Authors:
Hudis, C
Fornier, M
Riccio, L
Lebwohl, D
Crown, J
Gilewski, T
Surbone, A
Currie, V
Seidman, A
Reichman, B
Moynahan, M
Raptis, G
Sklarin, N
Theodoulou, M
Weiselberg, L
Salvaggio, R
Panageas, KS
Yao, TJ
Norton, L
Citation: C. Hudis et al., 5-year results of dose-intensive sequential adjuvant chemotherapy for women with high-risk node-positive breast cancer: A phase II study, J CL ONCOL, 17(4), 1999, pp. 1118-1126
Authors:
Khoo, K
Brandes, L
Reyno, L
Arnold, A
Dent, S
Vandenberg, T
Lebwohl, D
Fisher, B
Eisenhauer, E
Citation: K. Khoo et al., Phase II trial of N,N-diethyl-2-[4-(phenylmethyl)phenoxy]ethanamine. HCl and doxorubicin chemotherapy in metastatic breast cancer: A National Cancer Institute of Canada Clinical Trials Group Study, J CL ONCOL, 17(11), 1999, pp. 3431-3437
Authors:
Hudis, C
Seidman, A
Baselga, J
Raptis, G
Lebwohl, D
Gilewski, T
Moynahan, M
Sklarin, N
Fennelly, D
Crown, JPA
Surbone, A
Uhlenhopp, M
Riedel, E
Yao, TJ
Norton, L
Citation: C. Hudis et al., Sequential dose-dense doxorubicin, paclitaxel, and cyclophosphamide for resectable high-risk breast cancer: Feasibility and efficacy, J CL ONCOL, 17(1), 1999, pp. 93-100
Authors:
DeMario, MD
Ratain, MJ
Vogelzang, NJ
Mani, S
Vokes, EE
Fleming, GF
Melton, K
Johnson, S
Benner, S
Lebwohl, D
Citation: Md. Demario et al., A phase I study of oral uracil/ftorafur (UFT) plus leucovorin and bis-acetato-ammine-dichloro-cyclohexylamine-platinum IV (JM-216) each given over 14days every 28 days, CANC CHEMOT, 43(5), 1999, pp. 385-388