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A neuroendocrine carcinoma composed of small malignant cells which are often said to resemble "oat cells" under the microscope. Small cell carcinoma most often affects the lungs. Clinically, this is often a rapidly growing cancer that spreads to distant sites early.
No HPO annotations are available for this condition.
Retinoblastoma. The most common presenting sign is a white pupillary reflex (leukocoria). Strabismus is the second most common presenting sign and may accompany or precede leukocoria . Unusual presenting signs include glaucoma, orbital cellulitis, uveitis, hyphema, or vitreous hemorrhage. Most affected children are diagnosed before age five years. Atypical manifestations are more frequent in older children. Probands with retinoblastoma usually present in one of the following clinical settings:
Guidelines for diagnosis and care of children and families affected by retinoblastoma have been published .
Retinoblastoma should be suspected in children with any of the following:
Leukocoria (white pupil)
Strabismus
Change in eye appearance
No approved treatments are currently available for small cell carcinoma. The disease remains an area of unmet medical need.
Gene therapy approaches for small cell carcinoma have been reported in the published literature.
Guidelines for retinoblastoma care have been developed (see and Kenya National Retinoblastoma Strategy Best Practice Guidelines).
To establish the extent of disease and needs in an individual diagnosed with retinoblastoma, the following evaluations (if not performed as part of the evaluation that led to the diagnosis) are recommended:
Guidelines for clinical screening for children at risk have been published . Further information regarding medical surveillance for those who have had or are at risk of developing retinoblastoma is available in the guidelines for retinoblastoma care. Children who have undergone successful treatment require frequent follow-up examination for early detection of newly arising intraocular tumors, as indicated in the guidelines.
Table 3.
Retinoblastoma: Recommended Surveillance for Individuals at Risk and Affected Individuals
296 clinical trials registered, 40 recruiting. Interventions under study include drug therapy, procedural interventions, other interventions, and biologic therapy. Pipeline includes 2 PHASE4, 28 PHASE3, 106 PHASE2. Research is sponsored by a mix of industry and academic institutions.
NCT ID | Title | Phase | Sponsor | Status |
|---|---|---|---|---|
[NCT07454642](https://clinicaltrials.gov/study/NCT07454642) |
Data assembled from 4 of 12 sources · Last updated Nov 3, 2026, 3:00 PM UTC
Source: GeneReviews — "Retinoblastoma"
Reduced visual acuity
should be suspected in an individual with any of the following:
Diagnosis of retinoblastoma, including unilateral (unifocal and multifocal) and bilateral involvement
Retinoma
Family history of retinoblastoma
The diagnosis of retinoblastoma is established in a proband by retinal examination with full pupillary dilatation by an ophthalmologist or optometrist. Confirmation of the diagnosis and determination of the disease extent is accomplished by examination under anes...
Source: GeneReviews — "Retinoblastoma"
Several hereditary ocular conditions of childhood can clinically simulate retinoblastoma:
NDP-related persistent fetal vasculature and NDP-related Coats disease (See NDP-Related Retinopathies.)
• Tuberous sclerosis complex
Norrie disease (See NDP-Related Retinopathies.)
• Incontinentia pigmenti
Familial exudative vitreoretinopathy (See Phenotypic Series: Exudative Vitreoretinopathy.)
• Von Hippel-Lindau syndrome
Ocular infestation by Toxocara canis can also clinically simulate retinoblastoma.
Source: GeneReviews — "Retinoblastoma"
Biomarker and diagnostic research for small cell carcinoma has been reported in the published literature.
Source: GeneReviews — "Retinoblastoma"
296 trials found
System/Concern | Evaluation | Frequency
| • Eye exam under anesthesia (in young children)
Clinical eye exams w/o anesthesia once children are cooperative w/exam
| • Every 3-4 wks until age 6 mos
Every 2 mos from age 6 mos-3 yrs
Every 3-6 mos from age 3-7 yrs
Annually from age 7-10 yrs
Every 2 yrs from age 10 yrs
Prompt clinical investigation of any signs/symptoms of subsequent non-ocular malignant neoplasms1 | Ongoing education of affected persons caregivers w/clinical investigation as needed
| • Clinical eye exam (w/o anesthesia)
Eye ultrasound
| • Every 3-6 mos from diagnosis to 7 yrs
Every 2 yrs from age 7 yrs
| • Retinal exams
Photographic imaging to detect any change early
| Every 1-2 yrs
| Prompt clinical investigation of any signs/symptoms of malignant neoplasms1 |
Source: GeneReviews — "Retinoblastoma"
AVA6103 in Subjects With Locally Advanced or Metastatic Selected Solid Tumors |
PHASE1 |
Avacta Life Sciences Ltd |
RECRUITING |
[NCT05657873](https://clinicaltrials.gov/study/NCT05657873) | A Study of Targeted Radiation Therapy in People With Non-Small Cell Lung Cancer (NSCLC) | PHASE2 | Memorial Sloan Kettering Cancer Center | RECRUITING |
[NCT05234307](https://clinicaltrials.gov/study/NCT05234307) | PBF-1129 and Nivolumab for the Treatment of Recurrent or Metastatic Non-Small Cell Lung Cancer | PHASE1 | Dwight Owen | RECRUITING |
[NCT07276360](https://clinicaltrials.gov/study/NCT07276360) | Hypofractionated Radiotherapy for the Treatment of Locally Advanced Cervical Cancer in Uganda | PHASE2 | Uganda Cancer Institute | RECRUITING |
[NCT07405190](https://clinicaltrials.gov/study/NCT07405190) | Ivonescimab Alone And With Carboplatin/Pemetrexed For NSCLC | PHASE2 | Massachusetts General Hospital | RECRUITING |
427 publications have been identified in PubMed for small cell carcinoma. Research spans Case Report / Case Series (37%), Basic Science / Preclinical (15%), and Review / Meta-Analysis (13%).
Research Type | Count | % of Total |
|---|---|---|
Patient case studies | 157 | 37% |
Laboratory research | 66 | 15% |
Research summaries | 57 | 13% |
Disease patterns and progression | 50 | 12% |
Testing and diagnosis research | 45 | 11% |
Clinical study results | 32 | 7% |
New treatment approaches | 11 | 3% |
Other research | 9 | 2% |
Ozaki K (2026). [PMID: 41930198](https://pubmed.ncbi.nlm.nih.gov/41930198/). *Front Oncol*. [Case Report / Case Series]
Aceto G (2026). [PMID: 42297809](https://pubmed.ncbi.nlm.nih.gov/42297809/). *Nat Commun*. [Basic Science / Preclinical]
Perozziello F (2026). [PMID: 42377929](https://pubmed.ncbi.nlm.nih.gov/42377929/). *Clin Nucl Med*. [Case Report / Case Series]
Kok PS (2026). [PMID: 42293288](https://pubmed.ncbi.nlm.nih.gov/42293288/). *JTO Clin Res Rep*. [Clinical Trial Publication]
Mesmoudi S (2026). [PMID: 42592056](https://pubmed.ncbi.nlm.nih.gov/42592056/). *Oxf Med Case Reports*. [Case Report / Case Series]
Kourie HR (2026). [PMID: 41656191](https://pubmed.ncbi.nlm.nih.gov/41656191/). *BMC Cancer*. [Epidemiology / Natural History]
Al-Snayyan E (2026). [PMID: 41883749](https://pubmed.ncbi.nlm.nih.gov/41883749/). *Front Urol*. [Epidemiology / Natural History]
Reyes A (2026). [PMID: 42291370](https://pubmed.ncbi.nlm.nih.gov/42291370/). *Transl Lung Cancer Res*. [Basic Science / Preclinical]
Wang F (2026). [PMID: 42239895](https://pubmed.ncbi.nlm.nih.gov/42239895/). *Front Oncol*. [Case Report / Case Series]
Babadi M (2026). [PMID: 42291954](https://pubmed.ncbi.nlm.nih.gov/42291954/). *Cureus*. [Case Report / Case Series]
AI-curated news mentioning small cell carcinoma
Updated Oct 20, 2026
Recent research indicates that bladder preservation remains a viable option for patients with the rare aggressive subtype of small cell carcinoma. This finding could influence treatment strategies for this challenging cancer type.