Efficacy of combined radiotherapy and anti-programmed death 1 therapy in acral and mucosal melanoma.


Journal

The Journal of dermatology
ISSN: 1346-8138
Titre abrégé: J Dermatol
Pays: England
ID NLM: 7600545

Informations de publication

Date de publication:
Apr 2019
Historique:
received: 16 11 2018
accepted: 10 01 2019
pubmed: 14 2 2019
medline: 10 8 2019
entrez: 14 2 2019
Statut: ppublish

Résumé

Some studies showed that clinical response to immune check point inhibitors is lower in acral and mucosal melanoma than in cutaneous melanoma. Although the synergistic effect of radiotherapy (RT) and ipilimumab has been reported in patients with brain metastasis, the efficacy of combined RT and anti-programmed death 1 (PD-1) therapy for acral and mucosal melanoma is unclear. The present study aimed to evaluate the efficacy of combined RT and anti-PD-1 therapy for acral and mucosal melanoma. We retrospectively analyzed patients with acral or mucosal melanoma who were treated with anti-PD-1 and RT at Sapporo Medical University Hospital. In 10 patients (acral, 3; mucosal, 7), the response rate (RR) and the disease control rate (DCR) were 40% and 60%, respectively. As regards mucosal melanoma, four of the seven patients had achieved complete response + partial response, and three had progressive disease (RR = 57.1%). Meanwhile, two of the three patients with acral melanoma had stable disease and one had progressive disease (RR and DCR were 0% and 66.6%, respectively). Except for the patients treated with palliative RT for bone metastasis in the present study, the RR was 50% (4/8 patients), and the DCR was 75% (6/8 patients). Vitiligo developed after RT in five (50%) patients at a median duration of 2 months after RT. The clinical response and the high occurrence of vitiligo suggest that the combination of RT and anti-PD-1 therapy could be effective in some patients with mucosal melanoma.

Identifiants

pubmed: 30758859
doi: 10.1111/1346-8138.14805
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Antineoplastic Agents, Immunological 0
PDCD1 protein, human 0
Programmed Cell Death 1 Receptor 0
Nivolumab 31YO63LBSN
pembrolizumab DPT0O3T46P

Types de publication

Journal Article

Langues

eng

Pagination

328-333

Informations de copyright

© 2019 Japanese Dermatological Association.

Auteurs

Junji Kato (J)

Department of Dermatology, Sapporo Medical University School of Medicine, Sapporo, Japan.

Tokimasa Hida (T)

Department of Dermatology, Sapporo Medical University School of Medicine, Sapporo, Japan.

Masanori Someya (M)

Department of Radiology, Sapporo Medical University School of Medicine, Sapporo, Japan.

Sayuri Sato (S)

Department of Dermatology, Sapporo Medical University School of Medicine, Sapporo, Japan.

Masahide Sawada (M)

Department of Dermatology, Sapporo Medical University School of Medicine, Sapporo, Japan.

Kohei Horimoto (K)

Department of Dermatology, Sapporo Medical University School of Medicine, Sapporo, Japan.

Mao Fujioka (M)

Department of Dermatology, Sapporo Medical University School of Medicine, Sapporo, Japan.

Tomoyuki Minowa (T)

Department of Dermatology, Sapporo Medical University School of Medicine, Sapporo, Japan.

Yoshiyuki Matsui (Y)

Department of Dermatology, Sapporo Medical University School of Medicine, Sapporo, Japan.

Takaaki Tsuchiya (T)

Department of Radiology, Sapporo Medical University School of Medicine, Sapporo, Japan.

Mio Kitagawa (M)

Department of Radiology, Sapporo Medical University School of Medicine, Sapporo, Japan.

Kensei Nakata (K)

Department of Radiology, Sapporo Medical University School of Medicine, Sapporo, Japan.

Koh-Ichi Sakata (KI)

Department of Radiology, Sapporo Medical University School of Medicine, Sapporo, Japan.

Toshihiko Torigoe (T)

Department of Pathology, Sapporo Medical University School of Medicine, Sapporo, Japan.

Hisashi Uhara (H)

Department of Dermatology, Sapporo Medical University School of Medicine, Sapporo, Japan.

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Classifications MeSH