David J. Chung

ORCID: 0000-0003-0469-839X
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About
Contact & Profiles
Research Areas
  • Multiple Myeloma Research and Treatments
  • CAR-T cell therapy research
  • Protein Degradation and Inhibitors
  • Immunotherapy and Immune Responses
  • Cancer Treatment and Pharmacology
  • Hematopoietic Stem Cell Transplantation
  • Chronic Lymphocytic Leukemia Research
  • Acute Myeloid Leukemia Research
  • SARS-CoV-2 and COVID-19 Research
  • Immune Cell Function and Interaction
  • Chronic Myeloid Leukemia Treatments
  • Myeloproliferative Neoplasms: Diagnosis and Treatment
  • Peptidase Inhibition and Analysis
  • Monoclonal and Polyclonal Antibodies Research
  • Cancer Genomics and Diagnostics
  • Amyloidosis: Diagnosis, Treatment, Outcomes
  • vaccines and immunoinformatics approaches
  • Neutropenia and Cancer Infections
  • T-cell and B-cell Immunology
  • COVID-19 and healthcare impacts
  • COVID-19 Clinical Research Studies
  • Blood disorders and treatments
  • Glycosylation and Glycoproteins Research
  • Cholinesterase and Neurodegenerative Diseases
  • Cancer therapeutics and mechanisms

St Vincent's Hospital Sydney
2025

UNSW Sydney
2025

Memorial Sloan Kettering Cancer Center
2015-2024

Cornell University
2015-2024

University of Miami
2024

Kettering University
2012-2023

Massachusetts General Hospital
2023

Hadassah Medical Center
2023

City of Hope
2023

Sylvester Comprehensive Cancer Center
2023

Multiple myeloma is the most common indication for high-dose chemotherapy and autologous stem cell transplantation (ASCT), lenalidomide maintenance after transplant now standard. Although doubles progression-free survival, almost all patients eventually relapse. Posttransplant immunotherapy to improve outcomes ASCT therefore has great merit but first requires delineation of dynamics immune reconstitution. We evaluated lymphocyte composition function guide optimal timing identify potential...

10.1158/2326-6066.cir-15-0055 article EN Cancer Immunology Research 2015-10-14

Recently, the benefit of adding daratumumab to proteasome inhibitor-based, 3-drug combination bortezomib, lenalidomide, and dexamethasone for patients with newly diagnosed multiple myeloma who underwent high-dose melphalan chemotherapy autologous hemopoietic cell transplant was assessed. Here, we examine addition second-generation carfilzomib, dexamethasone.To assess safety effectiveness carfilzomib-lenalidomide-dexamethasone-daratumumab therapy myeloma, in absence transplant.Clinical...

10.1001/jamaoncol.2021.0611 article EN JAMA Oncology 2021-04-17

Abstract B-cell maturation antigen (BCMA)–targeting therapeutics have dramatically improved outcomes in relapsed/refractory multiple myeloma (RRMM). However, whether the mechanisms of resistance between these therapies are shared and how identification such before therapy initiation could refine clinical decision-making remains undefined. We analyzed for 72 RRMM patients treated with teclistamab, a CD3 × BCMA bispecific antibody, 42% (30/72) whom had prior BCMA-directed exposure. Malignant...

10.1182/blood.2023023557 article EN cc-by-nc-nd Blood 2024-07-25

We aimed to identify whether the use of autologous hematopoietic cell transplantation (HCT) impacts outcomes for multiple myeloma patients with gains chromosome 1q (+1q). retrospectively identified 95 patients, 21% having +1q. For +1q, overall response rate induction was 85%, 40% ≥ VGPR and 20% achieving a CR, similar non +1q (p = .64). The median PFS from diagnosis 2.1 years (95% CI: 1.2–not reached (NR)) vs 4.3 3.3 yrs–NR) without .003). Median OS 4.4 2.9–NR) not reached, respectively...

10.1080/10428194.2016.1260126 article EN Leukemia & lymphoma/Leukemia and lymphoma 2017-01-12

Abstract Multiple myeloma (MM) progression is characterized by the seeding of cancer cells in different anatomic sites. To characterize this evolutionary process, we interrogated, whole genome sequencing, 25 samples collected at autopsy from 4 patients with relapsed MM and an additional set 125 exomes 51 patients. Mutational signatures analysis showed how cytotoxic agents introduce hundreds unique mutations each surviving cell, detectable bulk sequencing only cases clonal expansion a single...

10.1038/s41467-020-17459-z article EN cc-by Nature Communications 2020-07-17

Abstract Purpose: Sustained minimal residual disease (MRD) negativity is associated with long-term survival in multiple myeloma. The gut microbiome affected by diet, and turn can modulate host immunity, for example through production of short-chain fatty acids including butyrate. We hypothesized that dietary factors affect the (abundance butyrate-producing bacteria or stool butyrate concentration) may be myeloma outcomes. Experimental Design: examined relationship (via a food frequency...

10.1158/1078-0432.ccr-22-0723 article EN Clinical Cancer Research 2022-09-28

Teclistamab, a B-cell maturation antigen (BCMA)- and CD3-targeting bispecific antibody, is an effective novel treatment for relapsed/refractory multiple myeloma (R/RMM), but efficacy in patients exposed to BCMA-directed therapies mechanisms of resistance have yet be fully delineated. We conducted real-world retrospective study commercial teclistamab, capturing both clinical outcomes immune correlates response cohort (n = 52) with advanced R/RMM. Teclistamab was highly overall rate (ORR) 64%,...

10.1182/bloodadvances.2023011225 article EN cc-by-nc-nd Blood Advances 2023-10-25

Despite being the mainstay of management for cytokine release syndrome (CRS) and immune effector cell-associated neurotoxicity (ICANS), there is limited data regarding impact tocilizumab (TCZ) corticosteroids (CCS) on chimeric antigen receptor (CAR) T-cell efficacy in multiple myeloma (MM). The present study aims to evaluate prognostic these immunosuppressants recipients BCMA- or GPRC5D-directed CAR T cells relapsed/refractory MM. Our retrospective cohort involved patients treated with...

10.1038/s41408-024-01048-0 article EN cc-by Blood Cancer Journal 2024-05-27

Abstract B-cell-maturation-antigen (BCMA)-directed therapies are highly active for multiple myeloma, but infections emerging as a major challenge. In this retrospective, single-center analysis we evaluated infectious complications after BCMA-targeted chimeric-antigen-receptor T-cell therapy (CAR-T), bispecific-antibodies (BsAb) and antibody-drug-conjugates (ADC). The primary endpoint was severe (grade ≥3) infection incidence. Amongst 256 patients, 92 received CAR-T, 55 BsAb 109 ADC....

10.1038/s41408-024-01043-5 article EN cc-by Blood Cancer Journal 2024-05-31

We compared the efficacy of human Langerhans cells (LC) as tumor immunogens in vivo with monocyte-derived dendritic (moDC) and investigated how interleukin 15 (IL15) supports optimal DC-stimulated antitumor immunity.American Joint Committee on Cancer stage III/IV melanoma patients participated this first clinical trial comparing peptide-pulsed LC moDC vaccines (NCT00700167, www.ClinicalTrials.gov). Correlative studies evaluated mechanisms mediating IL15 support immunity.Both DC were safe...

10.1158/1078-0432.ccr-10-3421 article EN Clinical Cancer Research 2011-02-26

Posttransplant vaccination targeting residual disease is an immunotherapeutic strategy to improve antigen-specific immune responses and prolong disease-free survival after autologous stem cell transplantation (ASCT) for multiple myeloma (MM). We conducted a phase 1 vaccine trial determine the safety, toxicity, immunogenicity of Langerhans-type dendritic cells (LCs) electroporated with CT7, MAGE-A3, Wilms tumor (WT1) messenger RNA (mRNA), ASCT MM. Ten patients received priming immunization...

10.1182/bloodadvances.2021005941 article EN cc-by-nc-nd Blood Advances 2022-01-31

Abstract Purpose: Vaccination with dendritic cell (DC)/multiple myeloma (MM) fusions has been shown to induce the expansion of circulating multiple myeloma–reactive lymphocytes and consolidation clinical response following autologous hematopoietic transplant (auto-HCT). Patients Methods: In this randomized phase II trial (NCT02728102), we assessed effect DC/MM fusion vaccination, GM-CSF, lenalidomide maintenance as compared control arms GM-CSF or alone on rates induction myeloma–specific...

10.1158/1078-0432.ccr-23-0235 article EN cc-by-nc-nd Clinical Cancer Research 2023-07-18
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