Major Cancer Regressions in Mesothelioma After Treatment with an Anti-Mesothelin Immunotoxin and Immune Suppression

被引:187
作者
Hassan, Raffit [1 ]
Miller, Andrew C. [2 ]
Sharon, Elad [3 ]
Thomas, Anish [4 ]
Reynolds, James C. [5 ]
Ling, Alexander [5 ]
Kreitman, Robert J. [1 ]
Miettinen, Markku M. [6 ]
Steinberg, Seth M. [7 ]
Fowler, Daniel H. [8 ]
Pastan, Ira [1 ]
机构
[1] NIH, NCI, CCR, Lab Mol Biol, Bethesda, MD 20892 USA
[2] NIH, Ctr Clin, Dept Crit Care Med, Bethesda, MD 20892 USA
[3] NIH, NCI, Div Canc Treatment & Diag, Canc Therapy Evaluat Program, Bethesda, MD 20892 USA
[4] NIH, NCI, CCR, Med Oncol Branch, Bethesda, MD 20892 USA
[5] NIH, Ctr Clin, Bethesda, MD 20892 USA
[6] NIH, NCI, CCR, Pathol Lab, Bethesda, MD 20892 USA
[7] NIH, NCI, CCR, Biostat & Data Management Sect, Bethesda, MD 20892 USA
[8] NIH, NCI, CCR, Expt Transplantat & Immunol Branch, Bethesda, MD 20892 USA
关键词
MALIGNANT PLEURAL MESOTHELIOMA; RESPONSE CRITERIA; SOLID TUMORS; RECOMBINANT IMMUNOTOXIN; PLUS CYCLOPHOSPHAMIDE; PHASE-I; THERAPY; RECIST; CHEMOTHERAPY; PENTOSTATIN;
D O I
10.1126/scitranslmed.3006941
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Immunotoxins are potent anticancer agents with an unusual mechanism of action: inhibition of protein synthesis resulting in apoptotic cell death. Immunotoxins have produced many durable complete responses in refractory hairy cell leukemia, where patients rarely form antibodies to the bacterial toxin component of the immunotoxin. Patients with mesothelioma, however, have normal immune systems and form antibodies after one cycle, and tumor responses to the immunotoxin have not been observed in this disease. We describe the results of a trial in which major antitumor responses were seen in patients with advanced mesothelioma who received the anti-mesothelin immunotoxin SS1P, together with pentostatin and cyclophosphamide, to deplete T and B cells. Of 10 patients with chemotherapy-refractory mesothelioma, 3 have had major tumor regressions with 2 ongoing at 15 months, and 2 others responded to chemotherapy after discontinuing immunotoxin therapy. Antibody formation was markedly delayed, allowing more SS1P cycles to be given, but this alone does not appear to account for the marked antitumor activity observed.
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页数:9
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