Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/57315
Title: The Effectiveness of Adjuvant PD-1 Inhibitors in Patients with Surgically Resected Stage III/IV Acral Melanoma
Authors: Arak, H.
Erkiliç, S.
Yaslikaya, Ş.
Eylemer, Mocan, E.
Aktaş, G.
Özdemir, M.
Semiz, H.S.
Kiliçkap, Saadettin
Özalp, Faruk Recep
Sever, Özlem Nuray
Akdaǧ, Goncagül
Aǧaoǧlu, Ahmet Burak
Özçelik, Melike
Sari, Murat
Arcagök, Murat
Anik, Hicran
Yayla, Şaziye Burçak
Sever, Nadiye
Açar, Fatma Pinar
Bayrakçi, İsmail
Turhal, Serdar
Ayhan, Murat
Kuş, Tülay
Keywords: acral malignant melanoma
adjuvant therapy
nivolumab
immune checkpoint inhibitor
MAS receptor
MAS1 protein, human
PDCD1 protein, human
programmed death 1 receptor
adjuvant chemotherapy
adult
aged
cancer staging
clinical trial
female
human
male
melanoma
middle aged
mortality
multicenter study
pathology
procedures
retrospective study
skin tumor
treatment outcome
very elderly
Adult
Aged
Aged, 80 and over
Chemotherapy, Adjuvant
Female
Humans
Immune Checkpoint Inhibitors
Male
Melanoma
Middle Aged
Neoplasm Staging
Programmed Cell Death 1 Receptor
Proto-Oncogene Mas
Retrospective Studies
Skin Neoplasms
Treatment Outcome
Publisher: Lippincott Williams and Wilkins
Abstract: Our aim was to assess the efficacy of adjuvant programmed cell death protein-1 (PD-1) inhibitors and compare the other adjuvant treatments in patients with surgically resected stage III or IV acral melanoma. This study is a multicenter, retrospective analysis. We included 114 patients with stage III or IV acral malignant melanoma who underwent surgery within the past 10 years. We analyzed the effect of adjuvant programmed cell death protein-1 inhibitors on disease-free survival (DFS). The mean follow-up was 40 months, during which 69 (59.5%) patients experienced recurrence. Among the participants, 64 (56.1%) received systemic adjuvant therapy. Specifically, 48.4% received anti-PD-1 therapy, 29.7% received interferon, 14.1% received tezozolomide, and 7.8% received B-Raf proto-oncogene/mitogen-activated protein kinase inhibitors. Patients who received adjuvant therapy had a median DFS of 24 (10.9-37.2) months, whereas those who did not receive adjuvant therapy had a median DFS of 15 (9.8-20.2) months. Multivariate analysis for DFS revealed that the receipt of adjuvant therapy and lymph node metastasis stage were independent significant parameters (P = 0.021, P = 0.018, respectively). No statistically significant difference was observed for DFS between programmed cell death protein-1 inhibitor treatment and other adjuvant treatments. Regarding overall survival (OS), patients who received adjuvant treatment had a median OS of 71 (30.4-111.7) months, whereas those who did not receive adjuvant treatment had a median OS of 38 (16.7-59.3; P = 0.023) months. In addition, there were no significant differences in OS observed between various adjuvant treatment agents (P = 0.122). In our study, we have shown that adjuvant therapy had a positive effect on both DFS and OS in patients with stages III-IV acral melanoma who underwent curative intent surgery. Notably, we found no significant differences between anti-PD-1 therapy and other adjuvant therapies. © 2024 Lippincott Williams and Wilkins. All rights reserved.
URI: https://doi.org/10.1097/CJI.0000000000000508
https://hdl.handle.net/11499/57315
ISSN: 1524-9557
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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