Therapy of patients with malignant melanoma using a monoclonal antimelanoma antibody-ricin A chain immunotoxin

We conducted a trial of a murine monoclonal antimelanoma antibody-ricin A chain immunotoxin (XOMAZYME-MEL) in 22 patients with metastatic malignant melanoma. The dose of immunotoxin administered ranged from 0.01 mg/kg daily for 5 days to 1 mg/kg daily for 4 days (total dose: 3.2 to 300 mg). Side eff...

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Veröffentlicht in:Cancer research (Chicago, Ill.) Ill.), 1987-03, Vol.47 (6), p.1717-1723
Hauptverfasser: SPITLER, L. E, DEL RIO, M, KAWAHATA, R. T, STOUDEMIRE, J. B, FRADKIN, L. B, BAUTISTA, E. E, SCANNON, P. J, KHENTIGAN, A, WEDEL, N. I, BROPHY, N. A, MILLER, L. L, HARKONEN, W. S, ROSENDORF, L. L, LEE, H. M, MISCHAK, R. P
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container_issue 6
container_start_page 1717
container_title Cancer research (Chicago, Ill.)
container_volume 47
creator SPITLER, L. E
DEL RIO, M
KAWAHATA, R. T
STOUDEMIRE, J. B
FRADKIN, L. B
BAUTISTA, E. E
SCANNON, P. J
KHENTIGAN, A
WEDEL, N. I
BROPHY, N. A
MILLER, L. L
HARKONEN, W. S
ROSENDORF, L. L
LEE, H. M
MISCHAK, R. P
description We conducted a trial of a murine monoclonal antimelanoma antibody-ricin A chain immunotoxin (XOMAZYME-MEL) in 22 patients with metastatic malignant melanoma. The dose of immunotoxin administered ranged from 0.01 mg/kg daily for 5 days to 1 mg/kg daily for 4 days (total dose: 3.2 to 300 mg). Side effects observed in most patients were a transient fall in serum albumin with an associated fall in serum protein, weight gain, and fluid shifts resulting in edema. In addition, patients experienced mild to moderate malaise, fatigue, myalgia, decrease in appetite, and fevers. There was a transient decrease in voltage on electrocardiograms without clinical symptoms, change in serial echocardiograms or elevation of creatine phosphokinase MB isozyme levels. Symptoms consistent with mild allergic reactions were observed in three patients. The side effects were related to the dose of immunotoxin administered and were generally transient and reversible. Encouraging clinical results were observed, even after a single course of a low dose of immunotoxin. In addition, localization of antibody and A chain to sites of metastatic disease was demonstrated by immunoperoxidase staining of biopsy specimens. Additional studies are being conducted to continue the evaluation of safety and efficacy of immunotoxin therapy for malignancy.
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E ; DEL RIO, M ; KAWAHATA, R. T ; STOUDEMIRE, J. B ; FRADKIN, L. B ; BAUTISTA, E. E ; SCANNON, P. J ; KHENTIGAN, A ; WEDEL, N. I ; BROPHY, N. A ; MILLER, L. L ; HARKONEN, W. S ; ROSENDORF, L. L ; LEE, H. M ; MISCHAK, R. P</creator><creatorcontrib>SPITLER, L. E ; DEL RIO, M ; KAWAHATA, R. T ; STOUDEMIRE, J. B ; FRADKIN, L. B ; BAUTISTA, E. E ; SCANNON, P. J ; KHENTIGAN, A ; WEDEL, N. I ; BROPHY, N. A ; MILLER, L. L ; HARKONEN, W. S ; ROSENDORF, L. L ; LEE, H. M ; MISCHAK, R. P</creatorcontrib><description>We conducted a trial of a murine monoclonal antimelanoma antibody-ricin A chain immunotoxin (XOMAZYME-MEL) in 22 patients with metastatic malignant melanoma. The dose of immunotoxin administered ranged from 0.01 mg/kg daily for 5 days to 1 mg/kg daily for 4 days (total dose: 3.2 to 300 mg). Side effects observed in most patients were a transient fall in serum albumin with an associated fall in serum protein, weight gain, and fluid shifts resulting in edema. In addition, patients experienced mild to moderate malaise, fatigue, myalgia, decrease in appetite, and fevers. There was a transient decrease in voltage on electrocardiograms without clinical symptoms, change in serial echocardiograms or elevation of creatine phosphokinase MB isozyme levels. Symptoms consistent with mild allergic reactions were observed in three patients. The side effects were related to the dose of immunotoxin administered and were generally transient and reversible. Encouraging clinical results were observed, even after a single course of a low dose of immunotoxin. In addition, localization of antibody and A chain to sites of metastatic disease was demonstrated by immunoperoxidase staining of biopsy specimens. Additional studies are being conducted to continue the evaluation of safety and efficacy of immunotoxin therapy for malignancy.</description><identifier>ISSN: 0008-5472</identifier><identifier>EISSN: 1538-7445</identifier><identifier>PMID: 3493066</identifier><identifier>CODEN: CNREA8</identifier><language>eng</language><publisher>Philadelphia, PA: American Association for Cancer Research</publisher><subject>Adult ; Aged ; Antibodies, Monoclonal - therapeutic use ; Antibodies, Neoplasm - immunology ; Antineoplastic agents ; Biological and medical sciences ; Bone Marrow - drug effects ; Chemotherapy ; Female ; Humans ; Immunotoxins - adverse effects ; Immunotoxins - therapeutic use ; Male ; Medical sciences ; Melanoma - immunology ; Melanoma - therapy ; Middle Aged ; Neoplasm Metastasis ; Pharmacology. 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B</creatorcontrib><creatorcontrib>BAUTISTA, E. E</creatorcontrib><creatorcontrib>SCANNON, P. J</creatorcontrib><creatorcontrib>KHENTIGAN, A</creatorcontrib><creatorcontrib>WEDEL, N. I</creatorcontrib><creatorcontrib>BROPHY, N. A</creatorcontrib><creatorcontrib>MILLER, L. L</creatorcontrib><creatorcontrib>HARKONEN, W. S</creatorcontrib><creatorcontrib>ROSENDORF, L. L</creatorcontrib><creatorcontrib>LEE, H. M</creatorcontrib><creatorcontrib>MISCHAK, R. P</creatorcontrib><title>Therapy of patients with malignant melanoma using a monoclonal antimelanoma antibody-ricin A chain immunotoxin</title><title>Cancer research (Chicago, Ill.)</title><addtitle>Cancer Res</addtitle><description>We conducted a trial of a murine monoclonal antimelanoma antibody-ricin A chain immunotoxin (XOMAZYME-MEL) in 22 patients with metastatic malignant melanoma. The dose of immunotoxin administered ranged from 0.01 mg/kg daily for 5 days to 1 mg/kg daily for 4 days (total dose: 3.2 to 300 mg). Side effects observed in most patients were a transient fall in serum albumin with an associated fall in serum protein, weight gain, and fluid shifts resulting in edema. In addition, patients experienced mild to moderate malaise, fatigue, myalgia, decrease in appetite, and fevers. There was a transient decrease in voltage on electrocardiograms without clinical symptoms, change in serial echocardiograms or elevation of creatine phosphokinase MB isozyme levels. Symptoms consistent with mild allergic reactions were observed in three patients. The side effects were related to the dose of immunotoxin administered and were generally transient and reversible. Encouraging clinical results were observed, even after a single course of a low dose of immunotoxin. In addition, localization of antibody and A chain to sites of metastatic disease was demonstrated by immunoperoxidase staining of biopsy specimens. Additional studies are being conducted to continue the evaluation of safety and efficacy of immunotoxin therapy for malignancy.</description><subject>Adult</subject><subject>Aged</subject><subject>Antibodies, Monoclonal - therapeutic use</subject><subject>Antibodies, Neoplasm - immunology</subject><subject>Antineoplastic agents</subject><subject>Biological and medical sciences</subject><subject>Bone Marrow - drug effects</subject><subject>Chemotherapy</subject><subject>Female</subject><subject>Humans</subject><subject>Immunotoxins - adverse effects</subject><subject>Immunotoxins - therapeutic use</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Melanoma - immunology</subject><subject>Melanoma - therapy</subject><subject>Middle Aged</subject><subject>Neoplasm Metastasis</subject><subject>Pharmacology. 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P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Therapy of patients with malignant melanoma using a monoclonal antimelanoma antibody-ricin A chain immunotoxin</atitle><jtitle>Cancer research (Chicago, Ill.)</jtitle><addtitle>Cancer Res</addtitle><date>1987-03-15</date><risdate>1987</risdate><volume>47</volume><issue>6</issue><spage>1717</spage><epage>1723</epage><pages>1717-1723</pages><issn>0008-5472</issn><eissn>1538-7445</eissn><coden>CNREA8</coden><abstract>We conducted a trial of a murine monoclonal antimelanoma antibody-ricin A chain immunotoxin (XOMAZYME-MEL) in 22 patients with metastatic malignant melanoma. The dose of immunotoxin administered ranged from 0.01 mg/kg daily for 5 days to 1 mg/kg daily for 4 days (total dose: 3.2 to 300 mg). Side effects observed in most patients were a transient fall in serum albumin with an associated fall in serum protein, weight gain, and fluid shifts resulting in edema. In addition, patients experienced mild to moderate malaise, fatigue, myalgia, decrease in appetite, and fevers. There was a transient decrease in voltage on electrocardiograms without clinical symptoms, change in serial echocardiograms or elevation of creatine phosphokinase MB isozyme levels. Symptoms consistent with mild allergic reactions were observed in three patients. The side effects were related to the dose of immunotoxin administered and were generally transient and reversible. Encouraging clinical results were observed, even after a single course of a low dose of immunotoxin. In addition, localization of antibody and A chain to sites of metastatic disease was demonstrated by immunoperoxidase staining of biopsy specimens. Additional studies are being conducted to continue the evaluation of safety and efficacy of immunotoxin therapy for malignancy.</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>3493066</pmid><tpages>7</tpages></addata></record>
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source MEDLINE; American Association for Cancer Research; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
subjects Adult
Aged
Antibodies, Monoclonal - therapeutic use
Antibodies, Neoplasm - immunology
Antineoplastic agents
Biological and medical sciences
Bone Marrow - drug effects
Chemotherapy
Female
Humans
Immunotoxins - adverse effects
Immunotoxins - therapeutic use
Male
Medical sciences
Melanoma - immunology
Melanoma - therapy
Middle Aged
Neoplasm Metastasis
Pharmacology. Drug treatments
Ricin - therapeutic use
Serum Albumin - analysis
title Therapy of patients with malignant melanoma using a monoclonal antimelanoma antibody-ricin A chain immunotoxin
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