Purpose: To determine the significance of both massive choroidal invasion and optic nerve invasion (retrolaminar [(RL]+cut end [CE]) as a criterion for classifying high metastatic potential retinoblastoma and their relationship with other known histopathological high-risk features. Methods: A retrospective review of 650 eyes diagnosed as retinoblastoma over a 10-year period. In our study, there is male predominance and a higher percentage of the poorly differentiated tumors. The age of most of the patients ranges from 1 month to 8 years with a median age of 2 years. Results: There were 24% of eyes with massive choroidal invasion and 18% of eyes with optic nerve invasion up to the cut end. On performing Cox-proportional hazard analysis, it was found that massive choroidal invasion in association with optic nerve invasion up to the cut end was an independent prognostic parameter. On Kaplan-Meier analysis, overall survival had reduced in patients having both massive choroidal invasion and an optic nerve cut end invasion along with orbital invasion (P < .05). Conclusion: The presence of massive choroidal invasion in association with optic nerve cut end invasion (RL+CE) could be used as a better prognostic predictor in assessing retinoblastoma patients with high metastatic potential and need to be kept for longer follow up. K E Y W O R D S histopathological high-risk factors, massive choroidal invasion, optic nerve invasion (retrolaminar+cut end), overall survival, retinoblastoma 1 INTRODUCTION Retinoblastoma (RB) is the most common intraocular tumor detected in early childhood with an annual incidence of 1 in 16 000-18 000 live births. The incidence of RB in the United States has been reported to involve 12.14 cases per million. According to Yahaya et al, the incidence of RB in developing countries is still higher compared to the developed countries. 1 It develops in response to the inactivation of the tumor suppressor gene RB1. RB can be unilateral or bilateral and may show either endophytic or exophytic growth. 2 Most patients are symptomatic with signs of leukocoria and strabismus, redness, decreased vision, orbital cellulitis, proptosis, lacrimation, and so on. 3 Parameters like massive choroidal invasion, scleral invasion, and optic nerve infiltration up to the resected end, iris, and ciliary body invasion are considered as histopathological high-risk factors (HRFs) in RB, which are associated with tumor progression, metastasis, and recurrence. Identification of HRFs may help in improving patient's survival. 4 With the advancement in early diagnosis, the treatment of RB patients has improved. The treatment of RB is based upon the age of the child, laterality, and extent of disease. 5 There are several e100 c