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ALK Positive Lung Cancer: Clinical Profile, Practice and Outcomes in a Developing Country
OBJECTIVES: To evaluate the performance and treatment profile of advanced EML4—ALK positive Non-small cell lung cancer (NSCLC) patients in a developing country with potentially restricted access to Crizotinib. MATERIALS AND METHODS: A retrospective analysis of advanced ALK positive NSCLC patients wh...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5026380/ https://www.ncbi.nlm.nih.gov/pubmed/27637025 http://dx.doi.org/10.1371/journal.pone.0160752 |
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author | Noronha, Vanita Ramaswamy, Anant Patil, Vijay M Joshi, Amit Chougule, Anuradha Kane, Subhadha Kumar, Rajiv Sahu, Arvind Doshi, Vipul Nayak, Lingaraj Mahajan, Abhishek Janu, Amit Prabhash, Kumar |
author_facet | Noronha, Vanita Ramaswamy, Anant Patil, Vijay M Joshi, Amit Chougule, Anuradha Kane, Subhadha Kumar, Rajiv Sahu, Arvind Doshi, Vipul Nayak, Lingaraj Mahajan, Abhishek Janu, Amit Prabhash, Kumar |
author_sort | Noronha, Vanita |
collection | PubMed |
description | OBJECTIVES: To evaluate the performance and treatment profile of advanced EML4—ALK positive Non-small cell lung cancer (NSCLC) patients in a developing country with potentially restricted access to Crizotinib. MATERIALS AND METHODS: A retrospective analysis of advanced ALK positive NSCLC patients who were treated from June 2012 to September 2015 was conducted. The primary goal was to evaluate outcomes of advanced ALK positive NSCLC in our practice and examine the logistic constraints in procuring Crizotinib. RESULTS: 94 patients were available for analysis. 21 (22.3%) patients were started on Crizotinib upfront, 60 (63.8%) on chemotherapy, 10 (10.6%) on Tyrosine kinase inhibitors (in view of poor PS) and 3 (3.2%) patients were offered best supportive care. Reasons for not starting Crizotinib upfront included symptomatic patients needing early initiation of therapy (23.3%), ALK not tested upfront (23.3%) and financial constraints (21.9%). 69 patients (73.4%) received Crizotinib at some stage during treatment. Dose interruptions (> 1 week) with Crizotinib were seen in 20 patients (29%), with drug toxicity being the commonest reason (85%). Median Progression free survival (PFS) on first line therapy for the entire cohort was 10 months, with a significant difference between patients receiving Crizotinib and those who did not ever receive Crizotinib (10 months vs. 2 months, p = 0.028). Median Overall Survival (OS) was not reached for the entire cohort, with 1 year survival being 81.2%. Patients with an ECOG Performance Status (PS) of >2 had a significantly reduced PFS compared to patients with PS < = 2 (1.5 months vs. 11 months, p< 0.001). 47 patients with financial constraints (68.1%) received Crizotinib completely free via various extramural support schemes. CONCLUSION: A majority of our ALK positive NSCLC patients were exposed to Crizotinib through the help of various support mechanisms and these patients had similar outcomes to that reported from previously published literature. |
format | Online Article Text |
id | pubmed-5026380 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-50263802016-10-10 ALK Positive Lung Cancer: Clinical Profile, Practice and Outcomes in a Developing Country Noronha, Vanita Ramaswamy, Anant Patil, Vijay M Joshi, Amit Chougule, Anuradha Kane, Subhadha Kumar, Rajiv Sahu, Arvind Doshi, Vipul Nayak, Lingaraj Mahajan, Abhishek Janu, Amit Prabhash, Kumar PLoS One Research Article OBJECTIVES: To evaluate the performance and treatment profile of advanced EML4—ALK positive Non-small cell lung cancer (NSCLC) patients in a developing country with potentially restricted access to Crizotinib. MATERIALS AND METHODS: A retrospective analysis of advanced ALK positive NSCLC patients who were treated from June 2012 to September 2015 was conducted. The primary goal was to evaluate outcomes of advanced ALK positive NSCLC in our practice and examine the logistic constraints in procuring Crizotinib. RESULTS: 94 patients were available for analysis. 21 (22.3%) patients were started on Crizotinib upfront, 60 (63.8%) on chemotherapy, 10 (10.6%) on Tyrosine kinase inhibitors (in view of poor PS) and 3 (3.2%) patients were offered best supportive care. Reasons for not starting Crizotinib upfront included symptomatic patients needing early initiation of therapy (23.3%), ALK not tested upfront (23.3%) and financial constraints (21.9%). 69 patients (73.4%) received Crizotinib at some stage during treatment. Dose interruptions (> 1 week) with Crizotinib were seen in 20 patients (29%), with drug toxicity being the commonest reason (85%). Median Progression free survival (PFS) on first line therapy for the entire cohort was 10 months, with a significant difference between patients receiving Crizotinib and those who did not ever receive Crizotinib (10 months vs. 2 months, p = 0.028). Median Overall Survival (OS) was not reached for the entire cohort, with 1 year survival being 81.2%. Patients with an ECOG Performance Status (PS) of >2 had a significantly reduced PFS compared to patients with PS < = 2 (1.5 months vs. 11 months, p< 0.001). 47 patients with financial constraints (68.1%) received Crizotinib completely free via various extramural support schemes. CONCLUSION: A majority of our ALK positive NSCLC patients were exposed to Crizotinib through the help of various support mechanisms and these patients had similar outcomes to that reported from previously published literature. Public Library of Science 2016-09-16 /pmc/articles/PMC5026380/ /pubmed/27637025 http://dx.doi.org/10.1371/journal.pone.0160752 Text en © 2016 Noronha et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Noronha, Vanita Ramaswamy, Anant Patil, Vijay M Joshi, Amit Chougule, Anuradha Kane, Subhadha Kumar, Rajiv Sahu, Arvind Doshi, Vipul Nayak, Lingaraj Mahajan, Abhishek Janu, Amit Prabhash, Kumar ALK Positive Lung Cancer: Clinical Profile, Practice and Outcomes in a Developing Country |
title | ALK Positive Lung Cancer: Clinical Profile, Practice and Outcomes in a Developing Country |
title_full | ALK Positive Lung Cancer: Clinical Profile, Practice and Outcomes in a Developing Country |
title_fullStr | ALK Positive Lung Cancer: Clinical Profile, Practice and Outcomes in a Developing Country |
title_full_unstemmed | ALK Positive Lung Cancer: Clinical Profile, Practice and Outcomes in a Developing Country |
title_short | ALK Positive Lung Cancer: Clinical Profile, Practice and Outcomes in a Developing Country |
title_sort | alk positive lung cancer: clinical profile, practice and outcomes in a developing country |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5026380/ https://www.ncbi.nlm.nih.gov/pubmed/27637025 http://dx.doi.org/10.1371/journal.pone.0160752 |
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