Specific targeting, biodistribution, and lack of immunogenicity of chimeric anti-GD3 monoclonal antibody KM871 in patients with metastatic melanoma: Results of a phase I trial

被引:57
作者
Scott, AM
Lee, FT
Hopkins, W
Cebon, JS
Wheatley, JM
Liu, ZQ
Smyth, FE
Murone, C
Sturrock, S
MacGregor, D
Hanai, N
Inoue, K
Yamasaki, M
Brechbiel, MW
Davis, ID
Murphy, R
Hannah, A
Lim-Joon, M
Chan, T
Chong, G
Ritter, G
Hoffman, EW
Burgess, AW
Old, LJ
机构
[1] Austin & Repatriat Med Ctr, Ludwig Inst Canc Res, Melbourne Tumor Biol Branch, Melbourne, Vic, Australia
[2] Austin & Repatriat Med Ctr, Dept Nucl Med, Melbourne, Vic, Australia
[3] Austin & Repatriat Med Ctr, Ctr Positron Emiss Tomog, Melbourne, Vic, Australia
[4] Austin & Repatriat Med Ctr, Dept Surg, Melbourne, Vic, Australia
[5] Austin & Repatriat Med Ctr, Dept Anat Pathol, Melbourne, Vic, Australia
[6] Kyowa Hakko Kogyo Co Ltd, Tokyo, Japan
[7] NCI, Radioimmune & Inorgan Chem Sect, NIH, Bethesda, MD 20892 USA
[8] Ludwig Inst Canc Res, New York, NY USA
关键词
D O I
10.1200/JCO.2001.19.19.3976
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: KM871 is a chimeric monoclonal antibody against the ganglioside antigen GD3, which is highly expressed on melanoma cells. We conducted an open-label, dose escalation phase I trial of KM871 in patients with metastatic melanoma. Patients and Methods: Seventeen patients were entered onto one of five dose levels (1, 5, 10, 20, and 40 mg/m(2)). Patients received three infusions of KM871 at 2-week intervals, with the first infusion of KM871 trace-labeled with indium-111 (In-111) to enable assessment of biodistribution in vivo. Biopsies of metastatic melanoma sites were performed on days 7 to 10. Results: Fifteen of 17 patients completed a cycle of three infusions of KM871. No dose-limiting toxicity was observed during the trial; the maximum-tolerated dose was therefore not reached. Three patients (at the 1-, 5-, and 40-mg/m(2) dose levels) developed pain and/or erythema at tumor sites consistent with an inflammatory response. No normal tissue uptake of In-111-KM871 was observed, and tumor uptake of In-111-KM871 was observed in all lesions greater than 1.5 cm (tumor biopsy (111)KM871 uptake results: range, 0.001% to 0.026% injected dose/g). The ratio of maximum tumor to normal tissue was 15:1. Pharmacokinetic analysis revealed a In-111-KM871 terminal half-life of 7.68 +/- 2.94 days. One patient had a clinical partial response that lasted 11 months. There was no serologic evidence of human antichimeric antibody in any patient, including one patient who received 16 infusions over a 12-month period. Conclusion: This study is the first to demonstrate the biodistribution and specific targeting of an anti-GD3 antibody to metastatic melanoma in patients. The long half-life and lack of immunogenicity of KM871 makes this antibody an attractive potential therapy for patients with metastatic melanoma. (C) 2001 by American Society of Clinical Oncology.
引用
收藏
页码:3976 / 3987
页数:12
相关论文
共 32 条
[1]   TREATMENT WITH HIGH-DOSE MOUSE MONOCLONAL (ANTI-GD3) ANTIBODY-R24 IN PATIENTS WITH METASTATIC MELANOMA [J].
BAJORIN, DF ;
CHAPMAN, PB ;
WONG, GY ;
CODY, BV ;
CORDONCARDO, C ;
DANTES, L ;
TEMPLETON, MA ;
SCHEINBERG, D ;
OETTGEN, HF ;
HOUGHTON, AN .
MELANOMA RESEARCH, 1992, 2 (5-6) :355-362
[2]  
BAJORIN DF, 1990, CANCER RES, V50, P7490
[3]   Phase II study of weekly intravenous recombinant humanized Anti-p185(HER2) monoclonal antibody in patients with HER2/neu-overexpressing metastatic breast [J].
Baselga, J ;
Tripathy, D ;
Mendelsohn, J ;
Baughman, S ;
Benz, CC ;
Dantis, L ;
Sklarin, NT ;
Seidman, AD ;
Hudis, CA ;
Moore, J ;
Rosen, PP ;
Twaddell, T ;
Henderson, IC ;
Norton, L .
JOURNAL OF CLINICAL ONCOLOGY, 1996, 14 (03) :737-744
[4]   PHASE-I TRIAL OF CISPLATIN, WR-2721, AND THE MURINE MONOCLONAL-ANTIBODY R24 IN PATIENTS WITH METASTATIC MELANOMA - CLINICAL AND BIOLOGIC EFFECTS [J].
BUKOWSKI, RM ;
MURTHY, SA ;
FINKE, J ;
CAULFIELD, MJ ;
TUBBS, R ;
HERZOG, P ;
STANLEY, J ;
EDINGER, M ;
TUASON, L ;
MCLAIN, D ;
BUDD, GT ;
OLENCKI, T ;
GANAPATHI, R .
JOURNAL OF IMMUNOTHERAPY, 1994, 15 (04) :273-282
[5]  
CARON PC, 1994, BLOOD, V83, P1760
[6]   Direct immobilization of gangliosides onto gold-carboxymethyldextran sensor surfaces by hydrophobic interaction: applications to antibody characterization [J].
Catimel, B ;
Scott, AM ;
Lee, FT ;
Hanai, N ;
Ritter, G ;
Welt, S ;
Old, LJ ;
Burgess, AW ;
Nice, EC .
GLYCOBIOLOGY, 1998, 8 (09) :927-938
[7]   LOCALIZATION OF THE GANGLIOSIDES GD2 AND GD3 IN ADHESION PLAQUES AND ON THE SURFACE OF HUMAN-MELANOMA CELLS [J].
CHERESH, DA ;
HARPER, JR ;
SCHULZ, G ;
REISFELD, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (18) :5767-5771
[8]   Antibody humanization: a case of the 'Emperor's new clothes'? [J].
Clark, M .
IMMUNOLOGY TODAY, 2000, 21 (08) :397-402
[9]   IMMUNOLOGICAL RESPONSE TO INTRATHECAL AND SYSTEMIC TREATMENT WITH GANGLIOSIDE ANTIBODY R-24 IN PATIENTS WITH MALIGNANT-MELANOMA [J].
DIPPOLD, W ;
BERNHARD, H ;
ZUMBUSCHENFELDE, KHM .
EUROPEAN JOURNAL OF CANCER, 1994, 30A (02) :137-144
[10]   CELL-SURFACE ANTIGENS OF HUMAN-MALIGNANT MELANOMA - DEFINITION OF 6 ANTIGENIC SYSTEMS WITH MOUSE MONOCLONAL-ANTIBODIES [J].
DIPPOLD, WG ;
LLOYD, KO ;
LI, LTC ;
IKEDA, H ;
OETTGEN, HF ;
OLD, LJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (10) :6114-6118