메뉴 건너뛰기




Volumn 18, Issue 2, 2000, Pages 429-436

Content and quality of currently published phase II cancer trials

Author keywords

[No Author keywords available]

Indexed keywords

ANTINEOPLASTIC AGENT;

EID: 0033984551     PISSN: 0732183X     EISSN: None     Source Type: Journal    
DOI: 10.1200/jco.2000.18.2.429     Document Type: Review
Times cited : (44)

References (30)
  • 1
    • 0030557614 scopus 로고    scopus 로고
    • Design and analysis of phase II cancer trials: A review of statistical methods and guidelines for medical researchers
    • Mariani L, Marubini E: Design and analysis of phase II cancer trials: A review of statistical methods and guidelines for medical researchers. Int Stat Rev 64:61-88, 1996
    • (1996) Int Stat Rev , vol.64 , pp. 61-88
    • Mariani, L.1    Marubini, E.2
  • 3
    • 0030923529 scopus 로고    scopus 로고
    • Publication bias: Evidence of delayed publication in a cohort study of clinical research projects
    • Stern JM, Simes RJ: Publication bias: Evidence of delayed publication in a cohort study of clinical research projects. Br Med J 315:640-645, 1997
    • (1997) Br Med J , vol.315 , pp. 640-645
    • Stern, J.M.1    Simes, R.J.2
  • 4
    • 0020108590 scopus 로고
    • One-sample multiple testing procedure for phase II clinical trials
    • Fleming TR: One-sample multiple testing procedure for phase II clinical trials. Biometrics 38:143-151, 1982
    • (1982) Biometrics , vol.38 , pp. 143-151
    • Fleming, T.R.1
  • 5
    • 0024536437 scopus 로고
    • Optimal two-stage designs for phase II clinical trials
    • Simon R: Optimal two-stage designs for phase II clinical trials. Control Clin Trials 10:1-10, 1989
    • (1989) Control Clin Trials , vol.10 , pp. 1-10
    • Simon, R.1
  • 6
    • 50549174560 scopus 로고
    • The determination of the number of patients required in a preliminary and a follow-up trial of a new chemotherapeutic agent
    • Gehan EA: The determination of the number of patients required in a preliminary and a follow-up trial of a new chemotherapeutic agent. J Chron Dis 13:346-353, 1961
    • (1961) J Chron Dis , vol.13 , pp. 346-353
    • Gehan, E.A.1
  • 7
    • 0020460601 scopus 로고
    • Statistics in medical journals
    • Altman DG: Statistics in medical journals. Stat Med 1:59-71, 1982
    • (1982) Stat Med , vol.1 , pp. 59-71
    • Altman, D.G.1
  • 8
    • 0026320717 scopus 로고
    • Statistics in medical journals: Developments in the 1980s
    • Altman DG: Statistics in medical journals: Developments in the 1980s. Stat Med 10:1897-1913, 1991
    • (1991) Stat Med , vol.10 , pp. 1897-1913
    • Altman, D.G.1
  • 9
    • 0029827296 scopus 로고    scopus 로고
    • Multistage designs for phase II clinical trials: Statistical issues in cancer research
    • Kramar A, Potvin D, Hill C: Multistage designs for phase II clinical trials: Statistical issues in cancer research. Br J Cancer 74:1317-1320, 1996
    • (1996) Br J Cancer , vol.74 , pp. 1317-1320
    • Kramar, A.1    Potvin, D.2    Hill, C.3
  • 10
    • 0031797332 scopus 로고    scopus 로고
    • Phase I and II trials of novel anticancer agents: Endpoints, efficacy and existentialism
    • Eisenhauer EA: Phase I and II trials of novel anticancer agents: Endpoints, efficacy and existentialism. Ann Oncol 9:1047-1052, 1998
    • (1998) Ann Oncol , vol.9 , pp. 1047-1052
    • Eisenhauer, E.A.1
  • 11
    • 0024600423 scopus 로고
    • How study design affects outcomes in comparisons of therapy
    • Colditz GA, Miller JN, Mosteller F: How study design affects outcomes in comparisons of therapy. I: Medical. Stat Med 8:441-454, 1989
    • (1989) I: Medical. Stat Med , vol.8 , pp. 441-454
    • Colditz, G.A.1    Miller, J.N.2    Mosteller, F.3
  • 12
    • 0032558314 scopus 로고    scopus 로고
    • Does quality of reports of randomized trials affect estimates of intervention efficacy reported in meta-analyses?
    • Moher D, Pham B, Jones A, et al: Does quality of reports of randomized trials affect estimates of intervention efficacy reported in meta-analyses? Lancet 352:609-613, 1998
    • (1998) Lancet , vol.352 , pp. 609-613
    • Moher, D.1    Pham, B.2    Jones, A.3
  • 13
    • 0032585188 scopus 로고    scopus 로고
    • The unpredictability paradox: Review of empirical comparisons of randomized and non-randomized clinical trials
    • Kunz R, Oxman AD: The unpredictability paradox: Review of empirical comparisons of randomized and non-randomized clinical trials. Br Med J 317:1185-1190, 1998
    • (1998) Br Med J , vol.317 , pp. 1185-1190
    • Kunz, R.1    Oxman, A.D.2
  • 15
    • 0030567189 scopus 로고    scopus 로고
    • Phase II studies: Which is worse, false positive or false negative?
    • Rogatko A, Litwin S: Phase II studies: Which is worse, false positive or false negative? J Natl Cancer Inst 88:462, 1996
    • (1996) J Natl Cancer Inst , vol.88 , pp. 462
    • Rogatko, A.1    Litwin, S.2
  • 16
    • 0026581740 scopus 로고
    • Planned versus attained designs in phase II clinical trials
    • Green SJ, Dahlberg S: Planned versus attained designs in phase II clinical trials. Stat Med 11:853-862, 1992
    • (1992) Stat Med , vol.11 , pp. 853-862
    • Green, S.J.1    Dahlberg, S.2
  • 17
    • 0032190034 scopus 로고    scopus 로고
    • A design alternative for two-stage, phase II, multicenter cancer clinical trials
    • Herndon JE: A design alternative for two-stage, phase II, multicenter cancer clinical trials. Control Clin Trials 19:440-450, 1998
    • (1998) Control Clin Trials , vol.19 , pp. 440-450
    • Herndon, J.E.1
  • 18
    • 0032582620 scopus 로고    scopus 로고
    • Optimal flexible designs in phase II clinical trials
    • Chen T, Ng TH: Optimal flexible designs in phase II clinical trials. Stat Med 17:2301-2312, 1998
    • (1998) Stat Med , vol.17 , pp. 2301-2312
    • Chen, T.1    Ng, T.H.2
  • 19
    • 0022124023 scopus 로고
    • Confidence limits for probability of response in multistage phase II clinical trials
    • Atkinson EN, Brown BW: Confidence limits for probability of response in multistage phase II clinical trials. Biometrics 41:741-744, 1985
    • (1985) Biometrics , vol.41 , pp. 741-744
    • Atkinson, E.N.1    Brown, B.W.2
  • 20
    • 0023176979 scopus 로고
    • Confidence intervals for a binomial parameter based on multistage tests
    • Duffy DE, Santner TJ: Confidence intervals for a binomial parameter based on multistage tests. Biometrics 43:81-93, 1987
    • (1987) Biometrics , vol.43 , pp. 81-93
    • Duffy, D.E.1    Santner, T.J.2
  • 21
    • 0022007270 scopus 로고
    • Methodologic guidelines for reports of clinical trials
    • Simon R, Wittes RE: Methodologic guidelines for reports of clinical trials. Cancer Treat Rep 69:1-3, 1985
    • (1985) Cancer Treat Rep , vol.69 , pp. 1-3
    • Simon, R.1    Wittes, R.E.2
  • 22
    • 1842294029 scopus 로고    scopus 로고
    • Optimal three-stage designs for phase II cancer clinical trials
    • Chen TT: Optimal three-stage designs for phase II cancer clinical trials. Stat Med 16:2701-2711, 1997
    • (1997) Stat Med , vol.16 , pp. 2701-2711
    • Chen, T.T.1
  • 23
    • 0030767683 scopus 로고    scopus 로고
    • Bayesian interim analysis of phase II cancer clinical trials
    • Heitjan DF: Bayesian interim analysis of phase II cancer clinical trials. Stat Med 16:1791-1802, 1997
    • (1997) Stat Med , vol.16 , pp. 1791-1802
    • Heitjan, D.F.1
  • 24
    • 0031898459 scopus 로고    scopus 로고
    • Sample size determination for phase II clinical trials based on Bayesian decision theory
    • Stallard N: Sample size determination for phase II clinical trials based on Bayesian decision theory. Biometrics 54:279-294, 1998
    • (1998) Biometrics , vol.54 , pp. 279-294
    • Stallard, N.1
  • 25
    • 0031697980 scopus 로고    scopus 로고
    • Approximately optimal designs for phase II clinical studies
    • Stallard N: Approximately optimal designs for phase II clinical studies. J Biopharm Stat 8:469-487, 1998
    • (1998) J Biopharm Stat , vol.8 , pp. 469-487
    • Stallard, N.1
  • 26
    • 0029591692 scopus 로고
    • Incorporating toxicity considerations into the design of two-stage phase II clinical trials
    • Bryant J, Day R: Incorporating toxicity considerations into the design of two-stage phase II clinical trials. Biometrics 51:1372-1383, 1995
    • (1995) Biometrics , vol.51 , pp. 1372-1383
    • Bryant, J.1    Day, R.2
  • 27
    • 0029117666 scopus 로고
    • Bivariate designs for phase II trials
    • Conaway MR, Petroni GR: Bivariate designs for phase II trials. Biometrics 51:656-664, 1995
    • (1995) Biometrics , vol.51 , pp. 656-664
    • Conaway, M.R.1    Petroni, G.R.2
  • 28
    • 0030459977 scopus 로고    scopus 로고
    • Designs for phase II trials allowing for a trade-off between response and toxicity
    • Conaway MR, Petroni GR: Designs for phase II trials allowing for a trade-off between response and toxicity. Biometrics 52:1375-1386, 1996
    • (1996) Biometrics , vol.52 , pp. 1375-1386
    • Conaway, M.R.1    Petroni, G.R.2
  • 29
    • 0028900407 scopus 로고
    • Bayesian sequential monitoring designs for single-arm clinical trials with multiple outcomes
    • Thall PF, Simon R, Estey EH: Bayesian sequential monitoring designs for single-arm clinical trials with multiple outcomes. Stat Med 14:357-379, 1995
    • (1995) Stat Med , vol.14 , pp. 357-379
    • Thall, P.F.1    Simon, R.2    Estey, E.H.3
  • 30
    • 0032581447 scopus 로고    scopus 로고
    • Some extensions and applications of a Bayesian strategy for monitoring multiple outcomes in clinical trials
    • Thall PF, Sung HG: Some extensions and applications of a Bayesian strategy for monitoring multiple outcomes in clinical trials. Stat Med 17:1563-1580, 1998
    • (1998) Stat Med , vol.17 , pp. 1563-1580
    • Thall, P.F.1    Sung, H.G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.