Clinical characteristics according to KRAS and TP53 status
Variable | KRAS-wt; TP53-wt(n = 20) | KRAS-m; TP53-wt(n = 31) | KRAS-wt; TP53-m(n = 33) | KRAS-m; TP53-m(n = 23) |
---|---|---|---|---|
Age | ||||
Median (IQR) | 71 (± 12) | 68 (± 11) | 63 (± 16) | 61 (± 14) |
Sex | ||||
Female | 9 (45%) | 8 (26%) | 11 (33%) | 9 (39%) |
Male | 11 (55%) | 23 (74%) | 22 (67%) | 14 (61%) |
Smoking status | ||||
Non-smoker | 4 (20%) | 2 (6%) | 2 (6%) | 1 (4%) |
Smoker | 15 (75%) | 29 (94%) | 31 (94%) | 22 (96%) |
Missing | 1 (5.0%) | 0 (0%) | 0 (0%) | 0 (0%) |
Histology | ||||
Squamous | 2 (10%) | 0 (0%) | 5 (15%) | 1 (4%) |
Non squamous | 18 (90%) | 31 (100%) | 28 (85%) | 22 (96%) |
Line of treatment | ||||
1 | 6 (30%) | 14 (45%) | 7 (21%) | 6 (26%) |
> 1 | 14 (70%) | 17 (55%) | 26 (79%) | 17 (74%) |
PD-L1 TPS % | ||||
0 | 3 (15%) | 5 (16%) | 4 (12%) | 2 (9%) |
1–49 | 6 (30%) | 6 (19%) | 6 (18%) | 5 (22%) |
> 50 | 7 (35%) | 15 (48%) | 12 (36%) | 10 (43%) |
Missing | 4 (20.0%) | 5 (16.1%) | 11 (33.3%) | 6 (26.1%) |
Number of mutation (s) | ||||
Median (IQR) | 0 (± 1.0) | 1.0 (± 0.50) | 2.0 (± 1.0) | 2.0 (± 0) |
KRAS mutation | ||||
Other than G12C | 22 (71%) | 14 (61%) | ||
G12C | 9 (29%) | 9 (39%) |
KRAS: Kirsten rat sarcoma viral oncogene homolog; KRAS-wt: KRAS wild type; KRAS-m: KRAS mutated; TP53: tumor protein p53; TP53-wt: TP53 wild type; TP53-m: TP53 mutated; PD-L1: programmed death ligand 1; TPS: tumor proportion score; ICR: confidence interval range
HDSB: Conceptualization, Investigation, Writing—original draft, Writing—review & editing. RE: Data curation, Writing—original draft, Writing—review & editing. ZM: Validation, Writing—review & editing. HB: Validation, Writing—review & editing, Supervision. RBD: Validation, Writing—review & editing. LG: Validation, Writing—review & editing. EF: Conceptualization, Investigation, Writing—original draft, Writing—review & editing, Supervision. All authors read and approved the submitted version.
The authors declare that they have no conflicts of interest.
The present study has been accepted and registered to the relevant institutional research (OncoHEGP: PRB-HEGP-URC NIF) and ethical committee (European Georges Pompidou Hospital) and has been conducted in accordance with the Declaration of Helsinki. All patients provided informed consent under the European Georges Pompidou Hospital approved protocol allowing collection and analysis of data.
Informed consent to participate in the study was obtained from all participants.
Informed consent to publication was obtained from relevant participants.
The raw data supporting the conclusions of this manuscript will be made available by the authors, without undue reservation, to any qualified researcher.
Not applicable.
© The Author(s) 2024.