Molecular Monitoring With Circulating Tumor DNA and Nivolumab Maintenance

NCT03311958 | Completed Early Phase 1 DMC FDA Drug

• 1 other identifier: HM-110
• Study Type: interventional
• Target: 15
• Locations: 1 country
• Sites: 1

Brief Summary

Patients suffering from diffuse large B-cell lymphoma (DLBCL) who relapse within 12 months of chemotherapy usually undergo salvage therapies, followed by autologous transplant with a low success rate. These treatments for relapse have significant toxicities and may not be tolerated well by the patients. These patients need an effective means of identifying relapse at an early time point to be treated effectively. Detection of circulating tumor DNA (ctDNA) has been reported to be a sensitive and more specific method to detect relapse at an early stage compared to PET/ CT scans. Purpose of this trial is to monitor patients who have undergone successful chemotherapy for the presence of ctDNA. Patients who test positive for ctDNA would be treated with Nivolumab for a period of 2 years to avoid complete relapse.

Conditions

Diffuse Large B Cell Lymphoma

Outcome Measures

Primary Outcomes (2)

• Evaluation of the rate of conversion from positive to negative ctDNA in nivolumab treated patients

  Regular monitoring of ctDNA positive patients on nivolumab until they become ctDNA negative

  2 years

• Evaluation of the rate of conversion from positive to negative ctDNA in nivolumab treated patients

  Regular testing of ctDNA in positive patients on nivoluman until clinical relapse

  2 years

Secondary Outcomes (4)

• To evaluate adverse events in patients on nivolumab as maintenance drug in post-induction, post-salvage and post-autologous transplant setting

  2 years

• Relapse free survival (RFS-ctDNA) for nivolumab treated patients

  2 years

• Proportion of patients who are able to convert from ctDNA positive to ctDNA negative after nivolumab treatment

  2 years

• To compare the ctDNA results of Clonoseq and Neolabs platform

  2 years

Study Arms (1)

Nivolumab

EXPERIMENTAL

Drug: Nivolumab, IV, 240 mg

Interventions

Nivolumab, IV, 240 mg DRUG

Patients would be given an infusion of 240 mg nivolumab over 30 min

Nivolumab

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Patients must have a tissue diagnosis of diffuse large B cell lymphoma, with a negative PET/CT scan performed within 28 days of study enrollment, with one of the following clinical features: high risk IPI, ABC-subtype DLBCL, Double hit/ triple hit DLBCL, Ki67\>90%, or MYC translocation.
• Patients can have any number of prior therapies and any amount of time period from the last therapy as long as they have complete response as seen in PET/CT at the time of enrolment.
• Patients with prior salvage chemo-immunotherapy, radiation therapy, autologous transplantation are included
• Prior radiation therapy must be completed at least 2 weeks prior to study enrollment
• Autologous transplant must have been done 100 days prior to the study enrollment
• Age \> 18 years.
• ECOG performance status ≤ 2
• Life expectancy of at least 3 months
• A formalin fixed tissue block or equivalent of 24 slides of the tumor sample for analyses by Adaptive Sequenta and NeoGenomics must be available for analysis.
• Patients must be off cancer-directed therapy for at least 3 weeks (2 weeks for oral agents prior to day 1 of the study
• Patients must have suitable organ and marrow function as defined below
• Absolute neutrophil count \> 500/mm3
• Platelets \> 20,000/mm3
• Total bilirubin \< 2.5 times the ULN
• AST/ALT (SGOT/SGPT) \< 2 times institutional normal limits

You may not qualify if:

• Patients with second malignancies (except monoclonal B cells of undetermined significance, antecendant indolent non Hodgkin lymphoma, non-melanomatous skin cancers, papillary thyroid carcinomas, ductal carcinoma in-situ, superficial bladder cancer, prostate cancer or in situ cervical cancers) are excluded unless a complete remission was achieved at least 3 years prior to enrollment and no additional therapy is required or anticipated to be required during the treatment.
• Subjects with active autoimmune disease or a syndrome that requires systemic corticosteroids
• Subjects who received non-oncology vaccine therapies for prevention of infectious disease within 4 weeks of study drug administration.
• Prior therapy with an anti-PD-1, anti-PD-L1, anti-PD-L2 agent
• Any contraindication to therapy with nivolumab
• Prior allogeneic transplantation
• Known hepatitis B virus (HBV) or hepatitis C virus (HCV) infection. Patients with documented cure from HCV infection will be included
• Known uncontrolled human immunodeficiency virus (HIV) infection or known acquired immunodeficiency syndrome (AIDS). Patients with documented controlled HIV infection (CD4 \> 200 and undetectable viral load) will be included.
• Any condition requiring systemic treatment with corticosteroids (\> 10 mg daily prednisone or equivalent) or other immunosuppressive medications within 14 days prior to first dose of study drug. Inhaled or topical steroids and adrenal replacement steroid doses \> 10 mg daily prednisone or equivalent are permitted in the absence of active autoimmune disease.
• History of anaphylactic reaction to monoclonal antibody therapy
• Poor psychiatric risk
• Patients receiving other investigational agents
• Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
• Pregnant or breast feeding. Refer to section 4.4 for further details

Sponsors & Collaborators

• Fox Chase Cancer Center: lead

Study Sites (1)

Fox Chase Cancer Center

Philadelphia, Pennsylvania, 19111, United States

Location

MeSH Terms

Conditions

Lymphoma, Large B-Cell, Diffuse

Interventions

Nivolumab

Condition Hierarchy (Ancestors)

Lymphoma, B-Cell; Lymphoma, Non-Hodgkin; Lymphoma; Neoplasms by Histologic Type; Neoplasms; Lymphoproliferative Disorders; Lymphatic Diseases; Hemic and Lymphatic Diseases; Immunoproliferative Disorders; Immune System Diseases

Intervention Hierarchy (Ancestors)

Antibodies, Monoclonal, Humanized; Antibodies, Monoclonal; Antibodies; Immunoglobulins; Immunoproteins; Blood Proteins; Proteins; Amino Acids, Peptides, and Proteins; Serum Globulins; Globulins

Study Officials

• Shazia Nakhoda, MD

  Fox Chase Cancer Center

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: early phase 1
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Model Details: Regular testing of DLBCL patients who have successfully undergone chemotherapy and are negative for ctDNA. Treatment of patients who become positive for ctDNA with Nivolumab

Study Record Dates

• First Submitted: October 5, 2017
• First Posted: October 17, 2017
• Study Start: May 15, 2018
• Primary Completion: January 26, 2024
• Study Completion: January 26, 2024
• Last Updated: April 6, 2025

Record last verified: 2025-04

Locations

US (1)