Abstract
Patients receiving intensive chemotherapy or marrow-ablative regimens as treatment for a variety of cancers require repetitive transfusions of platelets. Although death from hemorrhage is a rare event in such patients, minor episodes of bleeding are common, and there are appreciable potential complications from repeated platelet transfusions (Table 1). The most clinically ominous of these side effects is the development of alloimmunization with the requirement for identification and apheresis of histocompatible donors. Often, such compatible donors cannot be readily located, and the patient remains at risk of bleeding. Another serious problem is the frequent occurrence of febrile or allergic transfusion reactions, even in patients premedicated with antipyretics and/or antihistamines; these reactions can be quite discomfiting and frightening for the patient. In neutropenic patients, such transfusion reactions often mandate hospitalization and interim coverage with broad-spectrum antibiotics until culture results are available. Although transfusion reactions are common in alloimmunized patients, the presence in the plasma of a variety of different cytokines, elaborated because of damage to contaminating leukocytes during storage, is responsible for the frequent development of transfusion reactions in nonalloimmunized recipients (1).
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References
Heddle NM, Klama L, Singer J, et al. The role of plasma from platelet concentrates in transfusion reactions. N Engl J Med. 1994; 331: 625–628.
Buchholz DH, Young VM, Friedman NR, Reilly JA, Mardiney MR, Jr. Bacterial proliferation in platelet products stored at room temperature. Transfusion-induced enterobacter sepsis. N Engl J Med. 1971;285:429–433.
Braine HG, Kickler TS, Charache P, et al. Bacterial sepsis secondary to platelet transfusion: an adverse effect of extended storage at room temperature. Transfusion. 1986; 26: 391–393.
Ishibashi T, Kimura T, Uchida T, Kariyone S, Friese P, Burstein SA. Human interleukin 6 is a direct promoter of maturation of megakaryocytes in vitro. Proc Natl Acad Sci USA. 1989; 86: 5953–5957.
Musashi M, Yang YC, Paul SR, Clark SC, Sudo T, Ogawa M. Direct and synergistic effects of interleukin 11 on murine hemopoiesis in culture. Proc Natl Acad Sci USA. 1991; 88: 765–769.
Kaushansky K. Thrombopoietin: The primary regulator of platelet production. Blood. 1995; 86:419–431.
Bartley TD, Bogenberger J, Hunt P, et al. Identification and cloning of a megakaryocyte growth and development factor that is a ligand for the cytokine receptor Mpl. Cell. 1994; 77: 1117–1124.
Lok S, Kaushansky K, Holly RD, et al. Cloning and expression of murine thrombopoietin cDNA and stimulation of platelet production in vivo. Nature. 1994; 369: 565–568.
de Sauvage FJ, Hass PE, Spencer SD, et al. Stimulation of megakaryocytopoiesis and throm-bopoiesis by the c-Mpl ligand. Nature. 1994; 369: 533–538.
Ulich T, del Castillo J, Yin S, et al. Megakaryocyte growth and development factor ameliorates carboplatin-induced thrombocytopenia in mice. Blood. 1995; 86: 971–976.
Farese AM, Hunt P, Boone TC, MacVittie TJ. Recombinant human megakaryocyte growth and development factor stimulates thrombocytopoiesis in normal non-human primates. Blood. 1995; 86: 54–59.
Farese AM, Hunt P, Grab LB, MacVittie TJ. Combined administration of recombinant human megakaryocyte growth and development factor and granulocyte colony stimulating factor enhances multilineage hematopoietic reconstitution in nonhuman primates after radiation induced marrow aplasia. J Clin Invest. 1996; 97: 2145–2151.
Andrews RG, Winkler A, Woogerd P, et al. Recombinant human megakaryocyte growth and development factor (rHUMGDF) stimulates thrombopoiesis in normal baboons and accelerates platelet recovery after chemotherapy. Blood. 1995; 86: 371a (abstract no 1471).
Kaushansky K, Broudy VC, Grossmann A, et al. Thrombopoietin expands erythroid progenitors, increases red cell production, and enhances erythroid recovery after myelosuppressive therapy. J Clin Invest. 1995; 96: 1683–1687.
Hokom MM, Lacey D, Kinstler OB, et al. Peglayted megakaryocyte growth and development factor abrogates the lethal thrombocytopenia associated with carboplatin and irradiation in mice. Blood. 1995; 86: 4486–1492.
Molineux G, Hartley C, McElroy T, McCrea C, McNiece I. Megakaryocyte growth and development factor (MGDF) accelerates platelet recovery in peripheral blood progenitor cell (PBPC) transplant recipients. Blood. 1995; 86: 461a (abstract no 1831).
Basser R, Clarke K, Fox R, et al. Randomized, double-blind, placebo-controlled phase I trial of pegylated megakaryocyte growth and development factor (PEG-rHuMGDF) administered to patients with advanced cancer before and after chemotherapy-early results. Blood. 1995; 86: 257a (abstract no 1014).
Harker LA, Slichter SJ. The bleeding time as a screening test for evaluation of platelet function. N Engl J Med. 1972; 287: 155–159.
Bishop JF, Schiffer CA, Aisner J, Matthews JP, Wiernik PH. Surgery in acute leukemia: A review of 167 operations in thrombocytopenic patients. Am J Hematol 1987; 26: 147–155.
Dutcher J, Schiffer CA, Aisner J, Wiernik PH. Long-term follow-up of patients with leukemia receiving platelet transfusions: Identification of a large group of patients who do not become alloimmunized. Blood. 1981; 58: 1007–1011.
Dutcher J, Schiffer CA, Aisner J, Wiernik PH. Alloimmunization following platelet transfusion: the absence of a dose response relationship. Blood. 1981; 57: 395–398.
National Institutes of Health Consensus Development Consensus Conference. Platelet transfusion therapy. JAMA. 1987; 257: 1777–1780.
Gaydos LA, Freireich EJ, Mantel N. The quantitative relation between count and hemorrhage in patients with acute leukemia. N EnglJ Med. 1962; 266: 905–909.
Freireich EJ, Kliman A, Gaydos LA, et al. Response to repeated platelet transfusion from the same donor. Ann Intern Med. 1963; 59: 277–287.
Djerassi I, Farber S, Evans AE. Transfusions of fresh platelet concentrates to patients with secondary thrombocytopenia. N Engl J Med. 1963; 268: 221–226.
Schiffer CA. Prophylactic platelet transfusion. Transfusion. 1992; 32: 295–298.
Beutler E. Platelet transfusions: the 20,000/µL trigger. Blood. 1993; 81: 1411–1413.
Gmur J, Burger J, Schanz U, Fehr J, Schaffner A. Safety of stringent prophylactic platelet transfusion policy for patients with acute leukaemia. Lancet. 1991; 338: 1223–1226.
Heyman MR, Schiffer CA. Platelet transfusion therapy for the cancer patient. Semin Oncol. 1990; 17: 198–209.
Stone RM, Berg DT, George SL, et al. Granulocyte-macrophage colony stimulating factor after initial chemotherapy for elderly patients with primary acute myeloid leukemia. N Engl J Med. 1995; 332: 1671–1677.
Mayer RJ, Davis RB, Schiffer CA, et al. Intensive postremission chemotherapy in adults with acute myeloid leukemia. N Engl J Med. 1994; 331: 896–903.
Archimbaud E, Thomas X, Leblond V, et al. Timed sequential chemotherapy for previously treated patients with acute myeloid leukemia: long-term follow-up of the etoposide, mitoxantrone, and cytarabine-86 trial. J Clin Oncol. 1995; 13: 11–18.
Vigon I, Dreyfus F, Melle J, et al. Expression of the c-mpl proto-oncogene in human hematologic malignancies. Blood. 1993; 82: 877–883.
Matsumura I, Kanakura Y, Kato T, et al. Growth response of acute myeloblastic leukemia cells to recombinant human thrombopoietin. Blood. 1995; 86: 703–709.
Piacibello W, Sanavio F, Garetto L, et al. The effect of human megakaryocyte growth and development factor (MGDF) on human myeloid leukemia cell growth. Blood. 1995; 86: 45a (abstract no 168).
Slack JL, Baer MR, Bernstein SH, et al. Acute myeloid leukemia (AML) blast cell proliferation and differentiation in response to megakaryocyte growth and development factor (MGDF). Blood. 1995; 86: 520a (abstract no 2070).
Rowe JM, Andersen J, Mazza JJ, et al. A randomized placebo-controlled phase III of granulo-cyte-macrophage colony stimulating factor (GM-CSF) in adult patients (55 to 70 years) with acute myelogenous leukemia (AML). A study of the Eastern Cooperative Oncology Group (ECOG). Blood. 1995; 86: 257–262.
Dombret H, Chastang C, Feraux P, et al. A controlled study of recombinant human granulocyte colony stimulating factor in elderly patients after treatment for acute myeloid leukemia (AML). N Engl J Med. 1995; 332: 1678–1683.
Weaver CH, Buckner CK, Longin K, et al. Syngeneic transplantation with peripheral blood mononuclear cells collected after the administration of recombinant human granulocyte colony-stimulating factor. Blood. 1993; 82: 1981–1984.
Nichol JL, Hornkohl A, Selesi D, Wyres M, Hunt P. TPO levels in plasma of patients with thrombocytopenia or thrombocytosis. Blood. 1995; 86: 371a (abstract no 1474).
Nichol J, Hokom MM, Hornkohl, A, et al. Megakaryocyte growth and development factor. Analyses of in vitro effects on human megakaryopoiesis and endogenous serum levels during chemotherapy-induced thrombocytopenia. J Clin Invest. 1995; 95: 2973–2978.
Stein RS, Abels RI, Krantz SB. Pharmacologic doses of recombinant human erythropoietin in the treatment of myelodysplastic syndromes. Blood. 1991; 78: 1658–1665.
Negrin RS, Haeuber DH, Nagler A, et al. Maintenance treatment of patients with myelodysplastic syndromes using recombinant human granulocyte colony stimulating factor. Blood. 1990; 76: 36–43.
Hogge DE, Thompson BW, Schiffer CA. Platelet storage for seven days in second generation blood bags. Transfusion. 1986; 26: 131–135.
Schiffer CA, Lee EJ, Ness PM, Reilly J. Clinical evaluation of platelet concentrates stored for 1–5 days. Blood. 1986; 67: 1591–1594.
Schiffer CA, Aisner J, Wiernik PH. Frozen autologous platelet transfusion for patients with leukemia. N Engl J Med. 1978; 299: 7–12.
O’Connell BA, Lee EJ, Rothko K, Hussein MA, Schiffer CA. Selection of histocompatible apheresis platelet donors by cross-matching random donor platelet concentrates. Blood. 1992; 79:527–531.
Bensinger WI, Price TH, Dale DC, et al. The effects of daily recombinant human granulocyte colony-stimulating factor administration on normal granulocyte donors undergoing leukapheresis. Blood. 1993; 81: 1883–1888.
Korbling M, Huh YO, Durett A, et al. Allogeneic blood stem cell transplantation: peripheralization and yield of donor-derived primitive hematopoietic progenitor cells (CD34+Thy- ldim) and lymphoid subsets, and possible predictors of engraftment and graft-versus-host disease. Blood. 1995; 86: 2842–2848.
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Schiffer, C.A. (1997). Potential Clinical Applications of Thrombopoietic Growth Factors. In: Kuter, D.J., Hunt, P., Sheridan, W., Zucker-Franklin, D. (eds) Thrombopoiesis and Thrombopoietins. Humana Press. https://doi.org/10.1007/978-1-4612-3958-1_4
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DOI: https://doi.org/10.1007/978-1-4612-3958-1_4
Publisher Name: Humana Press
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