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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Veröffentlicht in:Ecancermedicalscience 2024, Vol.18, p.1654-1654
Hauptverfasser: 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
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Sprache:eng
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Zusammenfassung: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.
ISSN:1754-6605
1754-6605
DOI:10.3332/ecancer.2024.1654