Gefitinib with or without Transarterial Infusion Chemotherapy (Cisplatin) for Large Nonsmall Cell Lung Cancer with Epidermal Growth Factor Receptor Mutations |
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Authors: | Ying-Qiang Zhang Li-Juan Jiang Su-Xiang Jiang Yin-Feng Xu Bei-Bei Zhou Gui-Hua Huang Di-Min Liu Yu Wang Wen-Zhe Fan Jia-Ping Li Bo Wang |
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Affiliation: | 1. Department of Radiology, The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, China;2. Department of Oncology, The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, China;3. Department of Interventional Oncology, The First Affiliated Hospital, Sun Yat-sen University, Shenzhen, China;4. Department of Hand Surgery & Microsurgery, The First Affiliated Hospital, Sun Yat-sen University, Shenzhen, China;5. Department of Gastroenterology, The First Affiliated Hospital, Sun Yat-sen University, Shenzhen, China;6. State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University Cancer Center, Guangzhou, China;7. Department of Urology, Sun Yat-sen University Cancer Center, Guangzhou, China |
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Abstract: | PurposeTo retrospectively investigate the safety and benefit of gefitinib plus transarterial infusion (TAI) therapy as a first-line treatment compared to gefitinib alone for patients with large (>7 cm) nonsmall cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) mutations.Materials and MethodsBetween January 2010 and December 2013, 92 consecutive treatment-naïve patients with large NSCLC with EGFR mutations, who were treated using gefitinib plus TAI (G+T, n = 42) or gefitinib alone (G, n = 50) were reviewed. The primary endpoints were the objective response rate (ORR) and tumor reduction rate. The secondary endpoints were progression-free survival (PFS) and overall survival (OS), and safety was also assessed.ResultsThe baseline characteristics of the 2 groups were balanced, and no patients experienced treatment-related death. Toxicity outcomes did not differ between the G+T and G groups. The tumor reduction rate in the G+T group was significantly higher than that in the G group (42.9 vs 31.9%, P = .028). The ORR was 83% in the G+T group and 72% in the G group (P = .197). The median PFS was significantly longer in the G+T group than in the G group (14.0 vs 10.0 months, P = .023). The median OS was 30.0 months in the G+T group and 27.0 months in the G group (P = .235).ConclusionsThis study suggests that compared with gefitinib alone, combination therapy with gefitinib plus TAI was well tolerated and potentially improved the tumor reduction rate and PFS in patients with large NSCLC with EGFR mutations. |
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Keywords: | BAI transbronchial arterial infusion CR complete response CTCAE Common Terminology Criteria for Adverse Events DCR disease control rate ECOG Eastern Cooperative Oncology Group EGFR epidermal growth factor receptor G+T gefitinib plus transarterial infusion therapy NSCLC nonsmall cell lung cancer ORR objective response rate OS overall survival PFS progression-free survival PR partial response RECIST Response Evaluation Criteria in Solid Tumors SD stable disease TAI transarterial infusion therapy TKI tyrosine kinase inhibitor |
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