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Citation: Em. Jaffee et al., Novel allogeneic granulocyte-macrophage colony-stimulating factor-secreting tumor vaccine for pancreatic cancer: A phase I trial of safety and immuneactivation, J CL ONCOL, 19(1), 2001, pp. 145-156
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Citation: Ei. Heath et al., Phase I trial of the matrix metalloproteinase inhibitor BAY12-9566 in patients with advanced solid tumors, CANC CHEMOT, 48(4), 2001, pp. 269-274
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Citation: S. O'Reilly et al., Bioavailablility of penclomedine and systemic exposure to 4-O-demethylpenclomedine in patients receiving oral and intravenous penclomedine, CANC CHEMOT, 48(3), 2001, pp. 223-228
Citation: S. Lakhanpal et al., Phase II study of 4-ipomeanol, a naturally occurring alkylating furan, in patients with advanced hepatocellular carcinoma, INV NEW DR, 19(1), 2001, pp. 69-76
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Citation: Ec. Dees et al., A phase I and pharmacologic evaluation of the DNA intercalator CI-958 in patients with advanced solid tumors, CLIN CANC R, 6(10), 2000, pp. 3885-3894
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Citation: Ec. Dees et al., A prospective pharmacologic evaluation of age-related toxicity of adjuvantchemotherapy in women with breast cancer, CANCER INV, 18(6), 2000, pp. 521-529
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Citation: Sd. Baker et al., Phase I and pharmacologic study of oral fluorouracil on a chronic daily schedule in combination with the dihydropyrimidine dehydrogenase inactivator eniluracil, J CL ONCOL, 18(4), 2000, pp. 915-926
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Citation: A. Chakravarthy et al., Intensified adjuvant combined modality therapy for resected periampullary adenocarcinoma: Acceptable toxicity and suggestion of improved 1-year disease-free survival, INT J RAD O, 48(4), 2000, pp. 1089-1096
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Citation: Sd. Baker et al., Absorption, metabolism, and excretion of C-14-temozolomide following oral administration to patients with advanced cancer, CLIN CANC R, 5(2), 1999, pp. 309-317
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Citation: Jb. Nelson et al., Laparoscopic retroperitoneal lymph node dissection for clinical stage I nonseminomatous germ cell testicular tumors, UROLOGY, 54(6), 1999, pp. 1064-1067
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Citation: B. Mikhak et al., Long term follow-up of women treated with 16-week, dose-intensive adjuvantchemotherapy for high risk breast carcinoma, CANCER, 85(4), 1999, pp. 899-904