Evidence map›Paper›PMID 37316784›Full record

Trial reportBMC cancer2023

A multi-centre randomized controlled trial investigating Consolidation Chemotherapy with and without oxaliplatin in distal rectal cancer and Watch & Wait.

Angelita Habr-Gama, Guilherme Pagin São Julião, Cinthia D Ortega, Bruna Borba Vailati, Sergio Araujo, Thiago Jorge, Jorge Sabbaga, Gustavo L Rossi, Renata D'Alpino, Fabio Roberto Kater and 4 more

Registry-linked trialOpen access · goldAbstract readRandomized Controlled TrialMulticenter Study
In one paragraph

Trial report in BMC cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05000697 (Chemoradiation and Consolidation Chemotherapy With or Without Oxaliplatin for Distal Rectal Cancer and Watch and Wait. A Multi-center Prospective Randomized Controlled Trial.), 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
3.0field-weighted citation impact, top 8% 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.

NCT05000697 narecruitingnot on this map

Chemoradiation and Consolidation Chemotherapy With or Without Oxaliplatin for Distal Rectal Cancer and Watch and Wait. A Multi-center Prospective Randomized Controlled Trial. (CCHOWW)

TypeinterventionalSponsorHospital Alemão Oswaldo CruzRan2021 to 2027Enrolled216ConditionsRectal Cancer, ConsolidationArmsOxaliplatin, 5FU
3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Risks of Organ Preservation in Rectal Cancer: Data From Two International Registries on Rectal Cancer.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2025
    Article
  7. Review
  8. Article
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

14 authors at 10 institutions in 3 countries.

Angelita Habr-GamaUniversity of São Paulo School of Medicine, São Paulo, Brazil.
Guilherme Pagin São JuliãoAngelita and Joaquim Gama Institute, Praça Amadeu Amaral, 47 - conj.111, São Paulo, 01327-904, Brazil.
Cinthia D OrtegaDepartment of Radiology, Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, São Paulo, Brazil.
Bruna Borba VailatiAngelita and Joaquim Gama Institute, Praça Amadeu Amaral, 47 - conj.111, São Paulo, 01327-904, Brazil.
Sergio AraujoDepartment of Radiology and Diagnostic Imaging, Hospital Israelita Albert Einstein, São Paulo, Brazil.
Thiago JorgeDepartment of Medical Oncology, Hospital Alemão Oswaldo Cruz, São Paulo, Brazil.
Jorge SabbagaDepartment of Medical Oncology, Hospital Sírio Libanês, São Paulo, Brazil.
Gustavo L RossiServicio Cirugia General, Hospital Italiano de Buenos Aires, Sector de Coloproctologia, Buenos Aires, Argentina.
Renata D'AlpinoCentro Paulista de Oncologia, São Paulo, Brazil.
Fabio Roberto KaterDepartment of Medical Oncology, Hospital Beneficencia Portuguesa, São Paulo, Brazil.
Patricia Bailão AguilarDepartment of Radiation Oncology, Hospital Alemão Oswaldo Cruz, São Paulo, Brazil.
Adrian MattacheoHospital Gral. J. M. Ramos Mejia, Buenos Aires, Argentina.
Rodrigo Oliva PerezAngelita and Joaquim Gama Institute, Praça Amadeu Amaral, 47 - conj.111, São Paulo, 01327-904, Brazil. rodrigo.operez@gmail.com.ORCID http://orcid.org/0000-0003-1704-2277
Latin American Rectal Cancer Consortium (LARCC)
Hospital Alemão Oswaldo Cruz · BRHospital Israelita Albert Einstein · BRJorge Amado University Center · BRBeneficência Portuguesa de São Paulo · BRCentro Paulista de Investigação Clinica · BRHospital Italiano de Buenos Aires · ARHospital Ramos Mejía · ARHospital Sírio-Libanês · BRLudwig Cancer Research · BEUniversidade de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNeoadjuvant chemoradiation(nCRT) has been considered the preferred initial treatment strategy for distal rectal cancer. Advantages of this approach include improved local control after radical surgery but also the opportunity for organ preserving strategies (Watch and Wait-WW). Consolidation chemotherapy(cCT) regimens using fluoropyrimidine-based with or without oxalipatin following nCRT have demonstrated to increase complete response and organ preservation rates among these patients. However, the benefit of adding oxaliplatin to cCT compared to fluoropirimidine alone regimens in terms of primary tumor response remains unclear. Since oxalipatin-treatment may be associated with considerable toxicity, it becomes imperative to understand the benefit of its incorporation into standard cCT regimens in terms of primary tumor response. The aim of the present trial is to compare the outcomes of 2 different cCT regimens following nCRT (fluoropyrimidine-alone versus fluoropyrimidine + oxaliplatin) for patients with distal rectal cancer.

methodsIn this multi-centre study, patients with magnetic resonance-defined distal rectal tumors will be randomized on a 1:1 ratio to receive long-course chemoradiation (54 Gy) followed by cCT with fluoropyrimidine alone versus fluoropyrimidine + oxaliplatin. Magnetic resonance(MR) will be analyzed centrally prior to patient inclusion and randomization. mrT2-3N0-1 tumor located no more than 1 cm above the anorectal ring determined by sagittal views on MR will be eligible for the study. Tumor response will be assessed after 12 weeks from radiotherapy(RT) completion. Patients with clinical complete response (clinical, endoscopic and radiological) may be enrolled in an organ-preservation program(WW). The primary endpoint of this trial is decision to organ-preservation surveillance (WW) at 18 weeks from RT completion. Secondary endpoints are 3-year surgery-free survival, TME-free survival, distant metastases-free survival, local regrowth-free survival and colostomy-free survival. DISCUSSION: Long-course nCRT with cCT is associated with improved complete response rates and may be a very attractive alternative to increase the chances for organ-preservation strategies. Fluoropyrimidine-based cCT with or without oxaliplatin has never been investigated in the setting of a randomized trial to compare clinical response rates and the possibility of organ-preservation. The outcomes of this study may significantly impact clinical practice of patients with distal rectal cancer interested in organ-preservation.

trial registrationwww. CLINICALTRIALS: gov NCT05000697; registered on August 11

Indexed as

Intellectual DisabilityRectal NeoplasmsChemoradiotherapyConsolidation ChemotherapyHumansOxaliplatinOxaliplatinComplete Clinical ResponseConsolidation chemotherapyRectal CancerTotal neoadjuvant treatmentWatch and Wait

Identifiers

PMID37316784
PMCPMC10268479
OpenAlexW4380685536

What OpenQuestion holds

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LicenceCC BY
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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.