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Short-term Outcomes After Very Low-Dose Intravitreous Bevacizumab for Retinopathy of Prematurity.

Publication ,  Journal Article
Wallace, DK; Kraker, RT; Freedman, SF; Crouch, ER; Bhatt, AR; Hartnett, ME; Yang, MB; Rogers, DL; Hutchinson, AK; VanderVeen, DK; Haider, KM ...
Published in: JAMA Ophthalmol
June 1, 2020

IMPORTANCE: Intravitreous bevacizumab (0.25 mg to 0.625 mg) is commonly used to treat type 1 retinopathy of prematurity (ROP), but there are concerns about systemic toxicity, particularly the risk of neurodevelopmental delay. A much lower dose may be effective for ROP while reducing systemic risk. Previously, after testing doses of 0.25 mg to 0.031 mg, doses as low as 0.031 mg were found to be effective in small cohorts of infants. OBJECTIVE: To find the lowest dose of intravitreous bevacizumab effective for severe ROP. DESIGN, SETTING, AND PARTICIPANTS: Between April 2017 and May 2019, 59 premature infants with type 1 ROP in 1 or both eyes were enrolled in a masked, multicenter, dose de-escalation study. In cohorts of 10 to 14 infants, 1 eye per infant received 0.016 mg, 0.008 mg, 0.004 mg, or 0.002 mg of intravitreous bevacizumab. Diluted bevacizumab was prepared by individual research pharmacies and delivered using 300-µL syringes with 5/16-inch, 30-guage fixed needles. Analysis began July 2019. INTERVENTIONS: Bevacizumab intravitreous injections at 0.016 mg, 0.008 mg, 0.004 mg, or 0.002 mg. MAIN OUTCOMES AND MEASURES: Success was defined as improvement by 4 days postinjection and no recurrence of type 1 ROP or severe neovascularization requiring additional treatment within 4 weeks. RESULTS: Fifty-five of 59 enrolled infants had 4-week outcomes completed; the mean (SD) birth weight was 664 (258) g, and the mean (SD) gestational age was 24.8 (1.6) weeks. A successful 4-week outcome was achieved for 13 of 13 eyes (100%) receiving 0.016 mg, 9 of 9 eyes (100%) receiving 0.008 mg, 9 of 10 eyes (90%) receiving 0.004 mg, but only 17 of 23 eyes (74%) receiving 0.002 mg. CONCLUSIONS AND RELEVANCE: These data suggest that 0.004 mg may be the lowest dose of bevacizumab effective for ROP. Further investigation is warranted to confirm effectiveness of very low-dose intravitreous bevacizumab and its effect on plasma vascular endothelial growth factor levels and peripheral retinal vascularization.

Duke Scholars

Published In

JAMA Ophthalmol

DOI

EISSN

2168-6173

Publication Date

June 1, 2020

Volume

138

Issue

6

Start / End Page

698 / 701

Location

United States

Related Subject Headings

  • Treatment Outcome
  • Retinopathy of Prematurity
  • Retina
  • Receptors, Vascular Endothelial Growth Factor
  • Male
  • Intravitreal Injections
  • Infant, Newborn
  • Infant
  • Humans
  • Follow-Up Studies
 

Citation

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MLA
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Wallace, D. K., Kraker, R. T., Freedman, S. F., Crouch, E. R., Bhatt, A. R., Hartnett, M. E., … Pediatric Eye Disease Investigator Group (PEDIG). (2020). Short-term Outcomes After Very Low-Dose Intravitreous Bevacizumab for Retinopathy of Prematurity. JAMA Ophthalmol, 138(6), 698–701. https://doi.org/10.1001/jamaophthalmol.2020.0334
Wallace, David K., Raymond T. Kraker, Sharon F. Freedman, Eric R. Crouch, Amit R. Bhatt, M Elizabeth Hartnett, Michael B. Yang, et al. “Short-term Outcomes After Very Low-Dose Intravitreous Bevacizumab for Retinopathy of Prematurity.JAMA Ophthalmol 138, no. 6 (June 1, 2020): 698–701. https://doi.org/10.1001/jamaophthalmol.2020.0334.
Wallace DK, Kraker RT, Freedman SF, Crouch ER, Bhatt AR, Hartnett ME, et al. Short-term Outcomes After Very Low-Dose Intravitreous Bevacizumab for Retinopathy of Prematurity. JAMA Ophthalmol. 2020 Jun 1;138(6):698–701.
Wallace, David K., et al. “Short-term Outcomes After Very Low-Dose Intravitreous Bevacizumab for Retinopathy of Prematurity.JAMA Ophthalmol, vol. 138, no. 6, June 2020, pp. 698–701. Pubmed, doi:10.1001/jamaophthalmol.2020.0334.
Wallace DK, Kraker RT, Freedman SF, Crouch ER, Bhatt AR, Hartnett ME, Yang MB, Rogers DL, Hutchinson AK, VanderVeen DK, Haider KM, Siatkowski RM, Dean TW, Beck RW, Repka MX, Smith LE, Good WV, Kong L, Cotter SA, Holmes JM, Pediatric Eye Disease Investigator Group (PEDIG). Short-term Outcomes After Very Low-Dose Intravitreous Bevacizumab for Retinopathy of Prematurity. JAMA Ophthalmol. 2020 Jun 1;138(6):698–701.

Published In

JAMA Ophthalmol

DOI

EISSN

2168-6173

Publication Date

June 1, 2020

Volume

138

Issue

6

Start / End Page

698 / 701

Location

United States

Related Subject Headings

  • Treatment Outcome
  • Retinopathy of Prematurity
  • Retina
  • Receptors, Vascular Endothelial Growth Factor
  • Male
  • Intravitreal Injections
  • Infant, Newborn
  • Infant
  • Humans
  • Follow-Up Studies