| dc.contributor | Vall d'Hebron Barcelona Hospital Campus |
| dc.contributor.author | Canale, Matteo |
| dc.contributor.author | Angeli, Davide |
| dc.contributor.author | Tedaldi, Gianluca |
| dc.contributor.author | Priano, Ilaria |
| dc.contributor.author | Urbini, Milena |
| dc.contributor.author | Petracci, Elisabetta |
| dc.date.accessioned | 2025-04-25T05:57:36Z |
| dc.date.available | 2025-04-25T05:57:36Z |
| dc.date.issued | 2025-02-20 |
| dc.identifier.citation | Canale M, Urbini M, Petracci E, Angeli D, Tedaldi G, Priano I, et al. Genomic Profiling of Extensive Stage Small-Cell Lung Cancer Patients Identifies Molecular Factors Associated with Survival. Lung Cancer Targets Ther. 2025 Feb 20;16:11-23. |
| dc.identifier.issn | 1179-2728 |
| dc.identifier.uri | http://hdl.handle.net/11351/12987 |
| dc.description | Immunotherapy; Small-cell lung cancer; Tumor mutation burden |
| dc.description.abstract | Objective: Extensive stage Small-Cell Lung Cancer (ES-SCLC) is the most lethal lung cancer, and the addition of immunotherapy conferred a slight survival benefit for patients. Extensive molecular profiling of patients treated with chemotherapy (CT) or chemotherapy plus immunotherapy (CT+IO) would be able to identify molecular factors associated with patients' survival.
Material and methods: In this retrospective study, 99 ES-SCLC patients were considered. Of the 79 includible patients, 42 received CT (median age 71 y/o, I-IIIQ: 65-76), and 37 received CT+IO (median age 71 y/o, I-IIIQ 66-75). The FoundationOne CDx assay was performed on patients' tumor tissues.
Results: The most mutated genes were TP53 (99%), RB1 (78%), PTEN (23%) and MLL2 (20%), with no significant differences between the treatment groups. As a continuous variable, Tumor Mutation Burden (TMB) had an effect on patients' progression-free survival (PFS) by type of treatment (HR 1.81 (95%, CI: 0.99-3.31) and HR 0.84 (95%, CI: 0.56-1.26) for patients treated with CT and CT+IO, respectively). TMB was also computed and dichotomized using two different cut-offs: considering cut-offs of 10 mut/Mb and >16 mut/Mb, 45 patients (57%) and 68 patients (86.1%) had a low TMB, respectively. A high TMB (cut-off 10 mut/Mb) predicted worse PFS in patients treated with CT (p=0.046); even though not statistically significant, a high TMB (cut-off 16 mut/Mb) predicted a better survival in patients treated with CT+IO. Moreover, at univariate analysis, MLL2 mutations were associated with better prognosis in the overall case series (HRPFS = 0.51, 95% CI: 0.28-0.94), and overall survival (HROS = 0.52, 95% CI: 0.28-0.97).
Conclusion: In ES-SCLC, TMB is associated with worse survival in patients treated with CT alone, and with better survival in patients treated with CT+IO, whether considered as a continuous or a dichotomized variable, at different cut-offs. Alterations in epigenetic factors are also associated to better patient prognosis. |
| dc.language.iso | eng |
| dc.publisher | Dove Medical Press |
| dc.relation.ispartofseries | Lung Cancer: Targets and Therapy;16 |
| dc.rights | Attribution-NonCommercial 4.0 International |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc/4.0/ |
| dc.source | Scientia |
| dc.subject | Anomalies cromosòmiques |
| dc.subject | Pulmons - Càncer - Tractament |
| dc.subject | Pulmons - Càncer - Aspectes genètics |
| dc.subject | Quimioteràpia combinada |
| dc.subject | Pulmons - Càncer - Prognosi |
| dc.subject | Marcadors tumorals |
| dc.subject.mesh | Mutation |
| dc.subject.mesh | Small Cell Lung Carcinoma |
| dc.subject.mesh | /drug therapy |
| dc.subject.mesh | Antineoplastic Combined Chemotherapy Protocols |
| dc.subject.mesh | Prognosis |
| dc.subject.mesh | Biomarkers, Tumor |
| dc.title | Genomic Profiling of Extensive Stage Small-Cell Lung Cancer Patients Identifies Molecular Factors Associated with Survival |
| dc.type | info:eu-repo/semantics/article |
| dc.identifier.doi | 10.2147/LCTT.S492825 |
| dc.subject.decs | mutación |
| dc.subject.decs | carcinoma pulmonar de células pequeñas |
| dc.subject.decs | /farmacoterapia |
| dc.subject.decs | protocolos de quimioterapia antineoplásica combinada |
| dc.subject.decs | pronóstico |
| dc.subject.decs | marcadores tumorales |
| dc.relation.publishversion | https://doi.org/10.2147/LCTT.S492825 |
| dc.type.version | info:eu-repo/semantics/publishedVersion |
| dc.audience | Professionals |
| dc.contributor.organismes | Institut Català de la Salut |
| dc.contributor.authoraffiliation | [Canale M, Urbini M, Tedaldi G] Biosciences Laboratory, IRCCS Istituto Romagnolo per Lo Studio Dei Tumori (IRST) “dino Amadori”, Meldola, Italy. [Petracci E, Angeli D] Unit of Biostatistics and Clinical Trials, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) “Dino Amadori”, Meldola, Italy. [Priano I] Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. Servei d’Oncologia Mèdica, Vall d’Hebron Hospital Universitari, Barcelona, Spain |
| dc.identifier.pmid | 39995768 |
| dc.identifier.wos | 001429215900001 |
| dc.rights.accessrights | info:eu-repo/semantics/openAccess |