David S Ritchie

Summary

Affiliation: Peter MacCallum Cancer Centre
Country: Australia

Publications

  1. ncbi The role of second autografts in the treatment of Hodgkin lymphoma
    David S Ritchie
    Department of Haematology and Medical Oncology, Peter MacCallum Cancer Centre, East Melbourne, Australia
    Leuk Lymphoma 48:847-8. 2007
  2. ncbi Drug-mediated and cellular immunotherapy in multiple myeloma
    David S Ritchie
    Department of Haematology and Medical Oncology, Peter MacCallum Cancer Centre, East Melbourne, Vic, Australia
    Immunotherapy 2:243-55. 2010
  3. ncbi Complete molecular response of e6a2 BCR-ABL-positive acute myeloid leukemia to imatinib then dasatinib
    David S Ritchie
    Department of Haematology and Medical Oncology, Peter MacCallum Cancer Centre, No 1 A Beckett Street, Melbourne, Victoria 8006, Australia
    Blood 111:2896-8. 2008
  4. ncbi Plasma cell lysate as an antigen source in multiple myeloma immunotherapy
    David S Ritchie
    Department of Haematology and Medical Oncology, Peter MacCallum Cancer Centre, East Melbourne, Australia
    Leuk Lymphoma 48:1894-5. 2007
  5. ncbi A new therapeutic target for leukemia comes to the surface
    David S Ritchie
    Division of Haematology and Medical Oncology, Peter MacCallum Cancer Centre, East Melbourne, 3002, Victoria, Australia
    Cell 138:226-8. 2009
  6. ncbi DC research in Australia
    D S Ritchie
    Peter MacCallum Cancer Center, St Andrews Place, East Melbourne, Australia
    Cytotherapy 9:225-30. 2007
  7. ncbi The hyper-CVAD-rituximab chemotherapy programme followed by high-dose busulfan, melphalan and autologous stem cell transplantation produces excellent event-free survival in patients with previously untreated mantle cell lymphoma
    D S Ritchie
    Department of Haematology and Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia
    Ann Hematol 86:101-5. 2007
  8. ncbi Autologous dendritic cells pulsed with eluted peptide as immunotherapy for advanced B-cell malignancies
    David Ritchie
    Malaghan Institute of Medical Research, Wellington, New Zealand
    Leuk Lymphoma 47:675-82. 2006
  9. ncbi Prospective monitoring of tumor necrosis factor alpha and interferon gamma to predict the onset of acute and chronic graft-versus-host disease after allogeneic stem cell transplantation
    David Ritchie
    Malaghan Institute of Medical Research, Wellington, New Zealand
    Biol Blood Marrow Transplant 11:706-12. 2005
  10. ncbi Reactivation of DNA viruses in association with histone deacetylase inhibitor therapy: a case series report
    David Ritchie
    Department of Haematology and Medical Oncology, Peter MacCallum Cancer Centre and University of Melbourne, Melbourne, Victoria 3002, Australia
    Haematologica 94:1618-22. 2009

Collaborators

Detail Information

Publications33

  1. ncbi The role of second autografts in the treatment of Hodgkin lymphoma
    David S Ritchie
    Department of Haematology and Medical Oncology, Peter MacCallum Cancer Centre, East Melbourne, Australia
    Leuk Lymphoma 48:847-8. 2007
  2. ncbi Drug-mediated and cellular immunotherapy in multiple myeloma
    David S Ritchie
    Department of Haematology and Medical Oncology, Peter MacCallum Cancer Centre, East Melbourne, Vic, Australia
    Immunotherapy 2:243-55. 2010
    ..In addition, apoptosis-inducing therapies may prime endogenous antigen presentation via immunogenic cell death, which again may be enhanced by the addition of immunomodulatory drug therapy...
  3. ncbi Complete molecular response of e6a2 BCR-ABL-positive acute myeloid leukemia to imatinib then dasatinib
    David S Ritchie
    Department of Haematology and Medical Oncology, Peter MacCallum Cancer Centre, No 1 A Beckett Street, Melbourne, Victoria 8006, Australia
    Blood 111:2896-8. 2008
    ..Furthermore, we report that sustained molecular remission has been achieved despite withdrawal of tyrosine kinase inhibitor (TKI) therapy...
  4. ncbi Plasma cell lysate as an antigen source in multiple myeloma immunotherapy
    David S Ritchie
    Department of Haematology and Medical Oncology, Peter MacCallum Cancer Centre, East Melbourne, Australia
    Leuk Lymphoma 48:1894-5. 2007
  5. ncbi A new therapeutic target for leukemia comes to the surface
    David S Ritchie
    Division of Haematology and Medical Oncology, Peter MacCallum Cancer Centre, East Melbourne, 3002, Victoria, Australia
    Cell 138:226-8. 2009
    ..In this issue, Jaiswal et al. (2009) and Majeti et al. (2009) show that elevated CD47 expression by leukemic stem cells inhibits macrophage activity and is an indicator of poor prognosis for patients with acute myeloid leukemia...
  6. ncbi DC research in Australia
    D S Ritchie
    Peter MacCallum Cancer Center, St Andrews Place, East Melbourne, Australia
    Cytotherapy 9:225-30. 2007
    ..These collaborations have led to the emergence of DC research programs that extend from in vitro and animal models of DC biology through each step of clinical translation and into active clinical trials...
  7. ncbi The hyper-CVAD-rituximab chemotherapy programme followed by high-dose busulfan, melphalan and autologous stem cell transplantation produces excellent event-free survival in patients with previously untreated mantle cell lymphoma
    D S Ritchie
    Department of Haematology and Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia
    Ann Hematol 86:101-5. 2007
    ....
  8. ncbi Autologous dendritic cells pulsed with eluted peptide as immunotherapy for advanced B-cell malignancies
    David Ritchie
    Malaghan Institute of Medical Research, Wellington, New Zealand
    Leuk Lymphoma 47:675-82. 2006
    ..These results provide further evidence for the use of immunotherapy in the management of B-cell malignancies, but also suggest that sustained responses may only be possible in patients with low bulk disease early in the disease course...
  9. ncbi Prospective monitoring of tumor necrosis factor alpha and interferon gamma to predict the onset of acute and chronic graft-versus-host disease after allogeneic stem cell transplantation
    David Ritchie
    Malaghan Institute of Medical Research, Wellington, New Zealand
    Biol Blood Marrow Transplant 11:706-12. 2005
    ..These findings provide a means by which GVHD can be predicted before it is clinically evident, thus allowing for accurate diagnosis and monitoring of GVHD and possibly more cost-effective management of post-SCT immunosuppression...
  10. ncbi Reactivation of DNA viruses in association with histone deacetylase inhibitor therapy: a case series report
    David Ritchie
    Department of Haematology and Medical Oncology, Peter MacCallum Cancer Centre and University of Melbourne, Melbourne, Victoria 3002, Australia
    Haematologica 94:1618-22. 2009
    ..These observations suggest that vigilance for DNA virus reactivation is needed to quantify the risk in patients treated with histone deacetylase inhibitors...
  11. ncbi A high rate of durable responses with romidepsin, bortezomib, and dexamethasone in relapsed or refractory multiple myeloma
    Simon J Harrison
    Haematology Department, Peter MacCallum Cancer Centre, East Melbourne, Australia
    Blood 118:6274-83. 2011
    ..2 (95% CI: 5.5-19.6) months, and the median OS was > 36 months. This regimen shows activity with manageable toxicity and warrants further evaluation. This trial was registered at www.clinicaltrials.gov as NCT00431990...
  12. ncbi The immunostimulatory effect of lenalidomide on NK-cell function is profoundly inhibited by concurrent dexamethasone therapy
    Andy K Hsu
    Hematology Immunology Translational Research Laboratory, Peter MacCallum Cancer Centre, East Melbourne, Australia
    Blood 117:1605-13. 2011
    ..Our findings indicate that lenalidomide immunostimulatory effects on patient NK cells are severely blunted by concurrent dexamethasone administration...
  13. ncbi Graft-versus-host disease, donor chimerism, and organ toxicity in stem cell transplantation after conditioning with fludarabine and melphalan
    David S Ritchie
    Bone Marrow Transplant Service, Department of Clinical Haematology and Medical Oncology, Royal Melbourne Hospital, Melbourne, Australia
    Biol Blood Marrow Transplant 9:435-42. 2003
    ..Overall, the combination of fludarabine and melphalan is intensely immunosuppressive, leads to rapid T-cell engraftment and results in substantial toxicity and GVHD, particularly in heavily pretreated patients...
  14. ncbi Mantle cell lymphoma with central nervous system involvement: frequency and clinical features
    Saar Gill
    Department of Haematology and Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, Australia
    Br J Haematol 147:83-8. 2009
    ..While not routinely justified for all patients, CNS prophylaxis may particularly benefit patients with blastic histology at diagnosis, or those with systemic relapse after first-line treatment...
  15. ncbi The anti-cancer drug, phenoxodiol, kills primary myeloid and lymphoid leukemic blasts and rapidly proliferating T cells
    Patries M Herst
    Malaghan Institute of Medical Research, Wellington 6005, New Zealand
    Haematologica 94:928-34. 2009
    ....
  16. ncbi Biology and clinical observations of regulatory T cells in cancer immunology
    Michele W L Teng
    Cancer Immunology Program, Peter MacCallum Cancer Centre, East Melbourne, 3002, Vic, Australia
    Curr Top Microbiol Immunol 344:61-95. 2011
    ....
  17. ncbi Alloreactive natural killer cells in hematopoietic stem cell transplantation
    Hollie J Pegram
    Cancer Immunology Research Program, Peter MacCallum Cancer Centre, Melbourne, Australia
    Leuk Res 35:14-21. 2011
    ..Further understanding of conditioning and mechanisms to reduce graft versus host disease (GVHD) will improve our ability to manipulate NK cells in HSCT...
  18. ncbi Autoimmunity associated with immunotherapy of cancer
    Sally M Amos
    Cancer Immunology Research Program, Peter MacCallum Cancer Centre, Melbourne, Australia
    Blood 118:499-509. 2011
    ..This review introduces immunotherapeutic approaches to cancer treatment, provides details of toxicities arising from therapy, and discusses future potential ways to avoid or circumvent these side effects...
  19. ncbi The level of glycolytic metabolism in acute myeloid leukemia blasts at diagnosis is prognostic for clinical outcome
    Patries M Herst
    Malaghan Institute of Medical Research, Wellington, New Zealand
    J Leukoc Biol 89:51-5. 2011
    ..In conclusion, we found that the extent of myeloblast glycolysis may be an effective and easily applied method to determine the pretreatment prognosis of AML...
  20. ncbi Dendritic cells treated with lipopolysaccharide up-regulate serine protease inhibitor 6 and remain sensitive to killing by cytotoxic T lymphocytes in vivo
    Kate A Andrew
    Malaghan Institute of Medical Research, Wellington, New Zealand
    J Immunol 181:8356-62. 2008
    ..However, SPI-6 expression may provide DC with a survival advantage in some conditions, such as those modeled by in vitro cytotoxicity assays...
  21. ncbi In vivo tracking of dendritic cells in patients with multiple myeloma
    H Miles Prince
    Division of Haematology and Medical Oncology, Peter MacCallum Cancer Centre, St Andrew s Place, East Melbourne, VIC 3002, Australia
    J Immunother 31:166-79. 2008
    ..SC and ID routes produced similar levels of DC migration...
  22. ncbi Patients with multiple myeloma treated with thalidomide: evaluation of clinical parameters, cytokines,angiogenic markers, mast cells and marrow CD57+ cytotoxic T cells as predictors of outcome
    Linda Mileshkin
    Division of Haematology and Medical Oncology, Department of Haematology and Medical Oncology, Peter MacCallum Cancer Center, St Andrew s Place, East Melbourne, Vic, Australia
    Haematologica 92:1075-82. 2007
    ..We assessed laboratory and clinical parameters in patients with myeloma treated with thalidomide as potential prognostic markers and looked for changes with therapy...
  23. ncbi The role of ancestim (recombinant human stem-cell factor, rhSCF) in hematopoietic stem cell mobilization and hematopoietic reconstitution
    Kirsten E Herbert
    Peter MacCallum Cancer Centre, Department of Hematology and Medical Oncology, Victoria, Australia
    Expert Opin Biol Ther 10:113-25. 2010
    ..The emergence of other novel agents for HSPC mobilization such as plerixafor (AMD3100, Mozobil) will further demarcate the role of Ancestim as a second- or third-line mobilization agent for the mobilization-refractory patient...
  24. ncbi Tumour antigens on tap
    Franca Ronchese
    Malaghan Institute of Medical Research, Wellington School of Medicine, Wellington, New Zealand
    Lancet 360:268. 2002
  25. ncbi Improved survival for relapsed diffuse large B cell lymphoma is predicted by a negative pre-transplant FDG-PET scan following salvage chemotherapy
    Michael Dickinson
    Division of Haematology and Medical Oncology, Peter MacCallum Cancer Centre, East Melbourne, Vic, Australia
    Br J Haematol 150:39-45. 2010
    ..Although those with positive scans can still be salvaged with current treatments, PET may useful for selecting patients eligible for novel consolidation strategies after salvage therapies...
  26. ncbi [18F]fluorodeoxyglucose positron emission tomography scanning for staging, response assessment, and disease surveillance in patients with mantle cell lymphoma
    Saar Gill
    Division of Haematology and Medical Oncology, Peter MacCallum Cancer Centre, East Melbourne, Victoria, Australia
    Clin Lymphoma Myeloma 8:159-65. 2008
    ..Positron emission tomography (PET) is an important imaging modality in the staging and response assessment of patients with lymphoma, but data on its specific use in mantle cell lymphoma (MCL) are lacking...
  27. ncbi Preliminary evidence of disease response to the pan deacetylase inhibitor panobinostat (LBH589) in refractory Hodgkin Lymphoma
    Michael Dickinson
    Haematology Service, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia
    Br J Haematol 147:97-101. 2009
    ..This report describes the preliminary evidence of anti-tumour activity seen in the early phase of this study, which recently closed to accrual...
  28. ncbi Resting B cells suppress tumor immunity via an MHC class-II dependent mechanism
    Victoria Watt
    Malaghan Institute of Medical Research, Wellington, New Zealand
    J Immunother 30:323-32. 2007
    ..Together our findings indicate that the resting B cells are capable of limiting CD8+ T-cell effector function induced by DC vaccination via a mechanism that is dependent on the expression of MHC class-II molecules...
  29. ncbi Glycolytic metabolism confers resistance to combined all-trans retinoic acid and arsenic trioxide-induced apoptosis in HL60rho0 cells
    Patries M Herst
    Malaghan Institute of Medical Research, P O Box 7060, Wellington, New Zealand
    Leuk Res 32:327-33. 2008
    ..HL60rho0 cells were also significantly more resistant to apoptosis after combined ATO+ATRA treatment compared with HL60 cells, and this was associated with failure to upregulate Fas expression...
  30. ncbi Aplastic anemia as a late complication of thymoma in remission
    David S Ritchie
    Department of Clinical Haematology and Medical Oncology, Royal Melbourne Hospital, Melbourne, Australia
    Eur J Haematol 68:389-91. 2002
    ..This observation suggests that auto-reactive T cells may be produced by the thymoma but not induce clinical auto-immune disease until a later time, even after eradication of thymoma has been achieved...
  31. ncbi Disease status at autologous stem cell transplantation and the cell of origin phenotype are important predictors of outcome in patients with neurologic (central nervous system) relapse of diffuse large B-cell lymphoma undergoing autologous stem cell trans
    Sushrut Patil
    The Department of Malignant Haematology and Stem Cell Transplantation, Monash University, The Alfred Hospital, Melbourne, Australia
    Leuk Lymphoma 50:1964-8. 2009
    ..5 months and 5 months, respectively). Patients with neurological relapse of DLBCL have a poor outcome after ASCT; the outcome is worse for patients with non-GC phenotype irrespective of the disease stage at ASCT...
  32. ncbi Predicting durable remissions following thalidomide therapy for relapsed myeloma
    Hang Quach
    Division of Haematology and Medical Oncology, Peter MacCallum Cancer Centre, East Melbourne, Vic, Australia
    Leuk Lymphoma 50:223-9. 2009
    ..001). The OS for these groups were >69.8, 35.4 and 11.7 months, respectively (p < 0.001). These findings support the therapeutic goal of achieving 'maximum depth of response' in patients with relapsed myeloma...
  33. ncbi Therapeutic options in mantle cell lymphoma
    Saar Gill
    Department of Haematology and Medical Oncology, Peter MacCallum Cancer Centre
    Leuk Lymphoma 49:398-409. 2008
    ..Here we review the treatment options for patients with newly-diagnosed or relapsed MCL and discuss recent advances in management, including the role of autologous and allogeneic SCT...