Mony Ung1, Isabelle Rouquette2, Thomas Filleron3, Kristell Taillandy4, Laurent Brouchet5, Jaafar Bennouna6, Jean-Pierre Delord7, Julie Milia8, Julien Mazières9. 1. Department of Medical Oncology, Institut Curie, Hôpital René Huguenin, Saint-Cloud, France. 2. Department of Pathology, Institut Universitaire du Cancer de Toulouse-Oncopole, Centre Hospitalier Universitaire de Toulouse, Graduate Institute of Cancer Toulouse Oncopole, Toulouse, France. 3. Clinical Research Unit, Biostatistics, Institut Claudius Regaud, Institut Universitaire du Cancer, Oncopole, Graduate Institute of Cancer Toulouse Oncopole, Toulouse, France. 4. Centre Hospitalier Départemental de Vendée, Médecine Onco-Hématologie, La Roche-sur-Yon, France. 5. Thoracic Surgery Unit, Hôpital Larrey, Centre Hospitalier Universitaire, Université de Toulouse III, Toulouse, France. 6. Institut de Cancérologie de l'Ouest, Nantes-Angers, Nantes, France. 7. Department of Oncology and Clinical Research Unit, Institut Claudius Regaud, Institut Universitaire du Cancer, Graduate Institute of Cancer Toulouse Oncopole, Toulouse, France. 8. Pulmonary Medicine Unit, Hôpital Larrey, Centre Hospitalier Universitaire Toulouse, Université de Toulouse III, Toulouse, France. 9. Pulmonary Medicine Unit, Hôpital Larrey, Centre Hospitalier Universitaire Toulouse, Université de Toulouse III, Toulouse, France. Electronic address: mazieres.j@chu-toulouse.fr.
Abstract
BACKGROUND: Sarcomatoid carcinoma is a rare subtype of non-small-cell lung cancer, which has aggressive behavior. We present information on the clinicopathologic characteristics and clinical outcomes of these tumors. PATIENTS AND METHODS: From January 2000 to December 2012, the clinicopathologic data from 93 patients treated at 2 French cancer centers were retrospectively analyzed. A pathologic review was performed of all tumors. RESULTS: The patients were commonly male (77%), with a median age of 63 years and a history of smoking (84%). Most had symptoms, and about 70% presented with locally advanced or metastatic disease at diagnosis. Of the 93 cases, 41 were diagnosed by surgical resection. Pleomorphic carcinoma was the most common subtype (64%). With a median follow-up period of 30.7 months, the median survival of the patients who had undergone surgery was 16.4 months. Recurrence with distant metastases was common. Univariate analyses showed that advanced disease (pathologic stage > III) conferred a worse prognosis for recurrence-free and overall survival (P = .0024 and P < .0001, respectively). Twenty-eight patients received first-line chemotherapy for advanced disease. The progression rate was 72% at the first evaluation. The median time to progression and the median overall survival were poor (2.7 and 4.3 months, respectively). On univariate analysis, a platinum-based combination had significant influence on overall survival compared with monotherapy (P < .0001). CONCLUSION: Sarcomatoid carcinoma is associated with a poor prognosis. Surgical treatment should be carefully considered in the early stages. The high resistance to chemotherapy emphasizes the need to test for new strategies through collaborative programs dedicated to this population.
BACKGROUND:Sarcomatoid carcinoma is a rare subtype of non-small-cell lung cancer, which has aggressive behavior. We present information on the clinicopathologic characteristics and clinical outcomes of these tumors. PATIENTS AND METHODS: From January 2000 to December 2012, the clinicopathologic data from 93 patients treated at 2 French cancer centers were retrospectively analyzed. A pathologic review was performed of all tumors. RESULTS: The patients were commonly male (77%), with a median age of 63 years and a history of smoking (84%). Most had symptoms, and about 70% presented with locally advanced or metastatic disease at diagnosis. Of the 93 cases, 41 were diagnosed by surgical resection. Pleomorphic carcinoma was the most common subtype (64%). With a median follow-up period of 30.7 months, the median survival of the patients who had undergone surgery was 16.4 months. Recurrence with distant metastases was common. Univariate analyses showed that advanced disease (pathologic stage > III) conferred a worse prognosis for recurrence-free and overall survival (P = .0024 and P < .0001, respectively). Twenty-eight patients received first-line chemotherapy for advanced disease. The progression rate was 72% at the first evaluation. The median time to progression and the median overall survival were poor (2.7 and 4.3 months, respectively). On univariate analysis, a platinum-based combination had significant influence on overall survival compared with monotherapy (P < .0001). CONCLUSION:Sarcomatoid carcinoma is associated with a poor prognosis. Surgical treatment should be carefully considered in the early stages. The high resistance to chemotherapy emphasizes the need to test for new strategies through collaborative programs dedicated to this population.
Authors: Anette Szczepny; Kirstyn Carey; Lisa McKenzie; W Samantha N Jayasekara; Fernando Rossello; Alvaro Gonzalez-Rajal; Andrew S McCaw; Dean Popovski; Die Wang; Anthony J Sadler; Annabelle Mahar; Prudence A Russell; Gavin Wright; Rachael A McCloy; Daniel J Garama; Daniel J Gough; Stephen B Baylin; Andrew Burgess; Jason E Cain; D Neil Watkins Journal: Oncogene Date: 2018-01-25 Impact factor: 9.867