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Original Article
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Volume 336:404-409 February 6, 1997 Number 6
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Effects of Polyethylene Glycol–Conjugated 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.

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ABSTRACT

Background Polyethylene glycol (PEG)–conjugated recombinant human megakaryocyte growth and development factor (MGDF, also known as PEG-rHuMGDF), a recombinant molecule related to thrombopoietin, specifically stimulates megakaryopoiesis and platelet production and reduces the severity of thrombocytopenia in animals receiving myelosuppressive chemotherapy.

Methods We conducted a randomized, double-blind, placebo-controlled dose-escalation study of MGDF in 53 patients with lung cancer who were treated with carboplatin and paclitaxel. The patients were randomly assigned in blocks of 4 in a 1:3 ratio to receive either placebo or MGDF (0.03, 0.1, 0.3, 1.0, 3.0, or 5.0 µg per 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 cubic millimeter (range, 21,000 to 307,000) in 12 patients receiving placebo (P = 0.013). The platelet count recovered to base-line levels in 14 days in the treated patients as compared with more than 21 days in those receiving placebo (P<0.001). Among all 40 patients treated with MGDF, 1 had deep venous thrombosis and pulmonary embolism, and another had superficial thrombophlebitis.

Conclusions MGDF has potent stimulatory effects on platelet production in patients with chemotherapy-induced thrombocytopenia.


Source Information

From the Division of Hematology–Oncology, 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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