High-risk soft tissue sarcomas treated with perioperative chemotherapy: Improving prognostic classification in a randomised clinical trial

Patients with extremity and trunk wall soft tissue sarcoma (STS) with high malignancy grade and size >5 cm are at high-risk of death. This risk varies depending also on other patient and tumour features, including histologic subtype. This study investigated whether a prognostic nomogram can impro...

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Veröffentlicht in:European journal of cancer (1990) 2018-04, Vol.93, p.28-36
Hauptverfasser: Pasquali, Sandro, Colombo, Chiara, Pizzamiglio, Sara, Verderio, Paolo, Callegaro, Dario, Stacchiotti, Silvia, Martin Broto, Javier, Lopez-Pousa, Antonio, Ferrari, Stefano, Poveda, Andres, De Paoli, Antonino, Quagliuolo, Vittorio, Jurado, Josefina Cruz, Comandone, Alessandro, Grignani, Giovanni, De Sanctis, Rita, Palassini, Elena, Llomboart-Bosch, Antonio, Dei Tos, Angelo Paolo, Casali, Paolo G., Picci, Piero, Gronchi, Alessandro
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Sprache:eng
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Zusammenfassung:Patients with extremity and trunk wall soft tissue sarcoma (STS) with high malignancy grade and size >5 cm are at high-risk of death. This risk varies depending also on other patient and tumour features, including histologic subtype. This study investigated whether a prognostic nomogram can improve risk assessment of these patients. Data from high-risk STS patients enrolled in a randomised controlled trial investigating different perioperative chemotherapy regimens were analysed. Ten-year probability of overall survival (OS) and incidence of distant metastasis (DM) were computed using the prognostic nomogram Sarculator (pr-OS and inc-DM, respectively). Tumour response according to RECIST and Choi criteria was also investigated. Variation in pr-OS and inc-DM were observed and patients stratified in three prognostic groups. The 10-year OS in the low, intermediate, and high pr-OS categories were 0·42 (95%CI 0·32–0·52), 0·63 (95%CI 0·53–0·72), and 0·78 (95%CI 0·68–0·85), respectively. Patients in the intermediate (HR 0·51, P = 0·002) and high (HR 0·28, P 
ISSN:0959-8049
1879-0852
DOI:10.1016/j.ejca.2018.01.071