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KRAS G12 isoforms exert influence over up-front treatments: A retrospective, multicenter, Italian analysis of the impact of first-line immune checkpoint inhibitors in an NSCLC real-life population.
Fancelli, Sara; Caliman, Enrico; Mazzoni, Francesca; Paglialunga, Luca; Gatta Michelet, Marta Rita; Lavacchi, Daniele; Berardi, Rossana; Mentrasti, Giulia; Metro, Giulio; Birocchi, Ilaria; Delmonte, Angelo; Priano, Ilaria; Comin, Camilla Eva; Castiglione, Francesca; Bartoli, Caterina; Voltolini, Luca; Pillozzi, Serena; Antonuzzo, Lorenzo.
Afiliação
  • Fancelli S; Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
  • Caliman E; Clinical Oncology Unit, Careggi University Hospital, Florence, Italy.
  • Mazzoni F; Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
  • Paglialunga L; Clinical Oncology Unit, Careggi University Hospital, Florence, Italy.
  • Gatta Michelet MR; Medical Oncology Unit, Careggi University Hospital, Florence, Italy.
  • Lavacchi D; Clinical Oncology Unit, Careggi University Hospital, Florence, Italy.
  • Berardi R; Medical Oncology Unit, Careggi University Hospital, Florence, Italy.
  • Mentrasti G; Clinical Oncology Unit, Careggi University Hospital, Florence, Italy.
  • Metro G; Department of Medical Oncology, Università Politecnica delle Marche, Azienda Ospedaliero Universitaria (AOU) Ospedali Riuniti di Ancona, Ancona, Italy.
  • Birocchi I; Department of Medical Oncology, Università Politecnica delle Marche, Azienda Ospedaliero Universitaria (AOU) Ospedali Riuniti di Ancona, Ancona, Italy.
  • Delmonte A; Medical Oncology Unit, Santa Maria della Misericordia Hospital, Perugia, Italy.
  • Priano I; Medical Oncology Unit, Santa Maria della Misericordia Hospital, Perugia, Italy.
  • Comin CE; Scientific Institute of Romagna for the Study and Treatment of Tumors (IRST) Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Meldola, Italy.
  • Castiglione F; Scientific Institute of Romagna for the Study and Treatment of Tumors (IRST) Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Meldola, Italy.
  • Bartoli C; Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
  • Voltolini L; Surgery, Histopathology and Molecular Pathology Unit, Careggi University Hospital, Florence, Italy.
  • Pillozzi S; Pathological Histology and Molecular Diagnostics Unit, Careggi University Hospital, Florence, Italy.
  • Antonuzzo L; Pathological Histology and Molecular Diagnostics Unit, Careggi University Hospital, Florence, Italy.
Front Oncol ; 12: 968064, 2022.
Article em En | MEDLINE | ID: mdl-36452502
ABSTRACT

Background:

KRAS is commonly mutated in non-small cell lung cancer (NSCLC); however, the prognostic and predictive impact of each G12 substitution has not been fully elucidated. The approval of specific G12C inhibitors has modified the idea of KRAS "undruggability", and although the first-line standard consists of immune checkpoint inhibitors (ICIs) with or without chemotherapy, as suggested at ASCO 2022, the outcome in KRAS-mutated population is still controversial.

Methods:

We retrospectively described the clinical and pathological characteristics of a homogeneous G12 mutated cohort of 219 patients treated in four Italian oncologic units. We evaluated the outcome (PFS at 18 months and OS at 30 months) of those who underwent standard first-line treatment according to PD-L1 status, focusing on differences across single mutations.

Results:

In the study population, 47.9% of patients harbor the KRAS G12C mutation; 20.5%, G12V; 17.4%, G12D; and 8.2%, G12A. Smoking was a common behavior of patients harboring transversions and transition mutations. PD-L1 expression does not show particular distribution in the case series, although we recorded a prevalence of PD-L1 <1% in G12V (51.4%) compared to G12A (26.7%). ICIs alone was the clinician's choice in 32.7% of patients, and the chemo-immune combination in 17.3% of patients. We described the independent prognostic role of young age (p = 0.007), female gender (p = 0.016), and an ICI-based regimen (p = 0.034) regardless of mutations. Overall, our data confirm the worst prognostic value of G12V mutation apart from treatment choice unlike the other major mutations (C, D, and A) that showed a favorable trend in PFS.

Conclusions:

KRAS G12 mutations are confirmed to have different characteristics, and the outcome is influenced by ICI first-line regimen. This study provides valuable information for further analysis in the future.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Front Oncol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Front Oncol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Itália