Clinical outcomes of ROS1 -positive non-small cell lung cancer with limited access to ROS1 -tyrosine kinase inhibitors (TKIs): experience from an Indian tertiary referral centre
as a driver mutation is observed in approximately 1%-2% of all non-small cell lung cancer (NSCLC). Given its rarity, we share our experience regarding -positive NSCLC including the access to tyrosine kinase inhibitors (TKIs) in a low-middle income country like India. It is a retrospective analysis o...
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creator | Panda, Goutam Santosh Noronha, Vanita Patil, Vijay Joshi, Amit Menon, Nandini Kumar, Rajiv Pai, Trupti Shetty, Omshree Janu, Amit Chakrabarty, Nivedita Purandare, Nilendu Dey, Sayak Prabhash, Kumar |
description | as a driver mutation is observed in approximately 1%-2% of all non-small cell lung cancer (NSCLC). Given its rarity, we share our experience regarding
-positive NSCLC including the access to
tyrosine kinase inhibitors (TKIs) in a low-middle income country like India.
It is a retrospective analysis of
-positive NSCLC patients registered between January 2015 to December 2021 for demographics, treatment patterns and outcomes i.e., overall survival (OS) and progression free survival (PFS).
Baseline characteristics were available for 70 patients of 78 patients positive for
by fluorescent
hybridisation. Median age at presentation was 52 years, 39 (55.7%) were males, most (51, 72.86%) were non-smokers and ten patients (14.3%) had poor Eastern Cooperative Oncology Group (ECOG) performance status (PS) i.e., PS >2 at presentation. A total of 67 patients receiving cancer directed therapy were analysed for survival. The first line (1L) therapies included -
TKIs in 38, chemotherapy in 20, epidermal growth factor receptor TKI in eight and chemotherapy-bevacizumab in one only.
TKI was provided to 20 patients as part of an assistance programme. The median OS for patients who received
TKI was not attained (95% CI 37.85-NA), while it was 8.11 (95% CI 6.31-NA) months for those who did not (HR-0.1673). The median PFS for the 1L
TKI compared to the no-TKI group was 27.07 (95% CI 24.28-NA) months versus 5.78 (95% CI 3.42-12) months (HR: 0.2047). Poor ECOG PS at presentation was the only independent prognosticator for survival.
Using
TKI improves clinical outcomes in all-comers though statistically not significant. To further improve outcomes, future trials should pay special attention to patients with poor PS and find a way to increase the current limited access to TKI. |
doi_str_mv | 10.3332/ecancer.2024.1654 |
format | Article |
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-positive NSCLC including the access to
tyrosine kinase inhibitors (TKIs) in a low-middle income country like India.
It is a retrospective analysis of
-positive NSCLC patients registered between January 2015 to December 2021 for demographics, treatment patterns and outcomes i.e., overall survival (OS) and progression free survival (PFS).
Baseline characteristics were available for 70 patients of 78 patients positive for
by fluorescent
hybridisation. Median age at presentation was 52 years, 39 (55.7%) were males, most (51, 72.86%) were non-smokers and ten patients (14.3%) had poor Eastern Cooperative Oncology Group (ECOG) performance status (PS) i.e., PS >2 at presentation. A total of 67 patients receiving cancer directed therapy were analysed for survival. The first line (1L) therapies included -
TKIs in 38, chemotherapy in 20, epidermal growth factor receptor TKI in eight and chemotherapy-bevacizumab in one only.
TKI was provided to 20 patients as part of an assistance programme. The median OS for patients who received
TKI was not attained (95% CI 37.85-NA), while it was 8.11 (95% CI 6.31-NA) months for those who did not (HR-0.1673). The median PFS for the 1L
TKI compared to the no-TKI group was 27.07 (95% CI 24.28-NA) months versus 5.78 (95% CI 3.42-12) months (HR: 0.2047). Poor ECOG PS at presentation was the only independent prognosticator for survival.
Using
TKI improves clinical outcomes in all-comers though statistically not significant. To further improve outcomes, future trials should pay special attention to patients with poor PS and find a way to increase the current limited access to TKI.</description><identifier>ISSN: 1754-6605</identifier><identifier>EISSN: 1754-6605</identifier><identifier>DOI: 10.3332/ecancer.2024.1654</identifier><identifier>PMID: 38425761</identifier><language>eng</language><publisher>England: Cancer Intelligence</publisher><subject>Biopsy ; Chemotherapy ; Clinical outcomes ; FDA approval ; Immunotherapy ; Kinases ; Lung cancer ; Metastasis ; Mutation ; Patients ; Pleural effusion ; Radiation therapy ; Statistical analysis ; Survival analysis</subject><ispartof>Ecancermedicalscience, 2024, Vol.18, p.1654-1654</ispartof><rights>the authors; licensee ecancermedicalscience.</rights><rights>the authors; licensee e cancermedicalscience. 2024. This work is published under https://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>the authors; licensee cancermedicalscience. 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c428t-95f460af24bc205c5768573b8d515f6604fea32b84543eb2555980f3a12c417e3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10901635/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10901635/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,861,882,4010,27904,27905,27906,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38425761$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Panda, Goutam Santosh</creatorcontrib><creatorcontrib>Noronha, Vanita</creatorcontrib><creatorcontrib>Patil, Vijay</creatorcontrib><creatorcontrib>Joshi, Amit</creatorcontrib><creatorcontrib>Menon, Nandini</creatorcontrib><creatorcontrib>Kumar, Rajiv</creatorcontrib><creatorcontrib>Pai, Trupti</creatorcontrib><creatorcontrib>Shetty, Omshree</creatorcontrib><creatorcontrib>Janu, Amit</creatorcontrib><creatorcontrib>Chakrabarty, Nivedita</creatorcontrib><creatorcontrib>Purandare, Nilendu</creatorcontrib><creatorcontrib>Dey, Sayak</creatorcontrib><creatorcontrib>Prabhash, Kumar</creatorcontrib><title>Clinical outcomes of ROS1 -positive non-small cell lung cancer with limited access to ROS1 -tyrosine kinase inhibitors (TKIs): experience from an Indian tertiary referral centre</title><title>Ecancermedicalscience</title><addtitle>Ecancermedicalscience</addtitle><description>as a driver mutation is observed in approximately 1%-2% of all non-small cell lung cancer (NSCLC). Given its rarity, we share our experience regarding
-positive NSCLC including the access to
tyrosine kinase inhibitors (TKIs) in a low-middle income country like India.
It is a retrospective analysis of
-positive NSCLC patients registered between January 2015 to December 2021 for demographics, treatment patterns and outcomes i.e., overall survival (OS) and progression free survival (PFS).
Baseline characteristics were available for 70 patients of 78 patients positive for
by fluorescent
hybridisation. Median age at presentation was 52 years, 39 (55.7%) were males, most (51, 72.86%) were non-smokers and ten patients (14.3%) had poor Eastern Cooperative Oncology Group (ECOG) performance status (PS) i.e., PS >2 at presentation. A total of 67 patients receiving cancer directed therapy were analysed for survival. The first line (1L) therapies included -
TKIs in 38, chemotherapy in 20, epidermal growth factor receptor TKI in eight and chemotherapy-bevacizumab in one only.
TKI was provided to 20 patients as part of an assistance programme. The median OS for patients who received
TKI was not attained (95% CI 37.85-NA), while it was 8.11 (95% CI 6.31-NA) months for those who did not (HR-0.1673). The median PFS for the 1L
TKI compared to the no-TKI group was 27.07 (95% CI 24.28-NA) months versus 5.78 (95% CI 3.42-12) months (HR: 0.2047). Poor ECOG PS at presentation was the only independent prognosticator for survival.
Using
TKI improves clinical outcomes in all-comers though statistically not significant. 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Given its rarity, we share our experience regarding
-positive NSCLC including the access to
tyrosine kinase inhibitors (TKIs) in a low-middle income country like India.
It is a retrospective analysis of
-positive NSCLC patients registered between January 2015 to December 2021 for demographics, treatment patterns and outcomes i.e., overall survival (OS) and progression free survival (PFS).
Baseline characteristics were available for 70 patients of 78 patients positive for
by fluorescent
hybridisation. Median age at presentation was 52 years, 39 (55.7%) were males, most (51, 72.86%) were non-smokers and ten patients (14.3%) had poor Eastern Cooperative Oncology Group (ECOG) performance status (PS) i.e., PS >2 at presentation. A total of 67 patients receiving cancer directed therapy were analysed for survival. The first line (1L) therapies included -
TKIs in 38, chemotherapy in 20, epidermal growth factor receptor TKI in eight and chemotherapy-bevacizumab in one only.
TKI was provided to 20 patients as part of an assistance programme. The median OS for patients who received
TKI was not attained (95% CI 37.85-NA), while it was 8.11 (95% CI 6.31-NA) months for those who did not (HR-0.1673). The median PFS for the 1L
TKI compared to the no-TKI group was 27.07 (95% CI 24.28-NA) months versus 5.78 (95% CI 3.42-12) months (HR: 0.2047). Poor ECOG PS at presentation was the only independent prognosticator for survival.
Using
TKI improves clinical outcomes in all-comers though statistically not significant. To further improve outcomes, future trials should pay special attention to patients with poor PS and find a way to increase the current limited access to TKI.</abstract><cop>England</cop><pub>Cancer Intelligence</pub><pmid>38425761</pmid><doi>10.3332/ecancer.2024.1654</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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source | DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central Open Access; PubMed Central |
subjects | Biopsy Chemotherapy Clinical outcomes FDA approval Immunotherapy Kinases Lung cancer Metastasis Mutation Patients Pleural effusion Radiation therapy Statistical analysis Survival analysis |
title | Clinical outcomes of ROS1 -positive non-small cell lung cancer with limited access to ROS1 -tyrosine kinase inhibitors (TKIs): experience from an Indian tertiary referral centre |
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