William I. Bensinger
M.D., Northwestern University, 1973.
The Autologous Stem Cell Transplant Program at the FHCRC is focused on combining improved high dose therapy regimens, peripheral blood stem cells (PBSC) and post transplant immunotherapies designed to increase the fraction of patientswith malignant disease who can be cured. Some of the more innovative treatment strategies developed in the Autologous program have been used to pilot new safer treatment programs developed at the FHCRC are validated through a cooperative, high dose therapy group comprised of smaller, transplant centers in the northwest. In addition, as noted below, some of the treatment strategies developed in the Autologous Program are sufficiently promising to foster new conditioning regimens for patients who can undergo allogeneic transplantation. Due to the success of PBSC in autograft patients, studies of allogeneic PBSC have been underway and have demonstrated significant benefit of PBSC over marrow.
Targeted Radiotherapy Studies
This project involves the use of a radiometal 166-Holmium, which is a high energy beta particle emitting isotope with a relatively short half-life (26 hours). The isotope is coupled to a bone-seeking chelate DOTMP. When given intravenously, 166-Ho-DOTMP is taken up almost exclusively into bone, with negligible uptake in liver, lung, kidneys or gastrointestinal tract. This irradiates all of the marrow bearing areas where the overwhelming bulk of myeloma cells reside. At the FHCRC, a total of 38 patients have received 20-40 Gy of 166-Ho-DOTMP with melphalan of melphalan + TBI. The major toxicities as expected were marrow ablation with minor extramedullary toxicities. No treatment related deaths have occurred at the FHCRC. Approximately 45% of the evaluable patients (25 patients evaluable so far) have achieved complete remissions of their myeloma. Based on these encouraging data a phase III randomized study comparing 166-Ho-DOTMP + melphalan versus melphalan as a preparative regimen for patients with myeloma is planned to begin this summer. This unique approach should allow the delivery of higher doses of radiation to sites of disease while avoiding the dose limiting toxicities of high dose therapy.
If successful, this strategy could be extended to other diseases such as prostate cancer and is currently being studied in Ewing’s sarcoma and breast cancer. The treatment may also serve as a platform for the so named mini-transplants which use less intensive conditioning prior to allogeneic stem cell transplantation in order to avoid the relatively high transplant related mortality occuring after standard allografting. A protocol designed to provided targeted radiotherapy with 166-Ho-DOTMP in combination with allogeneic transplants is underway.
Promising studies utilizing interleukin-2 (IL-2) and GM-CSF are being investigated by Dr. Leona Holmberg. In an ongoing trial, autologous peripheral blood stem cells are thawed and incubated for 24 hours with IL-2 prior to transplant into recipients with breast canceror lymphoma. Lymphokine activated killer cell (LAK) cell and natural killer (NK) cell activity is greatly enhanced by this approach. Patients receive low dose IL-2 subcutaneously for up to 4 weeks following stem cell infusion. The treatment has been well tolerated and engraftment has been rapid in all patients. This approach appears to have significant activity in patients with chemotherapy-resistant breast cancer.
In a similar trial, 10 patients with multiple myeloma have received high-dose chemotherapy followed by IL-2 incubated PBSC and low dose IL-2 for 4 weeks. The treatment was well tolerated and all patients are surviving 1 to 4 years from transplant. Only 2 relapses have occurred. Additional studies are underway in patients with lymphomaand CML.
Pretransplant minimal residual disease predicts survival in mantle cell lymphoma patients undergoing autologous stem cell transplantation in complete remission.. Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.. 2015.
Carfilzomib, lenalidomide, and dexamethasone for relapsed multiple myeloma.. The New England journal of medicine. 372(2):142-52.. 2015.
Autologous transplant for relapsed follicular lymphoma: impact of pre-transplant rituximab sensitivity.. Leukemia & lymphoma. 56(1):92-6.. 2015.
Peripheral Blood Progenitor Cell Mobilization for Autologous and Allogeneic Hematopoietic Cell Transplantation: Guidelines of the American Society for Blood and Marrow Transplantation.. Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.. 2014.
A Preclinical Model of CD38-Pretargeted Radioimmunotherapy for Plasma Cell Malignancies.. Cancer research. 74(4):1179-89.. 2014.
Hepatitis B virus screening and potential reactivation in patients undergoing treatment for cancer.. Journal of the National Comprehensive Cancer Network : JNCCN. 12(12):1655-7.. 2014.
Lenalidomide Maintenance for High-Risk Multiple Myeloma after Allogeneic Hematopoietic Cell Transplantation.. Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.. 2014.
A prospective study of lenalidomide monotherapy for relapse after Allo-SCT for multiple myeloma.. Bone marrow transplantation. 49(4):492-5.. 2014.
Specific features identify patients with relapsed or refractory mantle cell lymphoma benefitting from autologous hematopoietic cell transplantation.. Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation. 19(9):1403-6.. 2013.
Optimizing Autologous Stem Cell Mobilization Strategies to Improve Patient Outcomes: Consensus Guidelines and Recommendations.. Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.. 2013.
Multiple Myeloma, Version 1.2013.. Journal of the National Comprehensive Cancer Network : JNCCN. 11(1):11-17.. 2013.
Phase Ib Dose-Escalation Study (PX-171-006) of Carfilzomib, Lenalidomide, and Low-Dose Dexamethasone in Relapsed or Progressive Multiple Myeloma.. Clinical cancer research : an official journal of the American Association for Cancer Research.. 2013.
Peripheral-blood stem cells versus bone marrow from unrelated donors.. The New England journal of medicine. 367(16):1487-96.. 2012.
Waldenstrom's Macroglobulinemia/Lymphoplasmacytic Lymphoma, Version 2.2013.. Journal of the National Comprehensive Cancer Network : JNCCN. 10(10):1211-1219.. 2012.
Allo-SCT for multiple myeloma: a review of outcomes at a single transplant center.. Bone marrow transplantation. 47(10):1312-7.. 2012.
Prevention and treatment of cancer-related infections.. Journal of the National Comprehensive Cancer Network : JNCCN. 10(11):1412-45.. 2012.
Allogeneic transplantation: peripheral blood vs. bone marrow.. Current opinion in oncology. 24(2):191-196.. 2012.
Phase I Trial of Anti-CS1 Monoclonal Antibody Elotuzumab in Combination With Bortezomib in the Treatment of Relapsed/Refractory Multiple Myeloma.. Journal of clinical oncology : official journal of the American Society of Clinical Oncology. 30(16):1965.. 2012.
Cytomegalovirus Viral Load and Virus-Specific Immune Reconstitution after Peripheral Blood Stem Cell versus Bone Marrow Transplantation.. Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation. 18(1):66-75.. 2012.
The effective use of plerixafor as a real-time rescue strategy for patients poorly mobilizing autologous CD34(+) cells.. Journal of clinical apheresis. 27(2):81-7.. 2012.