Outcome of patients with curative-intent treatment for primary pulmonary sarcoma: Results from an international multicenter retrospective study

. 2025 Dec ; 28 () : 565-573. [epub] 20250926

Status PubMed-not-MEDLINE Jazyk angličtina Země Nizozemsko Médium electronic-ecollection

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid41473068
Odkazy

PubMed 41473068
PubMed Central PMC12745123
DOI 10.1016/j.xjon.2025.06.024
PII: S2666-2736(25)00323-7
Knihovny.cz E-zdroje

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.

Département d'Oncologie Médicale Centre Léon Bérard Lyon France

Department of Clinical Oncology Cliniques Universitaires Saint Luc Institut Roi Albert 2 Université Catholique de Louvain Brussels Belgium

Department of Comprehensive Cancer Care Masaryk Memorial Cancer Institute and Faculty of Medicine Masaryk University Brno Czech Republic

Department of General Medical Oncology University Hospitals Leuven Leuven Cancer Institute Leuven Belgium

Department of Medical Oncology and Sarcoma Center West German Cancer Center University Hospital Essen Essen Germany

Department of Medical Oncology Centre Oscar Lambret University of Lille Lille France

Department of Medical Oncology Department of Medicine Hospital Clínico San Carlos School of Medicine Instituto de Investigación Sanitaria Madrid Spain

Department of Medicine and Surgery Università Campus Bio Medico di Roma Roma Italy

Department of Oncology Clinical Oncology Unit University Hospital Careggi Firenze Italy

Department of Soft Tissue Bone Sarcoma and Melanoma Maria Sklodowska Curie National Research Institute of Oncology Warsaw Poland

Department of Thoracic Surgery Francisco Gentil Portuguese Institute of Oncology Lisboa Portugal

Department of Thoracic Surgery Louis Pradel Hospital Hospices Civils de Lyon Lung and Heart Lung Transplantation Lyon France

Department of Thoracic Surgery Medical University of Vienna Vienna Austria

Department of Thoracic Surgery University of Witten Herdecke Kliniken der Stadt Koeln Lung Clinic Cologne Germany

Discovery Life Sciences Biomarker GmbH und Pathologie Nordhessen Kassel Deutschland

Division of Thoracic Surgery and Hyperbaric Surgery Department of Surgery Medical University of Graz Graz Austria

Institut du Thorax Curie Montsouris Institut Curie Paris France

Institute for Research in Operative Medicine University Witten Herdecke Cologne Germany

Laboratory of Experimental Oncology KU Leuven Leuven Cancer Institute Leuven Belgium

Medical Oncology 1 Unit Istituto Oncologico Veneto IOV IRCCS Padova Italy

Medical Oncology Department and INSERM U1339 CNRS UMR 3666 Institut Curie Paris France

Oncology Unit IRCCS AOUBO Bologna Italy

Operative Research Unit of Medical Oncology Fondazione Policlinico Universitario Campus Bio Medico Roma Italy

SSD Mesotelioma melanoma e tumori rari Azienda Ospedaliera Universitaria SS Antonio e Biagio e Cesare Arrigo Alessandria Italy

Thoracic Surgery Unit IRCCS National Cancer Institute Regina Elena Rome Italy

Unità Operativa Tumori Rari e Melanoma 1 R C C S Istituto Tumori Giovanni Paolo 2 Bari Italy

Zobrazit více v PubMed

Collaud S., Stork T., Schildhaus H.U., et al. Multimodality treatment including surgery for primary pulmonary sarcoma: size does matter. J Surg Oncol. 2020;122(3):506–514. doi: 10.1002/jso.25979. PubMed DOI

Sbaraglia M., Bellan E., Dei Tos A.P. The 2020 WHO Classification of. Soft Tissue Tumours: news and perspectives. Pathologica. 2021;113(2):70–84. doi: 10.32074/1591-951X-213. PubMed DOI PMC

Trojani M., Contesso G., Coindre J.M., et al. Soft-tissue sarcomas of adults; study of pathological prognostic variables and definition of a histopathological grading system. Int J Cancer. 1984;33(1):37–42. doi: 10.1002/ijc.2910330108. PubMed DOI

Robinson L.A., Babacan N.A., Tanvetyanon T., Henderson-Jackson E., Bui M.M., Druta M. Results of treating primary pulmonary sarcomas and pulmonary carcinosarcomas. J Thorac Cardiovasc Surg. 2021;162(1):274–284. doi: 10.1016/j.jtcvs.2020.03.179. PubMed DOI

Petrov D.B., Vlassov V.I., Kalaydjiev G.T., et al. Primary pulmonary sarcomas and carcinosarcomas—postoperative results and comparative survival analysis. Eur J Cardiothorac Surg. 2003;23(4):461–466. doi: 10.1016/S1010-7940(03)00024-1. PubMed DOI

Spraker M.B., Bair E., Bair R., Connell P.P., Mahmood U., Koshy M. An analysis of patient characteristics and clinical outcomes in primary pulmonary sarcoma. J Thorac Oncol. 2013;8(2):147–151. doi: 10.1097/JTO.0b013e318277401f. PubMed DOI

Huang Q., Li W., He X., et al. Prognostic visualization model for primary pulmonary sarcoma: a SEER-based study. Sci Rep. 2023;13(1):17774. doi: 10.1038/s41598-023-45058-7. PubMed DOI PMC

Gu H., Song R., Beeraka N.M., et al. SEER-based survival nomogram (1998-2015) based on “stage, lymph node dissection, tumor size and degree of differentiation, and therapies” for prognosis of primary pulmonary sarcoma. Technol Cancer Res Treat. 2023;22 doi: 10.1177/15330338221150732. 15330338221150732. PubMed DOI PMC

EURACAN Mission and goals. https://www.euracan.eu/about-us/about-euracan

Janssen J.P., Mulder J.J.S., Wagenaar S.S., Elbers H.R.J., van den Bosch J.M.M. Primary sarcoma of the lung: a clinical study with long-term follow-up. Ann Thorac Surg. 1994;58(4):1151–1155. doi: 10.1016/0003-4975(94)90476-6. PubMed DOI

Regnard J.F., Icard P., Guibert L., de Montpreville V.T., Magdeleinat P., Levasseur P. Prognostic factors and results after surgical treatment of primary sarcomas of the lung. Ann Thorac Surg. 1999;68(1):227–231. doi: 10.1016/S0003-4975(99)00398-7. PubMed DOI

Porte H.L., Metois D.G., Leroy X., Conti M., Gosselin B., Wurtz A. Surgical treatment of primary sarcoma of the lung. Eur J Cardiothorac Surg. 2000;18(2):136–142. doi: 10.1016/S1010-7940(00)00465-6. PubMed DOI

Etienne-Mastroianni B., Falchero L., Chalabreysse L., et al. Primary sarcomas of the lung: a clinicopathologic study of 12 cases. Lung Cancer. 2002;38(3):283–289. doi: 10.1016/S0169-5002(02)00303-3. PubMed DOI

Bacha E.A., Wright C.D., Grillo H.C., et al. Surgical treatment of primary pulmonary sarcomas. Eur J Cardiothorac Surg. 1999;15(4):456–460. doi: 10.1016/S1010-7940(99)00045-7. PubMed DOI

Collaud S., Stork T., Adámková Krákorová D., et al. 1732P Primary pulmonary sarcoma: a EURACAN project. Ann Oncol. 2024;35:S1037. doi: 10.1016/S0923-7534(24)03343-X. DOI

Yamada Y., Kaplan T., Soltermann A., et al. Surgical outcomes and risk analysis of primary pulmonary sarcoma. Thorac Cardiovasc Surg. 2021;69(1):101–108. doi: 10.1055/s-0039-1695784. PubMed DOI

Coindre J.M., Terrier P., Guillou L., et al. Predictive value of grade for metastasis development in the main histologic types of adult soft tissue sarcomas: a study of 1240 patients from the French Federation of Cancer Centers Sarcoma Group. Cancer. 2001;91(10):1914–1926. doi: 10.1002/1097-0142(20010515)91:10<1914::AID-CNCR1214>3.0.CO;2-3. PubMed DOI

Gamboa A.C., Gronchi A., Cardona K. Soft-tissue sarcoma in adults: an update on the current state of histiotype-specific management in an era of personalized medicine. CA Cancer J Clin. 2020;70(3):200–229. doi: 10.3322/caac.21605. PubMed DOI

Hashimoto H., Daimaru Y., Takeshita S., Tsuneyoshi M., Enjoji M. Prognostic significance of histologic parameters of soft tissue sarcomas. Cancer. 1992;70(12):2816–2822. PubMed

Lewis J.J., Leung D., Woodruff J.M., Brennan M.F. Retroperitoneal soft-tissue sarcoma: analysis of 500 patients treated and followed at a single institution. Ann Surg. 1998;228(3):355–365. doi: 10.1097/00000658-199809000-00008. PubMed DOI PMC

Gronchi A., Miah A.B., Dei Tos A.P., et al. Soft tissue and visceral sarcomas: ESMO-EURACAN-GENTURIS Clinical Practice Guidelines for diagnosis, treatment and follow-up(∗) Ann Oncol. 2021;32(11):1348–1365. doi: 10.1016/j.annonc.2021.07.006. PubMed DOI

Pasquali S., Pizzamiglio S., Touati N., et al. The impact of chemotherapy on survival of patients with extremity and trunk wall soft tissue sarcoma: revisiting the results of the EORTC-STBSG 62931 randomised trial. Eur J Cancer. 2019;109:51–60. doi: 10.1016/j.ejca.2018.12.009. PubMed DOI

Callegaro D., Miceli R., Bonvalot S., et al. Impact of perioperative chemotherapy and radiotherapy in patients with primary extremity soft tissue sarcoma: retrospective analysis across major histological subtypes and major reference centres. Eur J Cancer. 2018;105:19–27. doi: 10.1016/j.ejca.2018.09.028. PubMed DOI

von Mehren M., Randall R.L., Benjamin R.S., et al. Soft tissue sarcoma, version 2.2018, NCCN clinical practice guidelines in oncology. J Natl Compr Canc Netw. 2018;16(5):536–563. doi: 10.6004/jnccn.2018.0025. PubMed DOI

Transatlantic Australasian Retroperitoneal Sarcoma Working Group. https://tarpswg.org

Najít záznam

Citační ukazatele

Pouze přihlášení uživatelé

Možnosti archivace

Nahrávání dat ...