Postoperative complications and oncologic outcomes after multimodal therapy of localized high risk soft tissue sarcoma.


Journal

Radiation oncology (London, England)
ISSN: 1748-717X
Titre abrégé: Radiat Oncol
Pays: England
ID NLM: 101265111

Informations de publication

Date de publication:
21 Dec 2022
Historique:
received: 26 07 2022
accepted: 21 11 2022
entrez: 21 12 2022
pubmed: 22 12 2022
medline: 24 12 2022
Statut: epublish

Résumé

Standard therapy for localized high-risk soft tissue sarcoma includes surgical resection and neoadjuvant or adjuvant radiation therapy (± chemotherapy and locoregional hyperthermia). No difference in oncologic outcomes for patients treated with neoadjuvant and adjuvant radiation therapy was reported, whereas side effect profiles differ. The aim of this analysis was to analyse oncologic outcomes and postoperative complications in patients treated with multimodal treatment. Oncologic outcomes and major wound complications (MWC, subclassified as wound healing disorder, infection, abscess, fistula, seroma and hematoma) were evaluated in 74 patients with localized high-risk soft tissue sarcoma of extremities and trunk undergoing multimodal treatment, and also separately for the subgroup of lower extremity tumors. Clinical factors and treatment modalities (especially neoadjuvant vs. adjuvant radiotherapy) were evaluated regarding their prognostic value and impact on postoperative wound complications. Oncologic outcomes were dependent on number of high risk features (tumor size, depth to superficial fascia and grading), but not on therapy sequencing (however with higher risk patients in the neoadjuvant group). Different risk factors influenced different subclasses of wound healing complications. Slightly higher MWC-rates were observed in patients treated with neoadjuvant therapy, compared to adjuvant radiotherapy, although only with a trend to statistical significance (31.8% vs. 13.3%, p = 0.059). However, except for wound infections, no significant difference for other subclasses of postoperative complications was observed between neoadjuvant and adjuvant therapy. Diabetes was confirmed as a major risk factor for immune-related wound complications. Rates of major wound complications in this cohort are comparable to published data, higher rates of wound infections were observed after neoadjuvant radiotherapy. Tumor localization, patient age and diabetes seem to be major risk factors. The number of risk factors for high risk soft tissue sarcoma seem to influence DMFS. Neoadjuvant treatment increases the risk only for wound infection treated with oral or intravenous antibiotic therapy and appears to be a safe option at an experienced tertiary center in absence of other risk factors.

Sections du résumé

BACKGROUND BACKGROUND
Standard therapy for localized high-risk soft tissue sarcoma includes surgical resection and neoadjuvant or adjuvant radiation therapy (± chemotherapy and locoregional hyperthermia). No difference in oncologic outcomes for patients treated with neoadjuvant and adjuvant radiation therapy was reported, whereas side effect profiles differ. The aim of this analysis was to analyse oncologic outcomes and postoperative complications in patients treated with multimodal treatment.
METHODS METHODS
Oncologic outcomes and major wound complications (MWC, subclassified as wound healing disorder, infection, abscess, fistula, seroma and hematoma) were evaluated in 74 patients with localized high-risk soft tissue sarcoma of extremities and trunk undergoing multimodal treatment, and also separately for the subgroup of lower extremity tumors. Clinical factors and treatment modalities (especially neoadjuvant vs. adjuvant radiotherapy) were evaluated regarding their prognostic value and impact on postoperative wound complications.
RESULTS RESULTS
Oncologic outcomes were dependent on number of high risk features (tumor size, depth to superficial fascia and grading), but not on therapy sequencing (however with higher risk patients in the neoadjuvant group). Different risk factors influenced different subclasses of wound healing complications. Slightly higher MWC-rates were observed in patients treated with neoadjuvant therapy, compared to adjuvant radiotherapy, although only with a trend to statistical significance (31.8% vs. 13.3%, p = 0.059). However, except for wound infections, no significant difference for other subclasses of postoperative complications was observed between neoadjuvant and adjuvant therapy. Diabetes was confirmed as a major risk factor for immune-related wound complications.
CONCLUSION CONCLUSIONS
Rates of major wound complications in this cohort are comparable to published data, higher rates of wound infections were observed after neoadjuvant radiotherapy. Tumor localization, patient age and diabetes seem to be major risk factors. The number of risk factors for high risk soft tissue sarcoma seem to influence DMFS. Neoadjuvant treatment increases the risk only for wound infection treated with oral or intravenous antibiotic therapy and appears to be a safe option at an experienced tertiary center in absence of other risk factors.

Identifiants

pubmed: 36544149
doi: 10.1186/s13014-022-02166-4
pii: 10.1186/s13014-022-02166-4
pmc: PMC9768905
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

210

Subventions

Organisme : Deutsche Krebshilfe
ID : 70114187

Informations de copyright

© 2022. The Author(s).

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Auteurs

Vlatko Potkrajcic (V)

Department of Radiation Oncology, Eberhard-Karls-University Tuebingen, Hoppe-Seyler-Str. 3, 72076, Tübingen, Germany. vlatko.potkrajcic@med.uni-tuebingen.de.

Jonas Kolbenschlag (J)

Department of Hand, Plastic, Reconstructive and Burn Surgery, BG Unfallklinik, Eberhard-Karls-University Tuebingen, Schnarrenbergstraße 95, 72076, Tübingen, Germany.

Saskia Sachsenmaier (S)

Department of Orthopaedic Surgery, Eberhard-Karls-University Tuebingen, Hoppe-Seyler-Str. 3, 72076, Tübingen, Germany.

Adrien Daigeler (A)

Department of Hand, Plastic, Reconstructive and Burn Surgery, BG Unfallklinik, Eberhard-Karls-University Tuebingen, Schnarrenbergstraße 95, 72076, Tübingen, Germany.

Ruth Ladurner (R)

Department of General, Visceral and Transplant Surgery, Eberhard-Karls-University Tuebingen, Hoppe Seyler-Str. 3, 72076, Tübingen, Germany.

Alexander Golf (A)

Department of Internal Medicine, Medical Oncology and Pulmonology, Eberhard-Karls-University Tuebingen, Otfried-Müller-Straße 14, 72076, Tuebingen, Germany.

Cihan Gani (C)

Department of Radiation Oncology, Eberhard-Karls-University Tuebingen, Hoppe-Seyler-Str. 3, 72076, Tübingen, Germany.

Daniel Zips (D)

Department of Radiation Oncology, Eberhard-Karls-University Tuebingen, Hoppe-Seyler-Str. 3, 72076, Tübingen, Germany.
German Cancer Research Center (DKFZ), German Cancer Consortium (DKTK) Partnersite Tuebingen, Heidelberg, Germany.
Department of Radiation Oncology and Radiotherapy, Charité University Hospital, Charitépl. 1, 10117, Berlin, Germany.

Frank Paulsen (F)

Department of Radiation Oncology, Eberhard-Karls-University Tuebingen, Hoppe-Seyler-Str. 3, 72076, Tübingen, Germany.

Franziska Eckert (F)

Department of Radiation Oncology, Eberhard-Karls-University Tuebingen, Hoppe-Seyler-Str. 3, 72076, Tübingen, Germany.
Department of Radiation Oncology, Comprehensive Cancer Center, Medical University Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.

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