Abstract 497P
Background
The primary site of colorectal cancer (CRC) influences survival outcomes when metastasized to the liver or lung, with left-sided CRC being associated with longer survival than right-sided CRC. Additionally, the timing of metastasis, whether synchronous or metachronous, has been suggested as a factor for survival, with synchronous metastasis generally considered more aggressive than metachronous CRC with brain metastasis (BM). We investigated the effect of both CRC’s primary location and metastatic timing on overall survival (OS) upon metastasis to the brain.
Methods
We systematically searched PubMed, Embase, and the Cochrane Library. We included studies that described patients diagnosed with BM from CRC, with reports on survival outcomes based on different primary tumor sites (left vs right) or metastatic timing (synchronous vs metachronous). Within the eligible studies, we extracted hazard ratios (HR) for OS and conducted a meta-analysis by using the random-effect model.
Results
Out of 5836 studies identified through our search, 7 studies met the inclusion criteria for the meta-analysis. Similar to lung and liver metastasis of CRC, left-sided primary CRC exhibits better OS than right-sided CRC (multivariate HR = 0.71, 95% CI: 0.54-0.94, univariate HR = 0.75, 95% CI: 0.57-0.99) when metastasized to the brain. Regarding the timing of metastasis, we found no significant difference in OS between synchronous and metachronous metastasis (HR = 0.83, 95% CI: 0.48-1.43). Table: 497P
Hazard ratio of the included studies
Study | HR | 95% CI | |
Right colon vs left colon (reference = right), multivariate analysis | |||
Bergen 2021 | 0.65 | 0.46-0.92 | |
Chen 2022 | 0.94 | 0.56-1.57 | |
Chen 2023 | 0.49 | 0.18-1.34 | |
Total | 0.71 | 0.54-0.94 | I2: 0% |
Right colon vs left colon (reference = right), univariate analysis | |||
Bergen 2021 | 0.63 | 0.44-0.89 | |
Bonadio 2021 | 1.14 | 0.80-1.62 | |
Chen 2022 | 0.74 | 0.48-1.14 | |
Chen 2023 | 0.37 | 0.17-0.81 | |
Michl 2015 | 0.79 | 0.57-1.09 | |
Total | 0.75 | 0.57-0.99 | I2: 58% |
Synchronous vs metachronous (reference = metachronous), univariate analysis | |||
Chen 2023 | 0.83 | 0.44-1.58 | |
Mege 2013 | 0.50 | 0.10-2.60 | |
Tanriverdi 2014 | 1.14 | 0.31-4.13 | |
Total | 0.83 | 0.48-1.43 | I2: 0% |
Abbreviations: HR, hazard ratio; CI, confidence interval
Conclusions
Left-sided colon cancer exhibited higher OS compared to right-sided colon cancer, consistent with findings in lung and liver metastasis. However, OS did not differ between synchronous and metachronous metastasis. Further studies comparing the genotypes and mutations of CRC with BM based on their primary location and metastatic timing are warranted.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
478P - Molecular characterization of adult non-glioblastoma central nervous system (CNS) tumors to identify potential targettable alterations
Presenter: Marta Padovan
Session: Poster session 16
479P - The candidate novel markers PIV and PILE score to predict survival outcomes and therapeutic response in patients with primary central nervous system lymphoma
Presenter: Ling Duan
Session: Poster session 16
Resources:
Abstract
480P - Clinical utility of ctDNA detection by NGS for diagnosis of CNS lymphoma
Presenter: Ana Jiménez-Ubieto
Session: Poster session 16
481P - Integrating GWAS and transcriptomics prioritizes drug targets for meningioma
Presenter: Wan-Zhe Liao
Session: Poster session 16
482P - The prognostic impact of CDKN2A/B heterozygous deletions in meningioma: Insights of a multicenter analysis
Presenter: Franziska Ippen
Session: Poster session 16
483P - The use of steroids associated with PD1/PDL-1 blockage in patients with brain metastasis: A systematic review and meta-analysis
Presenter: Francisco Cezar Moraes
Session: Poster session 16
484P - EGFR amplification is the potential driver gene that accelerates brain metastases in NSCLC patients
Presenter: Hainan Yang
Session: Poster session 16
485P - A spatio-temporal evolution mathematical model of glioma growth: The influence of cellular and nutrient interactions on the tumor microenvironment
Presenter: Kalysta Borges
Session: Poster session 16
486P - Effects of a BBB-penetrating oligonucleotide drug, RBD8088, in mouse models of human glioblastoma
Presenter: Julia Grönros
Session: Poster session 16
487P - 3D-bioprinted co-cultures of glioblastoma and mesenchymal cells indicate a role for perivascular niche cells in shaping the chemotactic tumour microenvironment
Presenter: Radosław Zagożdżon
Session: Poster session 16