New drugs in advanced non-small-cell lung cancer: searching for the correct clinical development

被引:9
作者
Di Maio, Massimo [1 ]
Morabito, Alessandro [2 ]
Piccirillo, Maria Carmela [1 ]
Daniele, Gennaro [1 ]
Giordano, Pasqualina [1 ]
Costanzo, Raffaele [2 ]
Riccardi, Marita Georgia [3 ]
Rocco, Gaetano [2 ]
Normanno, Nicola [3 ]
Perrone, Francesco [1 ]
机构
[1] NCI, Clin Trials Unit, I-80131 Naples, Italy
[2] NCI, Dept Thorac Surg & Oncol, I-80131 Naples, Italy
[3] NCI, Cell Biol & Biotherapy Unit, I-80131 Naples, Italy
关键词
BIBW-2992; cediranib; crizotinib; figitumumab; mapatumumab; motesanib; PARP inhibitors; PF00299804; vorinostat; FACTOR TYROSINE KINASES; PHASE-II; INHIBITOR; PACLITAXEL; CARBOPLATIN; COMBINATION; VORINOSTAT; AZD2171; CP-751,871; GEFITINIB;
D O I
10.1517/13543784.2010.532122
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Importance of the field: Non-small-cell lung cancer (NSCLC) is one of the most active fields of research in oncology, with many drugs under clinical development. Most of these drugs offer novel mechanisms of action compared with drugs currently used in clinical practice. Areas covered in this review: In this article, results recently obtained with most promising new drugs for advanced NSCLC are briefly described. What the reader will gain: Most of the new drugs are currently being tested without a biomarker-driven selection, due to inadequate knowledge of predictive factors. A few drugs are tested in biologically selected samples of NSCLC patients. The results obtained with crizotinib in patients with ALK gene rearrangement are a good example of the speed with which biological discoveries can be translated to clinical testing. Take home message: Emerging clinical and molecular data demonstrate that NSCLC is a family of related but distinct diseases. Some drugs tested in unselected population will probably obtain an incremental benefit compared to the current standard, but this will not substantially change the unfavorable prognosis of NSCLC patients. By contrast, unprecedented and much more cost-effective results can be obtained when targeted agents are administered following appropriate biomarker-driven patient selection.
引用
收藏
页码:1503 / 1514
页数:12
相关论文
共 47 条
  • [1] [Anonymous], J CLIN ONCOL
  • [2] Clinical activity of the oral ALK inhibitor PF-02341066 in ALK-positive patients with non-small cell lung cancer (NSCLC)
    Bang, Y.
    Kwak, E. L.
    Shaw, A. T.
    Camidge, D. R.
    Iafrate, A. J.
    Maki, R. G.
    Solomon, B. J.
    Ou, S. I.
    Salgia, R.
    Clark, J. W.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (18)
  • [3] Blumenschein G R., 2010, J. Clin. Oncol, V28
  • [4] Phase 1b Study of Motesanib, an Oral Angiogenesis Inhibitor, in Combination with Carboplatin/Paclitaxel and/or Panitumumab for the Treatment of Advanced Non-Small Cell Lung Cancer
    Blumenschein, George R., Jr.
    Reckamp, Karen
    Stephenson, G. Joe
    O'Rourke, Timothy
    Gladish, Gregory
    McGreivy, Jesse
    Sun, Yu-Nien
    Ye, Yining
    Parson, Mandy
    Sandler, Alan
    [J]. CLINICAL CANCER RESEARCH, 2010, 16 (01) : 279 - 290
  • [5] PF-00299804 (PF299) patient (pt)-reported outcomes (PROs) and efficacy in adenocarcinoma (adeno) and nonadeno non-small cell lung cancer (NSCLC): A phase (P) II trial in advanced NSCLC after failure of chemotherapy (CT) and erlotinib (E)
    Campbell, A.
    Reckamp, K. L.
    Camidge, D. R.
    Giaccone, G.
    Gadgeel, S. M.
    Khuri, F. R.
    Engelman, J. A.
    Denis, L. J.
    O'Connell, J. P.
    Janne, P. A.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (15)
  • [6] Methodological aspects of lung cancer clinical trials in the era of targeted agents
    Di Maio, Massimo
    Gallo, Ciro
    De Maio, Ermelinda
    Morabito, Alessandro
    Piccirillo, Maria Carmela
    Gridelli, Cesare
    Perrone, Francesco
    [J]. LUNG CANCER, 2010, 67 (02) : 127 - 135
  • [7] Phase I clinical study of AZD2171, an oral vascular endothelial growth factor signaling inhibitor, in patients with advanced solid tumors
    Drevs, Joachim
    Siegert, Patrizia
    Medinger, Michael
    Mross, Klaus
    Strecker, Ralph
    Zirrgiebel, Ute
    Harder, Jan
    Blum, Hubert
    Robertson, Jane
    Juergensmeier, Juliane M.
    Puchalski, Thomas A.
    Young, Helen
    Saunders, Owain
    Unger, Clemens
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2007, 25 (21) : 3045 - 3054
  • [8] Biomarkers of Antiangiogenic Therapy: How Do We Move From Candidate Biomarkers to Valid Biomarkers
    Duda, Dan G.
    Ancukiewicz, Marek
    Jain, Rakesh K.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (02) : 183 - 185
  • [9] DY GK, 2010, J CLIN ONCOL, V28
  • [10] PF00299804, an irreversible pan-ERBB inhibitor, is effective in lung cancer models with EGFR and ERBB2 mutations that are resistant to gefitinib
    Engelman, Jeffrey A.
    Zejnullahu, Kreshnik
    Gale, Christopher-Michael
    Lifshits, Eugene
    Gonzales, Andrea J.
    Shimamura, Takeshi
    Zhao, Feng
    Vincent, Patrick W.
    Naumov, George N.
    Bradner, James E.
    Althaus, Irene W.
    Gandhi, Leena
    Shapiro, Geoffrey I.
    Nelson, James M.
    Heymach, John V.
    Meyerson, Matthew
    Wong, Kwok-Kin
    Janne, Pasi A.
    [J]. CANCER RESEARCH, 2007, 67 (24) : 11924 - 11932