Preoperative hypofractionated radiotherapy for soft tissue sarcomas: a systematic review

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Preoperative hypofractionated radiotherapy for soft tissue sarcomas: a systematic review. / Roohani, Siyer; Ehret, Felix; Kobus, Marta; Flörcken, Anne; Märdian, Sven; Striefler, Jana Käthe; Rau, Daniel; Öllinger, Robert; Jarosch, Armin; Budach, Volker; Kaul, David.

In: RADIAT ONCOL, Vol. 17, No. 1, 159, 14.09.2022.

Research output: SCORING: Contribution to journalSCORING: Review articleResearch

Harvard

Roohani, S, Ehret, F, Kobus, M, Flörcken, A, Märdian, S, Striefler, JK, Rau, D, Öllinger, R, Jarosch, A, Budach, V & Kaul, D 2022, 'Preoperative hypofractionated radiotherapy for soft tissue sarcomas: a systematic review', RADIAT ONCOL, vol. 17, no. 1, 159. https://doi.org/10.1186/s13014-022-02072-9

APA

Roohani, S., Ehret, F., Kobus, M., Flörcken, A., Märdian, S., Striefler, J. K., Rau, D., Öllinger, R., Jarosch, A., Budach, V., & Kaul, D. (2022). Preoperative hypofractionated radiotherapy for soft tissue sarcomas: a systematic review. RADIAT ONCOL, 17(1), [159]. https://doi.org/10.1186/s13014-022-02072-9

Vancouver

Bibtex

@article{50393b57272b42839cc66903fd78af3b,
title = "Preoperative hypofractionated radiotherapy for soft tissue sarcomas: a systematic review",
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 × 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.",
keywords = "Humans, Prospective Studies, Radiation Dose Hypofractionation, Retrospective Studies, Sarcoma/radiotherapy, Soft Tissue Neoplasms/radiotherapy",
author = "Siyer Roohani and Felix Ehret and Marta Kobus and Anne Fl{\"o}rcken and Sven M{\"a}rdian and Striefler, {Jana K{\"a}the} and Daniel Rau and Robert {\"O}llinger and Armin Jarosch and Volker Budach and David Kaul",
note = "{\textcopyright} 2022. The Author(s).",
year = "2022",
month = sep,
day = "14",
doi = "10.1186/s13014-022-02072-9",
language = "English",
volume = "17",
journal = "RADIAT ONCOL",
issn = "1748-717X",
publisher = "BioMed Central Ltd.",
number = "1",

}

RIS

TY - JOUR

T1 - Preoperative hypofractionated radiotherapy for soft tissue sarcomas: a systematic review

AU - Roohani, Siyer

AU - Ehret, Felix

AU - Kobus, Marta

AU - Flörcken, Anne

AU - Märdian, Sven

AU - Striefler, Jana Käthe

AU - Rau, Daniel

AU - Öllinger, Robert

AU - Jarosch, Armin

AU - Budach, Volker

AU - Kaul, David

N1 - © 2022. The Author(s).

PY - 2022/9/14

Y1 - 2022/9/14

N2 - 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 × 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.

AB - 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 × 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.

KW - Humans

KW - Prospective Studies

KW - Radiation Dose Hypofractionation

KW - Retrospective Studies

KW - Sarcoma/radiotherapy

KW - Soft Tissue Neoplasms/radiotherapy

U2 - 10.1186/s13014-022-02072-9

DO - 10.1186/s13014-022-02072-9

M3 - SCORING: Review article

C2 - 36104789

VL - 17

JO - RADIAT ONCOL

JF - RADIAT ONCOL

SN - 1748-717X

IS - 1

M1 - 159

ER -