Literature DB >> 12934656

Second-line chemotherapy for non-small cell lung cancer.

Frances A Shepherd1.   

Abstract

Several agents have been evaluated for the second-line treatment of patients with non-small cell lung cancer. The TAX 317 trial found that patients treated with docetaxel (Taxotere) 75 mg/m2 had significantly longer survival than those treated with best supportive care alone. In addition, symptom control was better for patients who received chemotherapy. The TAX 320 trial found that treatment with docetaxel 75 or 100 mg/m2 resulted in significantly higher response rates than treatment with vinorelbine (Navelbine) or ifosfamide (Mitoxana), and the 1-year survival rate was also significantly better for patients treated with docetaxel 75 mg/m2. A large randomized trial compared pemetrexed (LY-231514 or Alimta) 500 mg/m2 with docetaxel 75 mg/m2. Response and survival rates were similar in the two treatment arms, however, the toxicity profile of pemetrexed was superior to that of docetaxel with significantly less Grade 3/4 neutropenia and febrile neutropenia. Fewer patients in the pemetrexed arm required hospitalization. Topotecan (Hycamtin) 2.3 mg/m2/day orally for 5 days has been compared with docetaxel 75 mg/m2 in a large 800-patient study. The results of this trial are awaited. Gemcitabine (Gemzar) and irinotecan (Campto) have been evaluated both as single agents and in combination with each other and study results do not suggest that either of these drugs is superior to docetaxel or pemetrexed. The vinca alkaloid vinorelbine has proved to be inferior to docetaxel in a randomized trial. The epidermal growth factor receptor inhibitors gefitinib (ZD1839, Iressa) and erlotinib (CP-358774, OSI 774, Tarceva) have been evaluated in Phase II trials in the second- and third-line setting. Both drugs have demonstrated interesting response rates ranging from 10 to almost 20%. The results of placebo-controlled randomized trials of this family of drugs are awaited. In summary, several studies have now found a definite role for the second-line treatment of patients with non-small cell lung cancer.

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Year:  2003        PMID: 12934656     DOI: 10.1586/14737140.3.4.435

Source DB:  PubMed          Journal:  Expert Rev Anticancer Ther        ISSN: 1473-7140            Impact factor:   4.512


  6 in total

1.  Gefitinib in non-small-cell lung cancer-an old lesson new re-visited.

Authors:  Wolfram C M Dempke
Journal:  Transl Lung Cancer Res       Date:  2013-12

2.  Phase II trial of sequential gefitinib after minor response or partial response to chemotherapy in Chinese patients with advanced non-small-cell lung cancer.

Authors:  Jian Ming Xu; Yu Han; Yue Min Li; Chuan Hua Zhao; Yan Wang; Angelo Paradiso
Journal:  BMC Cancer       Date:  2006-12-16       Impact factor: 4.430

3.  Anticancer Activity of Novel Daphnane Diterpenoids from Daphne genkwa through Cell-Cycle Arrest and Suppression of Akt/STAT/Src Signalings in Human Lung Cancer Cells.

Authors:  Si-Kyoung Jo; Ji-Young Hong; Hyen Joo Park; Sang Kook Lee
Journal:  Biomol Ther (Seoul)       Date:  2012-11       Impact factor: 4.634

4.  Differential expression of circulating biomarkers of tumor phenotype and outcomes in previously treated non-small cell lung cancer patients receiving erlotinib vs. cytotoxic chemotherapy.

Authors:  Mary Jo Fidler; Casey Frankenberger; Richard Seto; Gabriela C Lobato; Cristina L Fhied; Selina Sayidine; Sanjib Basu; Mark Pool; Reem Karmali; Marta Batus; Wen-Rong Lie; David Hayes; Jehangir Mistry; Philip Bonomi; Jeffrey A Borgia
Journal:  Oncotarget       Date:  2017-04-28

5.  Real-world usage and clinical outcomes of alectinib among post-crizotinib progression anaplastic lymphoma kinase positive non-small-cell lung cancer patients in the USA.

Authors:  Marco D DiBonaventura; William Wong; Bijal Shah-Manek; Mathias Schulz
Journal:  Onco Targets Ther       Date:  2017-12-22       Impact factor: 4.147

6.  First- and second-line treatment of advanced metastatic non-small-cell lung cancer: a global view.

Authors:  Nicholas Thatcher
Journal:  BMC Proc       Date:  2008-09-24
  6 in total

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