Single-Center Experience with Trabectedin for the Treatment of Non-L-sarcomas.


Journal

Advances in therapy
ISSN: 1865-8652
Titre abrégé: Adv Ther
Pays: United States
ID NLM: 8611864

Informations de publication

Date de publication:
04 2022
Historique:
received: 29 11 2021
accepted: 17 01 2022
pubmed: 8 2 2022
medline: 12 4 2022
entrez: 7 2 2022
Statut: ppublish

Résumé

The effectiveness of trabectedin for the treatment of leiomyosarcoma and liposarcoma (commonly referred to as L-sarcomas) has been widely evidenced in clinical trials and real-world studies. Nevertheless, available literature on non-L-sarcomas is less abundant. The objective of the present study is to evaluate the effectiveness and safety of trabectedin in a cohort of patients with non-L-sarcomas in the real-world setting. This retrospective, observational study included 34 patients who received trabectedin in the Hospital de la Santa Creu i Sant Pau (Barcelona, Spain) between October 2013 and July 2020. The most frequent histologic subtypes were undifferentiated spindle cell/pleomorphic sarcoma (n = 11, 32.4%), synovial sarcoma (n = 6, 17.7%), myxofibrosarcoma (n = 5, 14.7%), and malignant peripheral nerve sheath tumor (n = 4, 11.8%). The mean number of cycles with trabectedin was 5.5 (range 2-28). Three patients achieved partial response (8.8%) and eight patients showed stable disease (23.5%). The objective response rate and disease control rate were 8.8% (95% confidence interval (CI), 95% CI 1.9-23.7) and 32.4% (95% CI 17.4-50.5), respectively. Overall, progression-free survival was 2.9 months (95% CI 2.1-3.4). The overall survival was 7.3 months (95% CI 4.7-12.8). The most common trabectedin-related grade 3 adverse events were observed in 10 patients (26.5%), mostly being neutropenia (14.7%) and elevated transaminases (5.9%), whereas one patient (2.9%) reported grade 4 febrile neutropenia that required hospitalization. The findings of this real-life study consistently support that trabectedin is an effective and safe option for the treatment of patients with non-L-sarcoma after failure of anthracyclines and ifosfamide, or in patients who are unsuited to receive these agents.

Identifiants

pubmed: 35129790
doi: 10.1007/s12325-022-02051-2
pii: 10.1007/s12325-022-02051-2
doi:

Substances chimiques

Antineoplastic Agents, Alkylating 0
Dioxoles 0
Tetrahydroisoquinolines 0
Trabectedin ID0YZQ2TCP

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Pagination

1596-1610

Informations de copyright

© 2022. The Author(s), under exclusive licence to Springer Healthcare Ltd., part of Springer Nature.

Références

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Auteurs

Paula Cerdà Serdà (P)

Medical Oncology Department, Hospital de la Santa Creu i Sant Pau, Carrer de Sant Quintí, 89, 08041, Barcelona, Spain. pcerda@santpau.cat.

Raúl Terés (R)

Medical Oncology Department, Hospital de la Santa Creu i Sant Pau, Carrer de Sant Quintí, 89, 08041, Barcelona, Spain.

Ana Sebio (A)

Medical Oncology Department, Hospital de la Santa Creu i Sant Pau, Carrer de Sant Quintí, 89, 08041, Barcelona, Spain.

Silvia Bagué (S)

Department of Pathology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.

Ruth Orellana (R)

Department of Pathology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.

María E Moreno (ME)

Pharmacy Department, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.

Mireia Riba (M)

Pharmacy Department, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.

Antonio López-Pousa (A)

Medical Oncology Department, Hospital de la Santa Creu i Sant Pau, Carrer de Sant Quintí, 89, 08041, Barcelona, Spain.

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