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Unexpected toxicity
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A phase II trial to compare the efficacy and safety of nivolumab and intermediate dose cytarabine with or without haploidentical lymphocyte infusion. To identify the role of haploidentical lymphocytes in the treatment of acute myeloid leukemia in older adults. The patients will be stratified based on the remission number (first or second)
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Ara-C+HaploLymphocyte+Nivo | Experimental | Patients treated with nivolumab, intermediate dose cytarabine and haploidentical lymphocyte infusion: [Cytarabine 500-1000 mg/m2 bid D-4, -3, -2 + G-CSF mobilized HLA-haploidentical donor peripheral blood stem cells infusion D0 + Nivolumab 40 mg D+5] Ñ… 2-3 cycles |
|
| Ara-C+ Nivo | Experimental | Patients treated with nivolumab and intermediate dose cytarabine: [Cytarabine 500-1000 mg/m2 bid D+1, +2, +3 + Nivolumab 40 mg D+1] Ñ… 2-3 cycles |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Cytarabine | Drug | Cytarabine 500-1000 mg/m2 bid IV infusion on D-4, -3, -2 |
|
| Measure | Description | Time Frame |
|---|---|---|
| Disease-free survival | DFS will be assessed with Kaplan-Meier method from the date of last remission before randomization until the date of relapse or the date of death | 2 years |
| Measure | Description | Time Frame |
|---|---|---|
| Overall survival | OS will be assessed with Kaplan-Meier method from the date of last remission before randomization until the date of death from any cause | 2 years |
| Incidence of graft-versus-host disease |
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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Boris V Afanasyev, MD, Prof. | Saint Petersburg | 197089 | Russia |
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| ID | Term |
|---|---|
| D015470 | Leukemia, Myeloid, Acute |
| ID | Term |
|---|---|
| D007951 | Leukemia, Myeloid |
| D007938 | Leukemia |
| D009370 | Neoplasms by Histologic Type |
| D009369 | Neoplasms |
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| ID | Term |
|---|---|
| D003561 | Cytarabine |
| D000077594 | Nivolumab |
| ID | Term |
|---|---|
| D003562 | Cytidine |
| D011741 | Pyrimidine Nucleosides |
| D011743 | Pyrimidines |
| D006573 | Heterocyclic Compounds, 1-Ring |
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| Nivolumab | Drug | Nivolumab 40 mg IV infusion on D+5 |
|
|
| Cytarabine | Drug | Cytarabine 500-1000 mg/m2 bid IV infusion on D+1, +2, +3 |
|
|
| Nivolumab | Drug | Nivolumab 40 mg IV infusion on D+1 |
|
|
| G-CSF mobilized HLA-haploidentical donor PBSC | Biological | G-CSF mobilized HLA-haploidentical donor peripheral blood stem cells IV infusion on D0 |
|
Incidence of acute GVHD, grades I-IV
| up to 12 months |
| Treatment-related adverse events as assessed by CTCAE v4.03 | Toxicity parameters based on NCI CTCAE 4.03 grades: hematological toxicity (CBC), hepatotoxicity (liver function tests), nephrotoxicity (creatinine), neurotoxicity (attending physician assessment), fatigue (attending physician assessment), rash (attending physician assessment), colitis (attending physician assessment), pneumonitis (attending physician assessment), autoimmune disorders (level of hormones, presence of autoimmune antibodies, attending physician assessment). | up to 12 months |
| D006402 |
| Hematologic Diseases |
| D006425 | Hemic and Lymphatic Diseases |
| D006571 |
| Heterocyclic Compounds |
| D001087 | Arabinonucleosides |
| D009705 | Nucleosides |
| D009706 | Nucleic Acids, Nucleotides, and Nucleosides |
| D061067 | Antibodies, Monoclonal, Humanized |
| D000911 | Antibodies, Monoclonal |
| D000906 | Antibodies |
| D007136 | Immunoglobulins |
| D007162 | Immunoproteins |
| D001798 | Blood Proteins |
| D011506 | Proteins |
| D000602 | Amino Acids, Peptides, and Proteins |
| D012712 | Serum Globulins |
| D005916 | Globulins |