Evidence map›Paper›PMID 41803359›Full record

ArticleLangenbeck's archives of surgery2026

Outcomes of patients with rectal cancer and pathological complete response as well as patients with tumor cell dedifferentiation. Two prognostic different groups of patients responding to pre-operative oncological therapy.

Tomáš Řezáč, Pavel Zbořil, Dušan Klos, Radek Vrba, Petr Špička, Lubomír Starý

Abstract read
In one paragraph

Article in Langenbeck's archives of surgery, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Tomáš ŘezáčDepartment of Surgery I, University Hospital Olomouc, Zdravotníku 248/7, Olomouc, 77900, Czech Republic.ORCID http://orcid.org/0000-0003-1326-0349
Pavel ZbořilDepartment of Surgery I, University Hospital Olomouc, Zdravotníku 248/7, Olomouc, 77900, Czech Republic. pavel.zboril@fnol.cz.ORCID http://orcid.org/0000-0002-7577-9990
Dušan KlosDepartment of Surgery I, University Hospital Olomouc, Zdravotníku 248/7, Olomouc, 77900, Czech Republic.ORCID http://orcid.org/0000-0002-3097-4418
Radek VrbaDepartment of Surgery I, Faculty of Medicine and Dentistry, Palacky University Olomouc, Hněvotínská 976/3, Olomouc, 77515, Czech Republic.ORCID http://orcid.org/0000-0003-1027-8949
Petr ŠpičkaDepartment of Surgery I, Faculty of Medicine and Dentistry, Palacky University Olomouc, Hněvotínská 976/3, Olomouc, 77515, Czech Republic.ORCID http://orcid.org/0000-0003-3166-2624
Lubomír StarýDepartment of Surgery I, Faculty of Medicine and Dentistry, Palacky University Olomouc, Hněvotínská 976/3, Olomouc, 77515, Czech Republic.ORCID http://orcid.org/0000-0003-4088-8801

Funding

Ministerstvo Zdravotnictví Ceské Republiky,Czechia FNOl, 00098892
6 · The paper itself

Abstract

introductionMultimodal treatment represents the standard of care for rectal adenocarcinoma. A subset of patients achieves a pathological complete response (pCR), while a different subset does not. While pCR is associated with improved overall survival (OS), non-responders suffer from not being treated in a way tailored to their needs and have worse overall survival. PURPOSE: To evaluate the factors responsible for pCR and tumor cell dedifferentiation. Additionally, the prognosis of patients with pCR and tumor cell dedifferentiation and the clinical impact of dedifferentiation.

resultsThe factor responsible for pCR was clinically negative lymph node status (cN0). The incidence of dedifferentiation of tumor cells was statistically significantly higher in the group of patients who were not treated with FOLFOX/FOLFIRI chemotherapy (p = 0.033), had cN1 lymph node status (p = 0.010), and primary tumor grade 2 (p < 0.0001). The clinical impact demonstrated an association between dedifferentiation and more advanced pT (p = 0.026) and pTNM stage (p = 0.035). Parameters identified as significant negative predictors of survival were: generalization (p = 0.01, HR 1.959, 95%CI 1.171–3.276), tumor budding (p = 0.001, HR 3.391, 95%CI 1.611–7.136), perineural spread (p = 0.015, HR 2.056, 95%CI 1.150–3. 676), number of positive lymph nodes (p = 0.047, HR 1.100, 95%CI 1.001–1.210), definitive pN (pN1 p = 0.003, HR 2.008, 95%CI 1.268–3.180), and stage III and IV (p = 0.037, HR 2.050, 95%CI 1.044–4.025, p = 0.001, HR 5.482, 95%CI 2.063–14.56).

conclusionThe genetics and biological characteristics of cancer cells make rectal cancer more challenging to treat. This shows why patients need personalized therapy.

Indexed as

AdenocarcinomaCell DedifferentiationRectal NeoplasmsAdultAgedAntineoplastic Combined Chemotherapy ProtocolsCombined Modality TherapyFemaleHumansMaleMiddle AgedNeoadjuvant TherapyNeoplasm StagingPathologic Complete ResponsePrognosisRetrospective Studiescell dedifferentiationneoadjuvant therapypathologic complete responcerectal neoplasm - prognosis

Identifiers

PMID41803359
PMCPMC13031231

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.