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Lung Cancer: Translational and Emerging Therapies by Kishan J. Pandya, Julie R. Brahmer, Manuel Hidalgo

By Kishan J. Pandya, Julie R. Brahmer, Manuel Hidalgo

Lung melanoma is the top reason behind cancer-related deaths within the usa. Filling a spot within the literature, this source interprets contemporary laboratory findings into functional functions for the prevention and keep an eye on of lung melanoma. that includes chapters via professional researchers within the box, this reference reports present advances in imaging, drug improvement, molecular therapeutics, genetics, immunotherapy, and chemotherapy, to face on the leading edge of applied sciences for sufferer analysis and remedy.

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Proteasome inhibition in small-cell lung cancer: preclinical rationale and clinical applications. Clin Lung Cancer 2005; 7(suppl 2): S67–S71. 80. Davies AM, Lara PN Jr, Mack PC, et al. Bortezomib-based combinations in the treatment of non–small-cell lung cancer. Clin Lung Cancer 2005; 7(suppl 2):S59–S63. 81. Brambilla E, Travis WD, Colby TV, et al. The new World Health Organization classification of lung tumours. Eur Respir J 2001; 18(6):1059–1068. 82. Johnson DH, Fehrenbacher L, Novotny WF, et al.

The continual reassessment method: comparison of Bayesian stopping rules for dose-ranging studies. Stat Med 2001; 20(19):2827–2843. 7. Thall PF, Estey EH, Sung HG. A new statistical method for dose-finding based on efficacy and toxicity in early phase clinical trials. Invest New Drugs 1999; 17(2):155–167. 8. Wolf M, Swaisland H, Averbuch S. Development of the novel biologically targeted anticancer agent gefitinib: determining the optimum dose for clinical efficacy. Clin Cancer Res 2004; 10(14):4607–4613.

Some of the most frequently cited are (i) the randomized discontinuation design (29,47,48), (ii) the phase-2 design with reference arm (50), (iii) the phase-2/3 design, (iv) the phase-2 selection design (52), and (v) the phase-2 screening design (32). A full discussion of these designs, their applications, strengths, and weakness is beyond the scope of this chapter. However, brief summary of these designs and relevant references are provided in Table 2. In summary, among the factors to be considered in designing a phase-2 study are (i) the anticipated activity of the agent/combination; (ii) the patient population of interest; (iii) the resources available to support the study; (iv) whether the outcome with standard therapy is very well defined such that there is a good historical control database; and (v) whether objective response rate is the end point of interest.

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