ORPHA:251595
Astrocytoma grade 2
Also known as: Diffuse astrocytoma
Publications
6,682
94.2th percentile
Trials
31
Interventional, condition-specific
Researchers
1,410
Distinct authors in sample
Gene link
—
Readiness
2/6
Stages with a signal
Clinical definition (Orphanet)
A rare low-grade astrocytoma characterized by a high degree of cellular differentiation, slow growth, and diffuse infiltration of adjacent brain structures, and corresponding to WHO grade II. The tumor typically affects young adults and has an intrinsic tendency for progression to high-grade glioma. Histological variants are fibrillary, gemistocytic, and protoplasmic astrocytoma. Patients most commonly present with , but also with other neurological or neuropsychological abnormalities, depending on the location.
How rare: 1-9 / 1 000 000 — roughly one to nine people per million. In a city the size of Kolkata, perhaps a few dozen.
Cross-references
Joined from Mondo / Orphanet. MeSH labels may enter searches; UMLS / OMIM / NCIT are stored for reference.
- MONDO:0016686
- UMLS:C0280785
- NCIT:C7173
Additional Mondo synonyms (8)
WHO grade II astrocytoma · astrocytoma, diffuse · astrocytoma, diffuse, malignant · diffuse astrocytoma · grade II astrocytic neoplasm · grade II astrocytic tumor · grade II astrocytic tumour · grade II astrocytoma
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
6,682 matched papers (4,563 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
31 matched on ClinicalTrials.gov (7 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
4
Drugs / clinical candidates · MONDO_0016686
- HILTONOL·phase 1
- TELAGLENASTAT·phase 1
- TEMOZOLOMIDE·phase 1
- TROTABRESIB·phase 1
CTD chemicals (MyDisease.info)
No CTD chemical associations returned for this Mondo ID.
Literature
Is anyone studying this?
6,682
6,682 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.
6,682 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).
4,563 in the last 10 years · high confidence · 94.2th percentile (publications denominator)
Phrase hits: 6,682 · MeSH hits: 0
Who's working on it?
1,410
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.
- 01Wang Y7 papers · 2025
Department of Radiation Oncology, The Fourth Hospital of Hebei Medical University, 12 Jiankang Road, Shijiazhuang 050011, China.
Papers in Europe PMC - 02Li Y5 papers · 2025
Department of Neurosurgery, Center for Malignant Brain Tumors, National Glioma MDT Alliance, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Papers in Europe PMC - 03Liu Y5 papers · 2026
Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Texas, USA.
Papers in Europe PMC - 04Li J4 papers · 2025
Department of Radiation Oncology, The Fourth Hospital of Hebei Medical University, 12 Jiankang Road, Shijiazhuang 050011, China.
Papers in Europe PMC - 05Wang J4 papers · 2026
Department of Neurosurgery, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Papers in Europe PMC - 06Abdullaev Z3 papers · 2026
Laboratory of Pathology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Papers in Europe PMC - 07Chung HJ3 papers · 2026
Laboratory of Pathology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Papers in Europe PMC - 08Dampier C3 papers · 2026
Laboratory of Pathology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Papers in Europe PMC - 09Ducray F3 papers · 2026
Neuro-Oncology Department, Hospices Civils of Lyon, 69500 Bron, France.
Papers in Europe PMC - 10Giannini C3 papers · 2026
Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
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; 7 currently recruiting in our sample.
Data as of 11 September 2026
31 interventional trials — more than 77.2% of diseases in the trials denominator have none at all (5501 of 7126; this disease is at the 96.1th percentile).
high confidence · 96.1th 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.
- NCT04065776·RECRUITING·Evaluation of Hippocampal-Avoidance Using Proton Therapy in Low-Grade Glioma
Not reviewed·Conditions: Glioma · Pilocytic Astrocytoma · Pilomyxoid Astrocytoma · Pleomorphic Xanthoastrocytoma·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
- NCT05190172·RECRUITING·PRO-GLIO: PROton Versus Photon Therapy in IDH-mutated Diffuse Grade II and III GLIOmas
Not reviewed·Conditions: Oligodendroglioma · Oligodendroglioma, Anaplastic · Diffuse Astrocytoma, IDH-Mutant·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
- NCT07223034·RECRUITING·A Study of 177Lu-PSMA-617 in People With Gliomas
Not reviewed·Conditions: Glioma · Diffuse Astrocytoma, IDH-Wildtype (Grade 2-4) · Glioblastoma, IDH-wildtype · Diffuse Midline Glioma, H3 K27-Altered·Matched via name phrase
- 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
- NCT06047379·RECRUITING·Safety and Efficacy of NEO212 in Patients With Astrocytoma IDH-mutant, Glioblastoma IDH-wildtype or Brain Metastasis
Not reviewed·Conditions: Diffuse Astrocytoma, IDH-Mutant · Glioblastoma, IDH-wildtype · Brain Metastases, Adult · Cervical Cancer·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.
Recruiting or not-yet-recruiting
- NCT05532969·NOT YET RECRUITING·Correlation Between Psychological Stress and Progression of Diffuse Astrocytoma Towards Secondary Glioma
Not reviewed·Conditions: Astrocytoma·Matched via name phrase
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)
- isrctn·ISRCTN12155285·Recruiting·Exploring energy patterns in brain tumours with new imaging technologies (LIFE-GlioB)
skipped — LLM skipped (--skip-llm)
- isrctn·ISRCTN45209900·No longer recruiting·A randomised study of radiotherapy and concomitant Temodal® (temozolomide) or neoadjuvant chemotherapy followed by radiotherapy and concomitant Temodal® in patients with high grade glioma
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·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)
- ctis·2023-504696-24-00·Authorised·The ALPINE trial: a phase 1-2 study of intra-arterial [177Lu]Lu-PSMA-I&T for progressive or recurrent intracranial adult type diffuse glioma
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 Astrocytoma grade 2 — 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.
"Astrocytoma grade 2" OR "Diffuse astrocytoma" OR "WHO grade II astrocytoma" OR "astrocytoma, diffuse" OR "astrocytoma, diffuse, malignant" OR "grade II astrocytic neoplasm" OR "grade II astrocytic tumor" OR "grade II astrocytic tumour" OR "grade II astrocytoma"
ClinicalTrials.gov query (quoted phrases + MeSH via query.cond, plus recall-expansion terms when used):
"Astrocytoma grade 2" OR "Diffuse astrocytoma" OR "WHO grade II astrocytoma" OR "astrocytoma, diffuse" OR "astrocytoma, diffuse, malignant" OR "grade II astrocytic neoplasm" OR "grade II astrocytic tumor" OR "grade II astrocytic tumour" OR "grade II astrocytoma"
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.
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
Ingested 2026-07-27T10:48:35.528Z
