dc.contributor.author
Roohani, Siyer
dc.contributor.author
Ehret, Felix
dc.contributor.author
Kobus, Marta
dc.contributor.author
Flörcken, Anne
dc.contributor.author
Märdian, Sven
dc.contributor.author
Striefler, Jana Käthe
dc.contributor.author
Rau, Daniel
dc.contributor.author
Öllinger, Robert
dc.contributor.author
Jarosch, Armin
dc.contributor.author
Budach, Volker
dc.contributor.author
Kaul, David
dc.date.accessioned
2024-02-15T12:50:23Z
dc.date.available
2024-02-15T12:50:23Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/42434
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-42158
dc.description.abstract
Background: Soft tissue sarcomas (STS) represent a diverse group of rare malignant tumors. Currently, five to six weeks of preoperative radiotherapy (RT) combined with surgery constitute the mainstay of therapy for localized high-grade sarcomas (G2-G3). Growing evidence suggests that shortening preoperative RT courses by hypofractionation neither increases toxicity rates nor impairs oncological outcomes. Instead, shortening RT courses may improve therapy adherence, raise cost-effectiveness, and provide more treatment opportunities for a wider range of patients. Presumed higher rates of adverse effects and worse outcomes are concerns about hypofractionated RT (HFRT) for STS. This systematic review summarizes the current evidence on preoperative HFRT for the treatment of STS and discusses toxicity and oncological outcomes compared to normofractionated RT.
Methods: We conducted a systematic review of clinical trials describing outcomes for preoperative HFRT in the management of STS using PubMed, the Cochrane library, the Cochrane Central Register of Controlled Trials, ClinicalTrials.gov, Embase, and Ovid Medline. We followed the 2020 Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. Trials on retroperitoneal sarcomas, postoperative RT, and hyperthermia were excluded. Articles published until November 30th, 2021, were included.
Results: Initial search yielded 94 articles. After removal of duplicate and ineligible articles, 13 articles qualified for analysis. Eight phase II trials and five retrospective analyses were reviewed. Most trials applied 5 x 5 Gy preoperatively in patients with high-grade STS. HFRT courses did not show increased rates of adverse events compared to historical trials of normofractionated RT. Toxicity rates were mostly comparable or lower than in trials of normofractionated RT. Moreover, HFRT achieved comparable local control rates with shorter duration of therapy. Currently, more than 15 prospective studies on HFRT + / - chemotherapy are ongoing.
Conclusions: Retrospective data and phase II trials suggest preoperative HFRT to be a reasonable treatment modality for STS. Oncological outcomes and toxicity profiles were favorable. To date, our knowledge is mostly derived from phase II data. No randomized phase III trial comparing normofractionated and HFRT in STS has been published yet. Multiple ongoing phase II trials applying HFRT to investigate acute and late toxicity will hopefully bring forth valuable findings.
en
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
Soft tissue sarcoma
en
dc.subject
Radiotherapy
en
dc.subject
Hypofractionation
en
dc.subject
Preoperative radiotherapy
en
dc.subject
Neoadjuvant radiotherapy
en
dc.subject
Wound complications
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
dc.title
Preoperative hypofractionated radiotherapy for soft tissue sarcomas: a systematic review
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.articlenumber
159
dcterms.bibliographicCitation.doi
10.1186/s13014-022-02072-9
dcterms.bibliographicCitation.journaltitle
Radiation Oncology
dcterms.bibliographicCitation.number
1
dcterms.bibliographicCitation.originalpublishername
Springer Nature
dcterms.bibliographicCitation.volume
17
refubium.affiliation
Charité - Universitätsmedizin Berlin
refubium.funding
Springer Nature DEAL
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.bibliographicCitation.pmid
36104789
dcterms.isPartOf.eissn
1748-717X