ORPHA:251630
Oligodendroglioma grade 3
Also known as: Anaplastic oligodendroglioma
Publications
5,381
Trials
97
Interventional, condition-specific
Researchers
1,294
Distinct authors in sample
Gene link
—
Readiness
2/6
Stages with a signal
Clinical definition (Orphanet)
A rare glial tumor characterized by a grade III oligodendroglial tumour with focal or diffuse anaplastic features. It typically occurs in the supratentorial white matter. Histologically, the cells are enlarged and epithelioid with pleomorphic and increased size nuclei, a vesicular chromatin pattern and prominent nucleoli. Most patients present with .
How rare: <1 / 1 000 000 — fewer than one in a million. In a city the size of Kolkata, that might mean on the order of fifteen people.
Cross-references
Joined from Mondo / Orphanet. MeSH labels may enter searches; UMLS / OMIM / NCIT are stored for reference.
- MONDO:0016696
- UMLS:C0334590
- NCIT:C4326
Additional Mondo synonyms (8)
WHO grade III oligodendroglial neoplasm · WHO grade III oligodendroglial tumor · WHO grade III oligodendroglial tumour · anaplastic oligodendroglioma · malignant oligodendroglioma · oligodendroglioma, anaplastic, malignant · oligodendroglioma, malignant · undifferentiated oligodendroglioma
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
5,381 matched papers (3,109 in last 10 years) Source
- Phenotype characterisedNot found
No HPO disease–phenotype associations via Monarch for these Mondo IDs
- Animal modelNot found
No Alliance genotype “model of” associations via Monarch for these Mondo IDs
- Orphan designationNot found
No FDA or EMA orphan-drug designation matched this disease via UMLS or preferred name Source
- Interventional trialPresent
97 matched on ClinicalTrials.gov (5 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)
None returned for this Mondo ID. That often means “not linked under this ID,” not “no clinical features.”
Animal models (Monarch / Alliance)
None returned for this Mondo ID. Empty here is not proof that no model organism work exists under another name or gene.
Monarch fetch 2026-07-29
Therapies
Designations, candidates, and chemicals
FDA OOPD and EMA orphan designations, Open Targets clinical candidates, and CTD chemical associations via MyDisease.info. These never change the interventional-trial headline.
Orphan designation (FDA · EMA)
No designation matched this disease via UMLS or preferred name on the FDA OOPD mirror or EMA orphan register. Absence here is not proof that none exists under another wording.
Open Targets candidates
30
Drugs / clinical candidates · MONDO_0016696
- LOMUSTINE·phase 3
- PROCARBAZINE·phase 3
- VINCRISTINE·phase 3
- 6-O-BENZYLGUANINE·phase 2
- BUSULFAN·phase 2
- CARMUSTINE·phase 2
- ETIRINOTECAN PEGOL·phase 2
- FILGRASTIM·phase 2
- IMATINIB MESYLATE·phase 2
- INTERFERON ALFA-2B·phase 2
- PROCARBAZINE HYDROCHLORIDE·phase 2
- TEMOZOLOMIDE·phase 2
- THALIDOMIDE·phase 2
- THIOTEPA·phase 2
- TOPOTECAN HYDROCHLORIDE·phase 2
CTD chemicals (MyDisease.info)
No CTD chemical associations returned for this Mondo ID.
Literature
Is anyone studying this?
5,381
5,381 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=3967) is 59.
5,381 papers since the earliest indexed year in this search — median last-10-year count for a rare disease in this dataset is 59 (publications denominator n=3967).
3,109 in the last 10 years · low confidence
Phrase hits: 5,381 · MeSH hits: 0
Who's working on it?
1,294
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.
- 01Chen D4 papers · 2026
Department of Neurosurgery, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.
Papers in Europe PMC - 02Liu S4 papers · 2026
Computational NeuroSurgery (CNS) Lab, Macquarie Medical School, Faculty of Medicine, Health and Human Sciences, Macquarie University, Sydney, NSW, Australia.
Papers in Europe PMC - 03Li J3 papers · 2025
Department of Radiation Oncology, The Second Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi 530000, P.R. China.
Papers in Europe PMC - 04Li X3 papers · 2026
Department of Radiation Oncology, The Second Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi 530000, P.R. China.
Papers in Europe PMC - 05Li Z3 papers · 2025
Department of Neurosurgery, Xuanwu Hospital Capital Medical University, Beijing, China.
Papers in Europe PMC - 06Lombardi G3 papers · 2026
Department of Oncology, Oncology 1, Veneto Institute of Oncology IOV-IRCCS, 35128 Padua, Italy.
Papers in Europe PMC - 07Wang H3 papers · 2025
Department of Medical Ultrasound, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China.
Papers in Europe PMC - 08Wang X3 papers · 2025
Jilin Provincial Key Laboratory of Radiation Oncology & Therapy, The First Hospital of Jilin University, Changchun, China.
Papers in Europe PMC - 09Wang Y3 papers · 2025
Department of Neurosurgery, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.
Papers in Europe PMC - 10Yoshida K3 papers · 2025
Department of Neurosurgery, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo, 160-8582, Japan.
Papers in Europe PMC
Clinical research
Is a treatment being tested?
97
interventional trials for this specific condition
97 interventional trials matched this specific condition name; 5 currently recruiting in our sample.
Data as of 11 September 2026
97 interventional trials — more than 77.2% of diseases in the trials denominator have none at all (5501 of 7126; this disease is at the 98.4th percentile).
low confidence · 98.4th percentile (trials denominator)
Recruiting interventional trials
From the matched ClinicalTrials.gov set
97 interventional trials matched after quoted-phrase search and title/condition post-filter.
- NCT04623931·RECRUITING·Chemotherapy and Radiation Therapy for the Treatment of IDH Wildtype Gliomas or Non-histological (Molecular) Glioblastomas
Not reviewed·Conditions: Anaplastic Astrocytoma, IDH-Wildtype · Anaplastic Oligoastrocytoma · Anaplastic Oligodendroglioma · Diffuse Astrocytoma, IDH-Wildtype·Matched via name phrase
- NCT04541082·RECRUITING·Phase I Study of Oral ONC206 in Recurrent and Rare Primary Central Nervous System Neoplasms
Not reviewed·Conditions: Central Nervous System Neoplasms · Glioblastoma · Gliosarcoma, Adult · Anaplastic Oligodendroglioma·Matched via name phrase
- NCT05698524·RECRUITING·A Study of Temodar With Abexinostat (PCI-24781) for Patients With Recurrent Glioma
Not reviewed·Conditions: Recurrent High Grade Glioma · Anaplastic Astrocytoma · Anaplastic Oligodendroglioma · Glioblastoma·Matched via name phrase
- NCT07468136·RECRUITING·Retifanlimab With or Without Difluoromethylornithine for the Treatment of Progressive High Grade Gliomas
Not reviewed·Conditions: Anaplastic Oligodendroglioma · Astrocytoma, IDH-Mutant, Grade 3 · Astrocytoma, IDH-Mutant, Grade 4 · Diffuse Astrocytoma·Matched via name phrase
- NCT04135807·RECRUITING·Implantable Microdevice In Primary Brain Tumors
Not reviewed·Conditions: Grade II Glioma · Grade III Glioma · Grade IV Glioma · Astrocytoma·Matched via name phrase
Observational and natural-history studies
6 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.
Other registries (secondary)
Broader net from EU CTIS, ISRCTN, and ICTRP when available — deduped against ClinicalTrials.gov IDs already counted above. Dual-model LLM relevance gates what we keep. These rows are not added to the interventional headline.
raw 6 · after dedupe 6 · already on CT.gov 0 · kept 0 · parent 0 · uncertain 6 · dropped 0 · fetched 2026-07-30
Source notes: ictrp: Error: ICTRP public search unavailable (WHO portal is SPA-only; SOAP needs partnership). Tried: https://apps.who.int/tri
No secondary-registry studies passed dual-model relevance for this condition name (after dedupe).
Uncertain / not reviewed (6)
- ctis·2023-509238-20-00·Cancelled·A Phase 1 Single Center Clinical Trial Evaluating Safety of 5-Aminolevulinic Acid (5-ALA) Combined With CV01 Delivery of Ultrasound for Sonodynamic Therapy (SDT) in Patients With Newly Diagnosed High-Grade Glioma (HGG) Prior to Resection and Standard Adjuvant Therapy
skipped — LLM skipped (--skip-llm)
- isrctn·ISRCTN19852453·No longer recruiting·Radiochemotherapy trial with radiotherapy and temozolomide chemotherapy for children and young adolescents 3 years and older to 18 years of age with primary high grade glioma, pontine glioma or gliomatosis cerebri
skipped — LLM skipped (--skip-llm)
- isrctn·ISRCTN45828668·No longer recruiting·A phase I - II, prospective, double blind, randomised study of the safety and efficacy of sulfasalazine for the treatment of progressing malignant gliomas
skipped — LLM skipped (--skip-llm)
- isrctn·ISRCTN17931175·No longer recruiting·A joint MRC/European Organisation for Research and Treatment of Cancer (EORTC) study of radiotherapy for low grade astrocytomas and oligodendrogliomas
skipped — LLM skipped (--skip-llm)
- isrctn·ISRCTN83176944·No longer recruiting·A prospective randomised trial comparing temozolomide with standard nitrosourea-based chemotherapy (PCV [procarbazine, CCNU, vincristine]/BCNU [bis-chloronitrosourea]) in the treatment of recurrent WHO astrocytic tumours grades III and IV (anaplastic astrocytoma and glioblastoma multiforme)
skipped — LLM skipped (--skip-llm)
- isrctn·ISRCTN32891249·No longer recruiting·A randomised trial of adjuvant procarbazine, CCNU, vincristine chemotherapy in patients with highly anaplastic oligodendroglioma (BR11) - EORTC
skipped — LLM skipped (--skip-llm)
Where to find support
Condition-specific patient organisations, when Orphanet lists them, are on the disease’s Orphanet page. We also link umbrella groups that support undiagnosed and ultra-rare families.
Orphanet entry for Oligodendroglioma grade 3 — check Associations / patient organisations on that page.
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.
"Oligodendroglioma grade 3" OR "Anaplastic oligodendroglioma" OR "WHO grade III oligodendroglial neoplasm" OR "WHO grade III oligodendroglial tumor" OR "WHO grade III oligodendroglial tumour" OR "malignant oligodendroglioma" OR "oligodendroglioma, anaplastic, malignant" OR "oligodendroglioma, malignant" OR "undifferentiated oligodendroglioma"
ClinicalTrials.gov query (quoted phrases + MeSH via query.cond, plus recall-expansion terms when used):
"Oligodendroglioma grade 3" OR "Anaplastic oligodendroglioma" OR "WHO grade III oligodendroglial neoplasm" OR "WHO grade III oligodendroglial tumor" OR "WHO grade III oligodendroglial tumour" OR "malignant oligodendroglioma" OR "oligodendroglioma, anaplastic, malignant" OR "oligodendroglioma, malignant" OR "undifferentiated oligodendroglioma"
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: 97 interventional · 6 observational · 1 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 multi-word and distinctive
- No synonyms dropped by stoplist
- No label/synonym collisions with other diseases in this corpus
- Publication count (5381) is implausibly high for prevalence class "<1 / 1 000 000" — treat as possible over-matching, not a measure of research intensity
Ingested 2026-07-27T10:50:44.444Z
