Evidence map›Paper›PMID 31943506›Full record

Trial reportThe oncologist2020

Predictive Impact of Mucinous Tumors on the Clinical Outcome in Patients with Poorly Differentiated, Stage II Colon Cancer: A TOSCA Subgroup Analysis.

Gerardo Rosati, Fabio Galli, Maurizio Cantore, Francesca Bergamo, Maria Banzi, Maria Giulia Zampino, Rodolfo Mattioli, Giovanni Gerardo Cardellino, Monica Ronzoni, Maria Di Bartolomeo and 12 more

Open access · bronzeAbstract readClinical Trial, Phase IIIMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in The oncologist, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

5 citing papers in PubMed, 11 citations in OpenAlex.

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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

22 authors at 16 institutions in 1 country.

Gerardo RosatiU.O. Oncologia Medica, Ospedale S. Carlo, Potenza, Italy.ORCID 0000-0001-7004-6862
Fabio GalliMethodology for Clinical Research Laboratory, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milan, Italy.
Maurizio CantoreU.O. Oncologia Medica, Azienda USL 1 di Massa e Carrara, Carrara, Italy.
Francesca BergamoU.O. Oncologia Medica 1, IRCCS Istituto Oncologico Veneto, Padova, Italy.
Maria BanziU.O. Oncologia Medica, Azienda USL-IRCCS, Reggio Emilia, Italy.
Maria Giulia ZampinoGastrointestinal Medical Oncology Unit and Neuroendocrine Tumors, IRCCS Istituto Europeo di Oncologia, Milan, Italy.
Rodolfo MattioliU.O. Oncologia Medica, Azienda Ospedaliera Marche Nord, Pesaro/Fano, Italy.
Giovanni Gerardo CardellinoU.O. Oncologia Medica, Azienda Ospedaliera Universitaria S. Maria della Misericordia, Udine, Italy.
Monica RonzoniU.O. Oncologia Medica, Ospedale San Raffaele, Milan, Italy.
Maria Di BartolomeoU.O. Oncologia Medica, Fondazione IRCCS INT, Milan, Italy.
Stefano TamberiU.O. Oncologia Medica, Ospedale degli Infermi, Faenza, Italy.
Paolo MarchettiU.O. Oncologia Medica, Ospedale Sant'Andrea, Università Sapienza, Roma e IRCCS Istituto Dermopatico dell'Immacolata, Rome, Italy.
Lorenza RimassaMedical Oncology and Hematology Unit, Humanitas Cancer Center, Humanitas Clinical and Research Center IRCCS, Rozzano, Italy.
Domenico CorsiU.O. Oncologia Medica, Ospedale S. Giovanni Calibita Fatebenefratelli, Rome, Italy.
Anna Maria BochicchioU.O. Oncologia Medica, Ospedale Oncologico Regionale CROB, Rionero in Vulture, Italy.
Fabrizio ArtioliU.O. Oncologia Medica, Ospedale B. Ramazzini, Carpi, Italy.
Roberto LabiancaCancer Center ASST Papa Giovanni XXIII, Bergamo, Italy.
Francesca GalliMethodology for Clinical Research Laboratory, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milan, Italy.
Eliana RulliMethodology for Clinical Research Laboratory, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milan, Italy.
Domenico BilanciaU.O. Oncologia Medica, Ospedale S. Carlo, Potenza, Italy.
Giacomo BregniU.O. Oncologia Medica, IRCCS San Martino-IST, Genova, Italy.
TOSCA (Three or Six Colon Adjuvant) Investigators
Mario Negri Institute for Pharmacological Research · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITOspedale San Carlo · ITCentro di Riferimento Oncologico della Basilicata · ITEuropean Institute of Oncology · ITFatebenefratelli Hospital · ITHumanitas University · ITIRCCS Ospedale San Raffaele · ITIstituto Dermopatico dell'Immacolata · ITIstituto Oncologico Veneto · ITIstituto Ramazzini · ITOspedale Papa Giovanni XXIII · ITOspedale per gli Infermi · ITOspedale Policlinico San Martino · ITOspedale Santa Maria della Misericordia di Udine · ITOspedali Riuniti Marche Nord · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlthough American Society of Clinical Oncology and European Society for Medical Oncology guidelines have identified the negative prognostic factors that clinicians have to consider when treating their patients with stage II colon cancer (CC), the role of histological subtype is controversial. SUBJECTS, MATERIALS, AND

methodsThe randomized, multicenter, phase III TOSCA trial compared 3 versus 6 months of fluoropyrimidine-oxaliplatin adjuvant chemotherapy in 3,759 patients with high-risk stage II or stage III CC. The objective of this substudy was to evaluate the influence of histological subtypes on the impact of the treatment duration of adjuvant chemotherapy in terms of relapse-free survival (RFS) and overall survival (OS) in 85 mucinous adenocarcinoma (MUC) and 389 nonmucinous adenocarcinoma (NMUC) patients with high-risk stage II, grade 3 CC.

resultsA significant interaction between treatment duration and histology was observed in both RFS (p = .027) and OS (p = .017). In the subgroup of patients with MUC, worse RFS (adjusted hazard ratio [HR], 3.95; 95% confidence interval [CI], 1.03-15.17; p = .045) and OS (HR, 9.56; 95% CI, 1.14-79.98; p = .037) were detected for patients treated in the 3-month arm. No statistically significant differences were found in the subgroup of patients with NMUC.

conclusionPatients with MUC, grade 3, stage II CC require special attention and may need 6 months of oxaliplatin-based chemotherapy. Larger studies are required to assess the combined use of histology and other prognostic/predictive factors to define the administration of chemotherapy in patients with stage II CC and to improve their prognosis. IMPLICATIONS FOR PRACTICE: Although ASCO and ESMO guidelines define the prognostic factors for patients with stage II colon cancer to establish the use of adjuvant chemotherapy, the influence of histological subtypes is controversial in this population. This study underscores that patients with grade 3 mucinous adenocarcinomas may need adjuvant chemotherapy with oxaliplatin and fluoropyrimidines for a duration of 6 months rather than 3 months.

Indexed as

AdenocarcinomaColonic NeoplasmsAntineoplastic Combined Chemotherapy ProtocolsChemotherapy, AdjuvantFluorouracilHumansNeoplasm Recurrence, LocalNeoplasm StagingOxaliplatinPrognosisFluorouracilOxaliplatinColorectal cancerHistological typeMucinous adenocarcinomaOxaliplatin-based adjuvant chemotherapyPoorly differentiated adenocarcinoma

Identifiers

PMID31943506
PMCPMC7288638
OpenAlexW3005816590

What OpenQuestion holds

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Registered trials

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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.