Evidence map›Paper›PMID 35268401›Full record

ReviewJournal of clinical medicine2022

Future Treatment Options in Systemic Sclerosis-Potential Targets and Ongoing Clinical Trials.

Anna Bohdziewicz, Katarzyna Karina Pawlik, Magdalena Maciejewska, Mariusz Sikora, Rosanna Alda-Malicka, Joanna Czuwara, Lidia Rudnicka

Open access · goldAbstract readReview
In one paragraph

Review in Journal of clinical medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
3.8field-weighted citation impact, top 6% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

  1. Pooled it
  2. Systemic sclerosis, main culprits and involved signaling pathways.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2025
    Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Blocking BAFF Alleviates Hepatic Fibrosis inPathogens (Basel, Switzerland) · 2023
    Article
  12. Article
  13. 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

7 authors at 2 institutions in 1 country.

Anna BohdziewiczDepartment of Dermatology, Medical University of Warsaw, Koszykowa 82A, 02-008 Warsaw, Poland.
Katarzyna Karina PawlikDepartment of Dermatology, Medical University of Warsaw, Koszykowa 82A, 02-008 Warsaw, Poland.ORCID 0000-0003-4342-4324
Magdalena MaciejewskaDepartment of Dermatology, Medical University of Warsaw, Koszykowa 82A, 02-008 Warsaw, Poland.ORCID 0000-0003-1009-6395
Mariusz SikoraNational Institute of Geriatrics, Rheumatology and Rehabilitation, Spartańska 1, 02-637 Warsaw, Poland.ORCID 0000-0002-6162-9916
Rosanna Alda-MalickaDepartment of Dermatology, Medical University of Warsaw, Koszykowa 82A, 02-008 Warsaw, Poland.
Joanna CzuwaraDepartment of Dermatology, Medical University of Warsaw, Koszykowa 82A, 02-008 Warsaw, Poland.
Lidia RudnickaDepartment of Dermatology, Medical University of Warsaw, Koszykowa 82A, 02-008 Warsaw, Poland.ORCID 0000-0002-8308-1023
Medical University of Warsaw · PLNational Institute of Geriatrics, Rheumatology and Rehabilitation · PL

Funding

Polish Ministry of Science and Higher Education MNiSW/2020/220/DIR/NN4
6 · The paper itself

Abstract

Systemic sclerosis is an autoimmune connective tissue disease characterized by vasculopathy and fibrosis of the skin and internal organs. The pathogenesis of systemic sclerosis is very complex. Mediators produced by immune cells are involved in the inflammatory processes occurring in the tissues. The currently available therapeutic options are often insufficient to halt disease progress. This article presents an overview of potential therapeutic targets and the pipeline of possible future therapeutic options. It is based on research of clinical trials involving novel, unestablished methods of treatment. Increasing knowledge of the processes and mediators involved in systemic scleroderma has led to the initiation of drug trials with therapeutic targets of CD28-CD80/86, CD19, CCL24, CD20, CD30, tumor necrosis factor (TNF), transforming growth factor β (TGF-β), B-cell activating factor (BAFF), lysophosphatidic acid receptor 1 (LPA1 receptor), soluble guanylate cyclase (sGC), Janus kinases (JAK), interleukin 6 (IL-6), endothelin receptor, and autotaxin. Data from clinical trials on these drugs indicate a significant potential for several new therapeutic options for systemic sclerosis in the upcoming future.

Indexed as

belimumabbrentuximab vedotinimatinibnilotinibnintedanibriociguatrituximabSAR100842systemic sclerosistofacitinib

Identifiers

PMID35268401
PMCPMC8911443
OpenAlexW4214535082

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.