Objective: The purpose of the study is to investigate chemoreduction a
nd adjuvant treatment (AT) for retinoblastoma and its effect on comple
te retinal tumor control, vitreous seed control, and subretinal seed c
ontrol. Design: The study design was a prospective, nonrandomized clin
ical trial. Participants: There were 130 intraocular retinoblastomas i
n 52 eyes of 32 consecutive patients observed for at least 1 year afte
r initiation of treatment. Intervention: Treatment with chemoreduction
using vincristine, etoposide, and carboplatin (VEC) and adjuvant trea
tment (+ AT) (cryotherapy, laser photocoagulation, thermotherapy, chem
othermotherapy, plaque radiation therapy, or external beam radiation t
herapy) were assessed. Main Outcome Measures: The effect of chemoreduc
tion for 6 cycles (VEC x 6) versus fewer than 6 cycles (VEC x < 6) on
retinoblastoma control was analyzed. Furthermore, the impact of adjuva
nt treatment (+ AT) versus no adjuvant treatment (no AT) on retinoblas
toma control was analyzed. Results: Retinal tumors showed favorable in
itial regression with chemoreduction. Adjuvant treatment was applied t
o 93% of the retinal tumors after chemoreduction and only 2% recurred
over the mean follow-up of 17 months (range 13-27 months). Vitreous se
eds and subretinal seeds showed initial regression and often complete
disappearance with chemoreduction. In those eyes with seeds before tre
atment, the addition of AT to VEC for 6 cycles decreased the vitreous
seed recurrence from 75% to 0% (P = 0.04) and also decreased the subre
tinal seed recurrence from 67% to 0% (P = 0.003). More important, when
considering that enucleation or external beam radiation therapy was t
he only other treatment option for these 52 eyes, the authors were suc
cessful in avoiding these methods in 42% of cases. Of the 36 eyes clas
sified as Reese-Ellsworth group 5, there was 78% ocular salvage, and e
xternal beam radiation therapy was avoided in 25% of these eyes. There
was a 100% ocular salvage in the group 5 eyes that received VEC for 6
cycles + AT to retinal tumors and seeds. Conclusions: Chemoreduction
and AT to intraocular retinoblastoma and its seeds provides good retin
al tumor control, even in eyes with advanced disease. Chemoreduction a
lone generally is not adequate to achieve complete tumor seed control.
Cautious follow-up of affected patients is recommended because the ri
sk for recurrent vitreous and subretinal seeds is substantial and prop
er treatment is critical for salvaging the eye.