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Molecular Cancer Therapeutics
Molecular Cancer Therapeutics
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Spotlight on Clinical Response

Response to Erlotinib in Patients with EGFR Mutant Advanced Non–Small Cell Lung Cancers with a Squamous or Squamous-like Component

Paul K. Paik, Anna M. Varghese, Camelia S. Sima, Andre L. Moreira, Marc Ladanyi, Mark G. Kris and Natasha Rekhtman
Paul K. Paik
1Thoracic Oncology Service, Division of Solid Tumor Oncology, Department of Medicine, and 2Department of Epidemiology and Biostatistics, and 3Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York, New York; 4Department of Medicine, Weill Cornell Medical College, New York, New York
1Thoracic Oncology Service, Division of Solid Tumor Oncology, Department of Medicine, and 2Department of Epidemiology and Biostatistics, and 3Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York, New York; 4Department of Medicine, Weill Cornell Medical College, New York, New York
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Anna M. Varghese
1Thoracic Oncology Service, Division of Solid Tumor Oncology, Department of Medicine, and 2Department of Epidemiology and Biostatistics, and 3Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York, New York; 4Department of Medicine, Weill Cornell Medical College, New York, New York
1Thoracic Oncology Service, Division of Solid Tumor Oncology, Department of Medicine, and 2Department of Epidemiology and Biostatistics, and 3Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York, New York; 4Department of Medicine, Weill Cornell Medical College, New York, New York
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Camelia S. Sima
1Thoracic Oncology Service, Division of Solid Tumor Oncology, Department of Medicine, and 2Department of Epidemiology and Biostatistics, and 3Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York, New York; 4Department of Medicine, Weill Cornell Medical College, New York, New York
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Andre L. Moreira
1Thoracic Oncology Service, Division of Solid Tumor Oncology, Department of Medicine, and 2Department of Epidemiology and Biostatistics, and 3Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York, New York; 4Department of Medicine, Weill Cornell Medical College, New York, New York
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Marc Ladanyi
1Thoracic Oncology Service, Division of Solid Tumor Oncology, Department of Medicine, and 2Department of Epidemiology and Biostatistics, and 3Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York, New York; 4Department of Medicine, Weill Cornell Medical College, New York, New York
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Mark G. Kris
1Thoracic Oncology Service, Division of Solid Tumor Oncology, Department of Medicine, and 2Department of Epidemiology and Biostatistics, and 3Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York, New York; 4Department of Medicine, Weill Cornell Medical College, New York, New York
1Thoracic Oncology Service, Division of Solid Tumor Oncology, Department of Medicine, and 2Department of Epidemiology and Biostatistics, and 3Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York, New York; 4Department of Medicine, Weill Cornell Medical College, New York, New York
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Natasha Rekhtman
1Thoracic Oncology Service, Division of Solid Tumor Oncology, Department of Medicine, and 2Department of Epidemiology and Biostatistics, and 3Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York, New York; 4Department of Medicine, Weill Cornell Medical College, New York, New York
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DOI: 10.1158/1535-7163.MCT-12-0163 Published November 2012
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Abstract

We previously reported that although EGFR mutations are not a feature of pure squamous cell carcinomas (SCC) of the lung, these mutations do occur in adenosquamous carcinomas (AD-SCC) and in rare solid adenocarcinomas, both of which can mimic SCC in small samples. Here we present an expanded series of these cases with a focus on sensitivity to erlotinib. The study included 13 patients with EGFR mutant lung carcinomas, which after detailed pathologic review were classified as AD-SCC (n = 11) or solid adenocarcinoma (n = 2). The majority received a diagnosis of SCC in at least 1 sample. All patients were treated with erlotinib. Eight of 11 patients with AD-SCC were evaluable for response. Their overall response rate was 88% (7/8; 95% CI, 47% to 99%). One of 2 solid adenocarcinoma patients responded to erlotinib. As a group, median progression-free survival was 12 months (95% CI, 8 to not reached); median overall survival was 29 months (95% CI, 27 to not reached). In conclusion, EGFR mutant AD-SCC and solid adenocarcinoma show a response to erlotinib that is comparable to that seen in patients with conventional adenocarcinoma. These tumors can mimic SCC in small samples. We propose an approach to increase the capture of these rare histology patients for EGFR mutation testing. Mol Cancer Ther; 11(11); 2535–40. ©2012 AACR.

  • Received February 17, 2012.
  • Revision received July 13, 2012.
  • Accepted July 26, 2012.
  • ©2012 American Association for Cancer Research.
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Molecular Cancer Therapeutics: 11 (11)
November 2012
Volume 11, Issue 11
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Response to Erlotinib in Patients with EGFR Mutant Advanced Non–Small Cell Lung Cancers with a Squamous or Squamous-like Component
Paul K. Paik, Anna M. Varghese, Camelia S. Sima, Andre L. Moreira, Marc Ladanyi, Mark G. Kris and Natasha Rekhtman
Mol Cancer Ther November 1 2012 (11) (11) 2535-2540; DOI: 10.1158/1535-7163.MCT-12-0163

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Response to Erlotinib in Patients with EGFR Mutant Advanced Non–Small Cell Lung Cancers with a Squamous or Squamous-like Component
Paul K. Paik, Anna M. Varghese, Camelia S. Sima, Andre L. Moreira, Marc Ladanyi, Mark G. Kris and Natasha Rekhtman
Mol Cancer Ther November 1 2012 (11) (11) 2535-2540; DOI: 10.1158/1535-7163.MCT-12-0163
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Molecular Cancer Therapeutics
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