The percentage of ALK-positive cells and the efficacy of first-line alectinib in advanced non-small cell lung cancer: is it a novel factor for stratification? (Turkish Oncology Group Study)
dc.authorid | gülmez, ahmet/0000-0002-3353-344X | |
dc.authorid | KESKİNKILIÇ, MERVE/0000-0002-3342-3144 | |
dc.authorid | Ergun, Yakup/0000-0003-4784-6743 | |
dc.authorid | bilgin, burak/0000-0003-1717-8246 | |
dc.authorid | Ak, Naziye/0000-0001-5790-7066 | |
dc.authorid | Ünal, Çağlar/0000-0003-3245-1570 | |
dc.authorid | Akkoc Mustafayev, Fatma Nihan/0000-0001-7024-4156 | |
dc.authorwosid | Sendur, Mehmet Ali Nahit/H-7555-2014 | |
dc.authorwosid | gülmez, ahmet/ABI-8218-2020 | |
dc.authorwosid | KESKİNKILIÇ, MERVE/HNR-2564-2023 | |
dc.authorwosid | Ergun, Yakup/N-3273-2018 | |
dc.authorwosid | Yumuk, Perran Fulden/A-6189-2018 | |
dc.authorwosid | bilgin, burak/A-9416-2018 | |
dc.authorwosid | Ay, Murat/GSI-4353-2022 | |
dc.contributor.author | Hizal, Mutlu | |
dc.contributor.author | Bilgin, Burak | |
dc.contributor.author | Paksoy, Nail | |
dc.contributor.author | Atci, Muhammed Mustafa | |
dc.contributor.author | Kahraman, Seda | |
dc.contributor.author | Kilickap, Saadettin | |
dc.contributor.author | Guven, Deniz Can | |
dc.date.accessioned | 2024-08-04T20:52:16Z | |
dc.date.available | 2024-08-04T20:52:16Z | |
dc.date.issued | 2023 | |
dc.department | İnönü Üniversitesi | en_US |
dc.description.abstract | Introduction Alectinib is an effective second-generation ALK tyrosine kinase inhibitor (TKI) used in the first-line treatment of patients with advanced ALK-positive NSCLC. Recent studies demonstrated that the percentage of ALK-positive tumor cells in patient groups receiving crizotinib might affect outcomes. This study aimed to investigate whether the percentage of ALK-positive cells had a predictive effect in patients with advanced NSCLC who received first-line Alectinib as ALK-TKI. Materials and methods This retrospective study included patients with advanced-stage NSCLC who received alectinib as a first-line ALK-TKI and whose percentage of ALK-positive cells was determined by FISH at 27 different centers. Patients who received any ALK-TKI before alectinib were not included in the study. Patients were separated into two groups according to the median (40%) value of the percentage of ALK-positive cells (high-positive group >= 40% and low-positive group < 40%). The primary endpoint was PFS, and the secondary endpoints were OS, ORR, and PFS of the subgroups based on different threshold values for the percentage of ALK-positive cells. Results 211 patients were enrolled (48.3% female, 51.7% male) to study. 37% (n = 78) of the patients had received chemotherapy previously. After a median of 19.4 months of follow-up, the median PFS was not reached in the high-positive group (n = 113), but it was 10.8 months in the low-positive group (n = 98) (HR 0.39; 95% CI 0.25-0.60, p < 0.001). The median OS in the high-positive group was not reached, whereas it was 22.8 months in the low-positive group (HR 0.37; 95% CI 0.22-0.63, p < 0.001). ORR was significantly higher in the high-positive group (87.2 vs. 68.5%; p = 0.002). According to the cut-off values of < 20%, 20-39%, 40-59%, and >= 60%, the median PFS was 4.5, 17.1, and 26 months, respectively, and could not be reached in the >= 60% group. Conclusion Our study demonstrated that the efficacy of alectinib varies significantly across patient subgroups with different percentages of ALK-positive cells. If these findings are prospectively validated, the percentage of ALK-positive cells may be used as a stratification factor in randomized trials comparing different ALK-TKIs. | en_US |
dc.identifier.doi | 10.1007/s00432-022-04252-2 | |
dc.identifier.endpage | 4148 | en_US |
dc.identifier.issn | 0171-5216 | |
dc.identifier.issn | 1432-1335 | |
dc.identifier.issue | 8 | en_US |
dc.identifier.pmid | 36048274 | en_US |
dc.identifier.scopus | 2-s2.0-85137039744 | en_US |
dc.identifier.scopusquality | Q1 | en_US |
dc.identifier.startpage | 4141 | en_US |
dc.identifier.uri | https://doi.org/10.1007/s00432-022-04252-2 | |
dc.identifier.uri | https://hdl.handle.net/11616/100863 | |
dc.identifier.volume | 149 | en_US |
dc.identifier.wos | WOS:000849293900006 | en_US |
dc.identifier.wosquality | Q2 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.language.iso | en | en_US |
dc.publisher | Springer | en_US |
dc.relation.ispartof | Journal of Cancer Research and Clinical Oncology | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Alectinib | en_US |
dc.subject | Percentage of ALK-positive cells | en_US |
dc.subject | Break-apart | en_US |
dc.subject | Predictive | en_US |
dc.subject | Response | en_US |
dc.title | The percentage of ALK-positive cells and the efficacy of first-line alectinib in advanced non-small cell lung cancer: is it a novel factor for stratification? (Turkish Oncology Group Study) | en_US |
dc.type | Article | en_US |