Evidence map›Paper›PMID 32511470›Full record

ArticlemedRxiv : the preprint server for health sciences2020

A systematic review and meta-analysis of cancer patients affected by a novel coronavirus.

B P Venkatesulu, V T Chandrasekar, P Girdhar, P Advani, A Sharma, T Elumalai, C Hsieh, H I Elghazawy, V Verma, S Krishnan

Open access · greenAbstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2020. 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
–field-weighted citation impact
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, 57 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 8 institutions in 4 countries.

B P VenkatesuluTransitional year residency, Department of Internal Medicine, Henry Ford Hospital, Detroit, MI 48202, United States.
V T ChandrasekarDepartment of Gastroenterology and Hepatology, University of Kansas Medical Center, Kansas City, KS 66160, United States.
P GirdharDepartment of Radiation Oncology, All India Institute of Medical Sciences, New Delhi, India.
P AdvaniRadiation Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Institutes of Health, National Cancer Institute, Bethesda, MD 20892, United States.
A SharmaDepartment of Experimental Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, United States.
T ElumalaiDepartment of Clinical Oncology, The Christie NHS Foundation Trust, Manchester, United Kingdom.
C HsiehDepartment of Radiation Oncology, Institute for Radiological Research, Chang Gung Memorial Hospital at Linkou and Chang Gung University, Taoyuan City, Taiwan.
H I ElghazawyDepartment of Clinical Oncology, Faculty of Medicine, Ain Shams University, Abbaseya, Cairo, Egypt.
V VermaDepartment of Radiation Oncology, Allegheny General Hospital, Pittsburgh, Pennsylvania.
S KrishnanDepartment of Radiation Oncology, Mayo Clinic Florida, 4500 San Pablo Road S, Mayo 1N, Jacksonville, FL 32224, USA.
The University of Texas MD Anderson Cancer Center · USAin Shams University · EGAllegheny General Hospital · USHenry Ford Hospital · USMayo Clinic in Florida · USNational Institutes of Health · USThe Christie NHS Foundation Trust · GBUniversity of Kansas Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCancer patients with COVID-19 disease have been reported to have double the case fatality rate of the general population. MATERIALS AND

methodsA systematic search of PubMed/MEDLINE, Embase, Cochrane Central, Google Scholar, and MedRxiv was done for studies on cancer patients with COVID-19. Pooled proportions were calculated for categorical variables. Odds ratio and forest plots were constructed for both primary and secondary outcomes. The random-effects model was used to account for heterogeneity between studies.

resultsThis systematic review of 31 studies and meta-analysis of 181,323 patients from 26 studies involving 23,736 cancer patients is the largest meta-analysis to the best of our knowledge assessing outcomes in cancer patients affected by COVID-19. Our meta-analysis shows that cancer patients with COVID-19 have a higher likelihood of death (odds ratio, OR 2.54), which was largely driven by mortality among patients in China. Cancer patients were more likely to be intubated, although ICU admission rates were not statistically significant. Among cancer subtypes, the mortality was highest in hematological malignancies (OR 2.43) followed by lung cancer (OR 1.8). There was no association between receipt of a particular type of oncologic therapy and mortality. Our study showed that cancer patients affected by COVID-19 are a decade older than the normal population and have a higher proportion of co-morbidities. There was insufficient data to assess the association of COVID-directed therapy and survival outcomes in cancer patients. Despite the heterogeneity of studies and inconsistencies in reported variables and outcomes, these data could guide clinical practice and oncologic care during this unprecedented global health pandemic.

conclusionCancer patients with COVID-19 disease are at increased risk of mortality and morbidity. A more nuanced understanding of the interaction between cancer-directed therapies and COVID-19-directed therapies is needed. This will require uniform prospective recording of data, possibly in multi-institutional registry databases.

Indexed as

cancerchemotherapyCOVID-19meta-analysisradiotherapy

Identifiers

PMID32511470
PMCPMC7265691
OpenAlexW3032078315

What OpenQuestion holds

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LicenceCC BY-NC
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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.