Clinical Trial Finder

Inclusion Criteria:

1. The patient's guardian signs an informed consent form and is willing to receive follow-up according to the schedule of the trial; 2. Children of more than 3 months and under 5 years of age who have not received any anti-cancer treatment; 3. The target eye must meet the following requirements: Clinically diagnosed as monocular retinoblastoma; According to the IIRC diagnostic criteria, the treatment eye is classified as Group E stage without clinical high-risk factors (Table 1); No refractive medium turbidity and/or pupillary abnormalities that affect the fundus examination; IOP≤21mmHg. 4. Sufficient organ function at baseline.

Exclusion Criteria:

Subjects with any of the following eye conditions: 1. Patients diagnosed as stage E retinoblastoma in one eye, but with high-risk factors: neovascular glaucoma; refractive interstitial opacity caused by anterior chamber, vitreous or subretinal hemorrhage; tumor invasion of optic nerve posterior to the cribriform plate and choroid (range of diameter> 2 mm), sclera, and anterior chamber; 2. Treatment-naïve pediatric patients; Patients with any of the following systemic diseases: 1. With a history of allergies or have allergic reactions to fluorescein sodium, with a history of allergies to protein products for treatment or diagnosis, and have allergic reactions to two or more drugs and/or non-drug factors, or suffering from allergic diseases; 2. Low birth weight children, and severely growth-stunted children; 3. Children who need systemic treatment for other system diseases; 4. Any condition that should be excluded from the study in the opinion of the investigator.

Arms

Experimental: Conbercept intravitreal Injection

Interventions

Drug: - Conbercept ophthalmic injection

Monthly injection of Conbercept from 0~5 months