» Articles » PMID: 33686688

The Efficacy of Anti-programmed Cell Death Protein 1 Therapy Among Patients with Metastatic Acral and Metastatic Mucosal Melanoma

Overview
Journal Cancer Med
Specialty Oncology
Date 2021 Mar 9
PMID 33686688
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Anti-programmed cell death protein 1 (PD-1) antibodies are a standard treatment for metastatic melanoma patients. However, the understanding of the efficacy of anti-PD-1 for acral melanoma (AM) and mucosal melanoma (MM) is limited as these subtypes are relatively rare compared to cutaneous melanoma (CM).

Methods: This single institution, retrospective cohort study included patients with advanced AM and MM who underwent anti-PD-1 therapy for metastatic melanoma between 2012 and 2018. Objective responses were determined using the investigator-assessed Response Evaluation Criteria in Solid Tumors version 1.1. Progression-free survival (PFS) and overall survival (OS) were assessed using the Kaplan-Meier method. A Cox regression analysis was performed to identify the factors associated with survival outcomes.

Results: Ninety-seven patients were identified, 38 (39%) with AM and 59 (61%) with MM. The objective response rates (ORRs) were 21.0% and 15.2% in patients with AM and MM, respectively. The median PFS and OS were 3.6 and 25.7 months for AM patients, and 3.0 and 20.1 months for MM patients, respectively. Elevated serum lactate dehydrogenase (LDH) (AM: hazard ratio [HR], 0.22; 95% confidence interval [CI], 0.06-0.87; p = 0.03, MM: HR, 0.20; 95% CI, 0.08-0.53; p = 0.001) was significantly associated with shorter OS for both subtypes.

Conclusions: The ORR, PFS, and OS with anti-PD-1 therapy were poor in patients with AM and MM compared to those previously reported clinical trials for nonacral CM. High serum LDH was associated with significantly shorter OS.

Citing Articles

Effectiveness of immune checkpoint inhibitors and other treatment modalities in patients with advanced mucosal melanomas: a systematic review and individual patient data meta-analysis.

Teo A, Yau C, Low C, Pereira J, Ng J, Soong T EClinicalMedicine. 2024; 77:102870.

PMID: 39416390 PMC: 11474374. DOI: 10.1016/j.eclinm.2024.102870.


A Narrative Review of the Evolution of Diagnostic Techniques and Treatment Strategies for Acral Lentiginous Melanoma.

Choi M, Choi E, Jung J, Lee W, Jo Y, Won C Int J Mol Sci. 2024; 25(19).

PMID: 39408752 PMC: 11477219. DOI: 10.3390/ijms251910414.


Current State of Melanoma Therapy and Next Steps: Battling Therapeutic Resistance.

Fateeva A, Eddy K, Chen S Cancers (Basel). 2024; 16(8).

PMID: 38672652 PMC: 11049326. DOI: 10.3390/cancers16081571.


Treatment outcomes of mucosal melanoma of head and neck: Efficacy of immune checkpoint inhibitors for advanced disease.

Ohshima S, Ueki Y, Yokoyama Y, Takahashi T, Shodo R, Yamazaki K Front Surg. 2023; 9:1032626.

PMID: 37082097 PMC: 10112385. DOI: 10.3389/fsurg.2022.1032626.


Nail Apparatus Melanoma: Current Management and Future Perspectives.

Ito T, Hashimoto H, Kaku-Ito Y, Tanaka Y, Nakahara T J Clin Med. 2023; 12(6).

PMID: 36983205 PMC: 10057171. DOI: 10.3390/jcm12062203.


References
1.
McLaughlin C, Wu X, Jemal A, Martin H, Roche L, Chen V . Incidence of noncutaneous melanomas in the U.S. Cancer. 2005; 103(5):1000-7. DOI: 10.1002/cncr.20866. View

2.
Eisenhauer E, Therasse P, Bogaerts J, Schwartz L, Sargent D, Ford R . New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1). Eur J Cancer. 2008; 45(2):228-47. DOI: 10.1016/j.ejca.2008.10.026. View

3.
Valsecchi M . Combined Nivolumab and Ipilimumab or Monotherapy in Untreated Melanoma. N Engl J Med. 2015; 373(13):1270. DOI: 10.1056/NEJMc1509660. View

4.
Tang B, Chi Z, Chen Y, Liu X, Wu D, Chen J . Safety, Efficacy, and Biomarker Analysis of Toripalimab in Previously Treated Advanced Melanoma: Results of the POLARIS-01 Multicenter Phase II Trial. Clin Cancer Res. 2020; 26(16):4250-4259. DOI: 10.1158/1078-0432.CCR-19-3922. View

5.
Curtin J, Busam K, Pinkel D, Bastian B . Somatic activation of KIT in distinct subtypes of melanoma. J Clin Oncol. 2006; 24(26):4340-6. DOI: 10.1200/JCO.2006.06.2984. View