Isolated thoracic perfusion in lung metastases from breast cancer: a retrospective observational study.


Journal

Updates in surgery
ISSN: 2038-3312
Titre abrégé: Updates Surg
Pays: Italy
ID NLM: 101539818

Informations de publication

Date de publication:
Mar 2019
Historique:
received: 17 09 2018
accepted: 05 12 2018
pubmed: 14 12 2018
medline: 30 7 2019
entrez: 14 12 2018
Statut: ppublish

Résumé

The median overall survival of metastatic breast cancer (MBC) patients is still approximately 2 years. This is even lower in triple-negative breast cancer (TNBC) patients with concomitant lung metastases. These patients are often not suitable for surgery and not responsive to systemic chemotherapy. Isolated thoracic perfusion (ITP) followed by chemofiltration has been used for palliation in selected specialised centres. A retrospective observational study evaluating 162 MBC patients who underwent 407 ITP procedures was performed. The primary objective was the evaluation of the feasibility, safety, tolerability and efficacy of ITP in the complete cohort of 162 patients with LM from breast cancer. The secondary objective of the study was the evaluation of responses and median survivals in 43 TNBC patients with LM. In the 162 patients, ITP appeared safe and well tolerated with MST from LM diagnosis to death or last contact of 19.5 months. In the subgroup of patients treated with systemic chemotherapy followed by ITP at progression, the MST from LM diagnosis to death or last contact was 29 months. In the subgroup of TNBC patients treated with systemic chemotherapy followed by ITP at progression, the MST from LM diagnosis to death or last contact was 19 months (ITP overall response rate was 65.52%). ITP followed by chemofiltration could be adopted in the sequential palliation treatments of BC patients with LM in progression after systemic chemotherapy, especially with TNBC. The present data allow interesting considerations about tolerability and responses, but do not allow robust conclusions about survival.

Identifiants

pubmed: 30542956
doi: 10.1007/s13304-018-00613-0
pii: 10.1007/s13304-018-00613-0
doi:

Substances chimiques

Mitomycin 50SG953SK6
Cisplatin Q20Q21Q62J

Types de publication

Journal Article Observational Study

Langues

eng

Pagination

165-177

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Auteurs

Stefano Guadagni (S)

Department of Applied Clinical Sciences and Biotechnology, University of L'Aquila, via Vetoio, 67100, L'Aquila, Italy. stefano.guadagni@univaq.it.

Karl Aigner (K)

Department of Surgical Oncology, Medias Klinikum, Burghausen, Germany.

Odisseas Zoras (O)

Department of Surgical Oncology, University of Crete, Heraklion, Greece.

Francesco Masedu (F)

Department of Applied Clinical Sciences and Biotechnology, University of L'Aquila, via Vetoio, 67100, L'Aquila, Italy.

Giammaria Fiorentini (G)

Department of Oncology and Hematology, Ospedali Riuniti Marche Nord, Pesaro, Italy.

Enrico Ricevuto (E)

Department of Applied Clinical Sciences and Biotechnology, University of L'Aquila, via Vetoio, 67100, L'Aquila, Italy.

Marcello Deraco (M)

Peritoneal Surface Malignancies Unit, Colon and Rectal Surgery, Fondazione IRCCS Istituto Nazionale Tumori, Milan, Italy.

Marco Clementi (M)

Department of Life, Health and Environmental Sciences, University of L'Aquila, L'Aquila, Italy.

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