메뉴 건너뛰기




Volumn 34, Issue 2, 2000, Pages 83-88

Clinical studies in the development of new anticancer agents exhibiting growth inhibition in models: Facing the challenge of a proper study design

Author keywords

Clinical studies; Cytostatic anticancer agents; Design; Phase I; Phase II; Phase III

Indexed keywords

ANGIOGENESIS INHIBITOR; ANTINEOPLASTIC AGENT; CYTOSTATIC AGENT; CYTOTOXIC AGENT; MATRIX METALLOPROTEINASE INHIBITOR; PROTEIN FARNESYLTRANSFERASE INHIBITOR; PROTEIN TYROSINE KINASE INHIBITOR;

EID: 0034058605     PISSN: 10408428     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1040-8428(00)00055-X     Document Type: Article
Times cited : (25)

References (13)
  • 1
    • 0029150669 scopus 로고
    • Inhibition of farnesyltransferase induces regression of mammary and salivary carcinomas in ras transgenic mice
    • Kohl N.E., Omer C.A., Conner M.W. et al. Inhibition of farnesyltransferase induces regression of mammary and salivary carcinomas in ras transgenic mice. Nat. Med. 1:1995;792-797.
    • (1995) Nat. Med. , vol.1 , pp. 792-797
    • Kohl, N.E.1    Omer, C.A.2    Conner, M.W.3
  • 2
    • 0032900619 scopus 로고    scopus 로고
    • Treatment with farnesyl protein transferase inhibitor induces regression of mammary tumors in transforming growth factor (TGF) α and TGFα/neu transgenic mice by inhibition of mitogenic activity and induction of apoptosis
    • Nørgaard P., Law B., Joseph H. et al. Treatment with farnesyl protein transferase inhibitor induces regression of mammary tumors in transforming growth factor (TGF) α and TGFα/neu transgenic mice by inhibition of mitogenic activity and induction of apoptosis. Clin. Cancer Res. 5:1999;35-42.
    • (1999) Clin. Cancer Res. , vol.5 , pp. 35-42
    • Nørgaard, P.1    Law, B.2    Joseph, H.3
  • 3
    • 14344254868 scopus 로고    scopus 로고
    • Tumor activity of SCH 66336, an orally bioavailable tricyclic inhibitor of farnesyl protein transferase in human tumor xenograft models in wap-ras transgenic mice
    • Liu M., Bryant M.S., Chen J. et al. Tumor activity of SCH 66336, an orally bioavailable tricyclic inhibitor of farnesyl protein transferase in human tumor xenograft models in wap-ras transgenic mice. Cancer Res. 58:1998;4947-4956.
    • (1998) Cancer Res. , vol.58 , pp. 4947-4956
    • Liu, M.1    Bryant, M.S.2    Chen, J.3
  • 4
    • 0001417046 scopus 로고    scopus 로고
    • A phase I and pharmacologic study of the farnesyl protein transferase (FPT) inhibitor SCH 66336 in patients with locally advanced or metastatic cancer
    • Adjei A.A., Erlichman C., Davis J.N. et al. A phase I and pharmacologic study of the farnesyl protein transferase (FPT) inhibitor SCH 66336 in patients with locally advanced or metastatic cancer. Proc. Am. Soc. Clin. Oncol. 18:1999;156a.
    • (1999) Proc. Am. Soc. Clin. Oncol. , vol.18
    • Adjei, A.A.1    Erlichman, C.2    Davis, J.N.3
  • 5
    • 0030723230 scopus 로고    scopus 로고
    • Matrixmetalloproteinase inhibitors: Present achievements and future prospects
    • Denis L.J., Verweij J. Matrixmetalloproteinase inhibitors: present achievements and future prospects. Invest. New Drugs. 15:1997;175-185.
    • (1997) Invest. New Drugs , vol.15 , pp. 175-185
    • Denis, L.J.1    Verweij, J.2
  • 6
    • 0000206174 scopus 로고    scopus 로고
    • Phase I and pharmacologic study with the novel farnesyl transferase inhibitor (FTI) R115777
    • (abstract 4780)
    • Schellens J., De Klerk G., Swart M. et al. Phase I and pharmacologic study with the novel farnesyl transferase inhibitor (FTI) R115777. Proc. Am. Ass. Cancer Res. 40:1999;724. (abstract 4780).
    • (1999) Proc. Am. Ass. Cancer Res. , vol.40 , pp. 724
    • Schellens, J.1    De Klerk, G.2    Swart, M.3
  • 7
    • 0031017851 scopus 로고    scopus 로고
    • Patient preferences for oral versus intravenous palliative chemotherapy
    • Liu G., Franssen E., Fitch M.I. et al. Patient preferences for oral versus intravenous palliative chemotherapy. J. Clin. Oncol. 15:1997;110-115.
    • (1997) J. Clin. Oncol. , vol.15 , pp. 110-115
    • Liu, G.1    Franssen, E.2    Fitch, M.I.3
  • 8
    • 0006599430 scopus 로고    scopus 로고
    • Dose escalation using the modified continual reassessment method (MCRM) in phase I clinical trials: A review of the San Antonio experience
    • Siu L.L., Rowinsky E.K., Clark G.M. et al. Dose escalation using the modified continual reassessment method (MCRM) in phase I clinical trials: a review of the San Antonio experience. Ann. Oncol. 2(Suppl. (2)):1998;127.
    • (1998) Ann. Oncol. , vol.2 , Issue.2 SUPPL. , pp. 127
    • Siu, L.L.1    Rowinsky, E.K.2    Clark, G.M.3
  • 9
    • 0003486931 scopus 로고
    • World Health Organization Geneva, Switzerland, WHO offset publication No 40
    • World Health Organization. WHO handbook for reporting results of cancer treatment. Geneva, Switzerland, WHO offset publication No 40, 1979.
    • (1979) WHO Handbook for Reporting Results of Cancer Treatment
  • 10
    • 0034594628 scopus 로고    scopus 로고
    • New guidelines to evaluate the response to treatment in solid tumors
    • (in press)
    • Therasse P, Arbuck SG, Eisenhauer E, et al. New guidelines to evaluate the response to treatment in solid tumors, J. Natl. Cancer Inst 2000 (in press).
    • (2000) J. Natl. Cancer Inst
    • Therasse, P.1    Arbuck, S.G.2    Eisenhauer, E.3
  • 11
    • 0342977110 scopus 로고
    • Combination therapy including a gelatinase inhibitor and cytotoxic agents reduces local invasion and metastasis of murine Lewis lung carcinoma
    • Anderson I.C., Shipp M.A., Docherty A.J.P. et al. Combination therapy including a gelatinase inhibitor and cytotoxic agents reduces local invasion and metastasis of murine Lewis lung carcinoma. Cancer Res. 53:1993;2087-2091.
    • (1993) Cancer Res. , vol.53 , pp. 2087-2091
    • Anderson, I.C.1    Shipp, M.A.2    Docherty, A.J.P.3
  • 12
    • 0032539559 scopus 로고    scopus 로고
    • Farnesyl transferase inhibitors cause enhanced mitotic sensitivity to taxol and epothilones
    • Moasser M.M., Sepp-Lorenzino L., Kohl N.E. et al. Farnesyl transferase inhibitors cause enhanced mitotic sensitivity to taxol and epothilones. Proc. Natl. Acad. Sci. USA. 95:1998;1369-1374.
    • (1998) Proc. Natl. Acad. Sci. USA , vol.95 , pp. 1369-1374
    • Moasser, M.M.1    Sepp-Lorenzino, L.2    Kohl, N.E.3
  • 13
    • 0007627465 scopus 로고    scopus 로고
    • Effective combination therapy with the non-thiol farnesyl transferase inhibitor FTI-2148 and taxol, gemcitabine or cisplatinum for human tumor xenografts in nude mice
    • (abstract 3443)
    • Sun J., Marfurt J., Blaskovich M.A. et al. Effective combination therapy with the non-thiol farnesyl transferase inhibitor FTI-2148 and taxol, gemcitabine or cisplatinum for human tumor xenografts in nude mice. Proc. Am. Ass. Cancer Res. 40:1999;522. (abstract 3443).
    • (1999) Proc. Am. Ass. Cancer Res. , vol.40 , pp. 522
    • Sun, J.1    Marfurt, J.2    Blaskovich, M.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.