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dc.contributor.authorParikh, Purvish
dc.contributor.authorChang, Alex
dc.contributor.authorNag, Shona
dc.contributor.authorDigumarti, Raghunadharao
dc.contributor.authorBhattacharyya, Gouri Shankar
dc.contributor.authorDoval, Dinesh Chandra
dc.contributor.authorBabu, Govind
dc.contributor.authorChacko, Raju Titus
dc.contributor.authorAdvani, Suresh
dc.contributor.authorRanade, Anantbhushan
dc.contributor.authorAggarwal, Shyam
dc.contributor.authorJagannathan, Ramesh
dc.contributor.authorHargreaves, Laura
dc.contributor.authorThatcher, Nick
dc.date.accessioned2009-04-02T16:11:37Z
dc.date.available2009-04-02T16:11:37Z
dc.date.issued2008-04
dc.identifier.citationClinical experience with gefitinib in Indian patients. 2008, 3 (4):380-5 J Thorac Oncolen
dc.identifier.issn1556-1380
dc.identifier.pmid18379356
dc.identifier.doi10.1097/JTO.0b013e318168f794
dc.identifier.urihttp://hdl.handle.net/10541/59253
dc.description.abstractINTRODUCTION: 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.isoenen
dc.subjectLung Canceren
dc.subjectRandomized Controlled Trialen
dc.subjectNon-Small-Cell Lung Canceren
dc.subject.meshAdenocarcinoma
dc.subject.meshAdult
dc.subject.meshAged
dc.subject.meshAntineoplastic Agents
dc.subject.meshCarcinoma, Large Cell
dc.subject.meshCarcinoma, Non-Small-Cell Lung
dc.subject.meshCarcinoma, Squamous Cell
dc.subject.meshClinical Trials as Topic
dc.subject.meshFemale
dc.subject.meshHumans
dc.subject.meshIndia
dc.subject.meshLung Neoplasms
dc.subject.meshMale
dc.subject.meshMaximum Tolerated Dose
dc.subject.meshMiddle Aged
dc.subject.meshPrognosis
dc.subject.meshQuinazolines
dc.subject.meshReceptor, Epidermal Growth Factor
dc.subject.meshRetrospective Studies
dc.subject.meshSurvival Rate
dc.titleClinical experience with gefitinib in Indian patients.en
dc.typeArticleen
dc.contributor.departmentTata Memorial Hospital, Mumbai, India. purvish@rediffmail.comen
dc.identifier.journalJournal of Thoracic Oncologyen
html.description.abstractINTRODUCTION: 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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