A multi‐institutional feasibility study of intra‐arterial chemotherapy in children with retinoblastoma. A Children's Oncology Group study (COG ARET12P1)

Author:

Chintagumpala Murali1ORCID,Piao Jin2,Gombos Dan3,Chevez‐Barrios Patricia4,Brock Lindsay5,Dunkel Ira J.6ORCID,Jubran Rima7ORCID,Leahey Ann M.8,Kim Jonathan9,O'Brien Joan10,Shields Carol L.11,Rodriguez‐Galindo Carlos12ORCID

Affiliation:

1. Division of Hematology‐Oncology Department of Pediatrics Texas Children's Cancer Center Baylor College of Medicine Houston Texas USA

2. Keck School of Medicine University of Southern California Los Angeles California USA

3. Department of Head and Neck Surgery Section of Ophthalmology University of Texas MD Anderson Cancer Center Houston Texas USA

4. Departments of Pathology and Genomic Medicine and Ophthalmology Houston Methodist Hospital Houston Texas USA

5. Children's Oncology Group Monrovia California USA

6. Department of Pediatrics Memorial Sloan Kettering Cancer Center New York New York USA

7. Department of Pediatrics Division of Hematology‐Oncology Cancer and Blood Disease Institute Children's Hospital Los Angeles Los Angeles California USA

8. Division of Oncology Children's Hospital of Philadelphia Philadelphia Pennsylvania USA

9. Kaiser Permanente Orange County California USA

10. Scheie Eye Institute Perelman School of Medicine University of Pennsylvania Philadelphia USA

11. Ocular Oncology Service Wills Eye Hospital Thomas Jefferson University Philadelphia Pennsylvania USA

12. Departments of Oncology and Global Pediatric Medicine St Jude Children's Research Hospital Memphis Tennessee USA

Abstract

AbstractBackgroundIntra‐arterial chemotherapy (IA) as a treatment to salvage the eye with advanced retinoblastoma is increasingly utilized based on successes reported by institutions around the world mainly through retrospective studies.ObjectiveTo study the feasibility of delivering melphalan directly into the ophthalmic artery in a multi‐institutional prospective study in children with newly diagnosed unilateral group D retinoblastoma.MethodsThe Children's Oncology Group (COG) initiated study ARET12P1 in 2014 and was open to nine institutions. Eligible patients older than six months of age were enrolled. The feasibility of delivering three injections of melphalan into the ophthalmic artery every 28 days was assessed.ResultsNine institutions participated in this trial. Fourteen patients were enrolled, two of whom were unevaluable for feasibility. Four patients experienced a feasibility failure. In two patients, the ophthalmic artery could not be accessed for the second IA injection, in one the artery could not be accessed for the first injection, and one patient experienced grade 4 hypotension during the procedure.ConclusionDelivery of prescribed therapy within the context of this study did not meet the feasibility goals of the study with only a 67% feasibility success rate. These results should caution centers that plan to initiate this treatment and suggest investment in training to achieve technical expertise or referral to centers with expertise.

Funder

National Cancer Institute

St. Baldrick's Foundation

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

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