Evidence map›Paper›PMID 36465081›Full record

ArticleRheumatology and immunology research2020

Risk of Malignancy and Biologic Therapy in Rheumatic Inflammatory Diseases: A Single-center Experience.

Laura Cometi, Cosimo Bruni, Saverio Passavanti, Lorenzo Tofani, Francesca Bartoli, Ginevra Fiori, Francesca Nacci, Gemma Lepri, Martina Orlandi, Daniela Melchiorre and 3 more

Open access · diamondAbstract read
In one paragraph

Article in Rheumatology and immunology research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–field-weighted citation impact, top 75% 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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 2 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
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

13 authors at 2 institutions in 1 country.

Laura CometiDepartment of Experimental and Clinical Medicine, Division of Rheumatology, University of Florence, Florence, Italy.
Cosimo BruniDepartment of Experimental and Clinical Medicine, Division of Rheumatology, University of Florence, Florence, Italy.
Saverio PassavantiDepartment of Internal Medicine, Division of Internal Medicine Unit III, Azienda Ospedaliera Universitaria Careggi, Florence, Italy.
Lorenzo TofaniDepartment of Experimental and Clinical Medicine, Division of Rheumatology, University of Florence, Florence, Italy.
Francesca BartoliDepartment of Geriatric Medicine, Division of Rheumatology Azienda Ospedaliera Universitaria Careggi, Florence, Italy.
Ginevra FioriDepartment of Geriatric Medicine, Division of Rheumatology Azienda Ospedaliera Universitaria Careggi, Florence, Italy.
Francesca NacciDepartment of Experimental and Clinical Medicine, Division of Rheumatology, University of Florence, Florence, Italy.
Gemma LepriDepartment of Experimental and Clinical Medicine, Division of Rheumatology, University of Florence, Florence, Italy.
Martina OrlandiDepartment of Experimental and Clinical Medicine, Division of Rheumatology, University of Florence, Florence, Italy.
Daniela MelchiorreDepartment of Experimental and Clinical Medicine, Division of Rheumatology, University of Florence, Florence, Italy.
Lorenzo AntonuzzoMedical Oncology Unit, Azienda Ospedaliera Universitaria Careggi, Florence, Italy.
Marco Matucci-CerinicDepartment of Experimental and Clinical Medicine, Division of Rheumatology, University of Florence, Florence, Italy.
Alberto Moggi-PignoneDepartment of Internal Medicine, Division of Internal Medicine Unit III, Azienda Ospedaliera Universitaria Careggi, Florence, Italy.
University of Florence · ITAzienda Ospedaliero-Universitaria Careggi · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Biologic disease modifying anti-rheumatic drugs (bDMARDs) have significantly improved the care of patients with rheumatic muscle-skeletal disorders (RMDs). Considering their immunosuppressive action, a theoretical increase of malignancy risk has been a major concern in the last few decades. The objective of this study is to analyze the incidence of malignancies in a cohort of patients affected by rheumatoid arthritis (RA), psoriathic arthritis (PsA), and ankylosing spondylitis (AS) treated with bDMARDs. Methods: The charts of bDMARD-treated RMD patients were reviewed, and data about bDMARD exposure and malignant cancers (excluding non-melanoma skin cancer) were collected. Results: 921 patients were included (median age: 50.59 years, 66.67% females); 1374 bDMARD treatments were administered, 87.12% were tumor necrosis factor inhibitors. A total of 21 malignant neoplasms were detected in 21 patients (61.90% females, median age at cancer diagnosis: 64.99 years), 66.67% in RA patients, 19.05% in PsA, and 14.28% in AS. Among them, 10 patients (47.62%) were treated with etanercept, 6 patients (28.57%) with adalimumab, and 1 case each with tocilizumab, certolizumab, golimumab, infliximab, and abatacept. The most common malignancies that we found were lung cancers, ductal mammary carcinomas, melanomas, and lymphomas. The incidence rate (IR) of malignancies in our cohort was 3.47 per 1000 person-years (p-y); the higher IRs were in RA patients (5.13 per 1000 p-y), in males (4.21 per 1000 p-y), and in patients aged >70 years (10.14 per 1000 p-y). Conclusions: The results of our study showed IR of malignancies in RMD patients treated with bDMARDs that is in agreement with literature data.

Indexed as

ankylosing spondylitisbiologicscancermalignancypsoriatic arthritisrheumatoid arthritis

Identifiers

PMID36465081
PMCPMC9524767
OpenAlexW3112863446

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.