This study is NOT currently recruiting participants.
Number
17-C-0149
Sponsoring Institute
National Cancer Institute (NCI)
Recruitment Detail
Type: No longer recruiting/follow-up only Gender: Male & Female Min Age: 18 Years Max Age: N/A
Referral Letter Required
No
Population Exclusion(s)
Pregnant Women;Children;Fetuses
Keywords
Monoclonal Antibody; PD-1 Receptor
Recruitment Keyword(s)
None
Condition(s)
Non-Hodgkin Lymphoma; Lymphoma; Diffuse Large B-Cell Lymphoma; gray-zone lymphoma; primary central nervous system lymphoma
Investigational Drug(s)
Investigational Device(s)
Intervention(s)
Biological/Vaccine: Pembrolizumab
Supporting Site
National Cancer Institute
B-cell lymphoma is a cancer of white blood cells that are found in lymph nodes. Some kinds of these cancers, such as gray-zone and extra-nodal, are rare and often aggressive. They are usually resistant to current treatments. Researchers want to see if a drug called pembrolizumab may treat these types of lymphoma.
Objective:
To collect data to see if it may be effective to give pembrolizumab to people with certain types of rare, aggressive B-cell lymphomas.
Eligibility:
People ages 18 and older who have a B-cell lymphoma, including gray-zone lymphoma or extra-nodal lymphoma
Design:
Participants will be screened with:
Medical history
Physical exam
Blood and urine tests
Scans. They will lie in a machine that takes images.
A tissue sample from a previous procedure will be tested.
The study will be done in 21-day cycles. During the study, participants:
Will repeat the screening tests.
Will get the study drug as an infusion into a vein over about 30 minutes.
Will have a cheek swab and/or saliva sample collected.
May have a bone marrow aspiration. A needle will be put into the hipbone, and a small amount of bone marrow will be taken out.
May have a lumbar puncture. If cerebrospinal fluid is collected, researchers will study it.
May have an eye exam.
May provide tissue samples.
May have tumor samples taken.
Participants will have a visit about 30 days after the last dose of the study drug. They will then have 4 visits in year 1, 2 visits a year in years 2-5, and once each year thereafter. They will also be contacted by phone.
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INCLUSION CRITERIA: -Patients must have a diagnosis of B-cell lymphoma confirmed by Laboratory of Pathology, NCI, that is relapsed from or refractory to prior therapy as follows: --Cohort 1: B-cell lymphoma, unclassifiable, with features intermediate between diffuse large B-cell lymphoma and classical Hodgkin lymphoma (i.e., Gray-zone lymphoma or GZL) --Cohort 2: Extranodal diffuse large B-cell lymphoma involving one or more of the specified extranodal sites (i.e., extranodal DLBCL). The following subtypes are included (they do not have to be confirmed as non-GCB subtype for study entry): ---Primary CNS lymphoma (PCNSL) ---Primary testicular lymphoma (PTL) ---Primary breast lymphoma (PBL) ---Primary cutaneous DLBCL, leg-type ---Intravascular large B-cell lymphoma (IVBCL) ---Diffuse large B-cell, NOS, activated B-cell type, involving 1 or more extranodal site NOTE: For GZL, diagnosis will be in accordance with the 2016 World Health Organization classification of lymphoid malignancies. Patients diagnosed with other extranodal DLBCL subtypes or that are not otherwise specified (NOS) must involved at least 1 extranodal site and must be considered non-GCB by local immunohistochemistry algorithms. Cases that are non-GCB by the Hans criteria are considered eligible as well as cases of DLBCL that are both CD10+ and MUM1+. -Evaluable disease by clinical exam (i.e., palpable lymphadenopathy, measurable skin lesions, etc.), laboratory assessment (i.e., lymphoma involvement of bone marrow or peripheral blood by morphology, cytology or flow cytometry), and/or imaging (measurable lymph nodes or masses on CT or MRI and/or evaluable FDG-avid lesions on PET) - Adequate tumor tissue (archival or fresh) must be available for correlative studies. NOTE: Tumor tissue may be from any previously collected tissue and adequacy is at the discretion of the Principal Investigator. If prior tissue is not available, patient must be willing to undergo baseline tumor biopsy. - Be 18 years of age or older on day of signing informed consent - Adequate performance status (PS) as follows: --Patients greater than or equal to 18 years must have ECOG 0-1 (and Karnofsky greater than or equal to 60%) NOTE: Patients greater than or equal to 18 years with an ECOG PS of 2 and Karnofsky greater than or equal to 60 will be considered eligible at the discretion of the Principal Investigator if decreased ECOG performance status is felt to be related to residual neurologic deficits caused by CNS disease involvement that are not progressive or anticipated to cause clinical managemnt problems during study participation. - Adequate organ function as evidenced by the following laboratory parameters (unless related to lymphoma infiltration at the discretion of the investigator): --Absolute neutrophil count (ANC) greater than or equal to 750 /mcL --Platelets greater than or equal to 50,000 / mcL (transfusions not permitted) --Hemoglobin greater than or equal to 9 g/dL (transfusions permitted) --Serum creatinine: Adults: less than or equal to 1.5 times upper limit of normal (ULN). Children: age greater than or equal to 14: less than or equal to 1.5 mg/dL OR Measured or calculated creatinine clearance (GFR can also be used in place of creatinine or CrCl): Greater than or equal to 30 mL/min/1.73 m(2) for subject with creatinine levels > 1.5 times institutional ULN (CrCl should be calculated per institutional standard) --Serum total bilirubin less than or equal to 1.5 times ULN OR Direct bilirubin less than or equal to ULN for patients with total bilirubin levels > 1.5 ULN --AST (SGOT) and ALT (SGPT) less than or equal to 3 times ULN (less than or equal to 5 X ULN if liver involvement) - The effects of pembrolizumab on the developing human fetus are unknown. For this reason, the following measures apply: --Women of childbearing potential must have a negative serum or urine pregnancy test within 72 hours prior to the first dose of pembrolizumab. --Men and women of childbearing potential (WOCBP) who are sexually active must agree to adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry, for the duration of study participation, and for at least 120 days after the last dose of pembrolizumab. Should a woman become pregnant or suspect she is pregnant while she or her partner is participating in this study, she should inform her treating physician immediately. --Participants must not be planning to conceive or father children within the projected duration of the trial, starting with the pre-screening/screening visit through 120 days after the last dose of pembrolizumab. --WOCBP is defined as any female who has experienced menarche and who has not undergone successful surgical sterilization or who is not postmenopausal. - Ability of patient or Legally Authorized Representative (LAR) to understand and the willingness to sign a written informed consent document EXCLUSION CRITERIA: - Patients with DLBCL who best fit the criteria of EBV+ DLBCL, NOS are not eligible -Current or prior anti-cancer treatment prior to the first dose of pembrolizumab as defined below: --Chemotherapy, targeted small molecule therapy, or other anti-cancer treatment not otherwise specified below within 2 weeks --Radiation therapy within 2 weeks --Anti-cancer monoclonal antibody (mAb) treatment within 4 weeks --Use of an investigational agent (e.g., biologic, drug, or other) within 4 weeks --Allogeneic stem cell transplant within 100 days --Prior therapy with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent at any time -No current use of systemic corticosteroids at physiologic doses > 10 mg/day of dexamethasone or equivalent are permitted. Patients receiving current systemic steroids must be on a stable steroid dose (i.e., less than or equal to 10 mg/day of dexamethasone or equivalent at the same dose for at least 7 days). Patients who recently discontinued systemic steroids must have completed them at least 7 days prior to entry. -Uncontrolled intercurrent illness including, but not limited to the following that may limit interpretation of results or that could increase risk to the patient at the discretion of the investigator: --Active autoimmune disease that has required systemic treatment in the past 2 years (i.e., with use of disease modifying agents, corticosteroids or immunosuppressive drugs). NOTE: Replacement therapy (e.g., thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a form of systemic treatment. --History of (non-infectious) pneumonitis that required steroids, evidence of interstitial lung disease or active, non-infectious pneumonitis. -Clinically significant history of liver disease, including viral or other hepatitis, current alcohol abuse, or cirrhosis; as well as active infection with HBV or HCV: ---Patients with occult or prior HBV infection (defined as positive total hepatitis B core antibody [HBcAb] and negative HBsAg) may be included if HBV DNA is undetectable. --Uncontrolled and/or symptomatic thyroid disease --Active graft-vs-host disease (GVHD) requiring treatment or any history of greater than or equal to grade II acute GVHD --Seizure activity within the past 4 weeks --Known mental or physical illness that would interfere with cooperation with the requirements of the trial or confound the results or interpretation of the results of the trial and, in the opinion of the treating investigator, would make the patient inappropriate for entry into the study. - Because there is an unknown but potential risk for adverse events in nursing infants secondary to treatment of the mother with pembrolizumab, breastfeeding must be discontinued if the mother is treated with pembrolizumab - Received a live vaccine within 30 days of planned start of study therapy. NOTE: Seasonal influenza vaccines for injection are generally inactivated flu vaccines and are allowed; however intranasal influenza vaccines (e.g., Flu-Mist ) are live attenuated vaccines, and are not allowed. -History of allergic reactions attributed to compounds of similar chemical or biologic composition to pembrolizumab unless felt to be in the best interests of the patient in the opinion of the investigator - Known additional malignancy that requires active systemic treatment
-Patients must have a diagnosis of B-cell lymphoma confirmed by Laboratory of Pathology, NCI, that is relapsed from or refractory to prior therapy as follows:
--Cohort 1: B-cell lymphoma, unclassifiable, with features intermediate between diffuse large B-cell lymphoma and classical Hodgkin lymphoma (i.e., Gray-zone lymphoma or GZL)
--Cohort 2: Extranodal diffuse large B-cell lymphoma involving one or more of the specified extranodal sites (i.e., extranodal DLBCL). The following subtypes are included (they do not have to be confirmed as non-GCB subtype for study entry):
---Primary CNS lymphoma (PCNSL)
---Primary testicular lymphoma (PTL)
---Primary breast lymphoma (PBL)
---Primary cutaneous DLBCL, leg-type
---Intravascular large B-cell lymphoma (IVBCL)
---Diffuse large B-cell, NOS, activated B-cell type, involving 1 or more extranodal site
NOTE: For GZL, diagnosis will be in accordance with the 2016 World Health Organization classification of lymphoid malignancies. Patients diagnosed with other extranodal DLBCL subtypes or that are not otherwise specified (NOS) must involved at least 1 extranodal site and must be considered non-GCB by local immunohistochemistry algorithms. Cases that are non-GCB by the Hans criteria are considered eligible as well as cases of DLBCL that are both CD10+ and MUM1+.
-Evaluable disease by clinical exam (i.e., palpable lymphadenopathy, measurable skin lesions, etc.), laboratory assessment (i.e., lymphoma involvement of bone marrow or peripheral blood by morphology, cytology or flow cytometry), and/or imaging (measurable lymph nodes or masses on CT or MRI and/or evaluable FDG-avid lesions on PET)
- Adequate tumor tissue (archival or fresh) must be available for correlative studies. NOTE: Tumor tissue may be from any previously collected tissue and adequacy is at the discretion of the Principal Investigator. If prior tissue is not available, patient must be willing to undergo baseline tumor biopsy.
- Be 18 years of age or older on day of signing informed consent
- Adequate performance status (PS) as follows:
--Patients greater than or equal to 18 years must have ECOG 0-1 (and Karnofsky greater than or equal to 60%)
NOTE: Patients greater than or equal to 18 years with an ECOG PS of 2 and Karnofsky greater than or equal to 60 will be considered eligible at the discretion of the Principal Investigator if decreased ECOG performance status is felt to be related to residual neurologic deficits caused by CNS disease involvement that are not progressive or anticipated to cause clinical managemnt problems during study participation.
- Adequate organ function as evidenced by the following laboratory parameters (unless related to lymphoma infiltration at the discretion of the investigator):
--Absolute neutrophil count (ANC) greater than or equal to 750 /mcL
--Platelets greater than or equal to 50,000 / mcL (transfusions not permitted)
--Hemoglobin greater than or equal to 9 g/dL (transfusions permitted)
--Serum creatinine: Adults: less than or equal to 1.5 times upper limit of normal (ULN). Children: age greater than or equal to 14: less than or equal to 1.5 mg/dL OR Measured or calculated creatinine clearance (GFR can also be used in place of creatinine or CrCl):
Greater than or equal to 30 mL/min/1.73 m(2) for subject with creatinine levels > 1.5 times institutional ULN (CrCl should be calculated per institutional standard)
--Serum total bilirubin less than or equal to 1.5 times ULN
OR
Direct bilirubin less than or equal to ULN for patients with total bilirubin levels > 1.5 ULN
--AST (SGOT) and ALT (SGPT) less than or equal to 3 times ULN (less than or equal to 5 X ULN if liver involvement)
- The effects of pembrolizumab on the developing human fetus are unknown. For this reason, the following measures apply:
--Women of childbearing potential must have a negative serum or urine pregnancy test within 72 hours prior to the first dose of pembrolizumab.
--Men and women of childbearing potential (WOCBP) who are sexually active must agree to adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry, for the duration of study participation, and for at least 120 days after the last dose of pembrolizumab. Should a woman become pregnant or suspect she is pregnant while she or her partner is participating in this study, she should inform her treating physician immediately.
--Participants must not be planning to conceive or father children within the projected duration of the trial, starting with the pre-screening/screening visit through 120 days after the last dose of pembrolizumab.
--WOCBP is defined as any female who has experienced menarche and who has not undergone successful surgical sterilization or who is not postmenopausal.
- Ability of patient or Legally Authorized Representative (LAR) to understand and the willingness to sign a written informed consent document
EXCLUSION CRITERIA:
- Patients with DLBCL who best fit the criteria of EBV+ DLBCL, NOS are not eligible
-Current or prior anti-cancer treatment prior to the first dose of pembrolizumab as defined below:
--Chemotherapy, targeted small molecule therapy, or other anti-cancer treatment not otherwise specified below within 2 weeks
--Radiation therapy within 2 weeks
--Anti-cancer monoclonal antibody (mAb) treatment within 4 weeks
--Use of an investigational agent (e.g., biologic, drug, or other) within 4 weeks
--Allogeneic stem cell transplant within 100 days
--Prior therapy with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent at any time
-No current use of systemic corticosteroids at physiologic doses > 10 mg/day of dexamethasone or equivalent are permitted. Patients receiving current systemic steroids must be on a stable steroid dose (i.e., less than or equal to 10 mg/day of dexamethasone or equivalent at the same dose for at least 7 days). Patients who recently discontinued systemic steroids must have completed them at least 7 days prior to entry.
-Uncontrolled intercurrent illness including, but not limited to the following that may limit interpretation of results or that could increase risk to the patient at the discretion of the investigator:
--Active autoimmune disease that has required systemic treatment in the past 2 years (i.e., with use of disease modifying agents, corticosteroids or immunosuppressive drugs). NOTE: Replacement therapy (e.g., thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a form of systemic treatment.
--History of (non-infectious) pneumonitis that required steroids, evidence of interstitial lung disease or active, non-infectious pneumonitis.
-Clinically significant history of liver disease, including viral or other hepatitis, current alcohol abuse, or cirrhosis; as well as active infection with HBV or HCV:
---Patients with occult or prior HBV infection (defined as positive total hepatitis B core antibody [HBcAb] and negative HBsAg) may be included if HBV DNA is undetectable.
--Uncontrolled and/or symptomatic thyroid disease
--Active graft-vs-host disease (GVHD) requiring treatment or any history of greater than or equal to grade II acute GVHD
--Seizure activity within the past 4 weeks
--Known mental or physical illness that would interfere with cooperation with the requirements of the trial or confound the results or interpretation of the results of the trial and, in the opinion of the treating investigator, would make the patient inappropriate for entry into the study.
- Because there is an unknown but potential risk for adverse events in nursing infants secondary to treatment of the mother with pembrolizumab, breastfeeding must be discontinued if the mother is treated with pembrolizumab
- Received a live vaccine within 30 days of planned start of study therapy. NOTE: Seasonal influenza vaccines for injection are generally inactivated flu vaccines and are allowed; however intranasal influenza vaccines (e.g., Flu-Mist ) are live attenuated vaccines, and are not allowed.
-History of allergic reactions attributed to compounds of similar chemical or biologic composition to pembrolizumab unless felt to be in the best interests of the patient in the opinion of the investigator
- Known additional malignancy that requires active systemic treatment
Principal Investigator
Referral Contact
For more information: