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Transcription regulators and ultra-rare and other rare translocation-related sarcomas treated with trabectedin: A proof of principle from a post-hoc analysis
BACKGROUND: Among sarcomas, which are rare cancers with an incidence of <6 per 100.000/year cases, ultra-rare sarcomas have an incidence of approximately ≤1/1,000,000/year cases and altogether account for ~20% of all soft tissue sarcomas (STS) and bone sarcomas. The Italian Sarcoma Group has rece...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9780071/ https://www.ncbi.nlm.nih.gov/pubmed/36568164 http://dx.doi.org/10.3389/fonc.2022.1042479 |
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author | Palmerini, Emanuela Sanfilippo, Roberta Grignani, Giovanni Buonadonna, Angela Romanini, Antonella Badalamenti, Giuseppe Ferraresi, Virginia Vincenzi, Bruno Comandone, Alessandro Pizzolorusso, Antonio Brunello, Antonella Gelsomino, Fabio De Pas, Tommaso Ibrahim, Toni Gurrieri, Lorena Grosso, Federica Zanelli, Francesca Pantaleo, Maria Abbondanza Milesi, Laura Ciuffreda, Libero Ferrari, Vittorio Marchesi, Emanuela Quattrini, Irene Righi, Alberto Setola, Elisabetta Carretta, Elisa Casali, Paolo G. Picci, Piero Ferrari, Stefano |
author_facet | Palmerini, Emanuela Sanfilippo, Roberta Grignani, Giovanni Buonadonna, Angela Romanini, Antonella Badalamenti, Giuseppe Ferraresi, Virginia Vincenzi, Bruno Comandone, Alessandro Pizzolorusso, Antonio Brunello, Antonella Gelsomino, Fabio De Pas, Tommaso Ibrahim, Toni Gurrieri, Lorena Grosso, Federica Zanelli, Francesca Pantaleo, Maria Abbondanza Milesi, Laura Ciuffreda, Libero Ferrari, Vittorio Marchesi, Emanuela Quattrini, Irene Righi, Alberto Setola, Elisabetta Carretta, Elisa Casali, Paolo G. Picci, Piero Ferrari, Stefano |
author_sort | Palmerini, Emanuela |
collection | PubMed |
description | BACKGROUND: Among sarcomas, which are rare cancers with an incidence of <6 per 100.000/year cases, ultra-rare sarcomas have an incidence of approximately ≤1/1,000,000/year cases and altogether account for ~20% of all soft tissue sarcomas (STS) and bone sarcomas. The Italian Sarcoma Group has recently performed a non-interventional, retrospective TrObs study with data from 512 anthracycline-pretreated patients with advanced multiple STS histologies and treated with trabectedin (Palmerini, Cancers 2021; ClinicalTrials.gov Identifier: NCT02793050). METHODS: A post-hoc analysis of case series to evaluate the efficacy and safety of trabectedin on patients with ultra-rare and other rare translocation-related sarcomas included in TrObs study was performed. Main outcomes comprised investigator-assessed overall response rate (ORR), disease control rate (DCR), progression-free survival (PFS) and safety. RESULTS: Thirty-six patients (18 women) with ultra-rare and other rare sarcoma and a median age of 53.0 years (range: 22-81) were included. Most patients had solitary fibrous tumor (SFT; n=11) followed by epithelioid sarcoma (n=5), malignant peripheral nerve sheath tumor (MPNST; n=4), extraskeletal myxoid chondrosarcoma (EMC; n=3), desmoplastic small round cell tumor (DSRCT; n=3), and alveolar soft part sarcoma (ASPS), rhabdomyosarcoma and clear cell sarcoma (n=2 each). Thirty-five patients had metastatic disease and 23 patients received trabectedin as a second-line treatment. Among 35 patients evaluable for response, two patients with SFT and ASPS had a partial response and one patient with DSRCT obtained a complete response, reaching an ORR of 8.6% (95% CI: 2.8-23.4%). Among patients with an ORR, 6-months PFS was 100% in patients with ASPS, 45.7% in patients with SFT and 33.3% in those with DSRCT. Two patients with epithelioid sarcoma and myoepithelioma had disease stabilization lasting >24 months. Nine patients had at least one grade 3/4 adverse event, mostly being bone marrow toxicity (n=6). CONCLUSIONS: Trabectedin has some anti-tumor activity in some ultra-rare and other rare sarcomas, particularly translocation-related sarcomas, with the well-known manageable safety profile. |
format | Online Article Text |
id | pubmed-9780071 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97800712022-12-24 Transcription regulators and ultra-rare and other rare translocation-related sarcomas treated with trabectedin: A proof of principle from a post-hoc analysis Palmerini, Emanuela Sanfilippo, Roberta Grignani, Giovanni Buonadonna, Angela Romanini, Antonella Badalamenti, Giuseppe Ferraresi, Virginia Vincenzi, Bruno Comandone, Alessandro Pizzolorusso, Antonio Brunello, Antonella Gelsomino, Fabio De Pas, Tommaso Ibrahim, Toni Gurrieri, Lorena Grosso, Federica Zanelli, Francesca Pantaleo, Maria Abbondanza Milesi, Laura Ciuffreda, Libero Ferrari, Vittorio Marchesi, Emanuela Quattrini, Irene Righi, Alberto Setola, Elisabetta Carretta, Elisa Casali, Paolo G. Picci, Piero Ferrari, Stefano Front Oncol Oncology BACKGROUND: Among sarcomas, which are rare cancers with an incidence of <6 per 100.000/year cases, ultra-rare sarcomas have an incidence of approximately ≤1/1,000,000/year cases and altogether account for ~20% of all soft tissue sarcomas (STS) and bone sarcomas. The Italian Sarcoma Group has recently performed a non-interventional, retrospective TrObs study with data from 512 anthracycline-pretreated patients with advanced multiple STS histologies and treated with trabectedin (Palmerini, Cancers 2021; ClinicalTrials.gov Identifier: NCT02793050). METHODS: A post-hoc analysis of case series to evaluate the efficacy and safety of trabectedin on patients with ultra-rare and other rare translocation-related sarcomas included in TrObs study was performed. Main outcomes comprised investigator-assessed overall response rate (ORR), disease control rate (DCR), progression-free survival (PFS) and safety. RESULTS: Thirty-six patients (18 women) with ultra-rare and other rare sarcoma and a median age of 53.0 years (range: 22-81) were included. Most patients had solitary fibrous tumor (SFT; n=11) followed by epithelioid sarcoma (n=5), malignant peripheral nerve sheath tumor (MPNST; n=4), extraskeletal myxoid chondrosarcoma (EMC; n=3), desmoplastic small round cell tumor (DSRCT; n=3), and alveolar soft part sarcoma (ASPS), rhabdomyosarcoma and clear cell sarcoma (n=2 each). Thirty-five patients had metastatic disease and 23 patients received trabectedin as a second-line treatment. Among 35 patients evaluable for response, two patients with SFT and ASPS had a partial response and one patient with DSRCT obtained a complete response, reaching an ORR of 8.6% (95% CI: 2.8-23.4%). Among patients with an ORR, 6-months PFS was 100% in patients with ASPS, 45.7% in patients with SFT and 33.3% in those with DSRCT. Two patients with epithelioid sarcoma and myoepithelioma had disease stabilization lasting >24 months. Nine patients had at least one grade 3/4 adverse event, mostly being bone marrow toxicity (n=6). CONCLUSIONS: Trabectedin has some anti-tumor activity in some ultra-rare and other rare sarcomas, particularly translocation-related sarcomas, with the well-known manageable safety profile. Frontiers Media S.A. 2022-12-08 /pmc/articles/PMC9780071/ /pubmed/36568164 http://dx.doi.org/10.3389/fonc.2022.1042479 Text en Copyright © 2022 Palmerini, Sanfilippo, Grignani, Buonadonna, Romanini, Badalamenti, Ferraresi, Vincenzi, Comandone, Pizzolorusso, Brunello, Gelsomino, De Pas, Ibrahim, Gurrieri, Grosso, Zanelli, Pantaleo, Milesi, Ciuffreda, Ferrari, Marchesi, Quattrini, Righi, Setola, Carretta, Casali, Picci and Ferrari https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Palmerini, Emanuela Sanfilippo, Roberta Grignani, Giovanni Buonadonna, Angela Romanini, Antonella Badalamenti, Giuseppe Ferraresi, Virginia Vincenzi, Bruno Comandone, Alessandro Pizzolorusso, Antonio Brunello, Antonella Gelsomino, Fabio De Pas, Tommaso Ibrahim, Toni Gurrieri, Lorena Grosso, Federica Zanelli, Francesca Pantaleo, Maria Abbondanza Milesi, Laura Ciuffreda, Libero Ferrari, Vittorio Marchesi, Emanuela Quattrini, Irene Righi, Alberto Setola, Elisabetta Carretta, Elisa Casali, Paolo G. Picci, Piero Ferrari, Stefano Transcription regulators and ultra-rare and other rare translocation-related sarcomas treated with trabectedin: A proof of principle from a post-hoc analysis |
title | Transcription regulators and ultra-rare and other rare translocation-related sarcomas treated with trabectedin: A proof of principle from a post-hoc analysis |
title_full | Transcription regulators and ultra-rare and other rare translocation-related sarcomas treated with trabectedin: A proof of principle from a post-hoc analysis |
title_fullStr | Transcription regulators and ultra-rare and other rare translocation-related sarcomas treated with trabectedin: A proof of principle from a post-hoc analysis |
title_full_unstemmed | Transcription regulators and ultra-rare and other rare translocation-related sarcomas treated with trabectedin: A proof of principle from a post-hoc analysis |
title_short | Transcription regulators and ultra-rare and other rare translocation-related sarcomas treated with trabectedin: A proof of principle from a post-hoc analysis |
title_sort | transcription regulators and ultra-rare and other rare translocation-related sarcomas treated with trabectedin: a proof of principle from a post-hoc analysis |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9780071/ https://www.ncbi.nlm.nih.gov/pubmed/36568164 http://dx.doi.org/10.3389/fonc.2022.1042479 |
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