Phase II Study of Propylene Glycol-Free Melphalan Combined with Carmustine, Etoposide, and Cytarabine for Myeloablative Conditioning in Lymphoma Patients Undergoing Autologous Stem Cell Transplantation.
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F. Gao | R. Vij | J. Dipersio | C. Abboud | A. Ghobadi | A. Cashen | K. Stockerl-Goldstein | T. Fletcher | C. Ceriotti
[1] P. Hari,et al. A Phase IIb, Multicenter, Open-Label, Safety, and Efficacy Study of High-Dose, Propylene Glycol-Free Melphalan Hydrochloride for Injection (EVOMELA) for Myeloablative Conditioning in Multiple Myeloma Patients Undergoing Autologous Transplantation. , 2015, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.
[2] Bruce D Cheson,et al. Recommendations for initial evaluation, staging, and response assessment of Hodgkin and non-Hodgkin lymphoma: the Lugano classification. , 2014, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[3] H. Prince,et al. The choice of multiple myeloma induction therapy affects the frequency and severity of oral mucositis after melphalan-based autologous stem cell transplantation. , 2014, Clinical lymphoma, myeloma & leukemia.
[4] J. McGuirk,et al. Phase IIa cross-over study of propylene glycol-free melphalan (LGD-353) and alkeran in multiple myeloma autologous transplantation , 2014, Bone Marrow Transplantation.
[5] J. Vose,et al. Phase III randomized study of rituximab/carmustine, etoposide, cytarabine, and melphalan (BEAM) compared with iodine-131 tositumomab/BEAM with autologous hematopoietic cell transplantation for relapsed diffuse large B-cell lymphoma: results from the BMT CTN 0401 trial. , 2013, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[6] H. Einsele,et al. Prospective oral mucositis audit: oral mucositis in patients receiving high-dose melphalan or BEAM conditioning chemotherapy--European Blood and Marrow Transplantation Mucositis Advisory Group. , 2008, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[7] M. Perazella,et al. Reviews: Recognition, Treatment, and Prevention of Propylene Glycol Toxicity , 2007, Seminars in dialysis.
[8] M. Mullins,et al. Osmol Gap as a Surrogate Marker for Serum Propylene Glycol Concentrations in Patients Receiving Lorazepam for Sedation , 2006, Pharmacotherapy.
[9] K. Wilson,et al. Propylene glycol toxicity: a severe iatrogenic illness in ICU patients receiving IV benzodiazepines: a case series and prospective, observational pilot study. , 2005, Chest.
[10] J. Fish,et al. Propylene Glycol‐Associated Renal Toxicity from Lorazepam Infusion , 2003, Pharmacotherapy.
[11] A. Goldman. Issues in designing sequential stopping rules for monitoring side effects in clinical trials. , 1987, Controlled clinical trials.
[12] J. Rossi,et al. Intensive chemotherapy with high doses of BCNU, etoposide, cytosine arabinoside, and melphalan (BEAM) followed by autologous bone marrow transplantation: toxicity and antitumor activity in 26 patients with poor-risk malignancies , 2004, Cancer Chemotherapy and Pharmacology.