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    INTREPID identifies ‘best responders’

    Fewer anti-VEGF injections among benefits of stereotactic radiotherapy for wet AMD

    The INTREPID trial results showed a significant benefit of stereotactic radiotherapy for reducing the need for further anti-vascular endothelial growth factor (VEGF) injections in eyes with active exudative age-related macular degeneration. Post-hoc responder analyses identified baseline characteristics associated with further reduction in need for anti-VEGF injections along with visual acuity benefits.

    By Cheryl Guttman Krader

    Reviewed by Timothy L. Jackson, PhD, FRCOphth

    London—Patients undergoing stereotactic radiotherapy for wet age-related macular degeneration (AMD) may experience a reduced need for anti-vascular endothelial growth factor (VEGF) injections, along with visual acuity benefits.

    Findings from post-hoc analyses of data collected through 12 months in the INTREPID trial indicate eyes with lesions that are actively leaking, fully within the radiotherapy treatment zone, and without significant fibrosis achieve the greatest benefit. The randomized, sham-controlled, double-masked trial is investigating stereotactic radiotherapy using a proprietary device (IRay, Oraya) in patients receiving anti-VEGF injections for AMD.

    “These ‘best responders’ represent about 25% to 50% of the enrolled population, depending on the number of defining criteria used,” said Timothy L. Jackson, PhD, FRCOphth, consultant ophthalmic surgeon, King’s College Hospital, London. “Overall, the data indicate that they can expect to need about 50% fewer anti-VEGF injections over the course of a year following the radiotherapy and achieve significantly better visual acuity improvements than their counterparts receiving anti-VEGF monotherapy.

    “However, these subset analyses need to be interpreted with caution and, of course, further follow-up is needed,” he added.

    The stereotactic radiotherapy is delivered using a slit lamp-type system. It delivers three X-ray beams that pass through the inferior sclera and overlap at the macula, coalescing over a 4-mm zone.

    Patient enrollment

    Patients were eligible to be enrolled in INTREPID if they had exudative AMD diagnosed within the past 3 years, had received at least three anti-VEGF injections in the prior year, were deemed to require further anti-VEGF therapy, and had a lesion measuring 6 mm or less.

    A total of 230 patients were randomly assigned to three groups to receive radiotherapy with a 16-Gy dose, 24-Gy dose, or sham exposure. The radiotherapy was administered as a one-time treatment and patients were seen monthly thereafter. Need for further anti-VEGF injection (ranibizumab; Lucentis, Genentech) was assessed based on predefined re-treatment criteria.

    For the responder analysis, eyes with actively leaking lesions were defined as those with macular volume >7.4 mm2, the macular volume which represented the median volume for the study population. Within this particular subgroup, patients who received stereotactic radiotherapy had a 45% reduction in the number of anti-VEGF injections received during the first 12 months of INTREPID along with a 5-letter greater gain in best-corrected visual acuity (BCVA) compared with the sham-treated controls.

    As a reference in the overall study population, stereotactic radiotherapy significantly reduced the number of anti-VEGF injections needed, but by only 32%, and was associated with a 1.6 letter BCVA benefit, which was not statistically significant.

    Eyes with both macular volume >7.4 mm2 and lesion diameter <4 mm represented about one-fourth of the study population. Within this subgroup, the radiotherapy-treated eyes required 54% fewer anti-VEGF injections than the sham-treated controls and had close to a 7-letter greater gain in visual acuity.

    Among eyes with lesions that were both actively leaking and that was within the treatment zone, only 20% of those receiving radiotherapy compared with 70% of controls received four or more anti-VEGF injections over the course of 12 months; while 100% of control eyes received at least one additional anti-VEGF injection after the mandatory baseline treatment, only 33% of the eyes in the radiation arm required anti-VEGF re-treatment, Dr. Jackson noted.OT

     

    FYI

    Timothy L. Jackson, PhD, FRCOphth

    E-mail: [email protected]

    Dr. Jackson receives lecture fees and grant support from Oraya. The proprietary stereotactic radiotherapy device is CE marked and investigational in the United States. This article is adapted from Dr. Jackson’s presentation at Retina 2012 during the annual meeting of the American Academy of Ophthalmology.

    Cheryl Guttman Krader
    Cheryl Guttman Krader is a contributor to Dermatology Times, Ophthalmology Times, and Urology Times.

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