ORPHA:213625
Leiomyosarcoma of the corpus uteri
Publications
3,980
Trials
31
Interventional, condition-specific
Researchers
1,332
Distinct authors in sample
Gene link
—
Readiness
2/6
Stages with a signal
Clinical definition (Orphanet)
Leiomyosarcoma of the corpus uteri is a rare, malignant, mesenchymal tumor of smooth muscle origin characterized, histologically, by spindle and/or pleomorphic cells, often forming disorganized fascicles, with tumor cell necrosis and, macroscopically, by a large, soft, usually intramural mass with irregular borders and necrotic and hemorrhagic areas, located in the uterus. Presenting signs and symptoms typically include dysfunctional vaginal bleeding, vaginal discharge, palpable pelvic mass and/or pelvic pain/pressure. Changes in bowel habits, frequent or painful urination and hematuria may also be associated.
Cross-references
Joined from Mondo / Orphanet. MeSH labels may enter searches; UMLS / OMIM / NCIT are stored for reference.
- MONDO:0016262
- UMLS:C0280631
- NCIT:C6340
Additional Mondo synonyms (16)
Uterine Leiomyosarcoma · body of uterus leiomyosarcoma · corpus uteri leiomyosarcoma · leiomyosarcoma - uterus · leiomyosarcoma of body of uterus · leiomyosarcoma of corpus uteri · leiomyosarcoma of the body of uterus · leiomyosarcoma of the corpus uteri · leiomyosarcoma of the uterine body · leiomyosarcoma of the uterine corpus · leiomyosarcoma of the uterus · leiomyosarcoma of uterine body · leiomyosarcoma of uterine corpus · leiomyosarcoma of uterus · uterine body leiomyosarcoma · uterine corpus leiomyosarcoma
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.
- Gene identifiedNot found
No GenCC disease–gene assertion in this build
- LiteraturePresent
3,980 matched papers (2,268 in last 10 years) Source
- Phenotype characterisedNot checked
Not yet enriched from Monarch / HPO
- Animal modelNot checked
Not yet enriched from Monarch / Alliance
- Orphan designationNot checked
FDA/EMA orphan-drug designation not enriched yet
- Interventional trialPresent
31 matched on ClinicalTrials.gov (3 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?
3,980
3,980 papers have been published on this condition. That is a real research literature — still far smaller than common diseases (breast cancer: over 700,000 papers). Median papers in the last 10 years for a rare disease in this dataset (publications denominator n=5449) is 41.
3,980 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).
2,268 in the last 10 years · low confidence
Phrase hits: 3,980 · MeSH hits: 0
Who's working on it?
1,332
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.
- 01Hayashi T9 papers · 2026
2Cancer Medicine, National Hospital Organization Kyoto Medical Centre; 3Medical R&D Promotion Project, The Japan Agency for Medical Research and Development (AMED), Tokyo, Japan.
Papers in Europe PMC - 02Konishi I9 papers · 2026
1Department of Obstetrics and Gynecology, National Hospital Organization Kyoto Medical Centre, Japan.
Papers in Europe PMC - 03Abiko K6 papers · 2024
1Department of Obstetrics and Gynecology, National Hospital Organization Kyoto Medical Centre, Japan.
Papers in Europe PMC - 04Lee B4 papers · 2026
Surgical Oncology, Department of Surgery, Stanford University School of Medicine, Stanford, CA, USA. byrnelee@stanford.edu.
Papers in Europe PMC - 05Nucci MR4 papers · 2026
Department of Pathology, Brigham and Women's Hospital/Harvard Medical School, Boston, MA.
Papers in Europe PMC - 06Wang Y4 papers · 2026
Department of Gynecology and Obstetrics, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, Fujian, China.
Papers in Europe PMC - 07Chen Z3 papers · 2025
Department of Obstetrics and Gynecology, The International Peace Maternity and Child Health Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
Papers in Europe PMC - 08Chiang S3 papers · 2026
Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, New York. Electronic address: chiangs@mskcc.org.
Papers in Europe PMC - 09Colombo N3 papers · 2026
Department of Gynecology, European Institute of Oncology (IEO) IRCCS, Milan, Italy.
Papers in Europe PMC - 10Croce S3 papers · 2026
Institut Bergonié, Comprehensive Cancer Center, Bordeaux, France.
Papers in Europe PMC
Clinical research
Is a treatment being tested?
31
interventional trials for this specific condition
31 interventional trials matched this specific condition name; 3 currently recruiting in our sample. 109 trials are registered for leiomyosarcoma, the broader category — shown separately because they may or may not enrol this specific subtype.
Data as of 27 July 2026
31 interventional trials — more than 73% of diseases in the trials denominator have none at all (5114 of 7003; this disease is at the 95.8th percentile).
low confidence · 95.8th percentile (trials denominator)
Recruiting interventional trials
From the matched ClinicalTrials.gov set
31 interventional trials matched after quoted-phrase search and title/condition post-filter.
- NCT06524583·RECRUITING·Interest of Post-operative Chemotherapy in Patients With Localised Uterine Leiomyosarcoma Suspected of Having a High Risk of Recurrence Based on a Biological Test Performed on the Tumour
Conditions: Leiomyosarcoma Uterus·Matched via name phrase
- NCT05649956·RECRUITING·Letrozole in Uterine Leiomyosarcoma
Conditions: Uterine Leiomyosarcoma·Matched via name phrase
- NCT07467772·RECRUITING·Ph 2 Elacestrant in ER Positive Uterine Sarcomas
Conditions: Uterine Sarcoma · Uterine Leiomyosarcoma · Endometrial Stromal Sarcoma · ESS·Matched via name phrase
Broader category: leiomyosarcoma
109
Interventional trials for the parent category, exclusive of NCT IDs already counted above. Eligibility for this subtype is not guaranteed.
Worth raising with a clinician. How we count trials.
Recruiting under the broader category
- NCT06498648·RECRUITING·Testing the Addition of an Anti-cancer Drug, Abemaciclib, to the Usual Chemotherapy Treatment (Gemcitabine) for Soft Tissue Sarcoma
Conditions: Advanced Dedifferentiated Liposarcoma · Advanced Leiomyosarcoma · Advanced Soft Tissue Sarcoma · Metastatic Dedifferentiated Liposarcoma·Matched via name phrase
- NCT07633756·NOT YET RECRUITING·A Phase 1b, Open-Label Study Of REC-617, A Selective CDK7 Inhibitor, In Patients With Metastatic Or Unresectable RB1-Negative Leiomyosarcoma After Prior Systemic Therapy
Conditions: Phase 1b · Open Label · REC-617 · RB1-Negative·Matched via name phrase
- NCT06957431·RECRUITING·Zanzalintinib Combined With Eribulin in Advanced Liposarcoma and Leiomyosarcoma
Conditions: Advanced Leiomyosarcoma · Adipocytic Sarcoma · Advanced Liposarcoma·Matched via name phrase
- NCT07405346·ENROLLING BY INVITATION·A Trial for Advanced Leiomyosarcoma With Human Organoid-guided Personalized Efficacy
Conditions: Advanced Leiomyosarcoma·Matched via name phrase
- NCT05711615·RECRUITING·Testing Low-Dose Common Chemotherapy (Liposomal Doxorubicin) in Combination With an Anti-Cancer Drug, Peposertib, in Advanced Sarcoma
Conditions: Metastatic Dedifferentiated Liposarcoma · Metastatic Leiomyosarcoma · Metastatic Myxofibrosarcoma · Metastatic Sarcoma·Matched via name phrase
- NCT06571734·RECRUITING·XL092 (Zanzalintinib) for the Treatment of Patients With Metastatic or Unresectable Leiomyosarcoma, Bone Sarcoma or Translocation-associated Soft Tissue Sarcoma
Conditions: Metastatic Leiomyosarcoma · Unresectable Leiomyosarcoma · Bone Sarcoma · Translocation-associated Soft Tissue Sarcoma·Matched via name phrase
- NCT06528769·RECRUITING·Study of All-Trans Retinoic Acid (ATRA) and Cemiplimab in Patients With Advanced Leiomyosarcoma
Conditions: Leiomyosarcoma · Sarcoma·Matched via name phrase
- NCT07169344·RECRUITING·Hypofractionated, 3-week, Preoperative Proton or X-ray Radiotherapy for Patients With Localized Soft Tissue Sarcoma
Conditions: Soft Tissue Sarcoma (Excluding GIST) · Soft Tissue Sarcoma Adult · Soft Tissue Sarcoma of the Trunk and Extremities · Synovial Sarcomas·Matched via name phrase
- NCT06849986·RECRUITING·IO Combined With AI as First-line Treatment for Patients With Soft Tissue Sarcoma(TAIS)
Conditions: Soft Tissue Sarcomas · Angiosarcoma · Fibrosarcoma · Leiomyosarcoma·Matched via name phrase
- NCT07173972·RECRUITING·Dose-escalated, Hypofractionated, Definitive Proton Radiotherapy for Patients With Inoperable Soft Tissue Sarcoma.
Conditions: Soft Tissue Sarcoma (STS) · Soft Tissue Sarcoma Adult · Soft Tissue Sarcoma of the Trunk and Extremities · Synovial Sarcomas·Matched via name phrase
- NCT06789172·RECRUITING·A Phase 1, First-in-human Study of OKN4395 and Pembrolizumab in Patients With Solid Tumors
Conditions: Solid Tumours · Sarcoma · HNSCC · Non Small Cell Lung Cancer·Matched via name phrase
- NCT04055220·RECRUITING·Efficacy and Safety of Regorafenib as Maintenance Therapy After First-line Treatment in Patients With Bone Sarcomas
Conditions: Bone Sarcoma · Osteosarcoma · Ewing Sarcoma · Chondrosarcoma·Matched via name phrase
- NCT04535271·RECRUITING·Metronomic Trabectedin, Gemcitabine, and Dacarbazine for Soft Tissue Sarcoma
Conditions: Leiomyosarcoma·Matched via name phrase
- NCT07516925·RECRUITING·A Study of Ivonescimab in People With Leiomyosarcoma
Conditions: Leiomyosarcoma·Matched via name phrase
- NCT06638931·RECRUITING·Agnostic Therapy in Rare Solid Tumors
Conditions: Urachal Cancer · Parathyroid Carcinoma · Fibrolamellar Carcinoma · Angiosarcoma·Matched via name phrase
Observational and natural-history studies
3 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.
None of the matched observational studies is currently listed as recruiting.
General rare disease registries you may be eligible for
These studies enroll across many rare conditions. They are not counted as evidence that anyone is studying this specific disease.
- NCT01793168·RECRUITING·Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford
Conditions: Rare Disorders · Undiagnosed Disorders · Disorders of Unknown Prevalence · Cornelia De Lange Syndrome
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 2026-07-26This 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.
"Leiomyosarcoma of the corpus uteri" OR "Leiomyosarcoma of corpus uteri" OR "Uterine Leiomyosarcoma" OR "body of uterus leiomyosarcoma" OR "body of the uterus leiomyosarcoma" OR "corpus uteri leiomyosarcoma" OR "leiomyosarcoma - uterus" OR "leiomyosarcoma of body of uterus" OR "leiomyosarcoma of the body of the uterus" OR "leiomyosarcoma of the body of uterus" OR "leiomyosarcoma of the uterine body" OR "leiomyosarcoma of uterine body" OR "leiomyosarcoma of the uterine corpus" OR "leiomyosarcoma of uterine corpus" OR "leiomyosarcoma of the uterus" OR "leiomyosarcoma of uterus" OR "uterine body leiomyosarcoma" OR "uterine corpus leiomyosarcoma"
ClinicalTrials.gov query (quoted phrases + MeSH via query.cond, plus recall-expansion terms when used):
"Leiomyosarcoma of the corpus uteri" OR "Leiomyosarcoma of corpus uteri" OR "Uterine Leiomyosarcoma" OR "body of uterus leiomyosarcoma" OR "body of the uterus leiomyosarcoma" OR "corpus uteri leiomyosarcoma" OR "leiomyosarcoma - uterus" OR "leiomyosarcoma of body of uterus" OR "leiomyosarcoma of the body of the uterus" OR "leiomyosarcoma of the body of uterus" OR "leiomyosarcoma of the uterine body" OR "leiomyosarcoma of uterine body" OR "leiomyosarcoma of the uterine corpus" OR "leiomyosarcoma of uterine corpus" OR "leiomyosarcoma of the uterus" OR "leiomyosarcoma of uterus" OR "uterine body leiomyosarcoma" OR "uterine corpus leiomyosarcoma"
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: 31 interventional · 3 observational · 0 expanded access. Only interventional studies enter the trial headline.
Parent-category trials query:
"leiomyosarcoma"
Query health: ok — strategies attempted: phrase; with hits: phrase
Run this search on ClinicalTrials.gov
Confidence reasoning
- Preferred label is multi-word and distinctive
- No synonyms dropped by stoplist
- No label/synonym collisions with other diseases in this corpus
- Publication count (3980) is extremely high with unknown/missing prevalence — treat as possible over-matching, not proven research intensity
Ingested 2026-07-27T09:35:31.330Z
