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Successful outcome with oral sirolimus treatment for complicated lymphatic malformations: a retrospective multicenter cohort study.
Cho, Yu Jeong; Kwon, Hyunhee; Ha, Suhyeon; Kim, Seong Chul; Kim, Dae Yeon; Namgoong, Jung-Man; Cho, Min Jeng; Lee, Ju Yeon; Jung, Eunyoung; Nam, So Hyun.
Afiliación
  • Cho YJ; Department of Surgery, Hanyang University Guri Hospital, Hanyang University School Medicine, Guri, Korea.
  • Kwon H; Department of Pediatric Surgery, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, Seoul, Korea.
  • Ha S; Department of Pediatric Surgery, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, Seoul, Korea.
  • Kim SC; Department of Pediatric Surgery, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, Seoul, Korea.
  • Kim DY; Department of Pediatric Surgery, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, Seoul, Korea.
  • Namgoong JM; Department of Pediatric Surgery, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, Seoul, Korea.
  • Cho MJ; Department of Surgery, Ulsan University Hospital, University of Ulsan College of Medicine, Ulsan, Korea.
  • Lee JY; Division of Pediatric Surgery, Department of Surgery, Chonnam National University Hospital, Gwangju, Korea.
  • Jung E; Department of Pediatric Surgery, Keimyung University Dongsan Hospital, Daegu, Korea.
  • Nam SH; Department of Surgery, Inje University Busan Paik Hospital, Busan, Korea.
Ann Surg Treat Res ; 106(3): 125-132, 2024 Mar.
Article en En | MEDLINE | ID: mdl-38435495
ABSTRACT

Purpose:

Sirolimus has emerged as a safe and effective treatment for complicated lymphatic malformations (LMs). We aim to prove the effectiveness and safety of sirolimus as a therapeutic option for patients with complicated LMs.

Methods:

Fifty-eight patients with complicated LMs treated with sirolimus for at least 6 months at multicenter between July 2018 and January 2023 were enrolled. All patients were administered oral sirolimus starting at 0.8 mg/m2 every 12 hours, with target serum concentration levels of 8-15 ng/mL. Evaluation for clinical symptoms and LMs volume on MRI were reviewed to assess treatment response and toxicities. Evaluation of disease response was divided into 3 values complete response, partial response (significant, moderate, and modest), and progressive disease.

Results:

The median age at the initiation of sirolimus treatment was 6.0 years (range, 1 month-26.7 years). The median duration of treatment was 2.0 years (range, 6 months-4.4 years). The most common lesions were head and neck (25 of 58, 43.1%). Forty-six patients (79.3%) demonstrated a reduction in LMs volume on MRI or improvement of clinical symptoms including 2 complete responses. The young age group and the patients who underwent few prior therapies showed better responses. None of the patients had toxicities attributable to sirolimus with a Common Terminology Criteria for Adverse Events grade of ≥3.

Conclusion:

Oral sirolimus treatment brought a successful outcome without severe adverse effects. It could be the first-line therapy, especially for the young age group of complicated LMs, and an additional option for refractory lesions that did not respond to conventional treatment.
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Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Ann Surg Treat Res Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Ann Surg Treat Res Año: 2024 Tipo del documento: Article