The efficacy of eribulin mesylate for patients with cutaneous angiosarcoma previously treated with taxane: a multicentre prospective observational study.


Journal

The British journal of dermatology
ISSN: 1365-2133
Titre abrégé: Br J Dermatol
Pays: England
ID NLM: 0004041

Informations de publication

Date de publication:
11 2020
Historique:
accepted: 18 03 2020
pubmed: 22 3 2020
medline: 15 5 2021
entrez: 22 3 2020
Statut: ppublish

Résumé

Taxanes are the current first-line treatment for advanced cutaneous angiosarcoma (CAS) for patients who are considered difficult to treat with doxorubicin owing to advanced age or comorbidity. However, no effective second-line therapy for such patients has been established. We designed a single-arm prospective observational study of eribulin mesylate (ERB) administered at a dose of 1·4 mg m We enrolled a total of 25 patients. The median OS and PFS were 8·6 months and 3·0 months, respectively. The best overall RR was 20% (five of 25). In total, 16 grade 3/4 severe adverse events (SAEs) occurred; however, all patients recovered. Patients who achieved partial response or stable disease as best response had longer OS than those with progressive disease (median OS not reached and 3·3 months, respectively; P < 0·001). Patients who did not experience SAEs showed longer OS than those who did (median OS 18·8 months and 7·5 months, respectively; P < 0·05). Patients with distant metastasis had shorter median OS than those with locoregional disease, but without statistically significant difference. ERB showed a promising RR and is a potential candidate for second-line treatment for patients with CAS, after treatment with taxanes. However, owing to the occurrence of SAEs in over half of the participants, caution should be exercised regarding ERB use in elderly patients. What is already known about this topic? Taxanes are the current first-line treatment for patients with advanced cutaneous angiosarcoma (CAS) who are considered difficult to treat with doxorubicin owing to advanced age or comorbidity. No effective therapy for taxane-resistant CAS has been established thus far. Eribulin suppresses microtubule polymerization and elicits an antitumour effect similar to that of taxanes. What does this study add? In our single-arm prospective observational study to evaluate the efficacy of eribulin for treating patients with advanced CAS who previously received taxanes, the median overall survival and progression-free survival were 8·6 and 3·0 months, respectively. Response rates at weeks 7, 13 and 25 were 20%, 17% and 14%, respectively. Although 16 grade 3/4 severe adverse events occurred, all patients recovered. Eribulin showed a promising response rate and is a potential candidate for second-line treatment in CAS after taxane treatment. Linked Comment: Smrke and Benson. Br J Dermatol 2020; 183:797-798.

Sections du résumé

BACKGROUND
Taxanes are the current first-line treatment for advanced cutaneous angiosarcoma (CAS) for patients who are considered difficult to treat with doxorubicin owing to advanced age or comorbidity. However, no effective second-line therapy for such patients has been established.
METHODS
We designed a single-arm prospective observational study of eribulin mesylate (ERB) administered at a dose of 1·4 mg m
RESULTS
We enrolled a total of 25 patients. The median OS and PFS were 8·6 months and 3·0 months, respectively. The best overall RR was 20% (five of 25). In total, 16 grade 3/4 severe adverse events (SAEs) occurred; however, all patients recovered. Patients who achieved partial response or stable disease as best response had longer OS than those with progressive disease (median OS not reached and 3·3 months, respectively; P < 0·001). Patients who did not experience SAEs showed longer OS than those who did (median OS 18·8 months and 7·5 months, respectively; P < 0·05). Patients with distant metastasis had shorter median OS than those with locoregional disease, but without statistically significant difference.
CONCLUSIONS
ERB showed a promising RR and is a potential candidate for second-line treatment for patients with CAS, after treatment with taxanes. However, owing to the occurrence of SAEs in over half of the participants, caution should be exercised regarding ERB use in elderly patients. What is already known about this topic? Taxanes are the current first-line treatment for patients with advanced cutaneous angiosarcoma (CAS) who are considered difficult to treat with doxorubicin owing to advanced age or comorbidity. No effective therapy for taxane-resistant CAS has been established thus far. Eribulin suppresses microtubule polymerization and elicits an antitumour effect similar to that of taxanes. What does this study add? In our single-arm prospective observational study to evaluate the efficacy of eribulin for treating patients with advanced CAS who previously received taxanes, the median overall survival and progression-free survival were 8·6 and 3·0 months, respectively. Response rates at weeks 7, 13 and 25 were 20%, 17% and 14%, respectively. Although 16 grade 3/4 severe adverse events occurred, all patients recovered. Eribulin showed a promising response rate and is a potential candidate for second-line treatment in CAS after taxane treatment. Linked Comment: Smrke and Benson. Br J Dermatol 2020; 183:797-798.

Identifiants

pubmed: 32198756
doi: 10.1111/bjd.19042
doi:

Substances chimiques

Bridged-Ring Compounds 0
Furans 0
Ketones 0
Taxoids 0
taxane 1605-68-1
eribulin LR24G6354G

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

831-839

Subventions

Organisme : Maruho Takagi Dermatology Foundation

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2020 British Association of Dermatologists.

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Auteurs

Y Fujisawa (Y)

Dermatology Division, University of Tsukuba, Tsukuba, Japan.

T Fujimura (T)

Department of Dermatology, Tohoku University Graduate School of Medicine, Sendai, Japan.

S Matsushita (S)

Department of Dermato-Oncology/Dermatology, National Hospital Organization Kagoshima Medical Center, Kagoshima, Japan.

Y Yamamoto (Y)

Department of Dermatology, Wakayama Prefectural Medical School, Wakayama, Japan.

H Uchi (H)

Department of Dermatology, Kyushu University, Fukuoka, Japan.

A Otsuka (A)

Department of Dermatology, Kyoto University, Kyoto, Japan.

T Funakoshi (T)

Department of Dermatology, Keio University, Tokyo, Japan.

T Miyagi (T)

Department of Dermatology, Graduate School of Medicine, University of the Ryukyus, Okinawa, Japan.

H Hata (H)

Department of Dermatology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Hokkaido, Japan.

M Gosho (M)

Department of Clinical Trial and Clinical Epidemiology, University of Tsukuba, Tsukuba, Japan.

Y Kambayashi (Y)

Department of Dermatology, Tohoku University Graduate School of Medicine, Sendai, Japan.

M Aoki (M)

Department of Dermato-Oncology/Dermatology, National Hospital Organization Kagoshima Medical Center, Kagoshima, Japan.

T Yanagi (T)

Department of Dermatology, Tokyo Metropolitan Cancer and Infectious Disease Center Komagome Hospital, Tokyo, Japan.

A Ohira (A)

Department of Dermatology, Graduate School of Medicine, University of the Ryukyus, Okinawa, Japan.

Y Nakamura (Y)

Dermatology Division, University of Tsukuba, Tsukuba, Japan.

T Maeda (T)

Department of Dermatology, Tokyo Metropolitan Cancer and Infectious Disease Center Komagome Hospital, Tokyo, Japan.

K Yoshino (K)

Department of Dermatology, Tokyo Metropolitan Cancer and Infectious Disease Center Komagome Hospital, Tokyo, Japan.

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