Evidence map›Paper›PMID 33643528›Full record

ArticleWorld journal of gastrointestinal oncology2021

Total neoadjuvant therapy

Mojca Tuta, Nina Boc, Erik Brecelj, Monika Peternel, Vaneja Velenik

Registry-linked trialOpen access · diamondAbstract read
In one paragraph

Article in World journal of gastrointestinal oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05054959 (Induction Versus Consolidation Chemotherapy in Total Neoadjuvant Therapy of Locally Advanced Rectal Cancer With High Risk of Recurrence), which is not on this map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 19% 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.

NCT05054959 phase2active not recruitingnot on this map

Induction Versus Consolidation Chemotherapy in Total Neoadjuvant Therapy of Locally Advanced Rectal Cancer With High Risk of Recurrence (ICONA Study)

TypeinterventionalSponsorInstitute of Oncology LjubljanaRan2021 to 2028Enrolled62ConditionsLocally Advanced Rectal CancerArmsConsolidation CAPOX Chemotherapy, Induction CAPOX Chemotherapy
3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 17 citations in OpenAlex.

  1. Trial
  2. Observational
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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

5 authors at 1 institution in 1 country.

Mojca TutaDivision of Radiology, Institute of Oncology, Ljubljana 1000, Slovenia.
Nina BocDivision of Radiology, Institute of Oncology, Ljubljana 1000, Slovenia.
Erik BreceljDivision of Surgery, Institute of Oncology, Ljubljana 1000, Slovenia.
Monika PeternelDivision of Radiotherapy, Institute of Oncology, Ljubljana 1000, Slovenia.
Vaneja VelenikFaculty of Medicine, University of Ljubljana, Ljubljana 1000, Slovenia.
University of Ljubljana · SI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFor locally advanced rectal cancer (LARC), standard therapy [consisting of neoadjuvant chemoradiotherapy (CRT), surgery, and adjuvant chemotherapy (ChT)] achieves excellent local control. Unfortunately, survival is still poor due to distant metastases, which remains the leading cause of death among these patients. In recent years, the concept of total neoadjuvant treatment (TNT) has been developed, whereby all systemic ChT-mainly affecting micrometastases-is applied prior to surgery.

aimTo compare standard therapy and total neoadjuvant therapy for LARC patients with high-risk factors for failure.

methodsIn a retrospective study, we compared LARC patients with high-risk factors for failure who were treated with standard therapy or with TNT. High-risk for failure was defined according to the presence of at least one of the following factors: T4 stage; N2 stage; positive mesorectal fascia; extramural vascular invasion; positive lateral lymph node. TNT consisted of 12 wk of induction ChT with capecitabine and oxaliplatin or folinic acid, fluorouracil and oxaliplatin, CRT with capecitabine, and 6-8 wk of consolidation ChT with capecitabine and oxaliplatin or folinic acid, fluorouracil and oxaliplatin prior to surgery. The primary endpoint was pathological complete response (pCR). In total, 72 patients treated with standard therapy and 89 patients treated with TNT were included in the analysis.

resultsCompared to standard therapy, TNT showed a higher proportion of pCR (23%

conclusionCompared to standard therapy, TNT provides better outcome for LARC patients with high-risk factors for failure, in terms of pCR and neoadjuvant rectal score.

Indexed as

Locally advanced rectal cancerNeoadjuvant rectal cancer scorePathological complete responseTotal neoadjuvant therapy

Identifiers

PMID33643528
PMCPMC7896420
OpenAlexW3127346343

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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Registered trials

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.