Electrochemotherapy for advanced cutaneous angiosarcoma: A European register-based cohort study from the International Network for Sharing Practices of electrochemotherapy (InspECT).


Journal

International journal of surgery (London, England)
ISSN: 1743-9159
Titre abrégé: Int J Surg
Pays: United States
ID NLM: 101228232

Informations de publication

Date de publication:
Dec 2019
Historique:
received: 03 08 2019
revised: 24 09 2019
accepted: 09 10 2019
pubmed: 17 10 2019
medline: 17 3 2020
entrez: 17 10 2019
Statut: ppublish

Résumé

Cutaneous angiosarcoma (cAS) is a highly aggressive malignancy that challenges the radicality of surgical treatment. Electrochemotherapy (ECT), a skin-directed treatment based on cytotoxic chemotherapy combined with local electric pulses, may be an intraoperative adjunct and a new opportunity in the therapeutic strategy. This cohort study reports the experience with ECT as an option. Data on patients with locally-advanced/metastatic cAS who underwent ECT between October 2013 and October 2018 at eight European centres were prospectively submitted to the InspECT (International network for sharing practices of ECT) register. Patients received therapy according to the European Standard Operating Procedures of ECT (ESOPE). Treatment feasibility was assessed based on tumour coverage with electrodes and recorded tissue current; treatment toxicity and tumour response were graded according to CTCAE v5.0 and RECIST v1.1 criteria, respectively; patient-reported outcomes (PRO) were evaluated using a visual analogue score (VAS) for pain, acceptance of retreatment and the EQ-5D questionnaire. We enrolled 20 patients with advanced cAS in the scalp/face (n = 7), breast/trunk (n = 10) or limbs (n = 3). Target tumours (n = 51) had a median size of 2.3 cm (range, 1-20). We administered 24 ECT courses using 1-4 cm treatment safety margin around tumours. In five patients, ECT was combined/sequenced with surgery. Median tissue current was 3 A (range, 1.5-10), tumour margins coverage rate was 75% (15/20 patients). The objective response rate (ORR) was 80% (complete, 40%). Grade-3 toxicity included skin ulceration (15%) and pain (10%), with no significant change of PRO scores. Bleeding control was achieved in 13/14 patients with ulcerated tumours. With a median overall survival of 12.5 months, the local progression-free survival (LPFS) was 10.9 months. ECT produces sustained response rate with minimal side effects and should be considered an option for advanced cAS. Palliative benefits include patient tolerability, local haemostasis and durable local control. Definition of optimal timing, treatment safety margins and combination with surgery need further investigation.

Sections du résumé

BACKGROUND BACKGROUND
Cutaneous angiosarcoma (cAS) is a highly aggressive malignancy that challenges the radicality of surgical treatment. Electrochemotherapy (ECT), a skin-directed treatment based on cytotoxic chemotherapy combined with local electric pulses, may be an intraoperative adjunct and a new opportunity in the therapeutic strategy. This cohort study reports the experience with ECT as an option.
METHODS METHODS
Data on patients with locally-advanced/metastatic cAS who underwent ECT between October 2013 and October 2018 at eight European centres were prospectively submitted to the InspECT (International network for sharing practices of ECT) register. Patients received therapy according to the European Standard Operating Procedures of ECT (ESOPE). Treatment feasibility was assessed based on tumour coverage with electrodes and recorded tissue current; treatment toxicity and tumour response were graded according to CTCAE v5.0 and RECIST v1.1 criteria, respectively; patient-reported outcomes (PRO) were evaluated using a visual analogue score (VAS) for pain, acceptance of retreatment and the EQ-5D questionnaire.
RESULTS RESULTS
We enrolled 20 patients with advanced cAS in the scalp/face (n = 7), breast/trunk (n = 10) or limbs (n = 3). Target tumours (n = 51) had a median size of 2.3 cm (range, 1-20). We administered 24 ECT courses using 1-4 cm treatment safety margin around tumours. In five patients, ECT was combined/sequenced with surgery. Median tissue current was 3 A (range, 1.5-10), tumour margins coverage rate was 75% (15/20 patients). The objective response rate (ORR) was 80% (complete, 40%). Grade-3 toxicity included skin ulceration (15%) and pain (10%), with no significant change of PRO scores. Bleeding control was achieved in 13/14 patients with ulcerated tumours. With a median overall survival of 12.5 months, the local progression-free survival (LPFS) was 10.9 months.
CONCLUSION CONCLUSIONS
ECT produces sustained response rate with minimal side effects and should be considered an option for advanced cAS. Palliative benefits include patient tolerability, local haemostasis and durable local control. Definition of optimal timing, treatment safety margins and combination with surgery need further investigation.

Identifiants

pubmed: 31618680
pii: S1743-9191(19)30278-X
doi: 10.1016/j.ijsu.2019.10.013
pii:
doi:

Substances chimiques

Antibiotics, Antineoplastic 0
Bleomycin 11056-06-7

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

34-42

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2019 IJS Publishing Group Ltd. Published by Elsevier Ltd. All rights reserved.

Auteurs

Luca G Campana (LG)

Department of Surgical Oncological and Gastroenterological Sciences - DISCOG, University of Padova, Padova, Italy. Electronic address: luca.campana@unipd.it.

Erika Kis (E)

Department of Dermatology and Allergology, University of Szeged, Hungary.

Krisztina Bottyán (K)

Department of Dermatology and Allergology, University of Szeged, Hungary.

Antonio Orlando (A)

Department of Plastic and Reconstructive Surgery, Southmead Hospital, North Bristol NHS Trust, Bristol, UK.

Francesca de Terlizzi (F)

Scientific and Medical Department, IGEA S.p.A., Carpi, Italy.

Grammatiki Mitsala (G)

Department of Plastic and Reconstructive Surgery, Southmead Hospital, North Bristol NHS Trust, Bristol, UK.

Rosanna Careri (R)

Department of Dermatology and Plastic Surgery, Dermatologic Clinic, University 'La Sapienza', Rome, Italy.

Pietro Curatolo (P)

Department of Dermatology and Plastic Surgery, Dermatologic Clinic, University 'La Sapienza', Rome, Italy.

Marko Snoj (M)

Department of Surgical Oncology, Institute of Oncology Ljubljana, Ljubljana, Slovenia.

Gregor Sersa (G)

Department of Experimental Oncology, Institute of Oncology Ljubljana, Ljubljana, Slovenia.

Sara Valpione (S)

The Christie NHS Foundation Trust, CRUK Manchester Institute, The University of Manchester, Manchester, UK.

Pietro Quaglino (P)

Department of Medical Sciences, Dermatologic Clinic, University of Turin, Turin, Italy.

David Mowatt (D)

Plastic Surgery Unit, The Christie NHS Foundation Trust, Manchester, UK.

Matteo Brizio (M)

Department of Medical Sciences, Dermatologic Clinic, University of Turin, Turin, Italy.

Hadrian Schepler (H)

Department of Dermatology, University Medical Center, Mainz, Germany.

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Classifications MeSH