Retrospective analysis of clinical characteristics of mCRC patients receiving three or more lines of chemotherapy.

Authors

null

Pilar Garcia Alfonso

Hospital General Universitario Gregorio Marañón, Madrid, Spain

Pilar Garcia Alfonso , Íñigo Martínez Delfrade , Javier Soto Alsar , Marianela Bringas Beranek , Natalia Gutiérrez Alonso , Laura Ortega , Gabriela Torres , Andres J. Muñoz Martín , Montserrat Blanco-Codesido , Aitana Calvo , Miguel Martin

Organizations

Hospital General Universitario Gregorio Marañón, Madrid, Spain, Instituto De Investigacion Sanitaria Gregorio Marañon, Madrid, Spain, H.G.U. Gregorio Marañon, Madrid, Spain

Research Funding

Other Foundation

Background: Prognostic and predictive factors are becoming more important in mCRC patients, and may have an impact in overall survival and in the number of lines of chemotherapy that a patient can receive. Methods: We conducted a retrospective analysis of 334 patients with mCRC. We analyzed the clinical characteristics of 113 (33.8%) mCRC patients who received ≥3 lines of chemotherapy. We apply the statistical test Chi square in order to identify significant association. Results: Several characteristics were significantly associated with receiving ≥ 3 lines of chemotherapy (n = 113): age < 80 years (n = 93, OR = 3.07, p = 0.001), ECOG 0-1 (n = 98, OR = 3.21, p = 0.055), primary tumor resection (n = 62, OR = 2.36, p = 0.000) and resection of metastases (n = 56, OR = 2.07, p = 0.002). Partial or complete response rate in the first line of chemotherapy was also significantly associated with receiving ≥ 3 lines of treatment (n = 65, p = 0.011). Tumor mutational status was analyzed in 333 patients: KRAS mutation was detected in 163 over 333 patients genotyped (48.9%), NRAS in 25/206 (12.1%), BRAF in 15/217 (6.9%) and PI3K in 31/213 (14.5%). In the group of patients receiving ≥ 3 lines of chemotherapy (n = 113): KRAS mutation was found in 60/113 patients (53.1%), NRAS in 5/77 (6.5 %), BRAF in 5/84 (5.9%) and PI3K in 8/80 (11.1%). Tumor mutations were not significantly associated with ≥ 3 lines of chemotherapy. No significant association was found between sex, tumor location (right [n = 33, 29.2%] or left [n = 76, 73%]), liver or lung isolated metastases and 3 or later lines of chemotherapy. We also performed in our database a survival analysis in the 334 patients: those who received ≥3 lines of chemotherapy had significantly higher survival rates (median OS 18 m in the group of < 3 lines of treatment vs. 37.2 m in the group of ≥ 3 lines of chemotherapy, HR = 1,6; CI 95% 1,2-2.1; p < 0,001). Conclusions: This retrospective analysis showed that mCRC patients with < 80 years, ECOG 0-1, primary tumor and or metastases resected and those with complete or partial response in the first line of treatment have a higher probability of receiving ≥ 3 lines of chemotherapy.

≥3 lines of chemotherapy

nMUTWTp
KRAS11360530.278
NRAS775720.055
BRAF845790.658
PI3K808720.144

Disclaimer

This material on this page is ©2024 American Society of Clinical Oncology, all rights reserved. Licensing available upon request. For more information, please contact licensing@asco.org

Abstract Details

Meeting

2019 Gastrointestinal Cancers Symposium

Session Type

Poster Session

Session Title

Poster Session C: Cancers of the Colon, Rectum, and Anus

Track

Cancers of the Colon, Rectum, and Anus

Sub Track

Multidisciplinary Treatment

Citation

J Clin Oncol 37, 2019 (suppl 4; abstr 682)

DOI

10.1200/JCO.2019.37.4_suppl.682

Abstract #

682

Poster Bd #

N7

Abstract Disclosures

Similar Abstracts

Abstract

2023 ASCO Annual Meeting

Frequency of KRAS, NRAS, and BRAF mutations in colorectal cancer in an Argentinian population.

First Author: Agustín Barbier

Abstract

2022 ASCO Gastrointestinal Cancers Symposium

Association of BRAF V600E mutation with survival in patients with metastatic mismatch repair-deficient colorectal cancer.

First Author: Elaine Tan

Abstract

2024 ASCO Gastrointestinal Cancers Symposium

Association of candidate alterations with primary resistance to KRAS G12D targeting in colorectal cancer.

First Author: Khalid Jazieh