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   <subfield code="a">10.1007/BF01741788</subfield>
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   <subfield code="a">Unique histological changes in lung metastases of osteosarcoma patients following therapy with liposomal muramyl tripeptide (CGP 19835A lipid)</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Eugenie Kleinerman, Austin Raymond, Corazon Bucana, Norman Jaffe, Michael Harris, Irwin Krakoff, Robert Benjamin, Isaiah Fidler]</subfield>
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   <subfield code="a">Summary: We have recently begun a phase II trial in patients with osteosarcoma who developed pulmonary metastases during adjuvant chemotherapy or who presented with pulmonary metastases that persisted despite chemotherapy. Eligible patients were rendered free of visible disease by surgery. Liposome-encapsulated muramyl tripeptide phosphatidylethanolamine (MTP-PE, CGP 19835A lipid) (2 mg/m2) was infused twice weekly for 3 months. In five patients, a single tumor nodule recurred within 6 weeks after completion of therapy. These lesions were resected and submitted for pathological examination. Tissue specimens obtained after therapy were compared to those obtained before therapy. All the patients showed a histological change in the characteristics of the pulmonary tumors. In three patients, peripheral fibrosis surrounded the tumor and inflammatory cell infiltration and neovascularization were present. This is in contrast to central necrosis, with viable peripheral tumor cells and no inflammatory response observed in lesions resected following chemotherapy. In a fourth case, evidence of early fibrotic changes was found. This and the fifth case showed a change in malignant characteristics, from high grade before liposomal therapy to low grade after therapy. The present study provides evidence for a biological effect of liposomal MTP-PE.</subfield>
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   <subfield code="a">Springer-Verlag, 1992</subfield>
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   <subfield code="a">Liposomal therapy</subfield>
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   <subfield code="a">Kleinerman</subfield>
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   <subfield code="u">Department of Cell Biology, The University of Texas M. D. Anderson Cancer Center, 1515 Holcombe Boulevard, Box 173, 77 030, Houston, Texas, USA</subfield>
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   <subfield code="a">Raymond</subfield>
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   <subfield code="u">Department of Pathology, The University of Texas M. D. Anderson Cancer Center, Houston, Texas, USA</subfield>
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   <subfield code="u">Department of Cell Biology, The University of Texas M. D. Anderson Cancer Center, 1515 Holcombe Boulevard, Box 173, 77 030, Houston, Texas, USA</subfield>
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   <subfield code="a">Jaffe</subfield>
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   <subfield code="u">Department of Pediatrics, The University of Texas M. D. Anderson Cancer Center, Houston, Texas, USA</subfield>
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   <subfield code="u">Tomorrow's Children's Institute, Hackensack, New Yersey, USA</subfield>
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   <subfield code="a">Krakoff</subfield>
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   <subfield code="u">Department of Division of Medicine, The University of Texas M. D. Anderson Cancer Center, Houston, Texas, USA</subfield>
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   <subfield code="a">Benjamin</subfield>
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   <subfield code="u">Department of Medical Oncology, The University of Texas M. D. Anderson Cancer Center, Houston, Texas, USA</subfield>
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   <subfield code="D">Isaiah</subfield>
   <subfield code="u">Department of Cell Biology, The University of Texas M. D. Anderson Cancer Center, 1515 Holcombe Boulevard, Box 173, 77 030, Houston, Texas, USA</subfield>
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   <subfield code="t">Cancer Immunology, Immunotherapy</subfield>
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   <subfield code="g">34/4(1992-07-01), 211-220</subfield>
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