RARE DISEASERESEARCH ATLAS

ORPHA:2030

Fibrosarcoma

low confidenceDisorder

Publications

53,665

Trials

34

Interventional, condition-specific

Researchers

1,339

Distinct authors in sample

Gene link

Readiness

2/6

Stages with a signal

How rare: How common this is has not been clearly measured.

Orphanet entry

Cross-references

Joined from Mondo / Orphanet. MeSH labels may enter searches; UMLS / OMIM / NCIT are stored for reference.

Additional Mondo synonyms (6)

fibrosarcoma · fibrosarcoma (disease) · fibrosarcoma (excluding infantile fibrosarcoma) · fibrosarcoma - not infantile · fibrosarcoma, malignant · malignant fibromatous neoplasm

Research stages

Trial readiness signals

Where this condition sits on an open-data research pipeline — not how close a treatment is, and not medical advice. Empty stages often mean “not in these databases under this Mondo ID,” not “impossible.”

2/6 stages with a signal

An interventional trial matched this condition name on ClinicalTrials.gov — see trials below.

  1. Gene identifiedNot found

    No GenCC disease–gene assertion in this build

  2. LiteraturePresent

    53,665 matched papers (22,637 in last 10 years) Source

  3. Phenotype characterisedNot checked

    Not yet enriched from Monarch / HPO

  4. Animal modelNot checked

    Not yet enriched from Monarch / Alliance

  5. Orphan designationNot checked

    FDA/EMA orphan-drug designation not enriched yet

  6. Interventional trialPresent

    34 matched on ClinicalTrials.gov (8 recruiting in sample)

Biology

Genes and phenotypes

Gene–disease validity from GenCC, plus phenotypes and animal models joined from Monarch Initiative via Mondo ID — not a clinical diagnosis aid.

Do we know what causes it?

Not yet — the cause hasn't been pinned down in GenCC.

No strong gene–disease assertion joined for this Orphanet entity.

Phenotypes (Monarch / HPO)

Not enriched in this build — Monarch phenotype joins were not run for this record.

Animal models (Monarch / Alliance)

Not enriched in this build.

Literature

Is anyone studying this?

53,665

53,665 papers — among the better-studied rare conditions, though still a fraction of common-disease literature (breast cancer: over 700,000). Median papers in the last 10 years for a rare disease in this dataset (publications denominator n=5449) is 41.

53,665 papers since the earliest indexed year in this search — median last-10-year count for a rare disease in this dataset is 41 (publications denominator n=5449).

22,637 in the last 10 years · low confidence

Phrase hits: 53,665 · MeSH hits: 0

Open Europe PMC search

Who's working on it?

1,339

Distinct author names in 200 sampled papers — named people below.

Who's working on it?

People publishing on this condition (sampled Europe PMC records). Affiliation is the most recent found in that sample.

  1. 01
    Wang Y6 papers · 2026

    Department of Otolaryngology Head and Neck Surgery, Xiangya Hospital, Central South University, Changsha, China. wangyvmin@csu.edu.cn.

    Papers in Europe PMC
  2. 02
    Kim MM5 papers · 2026

    Department of Cosmetics Engineering, and Graduate School of Applied Chemistry·Food Engineering, Dong-Eui University, Busan, Republic of Korea. mmkim@deu.ac.kr.

    Papers in Europe PMC
  3. 03
    Liu Y5 papers · 2026

    Department of Gynaecology and Obstetrics, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.

    Papers in Europe PMC
  4. 04
    Chen Y4 papers · 2026

    Department of Urology, Institute of Precision Drug Innovation and Cancer Center, Second Affiliated Hospital of Dalian Medical University, Dalian, China.

    Papers in Europe PMC
  5. 05
    Jiang Y4 papers · 2026

    TCM Prevention and Treatment of Metabolic and Chronic Diseases Key Laboratory of Sichuan Province, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China.

    Papers in Europe PMC
  6. 06
    Li W4 papers · 2026

    Department of Cardiovascular Surgery, Binzhou Medical University Hospital, Binzhou, Shandong, China.

    Papers in Europe PMC
  7. 07
    Li Z4 papers · 2026

    Department of Gastrointestinal Surgery, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.

    Papers in Europe PMC
  8. 08
    Wang J4 papers · 2026

    Department of Musculoskeletal Oncology, Sun Yat-Sen University Cancer Center, Guangzhou, 510060, People's Republic of China.

    Papers in Europe PMC
  9. 09
    Wang S4 papers · 2026

    Department of General Surgery, Peking University First Hospital, Peking University, Beijing, China.

    Papers in Europe PMC
  10. 10
    Zhang W4 papers · 2026

    Department of Orthopedic Surgery, West China Hospital, Sichuan University, Chengdu, Sichuan, China.

    Papers in Europe PMC

Clinical research

Is a treatment being tested?

34

interventional trials for this specific condition

34 interventional trials matched this specific condition name; 8 currently recruiting in our sample.

Data as of 27 July 2026

34 interventional trials — more than 73% of diseases in the trials denominator have none at all (5114 of 7003; this disease is at the 96th percentile).

low confidence · 96th percentile (trials denominator)

Recruiting interventional trials

From the matched ClinicalTrials.gov set

34 interventional trials matched after quoted-phrase search and title/condition post-filter.

Observational and natural-history studies

4 observational studies match this condition. These do not test a treatment and are not counted in the interventional-trial headline, but they are genuine research: natural-history work often defines the endpoints needed for a future rare-disease trial, and families may be able to enroll.

Recruiting or not-yet-recruiting

Open the complete matched search on ClinicalTrials.gov

Where to find support

We do not yet link condition-specific patient organisations. These umbrella groups support undiagnosed and ultra-rare families:

India — NPRD

Last verified 2026-07-26

This ORPHAcode is not on our curated NPRD list (direct or Mondo-parent match). That does not decide clinical eligibility; families in India should ask a notified Centre of Excellence about current coverage.

Hand-curated for this project. ORPHAcode mappings are best-effort and may be incomplete or imprecise for umbrella categories. Parent (Mondo) matches mean the policy lists a broader category — confirm eligibility with a Centre of Excellence. Financial entitlements summarised from public policy statements and may change. This is not official government guidance.

How we counted this

Europe PMC query (preferred label + any corrected label + Orphanet and Mondo exact synonyms, stoplisted; unioned with resolved MeSH labels when available). UMLS / OMIM / NCIT cross-references are stored on the overview but are not added to the query string.

"Fibrosarcoma" OR "fibrosarcoma (disease)" OR "fibrosarcoma (excluding infantile fibrosarcoma)" OR "fibrosarcoma - not infantile" OR "fibrosarcoma, malignant" OR "malignant fibromatous neoplasm"

Run this search on Europe PMC

ClinicalTrials.gov query (quoted phrases + MeSH via query.cond, plus recall-expansion terms when used):

"Fibrosarcoma" OR "fibrosarcoma (disease)" OR "fibrosarcoma (excluding infantile fibrosarcoma)" OR "fibrosarcoma - not infantile" OR "fibrosarcoma, malignant" OR "malignant fibromatous neoplasm"

Interventional trials matched via: phrase (mesh = registered under a MeSH descriptor no name phrase would catch; recall-expansion = gene / selected parent terms used only for trials).

Study-type breakdown: 34 interventional · 4 observational · 0 expanded access. Only interventional studies enter the trial headline.

Query health: ok — strategies attempted: phrase; with hits: phrase

Run this search on ClinicalTrials.gov

Confidence reasoning

  • Preferred label is short or not clearly distinctive
  • No synonyms dropped by stoplist
  • No label/synonym collisions with other diseases in this corpus
  • Publication count (53665) is extremely high with unknown/missing prevalence — treat as possible over-matching, not proven research intensity

Ingested 2026-07-26T18:49:09.910Z