Azacitidine Plus Nivolumab Following Reduced-intensity Allogeneic PBSC Transplantation for Patients With AML and High-risk Myelodysplasia

Aml Clinical Trial

Official title:

Phase I Trial of Azacitidine Plus Nivolumab Following Reduced-intensity Allogeneic PBSC Transplantation for Patients With AML and High-risk Myelodysplasia Big Ten Cancer Research Consortium BTCRC-AML18-342

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT04128020
• Other study ID #: BTCRC-AML18-342
• Status: Withdrawn
• Phase: Phase 1
• Start date: October 10, 2019
• Est. completion date: September 28, 2020

Study information

• Verified date: October 2020
• Source: Big Ten Cancer Research Consortium
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a phase I clinical trial that will define the maximum tolerated dose (MTD) and investigate the feasibility and safety of the combination of nivolumab and azacitidine after reduced-intensity allogeneic PBSC transplantation. Dose escalation will follow a traditional 3+3 design. The investigators will first escalate the dose of single agent nivolumab to determine its MTD (if any, at the doses tested), with an expanded cohort at the MTD or highest dose tested. The investigators will then combine escalating azacitidine in combination of with nivolumab at its determined MTD or highest dose tested in earlier cohorts, and expand the highest dose cohort tested with the combination. Patients will be treated according to the dose level cohorts described in the protocol.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: September 28, 2020
• Est. primary completion date: September 28, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Written informed consent and HIPAA authorization for release of personal health information. NOTE: HIPAA authorization may be included in the informed consent or obtained separately. Patients must be capable of understanding the investigational nature, potential risks and benefits of the study and provide valid informed consent.

• Age = 60 years at the time of consent who are deemed candidates (by their transplant physician) for reduced-intensity allogeneic PBSC transplantation. A recent randomized trial in patients aged 18-65 years demonstrated that myeloablative conditioning regimens are associated with improved overall survival in AML (largely due to a reduction in the risk of relapse), but resulted in equivalent survival in patients with MDS.4 However, it is acknowledged that some AML patients between 55-65 years may not tolerate myeloablative regimens due to associated comorbidities. Physicians should take the risks of the disease versus the patient's comorbidities in deciding on the appropriate preparative regimen in a given patient.

• Patients aged 18-59 years at the time of consent who are judged not to be candidates for myeloablative allogeneic PBSC transplantation by the transplant physician.

• Karnofsky performance status (KPS) = 70%

• Patients must have any of the following hematological malignancies at the time of transplantation:

• Acute myeloid leukemia (AML) in first (CR1) or subsequent complete remission (CR2, CR3 or beyond), as defined by less than 5% blasts in the bone marrow and peripheral blood.

• Myelodysplastic disorder (MDS) of high or very high-risk according to the revised International Prognostic Scoring System (IPSS-R).1

• Patients with MDS should have the bone marrow and the peripheral blood blast percentage reduced to <10% within at least 45 days of transplantation.

• The type of cytoreduction therapy used is at the discretion of the treating physician and may include use of hypomethylating drugs but not immune checkpoint inhibitors.

• Therapy-related MDS (regardless of IPSS score)

• Patients must receive a reduced-intensity conditioning (RIC) regimen as defined operationally by the National Marrow Donor Program and CIBMTR. RIC regimens are defined as those containing:

• = 500 cGy total-body irradiation (TBI)

• =9 mg/kg total busulfan dose (PO or IV)

• =140 mg/m2 total melphalan dose

• =10 mg/kg total thiotepa dose

• Usually includes a purine analogue (fludarabine, cladribine, or pentostatin).

• Use of fludarabine and cyclophosphamide (up to 200 mg/kg total dose) is also considered RIC.99

• Patients must have received GVHD prophylaxis with any of the regimens below. Accepted regimens are:

• Calcineurin inhibitor (tacrolimus or cyclosporine A) plus methotrexate

• Calcineurin inhibitor plus mycophenolate mofetil

• Calcineurin inhibitor plus sirolimus

• Post-transplant cyclophosphamide (PtCy) (in combination with calcineurin inhibitor or sirolimus, plus mycophenolate mofetil)

• Patients receiving the above regimens should be beginning to taper immunosuppression drugs between days +100 to +120 (in the absence of acute GVHD) with the goal of discontinuing immunosuppression by approximately day +180 as tolerated and according to institutional standards.

• Stem cell source must be mobilized peripheral blood (i.e., PBSC) and not bone marrow or cord blood.

• Allogeneic grafts from 6/6 HLA-matched siblings or from 10/10 HLA allele matched volunteer unrelated donors (matched for at least HLA-A, B, C and DRB1 and DQB1 by high resolution typing) are included.

• Are in complete remission defined as having <5% blasts in the bone marrow with normal karyotype and no extramedullary disease. This should be documented on a bone marrow biopsy performed within 14 days before study registration.

• Absolute neutrophil count (ANC) >1.5x109/l

• Platelet count >100x109/l (with no platelet transfusions in past 7 days)

• Serum creatinine <2.0 mg/dl

• Serum bilirubin < 2 x upper limit of normal

• AST and ALT <2.5 x upper limit of normal

• Non-pregnant and non-nursing.

• Women are considered of childbearing potential (WOCBP) unless they are surgically sterile (have undergone a hysterectomy, bilateral tubal ligation, or bilateral oophorectomy) or are post-menopausal. Menopause is defined clinically as 12 months of amenorrhea in a woman over 45 in the absence of other biological or physiological causes.

• Women of childbearing potential must be willing to abstain from heterosexual activity or use an effective method of contraception from the time of informed consent until 5 months after the last dose of study drug.

• Men who are sexually active with WOCBP must use any contraceptive method with a failure rate of less than 1% per year. Men receiving study drug and who are sexually active with WOCBP will be instructed to adhere to contraception from the first dose of study drug until 7 months after the last dose of study drug.

Exclusion Criteria:

• Use of a myeloablative preparative regimen

• Active central nervous system (CNS) leukemia. Patients with prior CNS leukemia that is now in remission are eligible.

• Prior allogeneic or autologous stem cell transplantation before current transplant

• Use of bone marrow or cord blood as stem cell source

• History of acute GvHD of any grade

• Use of systemic corticosteroids within 28 days prior to registration (except for use as replacement for adrenal insufficiency).

• Uncontrolled bacterial, viral or fungal infection at time of registration (defined as currently taking medication and progression or persistence of clinical symptoms). Patients with prior infection (e.g., fungal infection) that is resolved but need continuing prophylaxis can be included.

• HIV infection or disease at time of transplant. Patients with immune dysfunction are at a significantly higher risk of infection from intensive immunosuppressive therapies. Infectious disease testing will be performed according to local practice.

• Known additional malignancy that is active and/or progressive requiring treatment; exceptions include basal cell or squamous cell skin cancer, in situ cervical or bladder cancer, or other cancer for which the subject has been disease-free for at least three (3) years.

• Patients who have received a live/attenuated vaccine within 30 days of first expected treatment with nivolumab. However, it is recommended that patients who have received an allogeneic transplant should not receive live/attenuated vaccines within two years after allogeneic transplantation.

Related Conditions & MeSH terms

• Aml
• AML, Adult
• Myelodysplastic Syndromes
• Preleukemia

Intervention

Drug:
• Nivolumab
Nivolumab
• Azacitidine
Azacitidine

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Sherif Farag

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Maximum Tolerated Dose (MTD) of nivolumab	Maximum Tolerated Dose (MTD) of nivolumab	1 cycle (42 Days)
Primary	Maximum Tolerated Dose (MTD) of nivolumab and azacitidine	Maximum Tolerated Dose (MTD) of nivolumab and azacitidine	1 cycle (42 Days)
Secondary	Number of Subjects with Adverse Events	Describe grade 3 and 4 hematological and non-hematological toxicity associated with treatment with azacitidine and nivolumab maintenance treatment after allogeneic PBSC transplantation	2 years
Secondary	Incidence and severity of acute graft-versus-host disease (GvHD)	The overall cumulative incidence of acute GvHD (grades 2-4 and grades 3-4), with disease relapse or death from any cause other than GvHD as competing risks, will be described separately for those who receive post-transplant-treatment (at least one dose of either or both drugs), and for those treated at the MTD for nivolumab (Part A) and the combination of nivolumab and azacitidine (Part B) (i.e., including the 12 patients treated in each of the expansion cohorts).	5 years
Secondary	Incidence and severity of chronic GvHD	The cumulative incidence of chronic GvHD (mild, moderate, and severe as defined in Section 10.2.2.), with disease relapse or death from any cause other than GvHD as competing risks, will be described separately for those who receive post-transplant-treatment (at least one dose of either or both drugs), and for those treated at the MTD for nivolumab (Part A) and the combination of nivolumab and azacitidine (Part B) (i.e., including the 12 patients treated in each of the expansion cohorts).	5 years
Secondary	Incidence of infectious complications	The incidence and severity of infectious complications will be described for patients who receive at least one dose of either or both drugs. Summary data including the type of infections and severity occurring in each dose cohort will be tabulated and presented.	5 years
Secondary	Cumulative incidence of relapse	The cumulative incidence of relapse will be derived from calculations of the time from the date of transplantation to the date of confirmed relapse with those dying from causes other than relapse/progression of disease as a competing risk, and right censoring for patients alive and without relapse. The cumulative incidence of relapse will be described separately for those who receive at least one dose of either or both drugs, and for those treated at the MTD for nivolumab (Part A) and the combination of nivolumab and azacitidine (Part B) (i.e., including the 12 patients treated in each of the expansion cohorts).	5 years
Secondary	Cumulative incidence of non-relapse mortality	he cumulative incidence of non-relapse mortality will be derived from calculations of the time from the date of transplantation to the date of death from any cause other than disease relapse or progression, with relapse a competing risk, and right censoring for patients alive and without relapse. The cumulative incidence of non-relapse mortality will be described separately for those who receive at least one dose of either or both drugs, and for those treated at the MTD for nivolumab (Part A) and the combination of nivolumab and azacitidine (Part B) (i.e., including the 12 patients treated in each of the expansion cohorts).	5 years
Secondary	1 year Overall Survival (OS)	1-year and overall leukemia-free survival (LFS) will be calculated from the date of transplantation until the time of death from any cause or relapse of underlying disease using the Kaplan-Meier method. LFS will be described separately for those who receive at least one dose of either or both drugs, and for those treated at the MTD for nivolumab (Part A) and the combination of nivolumab and azacitidine (Part B) (i.e., including the 12 patients treated in each of the expansion cohorts).	1 year
Secondary	Overall Survival	Overall survival (OS) will be calculated from the date of transplantation until the time of death from any cause using the Kaplan-Meier method. OS will be described separately for those who receive at least one dose of either or both drugs, and for those treated at the MTD for nivolumab (Part A) and the combination of nivolumab and azacitidine (Part B) (i.e., including the 12 patients treated in each of the expansion cohorts).	5 years
Secondary	Leukemia-Free Survival	1-year and overall leukemia-free survival (LFS) will be calculated from the date of transplantation until the time of death from any cause or relapse of underlying disease using the Kaplan-Meier method. LFS will be described separately for those who receive at least one dose of either or both drugs, and for those treated at the MTD for nivolumab (Part A) and the combination of nivolumab and azacitidine (Part B) (i.e., including the 12 patients treated in each of the expansion cohorts).	1 year