Literature DB >> 24072220

Chemotherapy with Erlotinib or chemotherapy alone in advanced non-small cell lung cancer with acquired resistance to EGFR tyrosine kinase inhibitors.

Sarah B Goldberg1, Geoffrey R Oxnard, Subba Digumarthy, Alona Muzikansky, David M Jackman, Inga T Lennes, Lecia V Sequist.   

Abstract

Epidermal growth factor receptor (EGFR)-mutant non-small cell lung cancer has an oncogene-addicted biology that confers sensitivity to EGFR tyrosine kinase inhibitors (TKIs). Published data suggest that EGFR addiction persists after development of TKI acquired resistance, leading many clinicians to continue TKI with subsequent chemotherapy; however, this strategy has not been formally evaluated. Methods. We retrospectively reviewed an institutional database to identify patients with advanced EGFR mutation with acquired resistance who subsequently received chemotherapy. Patients were classified as receiving chemotherapy with continued erlotinib or chemotherapy alone. We assessed differences in outcomes between the two strategies. Results. Seventy-eight patients were included, 34 treated with chemotherapy and erlotinib and 44 treated with chemotherapy alone. Objective response rate was evaluable in 57 patients and was 41% for those treated with chemotherapy and erlotinib and 18% for those treated with chemotherapy alone. After adjusting for chemotherapy regimen and length of initial TKI course, the odds ratio for the response rate was 0.20 (95% confidence interval: 0.05-0.78; p = .02) favoring treatment with chemotherapy and erlotinib. The median progression-free survival was 4.4 months on chemotherapy and erlotinib and 4.2 months on chemotherapy alone (adjusted hazard ratio = 0.79; 95% confidence interval: 0.48-1.29; p = .34). There was no difference in overall survival. Conclusion. This is the first study, to our knowledge, to demonstrate that continuation of EGFR TKI with chemotherapy in patients with acquired resistance improves outcomes compared with chemotherapy alone. We observed an improved response rate but no difference in progression-free survival or overall survival. A larger prospective clinical trial is needed to evaluate this promising strategy further.

Entities:  

Keywords:  Drug resistance; Epidermal growth factor receptor; Non-small cell lung cancer; Protein kinase inhibitor

Mesh:

Substances:

Year:  2013        PMID: 24072220      PMCID: PMC3825307          DOI: 10.1634/theoncologist.2013-0168

Source DB:  PubMed          Journal:  Oncologist        ISSN: 1083-7159


  32 in total

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3.  Toxicity and response criteria of the Eastern Cooperative Oncology Group.

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Review 4.  Epidermal growth factor receptor mutation testing in the care of lung cancer patients.

Authors:  Lecia V Sequist; Victoria A Joshi; Pasi A Jänne; Daphne W Bell; Panos Fidias; Neal I Lindeman; David N Louis; Jeffrey C Lee; Eugene J Mark; Janina Longtine; Peter Verlander; Raju Kucherlapati; Matthew Meyerson; Daniel A Haber; Bruce E Johnson; Thomas J Lynch
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7.  Prospective assessment of discontinuation and reinitiation of erlotinib or gefitinib in patients with acquired resistance to erlotinib or gefitinib followed by the addition of everolimus.

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Journal:  Clin Cancer Res       Date:  2007-09-01       Impact factor: 12.531

8.  Gefitinib in combination with gemcitabine and cisplatin in advanced non-small-cell lung cancer: a phase III trial--INTACT 1.

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9.  Phase III study of erlotinib in combination with cisplatin and gemcitabine in advanced non-small-cell lung cancer: the Tarceva Lung Cancer Investigation Trial.

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10.  A randomized phase II study comparing erlotinib versus erlotinib with alternating chemotherapy in relapsed non-small-cell lung cancer patients: the NVALT-10 study.

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  58 in total

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5.  EGFR inhibitor and chemotherapy combinations for acquired TKI resistance in EGFR-mutant NSCLC models.

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6.  Chinese expert consensus on molecularly targeted therapy for advanced non-small cell lung cancer (2013 edition).

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Review 7.  Treatment Options for EGFR T790M-Negative EGFR Tyrosine Kinase Inhibitor-Resistant Non-Small Cell Lung Cancer.

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8.  Cationic lipoplexes for treatment of cancer stem cell-derived murine lung tumors.

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Review 9.  Management of tyrosine kinase inhibitor resistance in lung cancer with EGFR mutation.

Authors:  Kevin Becker; Yiqing Xu
Journal:  World J Clin Oncol       Date:  2014-10-10

10.  Local ablative therapy of oligoprogressive disease prolongs disease control by tyrosine kinase inhibitors in oncogene-addicted non-small-cell lung cancer.

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