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SHR Neuro Krebs Kardio Lipid Stoffw Microb

Collaud, S; Stork, T; Adamkova, D; Aigner, C; Bravio, I; Brunello, A; Cerbone, L; Clermidy, H; De Cock, L; Gasperoni, S; Girard, N; Mariuk-Jarema, A; Lefering, R; Melis, E; Marquina, G; Mazzeo, F; Mykoliuk, I; Pantaleo, MA; Penel, N; Schildhaus, HU; Strippoli, S; Vincenzi, B; Watson, S; Blay, JY; Bauer, S.
Outcome of patients with curative-intent treatment for primary pulmonary sarcoma: Results from an international multicenter retrospective study
JTCVS OPEN. 2025; 28: 565-573. Doi: 10.1016/j.xjon.2025.06.024 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Co-Autor*innen der Med Uni Graz
Mykoliuk Iurii
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Abstract:
OBJECTIVE: To evaluate outcome and prognostic factors of patients with primary pulmonary sarcoma (PPS) who underwent curative-intent surgery within multimodality treatment. METHODS: An international, multicenter, retrospective study including patients with PPS was performed through a network of sarcoma experts. Data on demographics, staging, treatment, and outcomes were retrieved. Overall survival was calculated from the date of diagnosis. Prognostic factors were assessed using uni- and multivariate analysis. RESULTS: Eighteen centers from 9 countries contributed, for a total of 173 patients. One hundred fifteen patients (66%) underwent curative-intent surgery within multimodality treatment. There were 58 male patients (50%). Twenty-two patients (20%) had metastases, mainly to lung (n = 7, 30%) and pleura (n = 9, 39%). Thirty-three patients (30%) underwent preoperative chemotherapy. Extent of lung resection was sublobar (n = 11, 10%), lobar (n = 58, 54%), or bilobar/pneumonectomy (n = 39, 36%). Median tumor size was 85 mm. Sixty-nine patients had grade 3 tumors (71%). Resection was complete in 85 patients (75%). Lymphadenectomy was performed in 70 patients (63%), with nodal involvement in 10 (14%). Thirty-seven (37%) patients received adjuvant chemotherapy, and 27 (27%) patients received adjuvant radiotherapy. Overall survival was 49% and 31% at 5 and 10 years, respectively. Median follow-up was 33 months. Male gender (P = .003), age older than 60 years (P = .021), presence of metastasis (P = . 002), tumor size >40 mm (P = . 046), and incomplete resections (P = . 008) were independent prognostic factors for poor survival. CONCLUSIONS: In patients with curative-intent multimodal treatment for PPS, an encouraging 5-year survival rate of 49% can be achieved in expert centers. Independent prognostic factors may aid in selecting patients for curative treatment.

Find related publications in this database (Keywords)
primary pulmonary sarcoma
surgery
EURACAN
chemotherapy
radiotherapy
outcome
soft-tissue sarcoma
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