Gemcitabine Re-challenge in Metastatic Soft Tissue Sarcomas: A Therapeutic Option for Selected Patients.


Journal

Anticancer research
ISSN: 1791-7530
Titre abrégé: Anticancer Res
Pays: Greece
ID NLM: 8102988

Informations de publication

Date de publication:
Jan 2019
Historique:
received: 25 11 2018
revised: 06 12 2018
accepted: 07 12 2018
entrez: 29 12 2018
pubmed: 29 12 2018
medline: 8 1 2019
Statut: ppublish

Résumé

Treatment options for patients with metastatic soft tissue sarcomas are limited. Re-challenge with a previously successful gemcitabine-based regimen is common. There are no published data to support this practice. We conducted a retrospective search to identify patients re-challenged with gemcitabine-based chemotherapy (GBC) from 2003 to 2015. Twenty-nine patients re-challenged with gemcitabine were identified. The response rate for initial GBC was 55% (n=15) and for re-challenge GBC 26% (n=6). The median progression-free survival was 11.1 months (95%CI=7.2-11.9) for initial GBC and 5.3 months (95%CI=2.0-7.5) for re-challenge GBC. Overall survival following gemcitabine re-challenge was 12.2 months (95%CI=7.0-18.2). Twelve out of 26 evaluable patients (46%) treated with re-challenge GBC experienced grade 3-4 adverse events (CTCAE 4.03) with 31% (n=8) of patients requiring dose reduction. In selected patients, gemcitabine re-challenge can be considered in advanced sarcomas, however, this approach is associated with toxicity.

Sections du résumé

BACKGROUND/AIM OBJECTIVE
Treatment options for patients with metastatic soft tissue sarcomas are limited. Re-challenge with a previously successful gemcitabine-based regimen is common. There are no published data to support this practice.
PATIENTS AND METHODS METHODS
We conducted a retrospective search to identify patients re-challenged with gemcitabine-based chemotherapy (GBC) from 2003 to 2015.
RESULTS RESULTS
Twenty-nine patients re-challenged with gemcitabine were identified. The response rate for initial GBC was 55% (n=15) and for re-challenge GBC 26% (n=6). The median progression-free survival was 11.1 months (95%CI=7.2-11.9) for initial GBC and 5.3 months (95%CI=2.0-7.5) for re-challenge GBC. Overall survival following gemcitabine re-challenge was 12.2 months (95%CI=7.0-18.2). Twelve out of 26 evaluable patients (46%) treated with re-challenge GBC experienced grade 3-4 adverse events (CTCAE 4.03) with 31% (n=8) of patients requiring dose reduction.
CONCLUSION CONCLUSIONS
In selected patients, gemcitabine re-challenge can be considered in advanced sarcomas, however, this approach is associated with toxicity.

Identifiants

pubmed: 30591479
pii: 39/1/347
doi: 10.21873/anticanres.13118
doi:

Substances chimiques

Deoxycytidine 0W860991D6
Gemcitabine 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

347-351

Informations de copyright

Copyright© 2019, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.

Auteurs

Ana Sebio (A)

Sarcoma Unit, Royal Marsden Hospital, London, U.K.

Anastasia Constantinidou (A)

Sarcoma Unit, Royal Marsden Hospital, London, U.K.
Medical School, University of Cyprus, Nicosia, Cyprus.

Charlotte Benson (C)

Sarcoma Unit, Royal Marsden Hospital, London, U.K.

Georgios Antoniou (G)

Sarcoma Unit, Royal Marsden Hospital, London, U.K.

Christina Messiou (C)

Sarcoma Unit, Royal Marsden Hospital, London, U.K.
Institute of Cancer Research, London, U.K.

Aisha Miah (A)

Sarcoma Unit, Royal Marsden Hospital, London, U.K.

Shane Zaidi (S)

Sarcoma Unit, Royal Marsden Hospital, London, U.K.

Ann Petruckevitch (A)

Statistics Department, Royal Marsden Hospital, London, U.K.

Omar Al-Muderis (O)

Sarcoma Unit, Royal Marsden Hospital, London, U.K.

Khin Thway (K)

Sarcoma Unit, Royal Marsden Hospital, London, U.K.
Institute of Cancer Research, London, U.K.

Winette T VAN DER Graaf (WT)

Sarcoma Unit, Royal Marsden Hospital, London, U.K.
Institute of Cancer Research, London, U.K.

Robin L Jones (RL)

Sarcoma Unit, Royal Marsden Hospital, London, U.K. robin.jones4@nhs.net.
Institute of Cancer Research, London, U.K.

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Classifications MeSH