Nivolumab and Tocilizumab for Relapsed Hematological Malignancy Post-allogeneic Transplant

Lymphoma Clinical Trial

Official title:

Phase 1 Study of Nivolumab in Combination With Tocilizumab for Treatment of Patients With Relapsed Hematological Malignancies Post-allogeneic Transplant

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT03588936
• Other study ID #: PRO32525
• Status: Terminated
• Phase: Phase 1
• Start date: September 14, 2018
• Est. completion date: July 15, 2020

Study information

• Verified date: October 2021
• Source: Medical College of Wisconsin
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a phase 1, interventional single arm, open label, treatment study designed to evaluate the safety combination programmed cell death protein 1 (PD-1) and interleukin 6 (IL-6) inhibition in participants with relapsed disease post-allogeneic transplant.

Description:

Study disease: Hematologic malignancies including, but not exclusive to,acute/chronic leukemia, lymphoma, and myelodysplastic syndrome that has relapsed after allogeneic transplant.

Study Rationale: Phase 1 Safety/Dose Finding Study: To determine the safety and maximum tolerated dose of Nivolumab in combination with Tocilizumab.

Study Agent Description:

Tocilizumab is a monoclonal antibody and immunosuppressant; specifically, tocilizumab is an IL-6 receptor antagonist.

Nivolumab is a human immunoglobulin G4 (IgG4) monoclonal antibody that binds to the PD-1 receptor of T cells blocking its interaction with PD-L1 and PD-L2, thereby enhancing T-cell proliferation and allowing the immune system to attack the tumor.

Number of Subjects: A maximum of 12 participants will be enrolled on this Phase 1 study.

Duration of Follow-up: Participants will be followed for up to one year post-treatment for survival and response.

Study Design: This is a 3 + 3 design. In a "3 + 3 design," three participants are initially enrolled into a given dose cohort. If there is no dose limiting toxicity (DLT) observed in any of these subjects, the trial proceeds to enroll additional subjects into the next higher dose cohort. If one subject develops a DLT at a specific dose, an additional three subjects are enrolled into that same dose cohort. Development of DLTs in more than one of six subjects in a specific dose cohort suggests that the maximum tolerated dose (MTD) has been exceeded, and further dose escalation is not pursued.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 2
• Est. completion date: July 15, 2020
• Est. primary completion date: July 15, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria

1. Age=18 years with hematological malignancies who have undergone allogeneic transplant for hematological malignancy and are =180 days post-transplant.

2. Relapsed disease post-allogeneic transplant defined as follows i. Acute or Chronic Leukemia or myelodysplastic or myeloproliferative disorders or natural killer (NK) cell neoplasms: Bone marrow (BM) with =5% disease involvement or peripheral blood evidence of overt relapse ii. Lymphoma: BM evidence of relapsed/persistent disease or PET/CT or CT evidence of persistent/progressive lymphadenopathy consistent with active lymphoma. Active disease defined as nodal lesions = 20 mm in the long axis or extranodal lesions=10 mm in long and short axis or bone marrow involvement that is biopsy proven

3. Karnofsky performance status =70 (See Appendix A for details)

4. Creatinine Clearance=60 ml/min

5. Adequate hepatic function, defined as aspartate aminotransferase (AST) and alanine aminotransferase (ALT) =3 x upper limit of normal (ULN). Serum bilirubin and alkaline phosphatase =3x x ULN, or considered not clinically significant (e.g. Gilbert's or indirect hyperbilirubinemia) or felt to be due to underlying disease.

6. Without evidence of active acute or chronic graft versus host disease (GVHD)

7. Off all immunosuppression and corticosteroids (other than replacement dose steroids defined as equivalent to a maximum of 10 mg Prednisone daily) for =28 days from first treatment.

8. Off all disease targeted treatments for =10 days to first treatment day

9. Able to provide written informed consent

10. Women of child-bearing potential and men must agree to use adequate contraception for the duration of study participation and for 120 days after the last treatment with nivolumab.

11. No FDA approved, more appropriate therapies available for disease control as determined by the treating physician

Exclusion Criteria

1. Positive beta-human chorionic gonadotropin (HCG) in female of child-bearing potential

2. Cluster of differentiation 3 (CD3) donor chimerism <5% within 4 weeks of starting study treatment

3. Prior administration of donor lymphocyte infusion post-allogeneic transplant within the last 6 months of study treatment

4. History of or active autoimmune disease, or other syndrome that requires systemic steroids.

5. History of allergic reactions attributed to compounds of similar chemical or biologic composition to nivolumab.

6. Uncontrolled or active infections on treatment

7. Confirmed active human immunodeficiency virus (HIV), Hepatitis B or C infection.

8. Presence of =grade 3 non-hematologic toxicities as per CTCAE version 5 from any previous treatment unless it is felt to be due to underlying disease.

9. Concurrent use of investigational therapeutic agents or enrollment on another therapeutic clinical trial at any institution.

a. Minimum of 4 weeks from last dose of investigational agent

10. Prior exposure to PD-1 or CTLA4 antibodies in the post-allogeneic transplant setting. Participants who received such agents pre-allogeneic transplant will NOT be excluded.

11. Prior exposure to daratumumab in the post-allogeneic transplant setting within two months of start date of treatment with this investigational protocol. Participants who received this agent pre-allogeneic transplant will NOT be excluded

12. Concurrent therapies targeted at disease relapse. However, previous treatments for relapsed disease are allowed.

13. Concurrent active malignancy (exceptions: treated solid malignancy in >2 years' remission, treated basal or squamous cell carcinomas of the skin)

14. History of Crohn's disease or ulcerative colitis

15. History of demyelinating disorder

16. Prior intolerance or allergy to tocilizumab

Related Conditions & MeSH terms

• Acute Leukemia
• Chronic Leukemia
• Hematologic Neoplasms
• Leukemia
• Lymphoma
• Myelodysplastic Syndromes

Intervention

Drug:
• Nivolumab (.25 mg/kg)
Participants will receive Nivolumab at one of two dose levels every 2 weeks for 4 treatments.
• Tocilizumab
Participants will receive 2 doses of tocilizumab
• Nivolumab (.5 mg/kg)
Participants will receive Nivolumab at one of two dose levels every 2 weeks for 4 treatments.

Locations

Country	Name	City	State
United States	Froedtert Hospital and the Medical College of Wisconsin	Milwaukee	Wisconsin

Sponsors (1)

Lead Sponsor	Collaborator
Medical College of Wisconsin

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Maximum-tolerated Dose	Determine the safety and the maximum tolerated dose among two candidate doses of nivolumab in combination with tocilizumab for treatment of relapsed hematological malignancy post-allogeneic transplant. Maximum-tolerated dose is based on the determination of dose-limiting toxicities.	Up to 4 weeks after last dose of study treatment (approximately 3 months)
Secondary	Response Rates Based on Imaging	The number of subjects with stable disease as evidenced by imaging (Diagnostic positron emission tomography (PET)-CT scans or CT of the neck, chest, abdomen, and pelvis).	End of study treatment (approximately 2 months)
Secondary	Response Rates Based on Pathologic Response	The number of subjects with bone marrow response (achievement of complete response; <5% blasts; stable disease; progressive disease).	End of study treatment (approximately 2 months)
Secondary	Overall Survival	The number of participants alive.	Up to 1 year from beginning of treatment
Secondary	Progression-Free Survival	Determine the number of subjects alive and in remission after treatment.	Up to 1 year from beginning of treatment
Secondary	Duration of response in responding participants	Number of subjects with complete response or stable disease.	Up to 1 year from the beginning of treatment
Secondary	Dose-limiting toxicities	The number of subjects with dose-limiting toxicities. This will be measured by the number of adverse events as defined by the NCI CTCAE version 4.03 non-hematologic = grade 3-5 signs/symptoms or by the development of steroid refractory grade 2-4 graft-versus-host disease or severe chronic graft-versus-host disease.	Up to 4 weeks after last dose of study treatment (approximately 3 months)