Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Review
  • Published:

Not too little, not too much—just right! (Better ways to give high dose melphalan)

Abstract

Of the 13 286 autologous haematopoietic cell transplant procedures reported in the US in 2010–2012 for plasma cell disorders, 10 557 used single agent, high-dose melphalan. Despite 30 years of clinical and pharmacokinetic (PK) experience with high-dose melphalan, and its continuing central role as cytoreductive therapy for large numbers of patients with myeloma, the pharmacodynamics and pharmacogenomics of melphalan are still in their infancy. The addition of protectant agents such as amifostine and palifermin allows dose escalation to 280 mg/m2, but at these doses it is cardiac, rather than gut, toxicity that is dose-limiting. Although combination with additional alkylating agents is feasible, the additional TRM may not be justified when so many post-consolidation therapies are available for myeloma patients. Current research should optimise the delivery of this single-agent chemotherapy. This includes the use of newer formulations and real-time PKs. These strategies may allow a safe and effective platform for adding synergistic novel therapies and provide a window of lymphodepletion for the addition of immunotherapies.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Figure 1

Similar content being viewed by others

References

  1. Lazarus HM, Phillips GL, Herzig RH, Hurd DD, Wolff SN, Herzig GP . High-dose melphalan and the development of hematopoietic stem-cell transplantation: 25 years later. J Clin Oncol 2008; 26: 2240–2243.

    CAS  PubMed  Google Scholar 

  2. Bayraktar UD, Bashir Q, Qazilbash M, Champlin RE, Ciurea SO . Fifty years of melphalan use in hematopoietic stem cell transplantation. Biol Blood Marrow Transplant. 2013; 19: 344–356.

    CAS  PubMed  Google Scholar 

  3. McElwain TJ, Hedley DW, Gordon MY, Jarman M, Millar JL, Pritchard J . High dose melphalan and non-cryopreserved autologous bone marrow treatment of malignant melanoma and neuroblastoma. Exp Hematol 1979; 7 (Suppl 5): 360–371.

    PubMed  Google Scholar 

  4. Lazarus HM, Herzig RH, Graham-Pole J, Wolff SN, Phillips GL, Strandjord S et al. Intensive melphalan chemotherapy and cryopreserved autologous bone marrow transplantation for the treatment of refractory cancer. J Clin Oncol 1983; 1: 359–367.

    CAS  PubMed  Google Scholar 

  5. Pritchard J, McElwain TJ, Graham-Pole J . High-dose melphalan with autologous marrow for treatment of advanced neuroblastoma. Br J Cancer 1982; 45: 86–94.

    CAS  PubMed  PubMed Central  Google Scholar 

  6. Vassal G, Tranchand B, Valteau-Couanet D, Mahe C, Couanet D, Schoeppfer C et al. Pharmacodynamics of tandem high-dose melphalan with peripheral blood stem cell transplantation in children with neuroblastoma and medulloblastoma. Bone Marrow Transplant 2001; 27: 471–477.

    CAS  PubMed  Google Scholar 

  7. McElwain TJ, Powles RL . High-dose intravenous melphalan for plasma-cell leukaemia and myeloma. Lancet 1983; 2: 822–824.

    Article  CAS  PubMed  Google Scholar 

  8. Selby PJ, McElwain TJ, Nandi AC, Perren TJ, Powles RL, Tillyer CR et al. Multiple myeloma treated with high dose intravenous melphalan. Br J Haematol 1987; 66: 55–62.

    CAS  PubMed  Google Scholar 

  9. Moreau P, Fiere D, Bezwoda WR, Facon T, Attal M, Laporte JP et al. Prospective randomized placebo-controlled study of granulocyte-macrophage colony-stimulating factor without stem-cell transplantation after high-dose melphalan in patients with multiple myeloma. J Clin Oncol 1997; 15: 660–666.

    CAS  PubMed  Google Scholar 

  10. Jagannath S, Vesole DH, Glenn L, Crowley J, Barlogie B . Low-risk intensive therapy for multiple myeloma with combined autologous bone marrow and blood stem cell support. Blood 1992; 80: 1666–1672.

    CAS  PubMed  Google Scholar 

  11. Gera S, Musch E, Osterheld HK, Loos U . Relevance of the hydrolysis and protein binding of melphalan to the treatment of multiple myeloma. Cancer Chemother Pharmacol 1989; 23: 76–80.

    CAS  PubMed  Google Scholar 

  12. Reece PA, Hill HS, Green RM, Morris RG, Dale BM, Kotasek D et al. Renal clearance and protein binding of melphalan in patients with cancer. Cancer Chemother Pharmacol 1988; 22: 348–352.

    CAS  PubMed  Google Scholar 

  13. Chang SY, Alberts DS, Melnick LR, Walson PD, Salmon SE . High-pressure liquid chromatographic analysis of melphalan in plasma. J. Pharm Sci 1978; 67: 679–682.

    CAS  PubMed  Google Scholar 

  14. Nath CE, Shaw PJ, Trotman J, Zeng LH, Duffull SB, Hegarty G et al. Population pharmacokinetics of melphalan in patients with multiple myeloma undergoing high dose therapy. Br J Clin Pharmacol 2010; 69: 484–497.

    CAS  PubMed  PubMed Central  Google Scholar 

  15. Kuhne A, Sezer O, Heider U, Meineke I, Muhlke S, Niere W et al. Population pharmacokinetics of melphalan and glutathione S-transferase polymorphisms in relation to side effects. Clin Pharmacol Ther 2008; 83: 749–757.

    CAS  PubMed  Google Scholar 

  16. Costa LJ, Micallef IN, Inwards DJ, Johnston PB, Porrata LF, Litzow MR et al. Effect of the dose per body weight of conditioning chemotherapy on severity of mucositis and risk of relapse after autologous haematopoietic stem cell transplantation in relapsed diffuse large B cell lymphoma. Br J Haematol 2008; 143: 268–273.

    CAS  PubMed  Google Scholar 

  17. Grazziutti ML, Dong L, Miceli MH, Krishna SG, Kiwan E, Syed N et al. Oral mucositis in myeloma patients undergoing melphalan-based autologous stem cell transplantation: incidence, risk factors and a severity predictive model. Bone Marrow Transplant 2006; 38: 501–506.

    CAS  PubMed  Google Scholar 

  18. Moreau P, Kergueris MF, Milpied N, Le Tortorec S, Mahe B, Bulabois CE et al. A pilot study of 220 mg/m2 melphalan followed by autologous stem cell transplantation in patients with advanced haematological malignancies: pharmacokinetics and toxicity. Br J Haematol 1996; 95: 527–530.

    CAS  PubMed  Google Scholar 

  19. Carlson K . Melphalan 200 mg/m2 with blood stem cell support as first-line myeloma therapy: impact of glomerular filtration rate on engraftment, transplantation-related toxicity and survival. Bone Marrow Transplant 2005; 35: 985–990.

    CAS  PubMed  Google Scholar 

  20. Badros A, Barlogie B, Siegel E, Roberts J, Langmaid C, Zangari M et al. Results of autologous stem cell transplant in multiple myeloma patients with renal failure. Br J Haematol 2001; 114: 822–829.

    CAS  PubMed  Google Scholar 

  21. Cibeira MT, Sanchorawala V, Seldin DC, Quillen K, Berk JL, Dember LM et al. Outcome of AL amyloidosis after high-dose melphalan and autologous stem cell transplantation: long-term results in a series of 421 patients. Blood 2011; 118: 4346–4352.

    CAS  PubMed  PubMed Central  Google Scholar 

  22. Gertz MA, Lacy MQ, Dispenzieri A, Ansell SM, Elliott MA, Gastineau DA et al. Risk-adjusted manipulation of melphalan dose before stem cell transplantation in patients with amyloidosis is associated with a lower response rate. Bone Marrow Transplant 2004; 34: 1025–1031.

    CAS  PubMed  Google Scholar 

  23. Palumbo A, Bringhen S, Bruno B, Falcone AP, Liberati AM, Grasso M et al. Melphalan 200 mg/m2 versus melphalan 100 mg/m2 in newly diagnosed myeloma patients: a prospective, multicenter phase 3 study. Blood 2010; 115: 1873–1879.

    CAS  PubMed  Google Scholar 

  24. Ploin DY, Tranchand B, Guastalla JP, Rebattu P, Chauvin F, Clavel M et al. Pharmacokinetically guided dosing for intravenous melphalan: a pilot study in patients with advanced ovarian adenocarcinoma. Eur J Cancer 1992; 28A: 1311–1315.

    CAS  PubMed  Google Scholar 

  25. Mougenot P, Pinguet F, Fabbro M, Culine S, Poujol S, Astre C et al. Population pharmacokinetics of melphalan, infused over a 24-hour period, in patients with advanced malignancies. Cancer Chemother Pharmacol 2004; 53: 503–512.

    CAS  PubMed  Google Scholar 

  26. Pinguet F, Martel P, Fabbro M, Petit I, Canal P, Culine S et al. Pharmacokinetics of high-dose intravenous melphalan in patients undergoing peripheral blood hematopoietic progenitor-cell transplantation. Anticancer Res 1997; 17: 605–611.

    CAS  PubMed  Google Scholar 

  27. Pinguet F, Culine S, Bressolle F, Astre C, Serre MP, Chevillard C et al. A phase I and pharmacokinetic study of melphalan using a 24-hour continuous infusion in patients with advanced malignancies. Clin Cancer Res 2000; 6: 57–63.

    CAS  PubMed  Google Scholar 

  28. Ninane J, Baurain R, de Selys A, Trouet A, Cornu G . High dose melphalan in children with advanced malignant disease. A pharmacokinetic study. Cancer Chemother Pharmacol 1985; 15: 263–267.

    CAS  PubMed  Google Scholar 

  29. Kergueris MF, Milpied N, Moreau P, Harousseau JL, Larousse C . Pharmacokinetics of high-dose melphalan in adults: influence of renal function. Anticancer Res 1994; 14: 2379–2382.

    CAS  PubMed  Google Scholar 

  30. Nath CE, Shaw PJ, Montgomery K, Earl JW . Population pharmacokinetics of melphalan in paediatric blood or marrow transplant recipients. Br J Clin Pharmacol 2007; 64: 151–164.

    CAS  PubMed  PubMed Central  Google Scholar 

  31. Tranchand B, Ardiet C, Bouffet E, Biron P, Philip I, Nasri F et al. [Effect of carboplatin on the pharmacokinetics of melphalan administered intravenously]. Bull Cancer 1994; 81: 43–46.

    CAS  PubMed  Google Scholar 

  32. Gouyette A, Hartmann O, Pico JL . Pharmacokinetics of high-dose melphalan in children and adults. Cancer Chemother Pharmacol 1986; 16: 184–189.

    CAS  PubMed  Google Scholar 

  33. Tricot G, Alberts DS, Johnson C, Roe DJ, Dorr RT, Bracy D et al. Safety of autotransplants with high-dose melphalan in renal failure: a pharmacokinetic and toxicity study. Clin Cancer Res 1996; 2: 947–952.

    CAS  PubMed  Google Scholar 

  34. Kastritis E, Terpos E, Dimopoulos MA . Current treatments for renal failure due to multiple myeloma. Expert Opin Pharmacother 2013; 14: 1477–1495.

    CAS  PubMed  Google Scholar 

  35. Russell JA, Kangarloo SB . Therapeutic drug monitoring of busulfan in transplantation. Curr Pharm Des 2008; 14: 1936–1949.

    CAS  PubMed  Google Scholar 

  36. Nieto Y, Vaughan WP . Pharmacokinetics of high-dose chemotherapy. Bone Marrow Transplant 2004; 33: 259–269.

    CAS  PubMed  Google Scholar 

  37. Shaw PJ, Nath CE, Nivison-Smith I, Joshua DE, Kerridge IH, Presgrave P et al. Higher melphalan exposure is associated with improved overall survival for myeloma patients undergoing autologous transplant. Biol Blood Marrow Transplant 2012; 18: S207.

    Google Scholar 

  38. Nath CE, Shaw PJ, Montgomery K, Earl JW . Melphalan pharmacokinetics in children with malignant disease: influence of body weight, renal function, carboplatin therapy and total body irradiation. Br J Clin Pharmacol 2005; 59: 314–324.

    CAS  PubMed  PubMed Central  Google Scholar 

  39. Tranchand B, Ploin YD, Minuit MP, Sapet C, Biron P, Philip T et al. High-dose melphalan dosage adjustment: possibility of using a test-dose. Cancer Chemother Pharmacol 1989; 23: 95–100.

    CAS  PubMed  Google Scholar 

  40. Parmar SR, Bookout R, Shapiro JF, Tombleson R, Perkins J, Kim J et al. Comparison of 1-day vs 2-day dosing of high-dose melphalan followed by autologous hematopoietic cell transplantation in patients with multiple myeloma. Bone Marrow Transplant 2014; 49: 761–766.

    CAS  PubMed  Google Scholar 

  41. Nath CE, Zeng L, Eslick A, Trotman J, Earl JW . An Isocratic UV HPLC Assay for Analysis of Total and Free Melphalan Concentrations in Human Plasma. Acta Chromatographica 2008; 20: 383–398.

    CAS  Google Scholar 

  42. Sweeney DJ, Greig NH, Rapoport SI . High-performance liquid chromatographic analysis of melphalan in plasma, brain and peripheral tissue by o-phthalaldehyde derivatization and fluorescence detection. J Chromatogr 1985; 339: 434–439.

    CAS  PubMed  Google Scholar 

  43. Ehrsson H, Eksborg S, Lindfors A . Quantitative determination of melphalan in plasma by liquid chromatography after derivatization with N-acetylcysteine. J Chromatogr 1986; 380: 222–228.

    CAS  PubMed  Google Scholar 

  44. Osterheld HK, Musch E, von Unruh GE, Loos U, Rauschecker H, Muhlenbruch BJ . A sensitive high-performance liquid chromatographic assay for melphalan and its hydrolysis products in blood and plasma. Cancer Chemother Pharmacol 1988; 21: 156–162.

    CAS  PubMed  Google Scholar 

  45. Springolo V, Borella F, Finardi GP, Gatti MT, Coppi G . High-performance liquid chromatographic determination of m-bis(chloroethyl)aminophenyl-L-alanine in plasma. J Chromatogr 1989; 490: 224–229.

    CAS  PubMed  Google Scholar 

  46. Silvestro L, Viano I, Baiocchi C, Saini G, Marmont F, Ferro R . Quantitation of melphalan in plasma of patients by reversed-phase high-performance liquid chromatography with electrochemical detection. J Chromatogr 1991; 563: 443–450.

    CAS  PubMed  Google Scholar 

  47. Sparidans RW, Martens I, Valkenburg-van Iersel LB, den Hartigh J, Schellens JH, Beijnen JH . Liquid chromatography-tandem mass spectrometric assay for the PARP-1 inhibitor olaparib in combination with the nitrogen mustard melphalan in human plasma. J Chromatogr B Analyt Technol Biomed Life Sci 2011; 879: 1851–1856.

    CAS  PubMed  Google Scholar 

  48. Vogl DT, Wang T, Perez WS, Stadtmauer EA, Heitjan DF, Lazarus HM et al. Effect of obesity on outcomes after autologous hematopoietic stem cell transplantation for multiple myeloma. Biol Blood Marrow Transplant 2011; 17: 1765–1774.

    PubMed  PubMed Central  Google Scholar 

  49. Bubalo J, Carpenter PA, Majhail N, Perales MA, Marks DI, Shaughnessy P et al. Conditioning chemotherapy dose adjustment in obese patients: a review and position statement by the American Society for Blood and Marrow Transplantation practice guideline committee. Biol Blood Marrow Transplant 2014; 20: 600–616.

    CAS  PubMed  Google Scholar 

  50. Shaw PJ, Nath CE, Trotman J, Gurney HP, Zeng L, Kwan YL et al. Actual weight to calculate surface area provides the best estimate of AUC for melphalan in myeloma. Biol Blood Marrow Transplant 2010; 16: S180.

    Google Scholar 

  51. Sharma M, Zhang M-J, Zhong X, Gasparetto CJ, Krishnan AY, Lonial S et al. Multiple myeloma (MM) in older (>70 year) patients - similar benefit from autologous hematopoietic cell transplantation (AHCT) compared with younger patients. Blood 2013; 122: 416–416.

    Google Scholar 

  52. Dasgupta RK, Adamson PJ, Davies FE, Rollinson S, Roddam PL, Ashcroft AJ et al. Polymorphic variation in GSTP1 modulates outcome following therapy for multiple myeloma. Blood 2003; 102: 2345–2350.

    CAS  PubMed  Google Scholar 

  53. Kuhne A, Kaiser R, Schirmer M, Heider U, Muhlke S, Niere W et al. Genetic polymorphisms in the amino acid transporters LAT1 and LAT2 in relation to the pharmacokinetics and side effects of melphalan. Pharmacogenet Genomics 2007; 17: 505–517.

    PubMed  Google Scholar 

  54. Dumontet C, Landi S, Reiman T, Perry T, Plesa A, Bellini I et al. Genetic polymorphisms associated with outcome in multiple myeloma patients receiving high-dose melphalan. Bone Marrow Transplant 2010; 45: 1316–1324.

    CAS  PubMed  Google Scholar 

  55. Vangsted A, Klausen TW, Vogel U . Genetic variations in multiple myeloma II: association with effect of treatment. Eur J Haematol 2012; 88: 93–117.

    CAS  PubMed  Google Scholar 

  56. Aljitawi OS, Ganguly S, Abhyankar S, Wolfe K, Daniels K, Ferree M et al. Phase IIa, open-label, randomized, pharmacokinetic comparative, cross-over study of melphalan Hcl for injection (propylene glycol-free) and alkeran for injection for myeloablative conditioning in multiple myeloma patients undergoing autologous transplantation. Biol Blood Marrow Transplantation 2012; 18: S257.

    Google Scholar 

  57. Rosenzweig M, Seldin DC, Remick DG, Skinner M, Quillen K, Oran B et al. Febrile reactions occurring with second cycle of high-dose melphalan and SCT in patients with AL amyloidosis: a 'melphalan recall' reaction. Bone Marrow Transplant 2010; 45: 21–24.

    CAS  PubMed  Google Scholar 

  58. McWilliams NB, Hayes FA, Green AA, Smith EI, Nitschke R, Altshuler GA et al. Cyclophosphamide/doxorubicin vs. cisplatin/teniposide in the treatment of children older than 12 months of age with disseminated neuroblastoma: a Pediatric Oncology Group Randomized Phase II study. Med Pediatr Oncol 1995; 24: 176–180.

    CAS  PubMed  Google Scholar 

  59. Pritchard J, Cotterill SJ, Germond SM, Imeson J, de Kraker J, Jones DR . High dose melphalan in the treatment of advanced neuroblastoma: results of a randomised trial (ENSG-1) by the European Neuroblastoma Study Group. Pediatr Blood Cancer 2005; 44: 348–357.

    PubMed  Google Scholar 

  60. Ladenstein R, Potschger U, Hartman O, Pearson AD, Klingebiel T, Castel V et al. 28 years of high-dose therapy and SCT for neuroblastoma in Europe: lessons from more than 4000 procedures. Bone Marrow Transplant 2008; 41 (Suppl 2): S118–S127.

    CAS  PubMed  Google Scholar 

  61. Matthay KK, Villablanca JG, Seeger RC, Stram DO, Harris RE, Ramsay NK et al. Treatment of high-risk neuroblastoma with intensive chemotherapy, radiotherapy, autologous bone marrow transplantation, and 13-cis-retinoic acid. Children's Cancer Group. N Engl J Med 1999; 341: 1165–1173.

    CAS  PubMed  Google Scholar 

  62. Matthay KK, Reynolds CP, Seeger RC, Shimada H, Adkins ES, Haas-Kogan D et al. Long-term results for children with high-risk neuroblastoma treated on a randomized trial of myeloablative therapy followed by 13-cis-retinoic acid: a children's oncology group study. J Clin Oncol 2009; 27: 1007–1013.

    CAS  PubMed  PubMed Central  Google Scholar 

  63. Kreissman SG, Seeger RC, Matthay KK, London WB, Sposto R, Grupp SA et al. Purged versus non-purged peripheral blood stem-cell transplantation for high-risk neuroblastoma (COG A3973): a randomised phase 3 trial. Lancet Oncol 2013; 14: 999–1008.

    CAS  PubMed  PubMed Central  Google Scholar 

  64. Ladenstein RL, Poetschger U, Luksch R, Brock P, Castel V, Yaniv I et al. Busulphan-melphalan as a myeloablative therapy (MAT) for high-risk neuroblastoma: Results from the HR-NBL1/SIOPEN trial. ASCO Meeting Abstracts 2011; 29 (18_suppl): 2.

    Google Scholar 

  65. Phillips GL, Meisenberg B, Reece DE, Adams VR, Badros A, Brunner J et al. Amifostine and autologous hematopoietic stem cell support of escalating-dose melphalan: a phase I study. Biol Blood Marrow Transplant 2004; 10: 473–483.

    CAS  PubMed  Google Scholar 

  66. Moreau P, Facon T, Attal M, Hulin C, Michallet M, Maloisel F et al. Comparison of 200 mg/m(2) melphalan and 8 Gy total body irradiation plus 140 mg/m(2) melphalan as conditioning regimens for peripheral blood stem cell transplantation in patients with newly diagnosed multiple myeloma: final analysis of the Intergroupe Francophone du Myelome 9502 randomized trial. Blood 2002; 99: 731–735.

    CAS  PubMed  Google Scholar 

  67. Zver S, Zadnik V, Cernelc P, Kozelj M . Cardiac toxicity of high-dose cyclophosphamide and melphalan in patients with multiple myeloma treated with tandem autologous hematopoietic stem cell transplantation. Int J Hematol 2008; 88: 227–236.

    PubMed  Google Scholar 

  68. Kozelj M, Zver S, Zadnik V . Long term follow-up report of cardiac toxicity in patients with multiple myeloma treated with tandem autologous hematopoietic stem cell transplantation. Radiol Oncol 2013; 47: 161–165.

    CAS  PubMed  PubMed Central  Google Scholar 

  69. Abidi MH, Agarwal R, Tageja N, Ayash L, Deol A, Al-Kadhimi Z et al. A phase I dose-escalation trial of high-dose melphalan with palifermin for cytoprotection followed by autologous stem cell transplantation for patients with multiple myeloma with normal renal function. Biol Blood Marrow Transplant 2013; 19: 56–61.

    CAS  PubMed  Google Scholar 

  70. Reece D, Song K, LeBlanc R, Mezzi K, Olujohungbe A, White D et al. Efficacy and safety of busulfan-based conditioning regimens for multiple myeloma. Oncologist 2013; 18: 611–618.

    CAS  PubMed  PubMed Central  Google Scholar 

  71. Moreau P, Attal M, Harousseau JL . New developments in conditioning regimens before auto-SCT in multiple myeloma. Bone Marrow Transplant 2011; 46: 911–915.

    CAS  PubMed  Google Scholar 

  72. Lahuerta JJ, Mateos MV, Martinez-Lopez J, Grande C, de la Rubia J, Rosinol L et al. Busulfan 12 mg/kg plus melphalan 140 mg/m2 versus melphalan 200 mg/m2 as conditioning regimens for autologous transplantation in newly diagnosed multiple myeloma patients included in the PETHEMA/GEM2000 study. Haematologica 2010; 95: 1913–1920.

    CAS  PubMed  PubMed Central  Google Scholar 

  73. Blanes M, Lahuerta JJ, Gonzalez JD, Ribas P, Solano C, Alegre A et al. Intravenous busulfan and melphalan as a conditioning regimen for autologous stem cell transplantation in patients with newly diagnosed multiple myeloma: a matched comparison to a melphalan-only approach. Biol Blood Marrow Transplant 2013; 19: 69–74.

    CAS  PubMed  Google Scholar 

  74. Yu AL, Gilman AL, Ozkaynak MF, London WB, Kreissman SG, Chen HX et al. Anti-GD2 antibody with GM-CSF, interleukin-2, and isotretinoin for neuroblastoma. N Engl J Med 2010; 363: 1324–1334.

    CAS  PubMed  PubMed Central  Google Scholar 

  75. Condomines M, Veyrune JL, Larroque M, Quittet P, Latry P, Lugagne C et al. Increased plasma-immune cytokines throughout the high-dose melphalan-induced lymphodepletion in patients with multiple myeloma: a window for adoptive immunotherapy. J Immunol 2010; 184: 1079–1084.

    CAS  PubMed  Google Scholar 

  76. Richardson PG, Lonial S, Jakubowiak AJ, Harousseau JL, Anderson KC . Monoclonal antibodies in the treatment of multiple myeloma. Br J Haematol 2011; 154: 745–754.

    CAS  PubMed  Google Scholar 

  77. Garfall AL, Vogl DT, Weiss BM, Stadtmauer EA . Cellular immunotherapy for plasma cell myeloma. Bone Marrow Transplant 2013; 48: 1377–1386.

    CAS  PubMed  Google Scholar 

  78. Lonial S, Kaufman J, Tighiouart M, Nooka A, Langston AA, Heffner LT et al. A phase I/II trial combining high-dose melphalan and autologous transplant with bortezomib for multiple myeloma: a dose- and schedule-finding study. Clin Cancer Res 2010; 16: 5079–5086.

    CAS  PubMed  Google Scholar 

  79. Miyamoto T, Yoshimoto G, Kamimura T, Muta T, Takashima S, Ito Y et al. Combination of high-dose melphalan and bortezomib as conditioning regimen for autologous peripheral blood stem cell transplantation in multiple myeloma. Int J Hematol 2013; 48: 1377–1386.

    Google Scholar 

  80. Popat R, Maharaj L, Oakervee H, Cavenagh J, Joel S . Schedule dependent cytotoxicity of bortezomib and melphalan in multiple myeloma. Br J Haematol 2013; 160: 111–114.

    CAS  PubMed  Google Scholar 

  81. Kaufman JL, Fabre C, Lonial S, Richardson PG . Histone deacetylase inhibitors in multiple myeloma: rationale and evidence for their use in combination therapy. Clin Lymphoma Myeloma Leuk 2013; 13: 370–376.

    CAS  PubMed  Google Scholar 

  82. Campbell RA, Sanchez E, Steinberg J, Shalitin D, Li ZW, Chen H et al. Vorinostat enhances the antimyeloma effects of melphalan and bortezomib. Eur J Haematol 2010; 84: 201–211.

    CAS  PubMed  Google Scholar 

  83. Peters WP, Stuart A, Klotman M, Gilbert C, Jones RB, Shpall EJ et al. High-dose combination cyclophosphamide, cisplatin, and melphalan with autologous bone marrow support. A clinical and pharmacologic study. Cancer Chemother Pharmacol 1989; 23: 377–383.

    CAS  PubMed  Google Scholar 

  84. Podar K, Tonon G, Sattler M, Tai YT, Legouill S, Yasui H et al. The small-molecule VEGF receptor inhibitor pazopanib (GW786034B) targets both tumor and endothelial cells in multiple myeloma. Proc Natl Acad Sci USA 2006; 103: 19478–19483.

    CAS  PubMed  PubMed Central  Google Scholar 

  85. Prince HM, Honemann D, Spencer A, Rizzieri DA, Stadtmauer EA, Roberts AW et al. Vascular endothelial growth factor inhibition is not an effective therapeutic strategy for relapsed or refractory multiple myeloma: a phase 2 study of pazopanib (GW786034). Blood 2009; 113: 4819–4820.

    CAS  PubMed  Google Scholar 

  86. Roussel M, Moreau P, Huynh A, Mary JY, Danho C, Caillot D et al. Bortezomib and high-dose melphalan as conditioning regimen before autologous stem cell transplantation in patients with de novo multiple myeloma: a phase 2 study of the Intergroupe Francophone du Myelome (IFM). Blood 2010; 115: 32–37.

    CAS  PubMed  Google Scholar 

  87. Nishihori T, Alekshun TJ, Shain K, Sullivan DM, Baz R, Perez L et al. Bortezomib salvage followed by a Phase I/II study of bortezomib plus high-dose melphalan and tandem autologous transplantation for patients with primary resistant myeloma. Br J Haematol 2012; 157: 553–563.

    CAS  PubMed  PubMed Central  Google Scholar 

  88. Rodriguez TE, Hari P, Stiff PJ, Zhong X, Sterrenberg D, Vesole DH . Busulfan / melphalan / bortezomib (Bu-Mel-Vel) vs. high dose melphalan as conditioning regimen for autologous hematopoietic cell transplantation in multiple myeloma (MM). Blood 2013; 122: 3357–3357.

    Google Scholar 

  89. Giralt S, Bensinger W, Goodman M, Podoloff D, Eary J, Wendt R et al. 166Ho-DOTMP plus melphalan followed by peripheral blood stem cell transplantation in patients with multiple myeloma: results of two phase 1/2 trials. Blood 2003; 102: 2684–2691.

    CAS  PubMed  Google Scholar 

  90. Christoforidou AV, Saliba RM, Williams P, Qazilbash M, Roden L, Aleman A et al. Results of a retrospective single institution analysis of targeted skeletal radiotherapy with (166)Holmium-DOTMP as conditioning regimen for autologous stem cell transplant for patients with multiple myeloma. Impact on transplant outcomes. Biol Blood Marrow Transplant 2007; 13: 543–549.

    PubMed  Google Scholar 

  91. Dispenzieri A, Wiseman GA, Lacy MQ, Hayman SR, Kumar SK, Buadi F et al. A Phase II study of (153)Sm-EDTMP and high-dose melphalan as a peripheral blood stem cell conditioning regimen in patients with multiple myeloma. Am J Hematol 2010; 85: 409–413.

    CAS  PubMed  PubMed Central  Google Scholar 

  92. Qazilbash MH, Saliba RM, Nieto Y, Parikh G, Pelosini M, Khan FB et al. Arsenic trioxide with ascorbic acid and high-dose melphalan: results of a phase II randomized trial. Biol Blood Marrow Transplant 2008; 14: 1401–1407.

    CAS  PubMed  PubMed Central  Google Scholar 

  93. Sharma M, Khan H, Thall PF, Orlowski RZ, Bassett RL Jr, Shah N et al. A randomized phase 2 trial of a preparative regimen of bortezomib, high-dose melphalan, arsenic trioxide, and ascorbic acid. Cancer 2012; 118: 2507–2515.

    CAS  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to P J Shaw.

Ethics declarations

Competing interests

Dr Shaw and Dr Nath have received funding from the National Heath and Research Council for their work on melphalan pharmacokinetics in myeloma Dr Lazarus declares no conflict of interest

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Shaw, P., Nath, C. & Lazarus, H. Not too little, not too much—just right! (Better ways to give high dose melphalan). Bone Marrow Transplant 49, 1457–1465 (2014). https://doi.org/10.1038/bmt.2014.186

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/bmt.2014.186

This article is cited by

Search

Quick links