Effects of Polyethylene GlycolConjugated Recombinant Human Megakaryocyte Growth and Development Factor on Platelet Counts after Chemotherapy for Lung Cancer
Michael Fanucchi, M.D., John Glaspy, M.D., Jeffrey Crawford, M.D., Jennifer Garst, M.D., Robert Figlin, M.D., William Sheridan, M.B., B.S., Dora Menchaca, Ph.D., Dianne Tomita, M.P.H., Howard Ozer, M.D., Ph.D., and Laurence Harker, M.D.
Background Polyethylene glycol (PEG)conjugated recombinanthuman megakaryocyte growth and development factor (MGDF, alsoknown as PEG-rHuMGDF), a recombinant molecule related to thrombopoietin,specifically stimulates megakaryopoiesis and platelet productionand reduces the severity of thrombocytopenia in animals receivingmyelosuppressive chemotherapy.
Methods We conducted a randomized, double-blind, placebo-controlleddose-escalation study of MGDF in 53 patients with lung cancerwho were treated with carboplatin and paclitaxel. The patientswere randomly assigned in blocks of 4 in a 1:3 ratio to receiveeither placebo or MGDF (0.03, 0.1, 0.3, 1.0, 3.0, or 5.0 µgper kilogram of body weight per day), injected subcutaneously.No other marrow-active cytokines were given.
Results In the 38 patients who received MGDF after chemotherapy,the median nadir platelet count was 188,000 per cubic millimeter(range, 68,000 to 373,000), as compared with 111,000 per cubicmillimeter (range, 21,000 to 307,000) in 12 patients receivingplacebo (P = 0.013). The platelet count recovered to base-linelevels in 14 days in the treated patients as compared with morethan 21 days in those receiving placebo (P<0.001). Amongall 40 patients treated with MGDF, 1 had deep venous thrombosisand pulmonary embolism, and another had superficial thrombophlebitis.
Conclusions MGDF has potent stimulatory effects on plateletproduction in patients with chemotherapy-induced thrombocytopenia.
Source Information
From the Division of HematologyOncology, Department of Medicine, and the Winship Cancer Center, Emory University School of Medicine, Atlanta (M.F., H.O., L.H.); the UCLA School of Medicine, Los Angeles (J. Glaspy, R.F.); the Comprehensive Cancer Center and Department of Medicine, Duke University, Durham, N.C. (J.C., J. Garst); and Amgen, Inc., Thousand Oaks, Calif. (W.S., D.M., D.T.).
Address reprint requests to Dr. Fanucchi at Emory University School of Medicine, 1365 Clifton Rd., Bldg. B, Rm. B6204, Atlanta, GA 30322.
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