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Prognostic value of specific KRAS mutations in patients with colorectal peritoneal metastases.
- Source :
-
ESMO open [ESMO Open] 2024 Apr; Vol. 9 (4), pp. 102976. Date of Electronic Publication: 2024 Apr 12. - Publication Year :
- 2024
-
Abstract
- Background: There is little evidence on KRAS mutational profiles in colorectal cancer (CRC) peritoneal metastases (PM). This study aims to determine the prevalence of specific KRAS mutations and their prognostic value in a homogeneous cohort of patients with isolated CRC PM treated with cytoreductive surgery and hyperthermic intraperitoneal chemotherapy.<br />Materials and Methods: Data were collected from 13 Italian centers, gathered in a collaborative group of the Italian Society of Surgical Oncology. KRAS mutation subtypes have been correlated with clinical and pathological characteristics and survival [overall survival (OS), local (peritoneal) disease-free survival (LDFS) and disease-free survival (DFS)].<br />Results: KRAS mutations occurred in 172 patients (47.5%) out of the 362 analyzed. Two different prognostic groups of KRAS mutation subtypes were identified: KRAS <superscript>MUT1</superscript> (G12R, G13A, G13C, G13V, Q61H, K117N, A146V), median OS > 120 months and KRAS <superscript>MUT2</superscript> (G12A, G12C, G12D, G12S, G12V, G13D, A59E, A59V, A146T), OS: 31.2 months. KRAS <superscript>MUT2</superscript> mutations mainly occurred in the P-loop region (P < 0.001) with decreased guanosine triphosphate (GTP) hydrolysis activity (P < 0.001) and were more frequently related to size (P < 0.001) and polarity change (P < 0.001) of the substituted amino acid (AA). When KRAS <superscript>MUT1</superscript> and KRAS <superscript>MUT2</superscript> were combined with other known prognostic factors (peritoneal cancer index, completeness of cytoreduction score, grading, signet ring cell, N status) in multivariate analysis, KRAS <superscript>MUT1</superscript> showed a similar survival rate to KRAS <superscript>WT</superscript> patients, whereas KRAS <superscript>MUT2</superscript> was independently associated with poorer prognosis (hazard ratios: OS 2.1, P < 0.001; DFS 1.9, P < 0.001; LDFS 2.5, P < 0.0001).<br />Conclusions: In patients with CRC PM, different KRAS mutation subgroups can be determined according to specific codon substitution, with some mutations (KRAS <superscript>MUT1</superscript> ) that could have a similar prognosis to wild-type patients. These findings should be further investigated in larger series.<br /> (Copyright © 2024 The Authors. Published by Elsevier Ltd.. All rights reserved.)
- Subjects :
- Humans
Male
Female
Middle Aged
Prognosis
Aged
Adult
Hyperthermic Intraperitoneal Chemotherapy
Disease-Free Survival
Retrospective Studies
Cytoreduction Surgical Procedures
Aged, 80 and over
Colorectal Neoplasms genetics
Colorectal Neoplasms pathology
Colorectal Neoplasms mortality
Peritoneal Neoplasms secondary
Peritoneal Neoplasms genetics
Proto-Oncogene Proteins p21(ras) genetics
Mutation
Subjects
Details
- Language :
- English
- ISSN :
- 2059-7029
- Volume :
- 9
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- ESMO open
- Publication Type :
- Academic Journal
- Accession number :
- 38613907
- Full Text :
- https://doi.org/10.1016/j.esmoop.2024.102976