Your browser doesn't support javascript.
loading
Baseline characteristics and treatment response predictive of nAMD outcomes with ranibizumab therapy in treatment-naive patients: the RACER subgroup analysis.
Tsai, Ching-Yao; Wu, Chien-Liang; Cheng, Cheng-Kuo; Shen, Yun-Dun; Wu, Wen-Chuan; Wu, Pei-Chang; Tsai, Arslan; Chen, Jiann-Torng.
  • Tsai CY; Taipei City Hospital, Taipei City, Taiwan.
  • Wu CL; Institute of Public Health, National Yang Ming Chiao Tung University, Taipei City, Taiwan.
  • Cheng CK; Department of Business Administration, Fu Jen Catholic University, New Taipei City, Taiwan.
  • Shen YD; Municipal Wan Fang Hospital, Taipei City, Taiwan.
  • Wu WC; Shin Kong Wu Ho-Su Memorial Hospital, Taipei City, Taiwan.
  • Wu PC; Taipei Medical University-Shung Ho Hospital, New Taipei City, Taiwan.
  • Tsai A; Kang-Ning General Hospital, Taipei City, Taiwan.
  • Chen JT; Kaohsiung Medical University Chung-Ho Memorial Hospital, Kaohsiung City, Taiwan.
BMC Ophthalmol ; 23(1): 39, 2023 Jan 27.
Article en En | MEDLINE | ID: mdl-36707779
ABSTRACT

BACKGROUND:

The Ranibizumab AMD Clinical Efficacy Study (RACER) conducted in treatment-naive adult Taiwanese patients with neovascular age-related macular degeneration (nAMD) suggested the importance of early and intensive dosing of ranibizumab for optimal treatment outcomes. This subgroup analysis aims to provide clinical information on treatment response that can potentially guide on maintaining the treatment or switching anti-VEGF agents in the real-world setting.

METHODS:

Visual acuity (VA) and central retinal thickness (CRT) were assessed in the RACER subgroup population. Subgroup analysis sets were categorised based on (1) baseline best-corrected VA (BCVA; ≤ 48 and > 48 letters); (2) baseline CRT (≤ 325 or > 325 µm); and (3) treatment response after three monthly initial injections < or ≥ 5-letter gain in BCVA and reduction of < or ≥ 50 µm in CRT.

RESULTS:

Patient age, sex, nAMD duration and number of ranibizumab injections did not differ significantly between the treatment subgroups. Poor baseline BCVA (≤ 48 letters) and baseline CRT severity (> 325 µm) were predictors of maximum BCVA gains (9.6 ± 12.9 letters [95%CI 6.3 to 12.9] and 5.1 ± 18.3 letters [95%CI - 0.5 to 10.8] at Months 3 and 12, respectively) and better CRT reductions (- 127.6 ± 104.2 µm and - 104.2 ± 107.4 µm at Months 3 and 12, respectively; both P < 0.001). For the subgroup showing favourable treatment improvement with BCVA gains ≥ 5 letters after three monthly initial injections, 75.6% of patients maintained follow-up at Month 12 with a mean of 6.5 ± 14.3 letter gains (95% CI 1.2 to 11.7). The BCVA gains < 5-letter subgroup nevertheless had stable BCVA (0.4 ± 12.1 letter gains) and CRT (- 41.9 ± 61.2 µm) at Month 12, respectively. In the subgroup with ≥ 50 µm CRT reduction after three monthly initial injections, there are significantly higher BCVA improvements vs. the < 50 µm CRT reduction subgroup at Month 3 (5.0 ± 8.6 letter gains vs. 1.5 ± 11.6 letter gains, respectively; intergroup P = 0.005).

CONCLUSION:

Lower baseline BCVA and higher baseline CRT were associated with BCVA gains and CRT reductions throughout the 12-month study period. Early CRT improvements after three monthly initial injections were associated with BCVA gains as early as Month 3.
Asunto(s)
Palabras clave

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Inhibidores de la Angiogénesis / Ranibizumab Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Adult / Humans Idioma: En Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Inhibidores de la Angiogénesis / Ranibizumab Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Adult / Humans Idioma: En Año: 2023 Tipo del documento: Article