Clinical characteristics and survival trends of patients with metastatic colorectal cancer (mCRC) and peritoneal carcinomatosis who receive metastases surgery in a Spanish cohort.

Authors

null

Marianela Bringas Sr.

Hospital General Universitario Gregorio Marañón, Madrid, Spain;

Marianela Bringas Sr., Javier Soto Sr., Natalia Gutiérrez Alonso , Andrés J. Muñoz Martín Sr., Aitana Calvo Ferrándiz , Gabriela Torres Pérez-Solero , Laura Ortega , Rocío Martín Lozano , Roberto Jiménez Rodríguez , Irene Gonzalez Caraballo , Ana Gutierrez Ortiz de la Tabla , Carlos López Jiménez , David Salomon Juliao Caamaño , María Palma Gómez , Mónica Benavente de Lucas , Marc Ariant Cañete Muñoz , Manuel Alva Bianchi Sr., Íñigo Martínez Delfrade , Miguel Martin , Pilar Garcia-Alfonso

Organizations

Hospital General Universitario Gregorio Marañón, Madrid, Spain; , Hospital General Universitario Gregorio Marañón, Instituto de Investigación Sanitaria Gregorio Marañón, Madrid, Spain; , Hospital General Universitario Gregorio Marañón, Universidad Complutense, Madrid, Spain; , Oncología Medica Hospital Gregorio Marañón, Madrid, Spain; , Servicio Oncología Médica, Hospital General Universitario Gregorio Marañón, IiSGM, Universidad Complutense, Madrid, Spain; , Servicio Oncología Médica. Hospital General Universitario Gregorio Marañón. IiSGM. Universidad Complutense, Madrid, Spain; , HGUGM, Madrid, Spain; , Gregorio Marañón University General Hospital, Madrid, Spain; , Servicio Oncología Médica, Hospital General Universitario Gregorio Marañon, IiSGM, Universidad Complutense, Madrid, Spain; , Hospital Universitario Ramón y Cajal, Madrid, Spain; , Instituto De Investigacion Sanitaria Gregorio Maranon, Madrid, Spain; , Hospital Gregorio Maranon, Madrid, Spain;

Research Funding

No funding received
None.

Background: Peritoneal metastases in patients with mCRC are commonly associated with poor outcomes. Some of these patients are candidates to undergo metastases surgery, which may result in better prognosis; however, clinical and molecular characteristics of these patients remain uncertain. Methods: We conducted a retrospective analysis of 166 patients with mCRC and peritoneal metastases in a tumor registry from 2015 to 2021, analyzing the clinical and molecular characteristics, as well as progression-free survival (PFS) and overall survival (OS) of patients who received peritoneal surgery versus those who did not. Results: From the whole population, 65 patients (39%) underwent peritoneal metastases surgery, and several characteristics were more frequent in this subgroup: ECOG 0 (n = 26, OR 2.75, p = 0,0069), age <65 years (n = 43, OR 2.29, p = 0,0162), absence of hepatic metastases (n = 56, OR 3.31, p = 0,0037), single metastatic location (n = 43, OR 3.48, p = 0,0002), normal CEA levels at diagnosis (n = 33, OR 2.02, p = 0,0455) and BRAF mutation (n = 12, OR 3.32, p = 0,0345). Moreover, these patients received more lines of systemic treatment (2.8 vs 2, p = 0,006) and more metastases surgeries (1.7 vs 0.9, p = 0,000). Significant differences in tumor mutational status regardless of BRAF (KRAS, NRAS, MSI, PI3K and HER2), sex and primary tumor location between groups were not found. PFS was longer in patients receiving metastases surgery (median, 13.68 vs 7.76 months; HR for progression 0.64; 95 % confidence interval (CI) 0.46 to 0.89; p = 0,009), as well as overall survival (median NR vs 29.53; HR for death 0.39; 95 % CI, 0.25 to 0.60; p = 0,000). Conclusions: In our cohort, patients with mCRC and peritoneal carcinomatosis who underwent metastases surgery had more frequently less than 65 years, ECOG 0, absence of liver metastases, single metastatic location, normal CEA levels at diagnosis and BRAF mutation. Moreover, this subgroup showed better outcomes with a statistically significant increase in PFS and OS.

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Abstract Details

Meeting

2023 ASCO Gastrointestinal Cancers Symposium

Session Type

Poster Session

Session Title

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

Track

Colorectal Cancer,Anal Cancer

Sub Track

Therapeutics

Citation

J Clin Oncol 41, 2023 (suppl 4; abstr 159)

DOI

10.1200/JCO.2023.41.4_suppl.159

Abstract #

159

Poster Bd #

H18

Abstract Disclosures

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