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March 4, 2026Drug Design Development and Therapy0 citationsOpen Access

Anti-Vascular Endothelial Growth Factor Combined with Dexamethasone Implant Therapy for Macular Edema: A Randomized Controlled Trial

YMYunxi MaJWJunwen WangMYMingzhu Yuan

Key Points

  • This research aims to evaluate the efficacy and safety of conbercept combined with dexamethasone versus conbercept alone for macular edema.
  • Randomized controlled trial design with 70 patients assigned to monotherapy or combination therapy.
  • Initial 12-week treatment with either conbercept alone or in combination with dexamethasone implant.
  • Follow-up assessments every 4 weeks for 48 weeks, focusing on best-corrected visual acuity and optical coherence tomography biomarkers.
  • Combination therapy showed improved best-corrected visual acuity and reduced central macular thickness at early follow-up points.
  • Fewer total injections were required for the combined treatment (P < 0.001), though there was a higher incidence of ocular hypertension.
  • Correlation exists between outcomes and the presence of hard exudate, indicating potential prognostic implications.

Abstract

Purpose: To compare the efficacy and safety of intravitreal conbercept monotherapy versus conbercept combined with dexamethasone implant in eyes with macular edema (ME). Methods: Patients diagnosed with ME secondary to diabetic retinopathy or retinal vein occlusion were enrolled and randomized 1:1 to the combined or monotherapy group. In initial 12 weeks, the combined group received 1 loading dose of conbercept concomitantly with dexamethasone implant (DEX), while the monotherapy group received 3 monthly loading doses of conbercept. Following initial phases, all patients received intravitreal injections of conbercept on demand, assessed every 4 weeks over a 48-week follow-up period. The primary outcome measure was changes in best-corrected visual acuity (BCVA). Secondary outcome measures encompassed changes in optical coherence tomography (OCT) biomarkers and the total number of injections administered. Clinical safety was evaluated based on the incidence and severity of adverse events. Results: 70 patients (70 eyes) were randomized to monotherapy (n=36) or combination therapy (n=34). Mean (SD) baseline BCVA and CMT were 44.60 (7.34) letters and 555.55 (150.87) μm in monotherapy group; 37.61 (13.47) letters and 581.80 (145.87) μm in combined group. The combined group showed greater BCVA improvement by week 8 and CMT reduction at weeks 4 and 8, and OCT biomarkers also improved more substantially during the first 12 weeks. The combination therapy required significantly fewer injections (P < 0.001) overall but a higher incidence of ocular hypertension. Outcomes of BCVA and CMT correlated with Hard Exudate (HE). Conclusion: Conbercept combined with DEX is an efficient and safe treatment for ME by providing accelerated visual and anatomical improvements in short term and maintaining similar long-term efficacy with fewer injections compared to conbercept monotherapy. OCT biomarkers display prognostic value. HE is associated with poor visual prognosis. Keywords: conbercept, dexamethasone implant, combination therapy, optical coherence tomography, biomarkers

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Cite This Study

Ma et al. (2026) studied this question.

synapsesocial.com/papers/69a7cc9fd48f933b5eed84ddhttps://doi.org/10.2147/dddt.s587166
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