Clinical experience with gefitinib in Indian patients.
dc.contributor.author | Parikh, Purvish | |
dc.contributor.author | Chang, Alex | |
dc.contributor.author | Nag, Shona | |
dc.contributor.author | Digumarti, Raghunadharao | |
dc.contributor.author | Bhattacharyya, Gouri Shankar | |
dc.contributor.author | Doval, Dinesh Chandra | |
dc.contributor.author | Babu, Govind | |
dc.contributor.author | Chacko, Raju Titus | |
dc.contributor.author | Advani, Suresh | |
dc.contributor.author | Ranade, Anantbhushan | |
dc.contributor.author | Aggarwal, Shyam | |
dc.contributor.author | Jagannathan, Ramesh | |
dc.contributor.author | Hargreaves, Laura | |
dc.contributor.author | Thatcher, Nick | |
dc.date.accessioned | 2009-04-02T16:11:37Z | |
dc.date.available | 2009-04-02T16:11:37Z | |
dc.date.issued | 2008-04 | |
dc.identifier.citation | Clinical experience with gefitinib in Indian patients. 2008, 3 (4):380-5 J Thorac Oncol | en |
dc.identifier.issn | 1556-1380 | |
dc.identifier.pmid | 18379356 | |
dc.identifier.doi | 10.1097/JTO.0b013e318168f794 | |
dc.identifier.uri | http://hdl.handle.net/10541/59253 | |
dc.description.abstract | INTRODUCTION: Treatment options are limited in patients with advanced or refractory non-small cell lung cancer and lead to suboptimal outcome and/or benefit. The epidermal growth factor tyrosine kinase inhibitor gefitinib (IRESSA) has been approved in many countries. Increased responsiveness to gefitinib has been demonstrated in particular subsets of patients, for example never smokers and patients of Asian origin. However, to date, little is known of its use specifically in patients from India. METHODS: Retrospective ad hoc analysis of clinical data from experience with gefitinib in patients with advanced NSCLC from India enrolled in the IRESSA Survival Evaluation in Lung (ISEL) study (n = 77) or included in the gefitinib expanded-access program in India (n = 133). RESULTS: Among Indian patients enrolled in the ISEL study, median survival was 6.4 months with gefitinib and 5.1 month with placebo. The objective response rate in Indian patients was 14% with gefitinib versus 0% with placebo. In ISEL, tolerability data from Indian patients were consistent with the overall study population. In the Indian gefitinib expanded-access program, median survival was 6 months and gefitinib was well tolerated. CONCLUSIONS: Gefitinib seems well tolerated in Indian patients with advanced NSCLC, with some clinical benefit observed. | |
dc.language.iso | en | en |
dc.subject | Lung Cancer | en |
dc.subject | Randomized Controlled Trial | en |
dc.subject | Non-Small-Cell Lung Cancer | en |
dc.subject.mesh | Adenocarcinoma | |
dc.subject.mesh | Adult | |
dc.subject.mesh | Aged | |
dc.subject.mesh | Antineoplastic Agents | |
dc.subject.mesh | Carcinoma, Large Cell | |
dc.subject.mesh | Carcinoma, Non-Small-Cell Lung | |
dc.subject.mesh | Carcinoma, Squamous Cell | |
dc.subject.mesh | Clinical Trials as Topic | |
dc.subject.mesh | Female | |
dc.subject.mesh | Humans | |
dc.subject.mesh | India | |
dc.subject.mesh | Lung Neoplasms | |
dc.subject.mesh | Male | |
dc.subject.mesh | Maximum Tolerated Dose | |
dc.subject.mesh | Middle Aged | |
dc.subject.mesh | Prognosis | |
dc.subject.mesh | Quinazolines | |
dc.subject.mesh | Receptor, Epidermal Growth Factor | |
dc.subject.mesh | Retrospective Studies | |
dc.subject.mesh | Survival Rate | |
dc.title | Clinical experience with gefitinib in Indian patients. | en |
dc.type | Article | en |
dc.contributor.department | Tata Memorial Hospital, Mumbai, India. purvish@rediffmail.com | en |
dc.identifier.journal | Journal of Thoracic Oncology | en |
html.description.abstract | INTRODUCTION: Treatment options are limited in patients with advanced or refractory non-small cell lung cancer and lead to suboptimal outcome and/or benefit. The epidermal growth factor tyrosine kinase inhibitor gefitinib (IRESSA) has been approved in many countries. Increased responsiveness to gefitinib has been demonstrated in particular subsets of patients, for example never smokers and patients of Asian origin. However, to date, little is known of its use specifically in patients from India. METHODS: Retrospective ad hoc analysis of clinical data from experience with gefitinib in patients with advanced NSCLC from India enrolled in the IRESSA Survival Evaluation in Lung (ISEL) study (n = 77) or included in the gefitinib expanded-access program in India (n = 133). RESULTS: Among Indian patients enrolled in the ISEL study, median survival was 6.4 months with gefitinib and 5.1 month with placebo. The objective response rate in Indian patients was 14% with gefitinib versus 0% with placebo. In ISEL, tolerability data from Indian patients were consistent with the overall study population. In the Indian gefitinib expanded-access program, median survival was 6 months and gefitinib was well tolerated. CONCLUSIONS: Gefitinib seems well tolerated in Indian patients with advanced NSCLC, with some clinical benefit observed. |
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Medical Oncology
Medical Oncology