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A systematic review of the safety and efficacy of currently used treatment modalities in the treatment of patients with PIK3CA-related overgrowth spectrum

  • Sarah M. Bernhard
  • , Luise Adam
  • , Hady Atef
  • , Dario Häberli
  • , Wichor M. Bramer
  • , Beatrice Minder
  • , Yvonne Döring
  • , Jessica E. Laine
  • , Taulant Muka
  • , Jochen Rössler
  • , Iris Baumgartner*
  • *Corresponding author for this work
  • Swiss Cardiovascular Center (Bern)
  • University of Bern
  • Cairo University
  • Institute of Social and Preventive Medicine (Bern)
  • Klinikum der Universität München
  • Partner Site Munich
  • University Hospital Bern

Research output: Contribution to journalReview articleAcademicpeer-review

9 Citations (Scopus)
107 Downloads (Pure)

Abstract

Background: PIK3CA (activating mutations of the p110α subunit of phosphatidylinositol 3-kinases)-related overgrowth spectrums (PROS) include a variety of clinical presentations that are associated with hypertrophy of different parts of the body. We performed a systematic literature review to assess the current treatment options and their efficacy and safety for PROS. Methods: A literature search was performed in Embase, MEDLINE (Ovid), Web of Science Core Collection, Cochrane Central Register of Controlled Trials, ClinicalTrials.gov, and Google Scholar to retrieve studies on the treatment of hypertrophy in PROS. Randomized controlled trials, cohort studies, and case series with ≥10 patients were included in the present review. The titles, abstracts, and full text were assessed by two reviewers independently. The risk of bias was assessed using the Newcastle-Ottawa scale. Results: We included 16 studies of the treatment of hypertrophy in PROS patients, 13 (81.3%) from clinical retrospective studies and 3 (13.7%) from prospective cohort studies. The risk of bias grade was low for 2, medium for 12, and high for 2 studies. Of the 16 studies, 13 reported on surgical treatment and 3 reported pharmacologic treatment using phosphatidylinositol-3-kinase (PI3K)/mammalian target of rapamycin (mTOR) pathway inhibitors in PROS patients. In 3 studies, PROS was defined by a mutation in the PIK3CA gene, and 13 studies relied on a clinical definition of PROS. Surgical therapy was beneficial for a specific subgroup of PROS (macrodactyly). However, little has been reported concerning surgery and the potential benefits for other PROS entities. The reported side effects after surgical therapy were mostly prolonged wound healing or scarring. PI3K/mTOR pathway inhibition was beneficial in patients with PROS by reducing hypertrophy and systemic symptoms. The adverse effects reported included infection, changes in blood count, liver enzymes, and metabolic measures. Conclusions: Surgery is a locally limited treatment option for specific types of PROS. A promising treatment option for PROS is pharmacologic PIK3CA inhibition. However, the level of evidence on the treatment of overgrowth in PROS patients is limited.

Original languageEnglish
Pages (from-to)527-538.e2
JournalJournal of Vascular Surgery: Venous and Lymphatic Disorders
Volume10
Issue number2
Early online date2 Aug 2021
DOIs
Publication statusPublished - 1 Mar 2022

Bibliographical note

Funding Information:
The work was funded by Swiss National Research Foundation CRSII5_193694 2021-2024 (PI: Prof. I. Baumgartner).

Publisher Copyright:
© 2021 The Authors

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