Evidence map›Paper›PMID 38809625›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2024

Prognostic Significance of Synchronous Colorectal Adenocarcinoma: A Matched-Pair Analysis.

Sahaphol Anannamcharoen, Thirayost Nimmanon, Piyapan Cheeranont, Chinakrit Boonya-Ussadorn

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Article in Asian Pacific journal of cancer prevention : APJCP, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Sahaphol AnannamcharoenDepartment of Surgery, Phramongkutklao Hospital, Bangkok, Thailand.ORCID 000000030274564X
Thirayost NimmanonDepartment of Pathology Phramongkutklao College of Medicine, Bangkok, Thailand.ORCID 0000000187651268
Piyapan CheeranontDepartment of Surgery, Phramongkutklao Hospital, Bangkok, Thailand.ORCID 0000000261332602
Chinakrit Boonya-UssadornDepartment of Surgery, Phramongkutklao Hospital, Bangkok, Thailand.ORCID 0000000247595916

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo determine the prognostic significance of the synchronous colorectal cancer (S-CRC) on survival and recurrence rate.

methodsAuthors conducted an analysis of 90 colorectal adenocarcinoma patients who received a curative (R0) resection with a full course of standard adjuvant treatment. A total of 45 patients diagnosed with S-CRC at the time of initial presentation were individually matched to a group of 45 solitary CRC patients in pair at a ratio of 1:1. The case-matched criteria included age (± 5 years), gender, tumor location, and tumor stage. For S-CRC, the most advanced pathologic lesion was defined as the index lesion, and the matching cancer stage was categorized according to the index lesion. The N-stage was determined based on all lymph nodes.

resultThere were a higher number of retrieved nodes in patients with S-CRC than those with solitary CRC. The median (min, max) of the total number of retrieved nodes for S-CRC was 18 (3, 53) nodes, compared to 14 (4, 45) nodes for solitary CRC (p < 0.01). All patients were without distant metastasis (stage I to III). The total accumulative number of patients experiencing tumor recurrence was 9 (20%) amongst the solitary CRC patients and 18 (40%) amongst the S-CRC patients at the 15-year surveillance period (p<0.05). The disease-free survival (DFS) (mean + SD) was 147.6 + 9.3 months in the solitary CRC group, compared to 110.5 + 11.7 months in the S-CRC group (p<0.05). Amongst S-CRC patients, those having primary and synchronous tumors located across anatomical segments had poorer DFS (70.5 months) and higher 15-year tumor recurrence rate (17.8%) than those with all tumors in the same or contiguous anatomical segments. In addition, the S-CRC patients with all tumors located in contiguous segment had a longer DFS (123.7 months) than the other types of anatomical correlation.

conclusionPatients with S-CRC had worse prognosis than those with solitary CRC. For S-CRC, the anatomical correlation between the primary and the synchronous tumors may influence DFS and recurrence rate.

Indexed as

AdenocarcinomaColorectal NeoplasmsNeoplasm Recurrence, LocalNeoplasms, Multiple PrimaryNeoplasm StagingAdultAgedCase-Control StudiesFemaleFollow-Up StudiesHumansLymphatic MetastasisMaleMatched-Pair AnalysisMiddle AgedPrognosisdisease-free survivalSolitary colorectal cancerTumor recurrence rate

Identifiers

PMID38809625
PMCPMC11318822

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