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NCT04342572CompletedPhase 1

Intra-arterial Chemotherapy for Retinoblastoma

Intra-arterial Chemotherapy for Retinoblastoma (IAC)

Source: ClinicalTrials.gov · Last updated 11 May 2025

Brief summary (registry, in English)

Children with retinoblastoma who may benefit from intra-arterial chemotherapy will receive up to 3 doses of melphalan and will be assessed for feasibility, toxicity, and response.

Status (registry)
Completed
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
5 (actual)
First submitted
8 Apr 2020
Start date
11 Aug 2020
Primary completion date
4 Jan 2023
Lead sponsor
Washington University School of Medicine
NCT number
NCT04342572

What you commit to

  • Study type: Interventional · Phase 1
  • Participants enrolled: 5
  • From 11 Aug 2020 to the primary completion date, 4 Jan 2023
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • New or recurrent retinoblastoma that can be controlled with other conservative measures such as cryotherapy, thermotherapy, or plaque radiotherapy.
  • Patients who would benefit from systemic chemotherapy.
  • Currently receiving any other investigational agents.

Other illness

  • A history of allergic reactions attributed to compounds of similar chemical or biologic composition to melphalan or other agents used in the study.
  • Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, or cardiac arrhythmia.

Lab values

  • Patients with HIV are eligible unless their CD4+ T-cell counts are \< 350 cells/mcL or they have a history of AIDS-defining opportunistic infection within the 12 months prior to registration. Concurrent treatment with effective ART according to DHHS treatment guidelines is recommended.

Other

  • Opaque or hazy media which precluded visualization of the fundus.
  • Unilateral COG group E retinoblastoma (refer to Appendix A) with very poor visual prognosis as defined by pediatric ophthalmologist.
  • Patients with clinical or radiological evidence suggestive of retinoblastoma invasion of the optic nerve, choroid, sclera, orbit or metastatic sites.
  • Pregnant and/or breastfeeding. Participants of childbearing potential must have a negative pregnancy test within 14 days of study entry.

Who the study is looking for

  • Patients diagnosed with retinoblastoma \>4 months of age16
  • Patients whose other treatment options would require systemic chemotherapy, radiotherapy, or enucleation
  • Patient or parent/legal guardian must sign a written informed consent
  • One of a, b, or c:
    • Patients who have bilateral COG stage B, C, D, or E retinoblastoma (refer to Appendix A) who have undergone systemic chemotherapy without resolution (meaning either has not had CR or has progressed despite systemic chemotherapy) and would have the following treatment options remaining:
    • IAC
    • enucleation of one eye
    • local radiation
    • Patients with non-germline retinoblastoma with unilateral disease who have COG A, B, C, or D tumors (refer to Appendix A).
    • Other patients may be considered on a case by case basis after discussion with pediatric ophthalmology, hematology/oncology, and interventional neuroradiology.

Age in the registry: 4 months to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Washington University School of Medicine/Saint Louis Children's Hospital
Coordinator of this site? Confirm its status
St LouisUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.