TTI-622 and TTI-621 in Combination With Pembrolizumab for the Treatment of Relapsed or Refractory Diffuse Large B-Cell Lymphoma
Study Details
Study Description
Brief Summary
This phase II trial tests the safety, side effects, and best dose of TTI-621 or TTI-622 in combination with pembrolizumab in treating patients with diffuse large B-Cell lymphoma that has come back (relapsed). TTI-621 and TTI-622 are called fusion proteins. A fusion protein includes two specialized proteins that are joined together. In TTI-621 and TTI-622, one of the proteins binds with other proteins found on the surface of certain cells that are part of the immune system. The other protein targets and blocks a protein called CD47. CD47 is present on cancer cells and is used by those cells to hide from the body's immune system. By blocking CD47, TTI-621 and TTI-622 may help the immune system find and destroy cancer cells. Pembrolizumab is a monoclonal antibody directed against human cell surface receptor PD-1 (programmed death-1 or programmed cell death-1) that works by helping the body's immune system attack the cancer and may interfere with the ability of cancer cells to grow and spread. Giving TTI-621 or TTI-622 in combination with pembrolizumab may kill more cancer cells in patients with relapsed or refractory diffuse large B-cell lymphoma.
Detailed Description
PRIMARY OBJECTIVES:
- To determine the toxicities of ontorpacept (TTI-621) or SIRPa-IgG4-Fc Fusion Protein TTI-622 (TTI-622) combined with pembrolizumab and to identify the recommended Phase 2 dose (RP2D) of TTI-621 and TTI-622, each combined with pembrolizumab. (Safety run in) II. To estimate preliminary efficacy of pembrolizumab in combination with TTI-621 (Arm A) or TTI-622 (Arm B) as measured by overall response rate (ORR). (Phase II).
SECONDARY OBJECTIVE:
- To estimate efficacy of pembrolizumab in combination with TTI-621 or TTI-622 as measured by duration of response (DOR), progression free survival (PFS), and overall survival (OS).
CORRELATIVE OBJECTIVE:
- Correlation of biomarkers measured in serial peripheral blood samples and tumor tissues with clinical responses, which may include but are not limited to: SIRPalpha expression, monocyte/macrophage markers in tumor micro-environment, tumor infiltrating lymphocytes (TILs), PD-1/PDL-1 expression.
OUTLINE: Patients are assigned to 1 of 2 arms.
ARM A: Patients receive pembrolizumab intravenously (IV) over 30 minutes on day 1 of each cycle and TTI-621 IV over 60-120 minutes on day 1 of each cycle. Treatment repeats every 21 days for up to 12 cycles in the absence of disease progression or unacceptable toxicity. Patients also undergo positron emission tomography/computed tomography (PET/CT) scans or CT scans of the chest, abdomen, and pelvis prior to cycle 3 and every 4 cycles thereafter. If no disease progression after cycle 12, patients then receive pembrolizumab IV over 30 minutes on days 1 of each cycle and TTI-621 IV over 60-120 minutes on day 1 of each cycle. Treatment repeats every 21 days for up to 23 cycles in the absence of disease progression or unacceptable toxicity.
ARM B: Patients receive pembrolizumab IV over 30 minutes on day 1 of each cycle and TTI-622 IV over 60-90 minutes on day 1 of each cycle. Treatment repeats every 21 days for up to 12 cycles in the absence of disease progression or unacceptable toxicity. Patients also undergo PET/CT scans or CT scans of the chest, abdomen, and pelvis prior to cycle 3 and every 4 cycles thereafter. If no disease progression after cycle 12, patients then receive pembrolizumab IV over 30 minutes on days 1 of each cycle and TTI-622 IV over 60-90 minutes on day 1 of each cycle. Treatment repeats every 21 days for up to 23 cycles in the absence of disease progression or unacceptable toxicity.
After completion of the study treatment, patients are followed every 6 months for up to 2 years from registration.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Arm A (pembrolizumab, TTI-621) Patients receive pembrolizumab IV over 30 minutes on day 1 of each cycle and TTI-621 IV over 60-120 minutes on day 1 of each cycle. Treatment repeats every 21 days for up to 12 cycles in the absence of disease progression or unacceptable toxicity. Patients also undergo PET/CT scans or CT scans of the chest, abdomen, and pelvis prior to cycle 3 and every 4 cycles thereafter. If no disease progression after cycle 12, patients then receive pembrolizumab IV over 30 minutes on days 1 of each cycle and TTI-621 IV over 60-120 minutes on day 1 of each cycle. Treatment repeats every 21 days for up to 23 cycles in the absence of disease progression or unacceptable toxicity. |
Procedure: Biospecimen Collection
Undergo correlative studies
Other Names:
Procedure: Computed Tomography
Undergo PET/CT or CT scans of the chest, abdomen, and pelvis
Other Names:
Drug: Ontorpacept
Given IV
Other Names:
Biological: Pembrolizumab
Given IV
Other Names:
Procedure: Positron Emission Tomography
Undergo PET/CT scans
Other Names:
|
| Experimental: Arm B (pembrolizumab, TTI-622) Patients receive pembrolizumab IV over 30 minutes on day 1 of each cycle and TTI-622 IV over 60-90 minutes on day 1 of each cycle. Treatment repeats every 21 days for up to 12 cycles in the absence of disease progression or unacceptable toxicity. Patients also undergo PET/CT scans or CT scans of the chest, abdomen, and pelvis prior to cycle 3 and every 4 cycles thereafter. If no disease progression after cycle 12, patients then receive pembrolizumab IV over 30 minutes on days 1 of each cycle and TTI-622 IV over 60-90 minutes on day 1 of each cycle. Treatment repeats every 21 days for up to 23 cycles in the absence of disease progression or unacceptable toxicity. |
Procedure: Biospecimen Collection
Undergo correlative studies
Other Names:
Procedure: Computed Tomography
Undergo PET/CT or CT scans of the chest, abdomen, and pelvis
Other Names:
Biological: Pembrolizumab
Given IV
Other Names:
Procedure: Positron Emission Tomography
Undergo PET/CT scans
Other Names:
Drug: SIRPa-IgG4-Fc Fusion Protein TTI-622
Given IV
Other Names:
|
Outcome Measures
Primary Outcome Measures
- Recommended phase 2 dose of TTI-621 and TTI-622 when given in combination with pembrolizumab (Safety run-in) [Up to 6 weeks]
Defined as the highest dose for which at most 1 out of 6 subjects experience significant toxicity during the 6-week safety assessment period. Toxicity will be measured per National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE) version 5. Significant toxicity is defined as an adverse event occurring during the first cycle of treatment that is possibly, probably, or definitely related to study treatment.
- Overall response (Phase 2) [Up to 2 years]
A success is defined as an objective status of partial metabolic response (PMR) or complete metabolic response (CMR) by positron emission tomography-computed tomography (PET-CT) based criteria at any time. The proportion of successes will be estimated by the number of successes divided by the total number of evaluable patients. 95% confidence intervals for the true success proportion will be calculated according to the approach of Duffy and Santner (1987). Note: For patients where PET/CT scan was not available due to insurance coverage and who received a CT scan only, they will still be considered evaluable for the primary endpoint and will be included in the denominator for estimating overall response rate. In these patients, the CT-based responses will be reported descriptively.
Secondary Outcome Measures
- Duration of response (DOR) (Phase 2) [Up to 2 years]
Defined for all evaluable patients who have achieved an objective response as the date at which the patient's objective status is first noted to be either a CMR or PMR to first documentation of disease progression. DOR will be descriptively summarized.
- Progression-free survival (PFS) (Phase 2) [Time from registration to first documentation of disease progression (progressive metabolic disease [PMD] or progressive disease [PD]) or death due to any cause in the absence of documented progression, assessed up to 2 years]
For patients who receive subsequent treatment before disease progression, the patient will be censored at their last disease assessment. The distribution of PFS will be estimated using the method of Kaplan-Meier (1958). Median and landmark estimates along with two-sided 95% confidence intervals will be reported.
- Overall survival (OS) (Phase 2) [Time from registration to death due to any cause, assessed up to 2 years]
Patients still alive by the analysis cutoff will be censored at their last date known to be alive. The distribution of OS will be estimated using the method of Kaplan-Meier. Median and landmark estimates along with two-sided 95% confidence intervals will be reported.
- Incidence of adverse events (AEs) (Phase 2) [Up to 2 years]
All eligible patients that have initiated treatment will be considered evaluable for assessing AE rate(s). The maximum grade for each type of AE will be recorded for each patient, and frequency tables will be reviewed to determine patterns. Additionally, the relationship of the AE(s) to the study treatment will be taken into consideration.
Eligibility Criteria
Criteria
Inclusion Criteria:
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Age >= 18 years
-
Documented CD20+ mature B-cell neoplasm according to World Health Organization (WHO) classification (Swerdlow et al., 2016) as one of the following:
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Diffuse large B-cell lymphoma not otherwise specified (NOS) including
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Transformed lymphoma
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Richter's transformation
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Germinal center B-cell type
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Activated B-cell type
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High-grade B-cell lymphoma (HGBCL), NOS
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Primary mediastinal (thymic) large B-cell lymphoma
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Patients with "double-hit" or "triple-hit" diffuse large B-cell lymphoma (DLBCL) (technically as HGBCL, with MYC and BCL2 and/or BCL6 rearrangements)
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Follicular lymphoma 3B
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T-cell/histiocyte-rich large B cell lymphoma
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Large B-cell lymphoma with IRF4 rearrangement
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Primary cutaneous DLBCL, leg type
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Epstein-Barr virus (EBV) positive DLBCL, NOS
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DLBCL associated with chronic inflammation
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Intravascular large B-cell lymphoma
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ALK positive large B-cell lymphoma
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Relapsed, progressive and/or refractory disease (Cheson et al., 2007) following treatment with an anti-CD20 monoclonal antibody (e.g., rituximab) in combination with chemotherapy
-
Measurable disease as defined below:
-
Fluorodeoxyglucose (FDG)-avid lymphomas: Measurable disease with computerized tomography (CT) (or magnetic resonance imaging [MRI]) scan with involvement of 2 or more clearly demarcated lesions/nodes with a long axis > 1.5 cm and short axis
1.0 cm (or 1 clearly demarcated lesion/node with a long axis > 2.0 cm and short axis >= 1.0 cm) AND FDG positron emission tomography (PET) scan that demonstrates positive lesion(s) compatible with CT (or MRI) defined anatomical tumor sites
-
FDG-nonavid lymphomas: Measurable disease with CT (or MRI) scan with involvement of 2 or more clearly demarcated lesions/nodes with a long axis > 1.5 cm and short axis > 1.0 cm or 1 clearly demarcated lesion/node with a long axis > 2.0 cm and short axis >= 1.0 cm.
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Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) 0 or 1
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= 4 weeks from last dose of anti-CD20 targeting therapy
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= 12 weeks post chimeric antigen receptor (CAR) T-cell therapy
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Resolution of all adverse events due to prior therapy to =< Grade 1 or baseline NOTE: Patients with =< Grade 2 neuropathy may be eligible. Patients with endocrine-related adverse events (AEs) Grade =< 2 requiring treatment or hormone replacement may be eligible
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If receiving glucocorticoid treatment at screening, treatment must be tapered down and administered with a maximum of 10 mg daily in the last 14 days prior to registration
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Absolute neutrophil count (ANC) >= 500/mm^3; growth factor support allowed in case of bone marrow involvement (obtained =< 7 days prior to registration)
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Absolute lymphocyte count >= 200/mm^3 (obtained =< 7 days prior to registration)
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Platelet count >= 75,000/mm^3 (obtained =< 7 days prior to registration)
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Hemoglobin >= 8.0 g/dL (obtained =< 7 days prior to registration)
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International normalized ratio (INR) or partial thromboplastin time (PTT)/activated partial thromboplastin time (aPTT) =< 1.5 × upper limit of normal (ULN) unless participant is receiving anticoagulant therapy as long as prothrombin time (PT) or PTT is within therapeutic range of intended use of anticoagulants (obtained =< 7 days prior to registration)
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Total bilirubin =< 1.5 x upper limit of normal (ULN), unless due to Gilbert's disease (direct bilirubin [bili] =< ULN) (obtained =< 7 days prior to registration)
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Aspartate transaminase (AST/serum glutamic oxaloacetic transaminase [SGOT]) and alanine transaminase (ALT/serum glutamic pyruvic transaminase [SGPT]) =< 2.5 x ULN (obtained =< 7 days prior to registration)
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Calculated creatinine clearance >=30 mL/min using the Cockcroft-Gault formula (obtained =< 7 days prior to registration)
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Provide informed written consent
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Negative pregnancy test done =< 3 days prior to registration, for persons of childbearing potential only
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Female of childbearing must agree to use a highly effective method of contraception during the treatment and for 120 days after the last dose of study treatment
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Male participants with female partners of childbearing potential must agree to refrain from donating sperm and one of the conception methods during the treatment and for 120 days after last dose study treatment
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Willing to return to the enrolling institution for follow-up (during the active monitoring phase of the study)
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Willing to provide mandatory tissue and blood samples for correlative research purposes
Exclusion Criteria:
-
Primary central nervous system (CNS) lymphoma or known CNS involvement by lymphoma at screening as confirmed by magnetic resonance imaging (MRI)/computed tomography (CT) scan (brain) and, if clinically indicated, by lumbar puncture
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Known past or current malignancy other than inclusion diagnosis, except for:
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Cervical carcinoma of Stage 1B or less
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Non-invasive basal cell or squamous cell skin carcinoma
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Non-invasive, superficial bladder cancer
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Prostate cancer with a current prostate specific antigen (PSA) level < 0.1 ng/mL
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Any curable cancer with a complete response (CR) of > 2 years duration
-
Received < 2 prior systemic anti-cancer therapy including investigational agents =< 4 weeks or =< 5 half-lives, whichever is shorter, prior to registration
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Received prior therapy with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent or with an agent directed to another stimulatory or co-inhibitory T-cell receptor (e.g., CTLA-4, OX-40, CD137) =< 4 weeks prior to registration
-
Known clinically significant cardiac disease, including:
-
Onset of unstable angina pectoris within 6 months of signing informed consent form (ICF)
-
Acute myocardial infarction within 6 months of signing ICF
-
Congestive heart failure (grade III or IV as classified by the New York Heart Association and/or known decrease ejection fraction of < 45%)
-
Chronic ongoing infectious diseases (except hepatitis B or hepatitis C) requiring treatment (excluding prophylactic treatment) at the time of enrollment or =< the previous 2 weeks
-
Confirmed history or current autoimmune disease or other diseases resulting in permanent immunosuppression or requiring permanent immunosuppressive therapy or primary immunodeficiency disorder. Low-dose steroids (=< 10 mg daily of prednisone equivalent) is allowed
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Seizure disorder requiring therapy (such as steroids or anti-epileptics)
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Autologous hematopoietic stem cell transplant (HSCT) =< 100 days prior or any prior allogeneic HSCT or solid organ transplantation
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Known human immunodeficiency virus (HIV) infection
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Exposed to live or live attenuated vaccine =< 4 weeks prior to registration
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Any of the following because this study involves an investigational agent whose genotoxic, mutagenic and teratogenic effects on the developing fetus and newborn are unknown:
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Pregnant persons
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Nursing persons
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Persons of childbearing potential who are unwilling to employ adequate contraception
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Patient has any condition for which, in the opinion of the investigator, participation would not be in the best interest of the patient (e.g., compromise the well-being) or that could prevent, limit, or confound the protocol-specified assessments
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Co-morbid systemic illnesses or other severe concurrent disease which, in the judgment of the investigator, would make the patient inappropriate for entry into this study or interfere significantly with the proper assessment of safety and toxicity of the prescribed regimens
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Uncontrolled intercurrent illness including, but not limited to:
-
ongoing or active infection
-
uncontrolled infection requiring ongoing antibiotics
-
symptomatic congestive heart failure
-
unstable angina pectoris
-
cardiac arrhythmia
-
or psychiatric illness/social situations that would limit compliance with study requirements
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known substance abuse disorder
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Known hypersensitivity to pembrolizumab
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Major surgery other than diagnostic surgery =< 4 weeks prior to registration
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Prior radiation therapy =< 2 weeks prior to registration or who has not recovered from all radiation-related toxicities, not require corticosteroids, and not have had radiation pneumonitis. Note: A 1-week washout is permitted for palliative radiation (=< 2 weeks of radiotherapy) to non-CNS disease
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Active autoimmune disease such as Crohn's disease, rheumatoid arthritis, Sjogren's disease, systemic lupus erythematosus, or similar conditions requiring systemic treatment =< the past 3 months or a documented history of clinically severe autoimmune disease/syndrome difficult to control in the past.
EXCEPTIONS:
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Vitiligo or resolved childhood asthma/atopy
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Intermittent use of bronchodilators or local steroid injections
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Hypothyroidism stable on hormone replacement,
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Diabetes stable with current management
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History of positive Coombs test but no evidence of hemolysis
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Psoriasis not requiring systemic treatment
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Conditions not expected to recur in the absence of an external trigger
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Has a known history of hepatitis B (defined as hepatitis B surface antigen [HBsAg] reactive) or known active hepatitis C virus (HCV) (defined as HCV ribonucleic acid [RNA] is detected) infection
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Prior anti CD47 therapy
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Active use of anticoagulant like warfarin. Use of low molecular weight heparin and factor Xa inhibitors will be permitted on case by case basis. There will be no restriction for daily aspirin < 81mg daily
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Mayo Clinic in Rochester | Rochester | Minnesota | United States | 55905 |
Sponsors and Collaborators
- Mayo Clinic
- National Cancer Institute (NCI)
Investigators
- Principal Investigator: Stephen M Ansell, Mayo Clinic in Rochester
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- MC200802
- NCI-2022-06277
- MC200802
- P30CA015083