Evidence map›Paper›PMID 35398759›Full record

ArticleEuropean journal of cancer (Oxford, England : 1990)2022

Clinical profile and mortality of Sars-Cov-2 infection in cancer patients across two pandemic time periods (Feb 2020-Sep 2020; Sep 2020-May 2021) in the Veneto Oncology Network: The ROVID study.

Maria V Dieci, Giuseppe Azzarello, Vittorina Zagonel, Franco Bassan, Stefania Gori, Giuseppe Aprile, Vanna Chiarion-Sileni, Sara Lonardi, Cristina Oliani, Marta Zaninelli and 16 more

Open access · bronzeAbstract read
In one paragraph

Article in European journal of cancer (Oxford, England : 1990), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 42% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

26 authors at 11 institutions in 1 country.

Maria V DieciOncology 2, Veneto Institute of Oncology IOV-IRCCS, Padova, Italy; Department of Surgery, Oncology and Gastroenterology, University of Padova, Italy. Electronic address: mariavittoria.%20dieci@unipd.it.
Giuseppe AzzarelloOncology and Oncologic Hematology, AULSS 3 Serenissima, Mirano Hospital, Mirano (Venice), Italy.
Vittorina ZagonelOncology 1, Veneto Institute of Oncology IOV-IRCCS, Padova, Italy.
Franco BassanOncology, AULSS 7 Pedemontana, Santorso Hospital and Bassano Hospital, Vicenza, Italy.
Stefania GoriOncology, IRCCS Ospedale Don Calabria-Sacro Cuore, Negrar di Valpolicella, (Verona), Italy.
Giuseppe AprileDepartment of Oncology, San Bortolo General Hospital, AULSS 8 Berica, Vicenza, Italy.
Vanna Chiarion-SileniMelanoma Oncology Unit, Veneto Institute of Oncology IOV-IRCCS, Padova, Italy.
Sara LonardiOncology 1, Veneto Institute of Oncology IOV-IRCCS, Padova, Italy.
Cristina OlianiOncology, AULSS 5 Polesana, Santa Maria Della Misericordia Hospital, Rovigo, Italy.
Marta ZaninelliOncology, AULSS 9 Scaligera, Villafranca Hospital, Villafranca, (VR), Italy.
Rita ChiariOncology, AULSS 6 Euganea, South Padova Hospital, Monselice, (PD), Italy.
Adolfo FavarettoDepartment of Oncology, AULSS 2 Marca Trevigiana, Ca'Foncello Hospital, Treviso, Italy.
Alberto PavanOncology Department, AULSS 3 Serenissima, Sant'Angelo General Hospital, Mestre and SS Giovanni e Paolo General Hospital, Venezia, Italy.
Elisabetta Di LisoOncology 2, Veneto Institute of Oncology IOV-IRCCS, Padova, Italy.
Eleonora MioranzaOncology 2, Veneto Institute of Oncology IOV-IRCCS, Padova, Italy.
Alessandra BaldoniOncology and Oncologic Hematology, AULSS 3 Serenissima, Mirano Hospital, Mirano (Venice), Italy.
Francesca BergamoOncology 1, Veneto Institute of Oncology IOV-IRCCS, Padova, Italy.
Marco MaruzzoOncology 1, Veneto Institute of Oncology IOV-IRCCS, Padova, Italy.
Stamatia ZiampiriOncology, AULSS 7 Pedemontana, Santorso Hospital and Bassano Hospital, Vicenza, Italy.
Alessandro InnoOncology, IRCCS Ospedale Don Calabria-Sacro Cuore, Negrar di Valpolicella, (Verona), Italy.
Filomena GrazianiDepartment of Oncology, San Bortolo General Hospital, AULSS 8 Berica, Vicenza, Italy.
Giusy SinigagliaOncology, AULSS 5 Polesana, Santa Maria Della Misericordia Hospital, Rovigo, Italy.
Michele CelestinoOncology 2, Veneto Institute of Oncology IOV-IRCCS, Padova, Italy.
Pierfranco ConteOncology 2, Veneto Institute of Oncology IOV-IRCCS, Padova, Italy; Department of Surgery, Oncology and Gastroenterology, University of Padova, Italy.
Valentina GuarneriOncology 2, Veneto Institute of Oncology IOV-IRCCS, Padova, Italy; Department of Surgery, Oncology and Gastroenterology, University of Padova, Italy.
Veneto Oncology Network
Istituto Oncologico Veneto · ITUniversity of Padua · ITOspedale di Mirano · ITOspedale Sacro Cuore Don Calabria · ITOspedale San Bassiano · ITOspedale San Bortolo · ITOspedale Santa Maria della Misericordia di Rovigo · ITCa' Foncello Hospital · ITOspedale dell' Angelo · ITSanta Maria Nuova Hospital · ITVilla Torri Hospital · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionWe analyzed a cohort of patients with cancer and Sars-Cov-2 infection from the Veneto Oncology Network registry across two pandemic time periods. MATERIALS AND

methods761 patients with cancer and SARS-CoV-2 infection were included.

results198 patients were diagnosed during the first pandemic time period (TP1; February 2020 September 2020), 494 during TP2 before the vaccination campaign (TP2/pre-vaccination; September 2020-21 February 2021) and 69 in TP2/post-vaccination (22 February 2021-15 May 2021). TP2 vs TP1 patients were younger (p = 0.004), showed more frequently a good performance status (p < 0.001) and <2 comorbidities (p = 0.002), were more likely to be on active anticancer therapy (p = 0.006). Significantly fewer patients in TP2 (3-4%) vs TP1 (22%) had an in-hospital potential source of infection (p < 0.001). TP2 patients were more frequently asymptomatic (p = 0.003). Significantly fewer patients from TP2 were hospitalized (p < 0.001) or admitted to intensive care unit (p = 0.006). All-cause mortality decreased from 30.3% in TP1, to 8.9% and 8.7% in the two TP2 periods (p < 0.001), reflected by a significant reduction in Sars-Cov-2-related mortality (15.2%, 7.5% and 5.8% in the three consecutive time periods, p = 0.004).

conclusionsDifferences in clinical characteristics and features of Sars-Cov-2 infection between TP1 and TP2 reflect the effects of protective measures and increased testing capacity. The lower mortality in TP2 is in line with a less frail population. However, the vast majority of death events in TP2 were related to COVID-19, reinforcing the priority to protect cancer patients.

Indexed as

COVID-19NeoplasmsHospitalizationHumansPandemicsSARS-CoV-2CancerCOVID-19Sars-Cov-2

Identifiers

PMID35398759
PMCPMC8930432
OpenAlexW4221128319

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.