subject has an active infection requiring therapy.
8. Subject has had an allogeneic tissue/solid organ transplant.
9. Subject has active autoimmune disease that has required systemic treatment within the past 2 years (eg, with use of disease modifying agents, corticosteroids or immunosuppressive drugs). Replacement therapy (eg, thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a form of systemic treatment.
10. Subject has known active Hepatitis B, Hepatitis C or tuberculosis. Active Hepatitis B is defined as a known positive HBsAg result. Active Hepatitis C is defined by a known positive Hep C Ab result and known quantitative HCV ribonucleic acid (RNA) results greater than the lower limits of detection of the assay.
11. Concomitant comorbidities that are uncontrolled that would preclude the patient from being a surgical candidate including uncontrolled CHF, diabetes or heart disease
12. Women with a positive serum or urine pregnancy test at baseline, or are pregnant or breastfeeding.
\-
Eligible Sex
ALL
Accepts Healthy Volunteers
No
Sponsors
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Icahn School of Medicine at Mount Sinai
OTHER
Sponsor Role
collaborator
Oncovir, Inc.
INDUSTRY
Sponsor Role
lead
Responsible Party
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Responsibility Role
SPONSOR
Principal Investigators
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Thomas Marron, MD
Role: STUDY_DIRECTOR
Assistant Director
Locations
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Icahn School of Medicine Mount Sinai
New York, New York, United States
Site Status
Countries
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United States
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Other Identifiers
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GCO#19-2701
Identifier Type: -
Identifier Source: org_study_id
NCT04345705
Identifier Type: -
Identifier Source: nct_alias
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