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Volumn 2, Issue 2, 2017, Pages

Patient-reported tolerability of adverse events in phase 1 trials

Author keywords

adverse event; Dose limiting toxicity; patient reported outcome; phase 1; tolerability

Indexed keywords


EID: 85051252335     PISSN: None     EISSN: 20597029     Source Type: Journal    
DOI: 10.1136/esmoopen-2016-000148     Document Type: Article
Times cited : (21)

References (14)
  • 1
    • 0029793053 scopus 로고    scopus 로고
    • Workshop on phase i study design
    • Amsterdam, March 12, 1996. Ann Oncol
    • Arbuck SG. Workshop on phase I study design. Ninth NCI/EORTC new drug development symposium, Amsterdam, March 12, 1996. Ann Oncol 1996;7:567-73.
    • (1996) Ninth NCI/EORTC New Drug Development Symposium , vol.7 , pp. 567-573
    • Arbuck, S.G.1
  • 2
    • 66849118694 scopus 로고    scopus 로고
    • Dose escalation methods in phase i cancer clinical trials
    • Le Tourneau C, Lee JJ, Siu LL. Dose escalation methods in phase I cancer clinical trials. J Natl Cancer Inst 2009;101:708-20.
    • (2009) J Natl Cancer Inst , vol.101 , pp. 708-720
    • Le Tourneau, C.1    Lee, J.J.2    Siu, L.L.3
  • 3
    • 79958777006 scopus 로고    scopus 로고
    • Heterogeneity in the definition of dose-limiting toxicity in phase i cancer clinical trials of molecularly targeted agents: A review of the literature
    • Le Tourneau C, Razak AR, Gan HK, et al. Heterogeneity in the definition of dose-limiting toxicity in phase I cancer clinical trials of molecularly targeted agents: a review of the literature. Eur J Cancer 2011;47:1468-75.
    • (2011) Eur J Cancer , vol.47 , pp. 1468-1475
    • Le Tourneau, C.1    Razak, A.R.2    Gan, H.K.3
  • 4
    • 79955617684 scopus 로고    scopus 로고
    • Phase i trials of molecularly targeted agents: Should we pay more attention to late toxicities?
    • Postel-Vinay S, Gomez-Roca C, Molife LR, et al. Phase I trials of molecularly targeted agents: should we pay more attention to late toxicities? J Clin Oncol 2011;29:1728-35.
    • (2011) J Clin Oncol , vol.29 , pp. 1728-1735
    • Postel-Vinay, S.1    Gomez-Roca, C.2    Molife, L.R.3
  • 5
    • 79958774831 scopus 로고    scopus 로고
    • Phase 1 trials of molecular targeted therapies: Are we evaluating toxicities properly?
    • Soria JC. Phase 1 trials of molecular targeted therapies: are we evaluating toxicities properly? Eur J Cancer 2011;47:1443-5.
    • (2011) Eur J Cancer , vol.47 , pp. 1443-1445
    • Soria, J.C.1
  • 6
    • 84904042903 scopus 로고    scopus 로고
    • Towards new methods for the determination of dose limiting toxicities and the assessment of the recommended dose for further studies of molecularly targeted agents-dose-limiting toxicity and toxicity assessment recommendation group for early trials of targeted therapies, an european organisation for research and treatment of cancer-led study
    • Postel-Vinay S, Collette L, Paoletti X, et al. Towards new methods for the determination of dose limiting toxicities and the assessment of the recommended dose for further studies of molecularly targeted agents-dose-limiting toxicity and toxicity assessment recommendation group for early trials of targeted therapies, an european organisation for research and treatment of cancer-led study. Eur J Cancer 2014;50:2040-9.
    • (2014) Eur J Cancer , vol.50 , pp. 2040-2049
    • Postel-Vinay, S.1    Collette, L.2    Paoletti, X.3
  • 7
    • 84904071224 scopus 로고    scopus 로고
    • Defining dose-limiting toxicity for phase 1 trials of molecularly targeted agents: Results of a DLT-TARGETT international survey
    • Paoletti X, Le Tourneau C, Verweij J, et al. Defining dose-limiting toxicity for phase 1 trials of molecularly targeted agents: results of a DLT-TARGETT international survey. Eur J Cancer 2014;50:2050-6.
    • (2014) Eur J Cancer , vol.50 , pp. 2050-2056
    • Paoletti, X.1    Le Tourneau, C.2    Verweij, J.3
  • 8
    • 84965094526 scopus 로고    scopus 로고
    • Validity and reliability of the US national cancer institute's patient-reported outcomes version of the common terminology criteria for adverse events (PROCTCAE)
    • Dueck AC, Mendoza TR, Mitchell SA, et al. Validity and reliability of the US national cancer institute's patient-reported outcomes version of the common terminology criteria for adverse events (PROCTCAE). JAMA Oncol 2015;1:1051-9.
    • (2015) JAMA Oncol , vol.1 , pp. 1051-1059
    • Dueck, A.C.1    Mendoza, T.R.2    Mitchell, S.A.3
  • 9
    • 67049087117 scopus 로고    scopus 로고
    • Prevalence, determinants, and outcomes of nonadherence to imatinib therapy in patients with chronic myeloid leukemia: The ADAGIO study
    • Noens L, van Lierde MA, De Bock R, et al. Prevalence, determinants, and outcomes of nonadherence to imatinib therapy in patients with chronic myeloid leukemia: the ADAGIO study. Blood 2009;113:5401-11.
    • (2009) Blood , vol.113 , pp. 5401-5411
    • Noens, L.1    Van Lierde, M.A.2    De Bock, R.3
  • 10
    • 84978193438 scopus 로고    scopus 로고
    • Treatment adherence and its impact on disease-free survival in the Breast International Group 1-98 trial of tamoxifen and letrozole, alone and in sequence
    • Chirgwin JH, Giobbie-Hurder A, Coates AS, et al. Treatment adherence and its impact on disease-free survival in the Breast International Group 1-98 trial of tamoxifen and letrozole, alone and in sequence. J Clin Oncol 2016;34:2452-9.
    • (2016) J Clin Oncol , vol.34 , pp. 2452-2459
    • Chirgwin, J.H.1    Giobbie-Hurder, A.2    Coates, A.S.3
  • 11
    • 84978198934 scopus 로고    scopus 로고
    • Sticking to it: Improving outcomes by increasing adherence
    • Hershman DL. Sticking to it: improving outcomes by increasing adherence. J Clin Oncol 2016;34:2440-2.
    • (2016) J Clin Oncol , vol.34 , pp. 2440-2442
    • Hershman, D.L.1
  • 12
    • 36849093844 scopus 로고    scopus 로고
    • Patient-reported outcomes and the evolution of adverse event reporting in oncology
    • Trotti A, Colevas AD, Setser A, et al. Patient-reported outcomes and the evolution of adverse event reporting in oncology. J Clin Oncol 2007;25:5121-7.
    • (2007) J Clin Oncol , vol.25 , pp. 5121-5127
    • Trotti, A.1    Colevas, A.D.2    Setser, A.3
  • 13
    • 84909994482 scopus 로고    scopus 로고
    • Development of the National Cancer Institute's patient-reported outcomes version of the common terminology criteria for adverse events (PRO-CTCAE)
    • Basch E, Reeve BB, Mitchell SA, et al. Development of the National Cancer Institute's patient-reported outcomes version of the common terminology criteria for adverse events (PRO-CTCAE). JNCI 2014;106:dju244.
    • (2014) JNCI , vol.106 , pp. dju244
    • Basch, E.1    Reeve, B.B.2    Mitchell, S.A.3
  • 14
    • 84976628075 scopus 로고    scopus 로고
    • An explorative study to assess the association between health-related quality of life and the recommended phase II dose in a phase i trial: Idarubicin-loaded beads for chemoembolisation of hepatocellular carcinoma
    • Anota A, Boulin M, Dabakuyo-Yonli S, et al. An explorative study to assess the association between health-related quality of life and the recommended phase II dose in a phase I trial: idarubicin-loaded beads for chemoembolisation of hepatocellular carcinoma. BMJ Open 2016;6:e010696.
    • (2016) BMJ Open , vol.6 , pp. e010696
    • Anota, A.1    Boulin, M.2    Dabakuyo-Yonli, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.