التفاصيل البيبلوغرافية
| العنوان: |
Impact of KRAS G12C mutation in patients with advanced non-squamous non-small cell lung cancer treated with first-line pembrolizumab monotherapy. |
| المؤلفون: |
Justeau, Grégoire1,2 (AUTHOR) gregoire.justeau@inserm.fr, Huchot, Eric3 (AUTHOR), Simonneau, Yannick4 (AUTHOR), Roa, Magali5 (AUTHOR), Le Treut, Jacques6 (AUTHOR), Le Garff, Gwenaelle7 (AUTHOR), Bylicki, Olivier8 (AUTHOR), Schott, Roland9 (AUTHOR), Bravard, Anne-Sophie10 (AUTHOR), Tiercin, Marie11 (AUTHOR), Lamy, Régine12 (AUTHOR), De Chabot, Gonzague13 (AUTHOR), Marty, Adina14 (AUTHOR), Moreau, Diane3 (AUTHOR), Locher, Chrystèle15 (AUTHOR), Bernier, Cyril16 (AUTHOR), Chouaid, Christos17 (AUTHOR), Descourt, Renaud18 (AUTHOR) |
| المصدر: |
Lung Cancer (01695002). Dec2022, Vol. 174, p45-49. 5p. |
| مصطلحات موضوعية: |
*NON-small-cell lung carcinoma, *RAS oncogenes |
| مصطلحات جغرافية: |
FRANCE |
| مستخلص: |
• In 681 non-squamous aNSCLC PD-L1 ≥ 50 % patients, 12.5 % had a KRAS G12C mutation. • No clinical or biological difference between KRAS G12C and KRAS non-G12C patients. • KRAS G12C had no impact on first-line pembrolizumab efficacy in non-squamous aNSCLC. Few data are available on the impact of KRAS mutation in patients with advanced non-squamous non-small cell lung cancer (aNSCLC) treated with immunotherapy. This analysis assessed the impact of KRAS mutation on the efficiency of first-line pembrolizumab immunotherapy in aNSCLC patients with PD-L1 ≥ 50 %. This was a secondary analysis of the ESCKEYP study, a retrospective, national, multicenter study which included consecutively all metastatic NSCLC patients who initiated first-line treatment with pembrolizumab monotherapy from May 2017 (date of pembrolizumab availability in this indication in France) to November 22, 2019 (pembrolizumab-chemotherapy combination approval). Progression-free survival (PFS) and overall survival (OS) were calculated from the start of pembrolizumab treatment by the Kaplan-Meier method. Tumor response and PFS were assessed locally. Among the 681 non-squamous aNSCLC PD-L1 ≥ 50 % patients treated with pembrolizumab in the first line, 227 (33.0 %) had a KRAS mutation (KRAS G12C, 12.5 %; KRAS non-G12C, 20.5 %). Except among non-smokers (KRAS G12C, 0 %; KRAS non-G12C, 2.9 %; no KRAS mutation, 9.2 %), patients presented no differences in terms of sex, age, number and sites of metastatic disease at diagnosis, use of corticosteroids, use of antibiotics, and for biological factors between wild-type KRAS , KRAS G12C and non- KRAS G12C groups. Median (95 % CI) PFS in months were 7.0 (3.7–14) for KRAS G12C, 4.8 (3.4–6.7) for KRAS non-G12C and 8.5 (7.3–10.6) for wild-type KRAS genotypes (p = 0.23). Median OS were 18.4 (12.6-NR), 20.6 (11.4-NR) and 27.1 (18.7–34.2) months, respectively (p = 0.57). No difference in efficacy was observed in non-squamous aNSCLC patients treated with first-line pembrolizumab immunotherapy whether they presented a KRAS G12C, non KRAS G12C or wild-type KRAS genotype. [ABSTRACT FROM AUTHOR] |
| قاعدة البيانات: |
Academic Search Index |
