Evidence map›Paper›PMID 37468881›Full record

ArticleBMC cancer2023

Persistent high levels of carcinoembryonic antigen after tumor resection are associated with poorer survival outcomes in patients with resected colon cancer.

Wendy R Muñoz-Montaño, Horacio N López-Basave, Alison Castillo-Morales, Carolina Castillo-Morales, Karen Sánchez-Trejo, Rodrigo Catalán, Consuelo Díaz-Romero, Leonardo S Lino-Silva, Andrea Maliachi-Díaz, Erika Ruiz-García and 2 more

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. CEA vaccines.Human vaccines & immunotherapeutics · 2023
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 1 institution in 1 country.

Wendy R Muñoz-MontañoDepartment of Medical Oncology, Instituto Nacional de Cancerología, Av. San Fernando 22, Belisario Domínguez Secc. 16, Tlalpan, 14080, Ciudad de México, Mexico.
Horacio N López-BasaveDepartment of Medical Oncology, Instituto Nacional de Cancerología, Av. San Fernando 22, Belisario Domínguez Secc. 16, Tlalpan, 14080, Ciudad de México, Mexico.
Alison Castillo-MoralesDepartment of Medical Oncology, Instituto Nacional de Cancerología, Av. San Fernando 22, Belisario Domínguez Secc. 16, Tlalpan, 14080, Ciudad de México, Mexico.
Carolina Castillo-MoralesDepartment of Medical Oncology, Instituto Nacional de Cancerología, Av. San Fernando 22, Belisario Domínguez Secc. 16, Tlalpan, 14080, Ciudad de México, Mexico.
Karen Sánchez-TrejoMexican Agency for the Evaluation of Health Technologies, Mexico City, Mexico.
Rodrigo CatalánDepartment of Medical Oncology, Instituto Nacional de Cancerología, Av. San Fernando 22, Belisario Domínguez Secc. 16, Tlalpan, 14080, Ciudad de México, Mexico.
Consuelo Díaz-RomeroDepartment of Medical Oncology, Instituto Nacional de Cancerología, Av. San Fernando 22, Belisario Domínguez Secc. 16, Tlalpan, 14080, Ciudad de México, Mexico.
Leonardo S Lino-SilvaDepartment of Medical Oncology, Instituto Nacional de Cancerología, Av. San Fernando 22, Belisario Domínguez Secc. 16, Tlalpan, 14080, Ciudad de México, Mexico.
Andrea Maliachi-DíazDepartment of Medical Oncology, Instituto Nacional de Cancerología, Av. San Fernando 22, Belisario Domínguez Secc. 16, Tlalpan, 14080, Ciudad de México, Mexico.
Erika Ruiz-GarcíaDepartment of Medical Oncology, Instituto Nacional de Cancerología, Av. San Fernando 22, Belisario Domínguez Secc. 16, Tlalpan, 14080, Ciudad de México, Mexico.
Marytere Herrera-MartínezDepartment of Medical Oncology, Instituto Nacional de Cancerología, Av. San Fernando 22, Belisario Domínguez Secc. 16, Tlalpan, 14080, Ciudad de México, Mexico.
German Calderillo-RuízDepartment of Medical Oncology, Instituto Nacional de Cancerología, Av. San Fernando 22, Belisario Domínguez Secc. 16, Tlalpan, 14080, Ciudad de México, Mexico. calderilloruizgerman@gmail.com.
Instituto Nacional de Cancerología · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInterindividual survival and recurrence rates in cases of locoregional colon cancer following surgical resection are highly variable. The aim of the present study was to determine whether elevated pre-operative and post-operative CEA values are useful prognostic biomarkers for patients with stage I-III colon cancer who underwent surgery with curative intent.

methodsWe conducted a retrospective study in patients with histologically confirmed stage I-III primary colonic adenocarcinoma who underwent radical surgical resection at Mexico's National Cancer Institute, between January 2008 and January 2020. We determined pre-operative and post-operative CEA and analyzed the association of scores with poorer survival outcomes in patients with resected colon cancer, considering overall survival (OS) and disease-free survival (DFS).

resultsWe included 640 patients with stage I-III colon cancer. Pre-operative CEA levels were in the normal range in 460 patients (group A) and above the reference value in the other 180. Of the latter, 134 presented normalized CEA levels after surgery, but 46 (group C) continued to show CEA levels above the reference values after surgery. Therefore, propensity score matching (PSM) was carried out to reduce the bias. Patients were adjusted at a 1:1:1 ratio with 46 in each group, to match the number in the smallest group. Median follow- up was 46.4 months (range, 4.9-147.4 months). Median DFS was significantly shorter in Group C: 55.5 months (95% CI 39.6-71.3) than in the other two groups [Group A: 77.1 months (95% CI 72.6-81.6). Group B: 75.7 months (95% CI 66.8-84.5) (p-value < 0.001)]. Overall survival was also significantly worse in group C [57.1 (95% CI 37.8-76.3) months] than in group A [82.8 (95% CI 78.6-86.9 months] and group B [87.1 (95% CI 79.6-94.5 months] (p-value = 0.002). To identify whether change in CEA levels operative and post-surgery was an independent prognostic factor for survival outcomes, a Cox proportional hazard model was applied. In multivariate analysis, change in CEA level was a statistically significant, independent prognostic factor for overall survival (p-value = 0.031).

conclusionsWhen assessed collectively, pre-operative and post-operative CEA values are useful biomarkers for predicting survival outcomes in patients with resected colon cancer. Prognoses are worse for patients with elevated pre-operative and post-surgical CEA values, but similar in patients with normal post-surgical values, regardless of their pre-surgery values.

Indexed as

Carcinoembryonic AntigenColonic NeoplasmsBiomarkers, TumorDisease-Free SurvivalHumansNeoplasm StagingPrognosisRetrospective StudiesBiomarkers, TumorCarcinoembryonic AntigenCEA valuesColon cancerPre-operative and post-surgical

Identifiers

PMID37468881
PMCPMC10354962
OpenAlexW4384819776

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.