Real-World Data on Clinical Outcomes and Treatment Management of Advanced Melanoma Patients: Single-Center Study of a Tertiary Cancer Center in Switzerland.

BRAF and MEK inhibitors adjuvant treatment immune checkpoint inhibitors melanoma real-world evidence targeted therapy unresectable melanoma

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
20 Feb 2024
Historique:
received: 31 01 2024
revised: 13 02 2024
accepted: 15 02 2024
medline: 13 3 2024
pubmed: 13 3 2024
entrez: 13 3 2024
Statut: epublish

Résumé

Immune checkpoint inhibitors (ICIs) and BRAF/MEK inhibitors (BRAF/MEKi) have drastically changed the outcomes of advanced melanoma patients in both the resectable/adjuvant and unresectable/metastatic setting. In this follow-up analysis of real-world data, we aimed to investigate the clinical management and outcomes of advanced melanoma patients in a tertiary referral center in Switzerland approximately a decade after the introduction of ICIs and BRAF/MEKi into clinical use. Moreover, we aimed to compare the results with seminal phase 3 trials and to identify areas of high unmet clinical need. This single-center retrospective cohort study analyzed the melanoma registry of the University Hospital Zurich, a tertiary cancer center in Switzerland, and included patients treated in the resectable/adjuvant (n = 331) or unresectable/metastatic setting (n = 375). In the resectable setting, adjuvant anti-PD1 or BRAF/MEKi showed a 3-year relapse-free survival (RFS) of 53% and 67.6%, respectively, and the overall median RFS was 50 months. Patients with lymph node plus in-transit metastases or with distant metastases prior to commencing adjuvant treatment had a significantly reduced overall survival (OS). In 10.9% of patients, the treatment was stopped due to toxicity, which did not affect RFS/OS, unless the duration of the treatment was <3 months. Following a relapse of the disease during the first adjuvant treatment, the median progression-free survival (PFS2) was only 6.6 months; outcomes were particularly poor for relapses that were unresectable (median PFS2 3.9 months) or occurred within the first 2 months (median PFS2 2.7 months). A second adjuvant treatment for patients with resectable relapses still showed efficacy (median RFS2 43.7 months). Elevated LDH levels in patients with an unresectable relapse was correlated with a strong reduction in OS2 (HR 9.84, Our study offers real-world insights into the clinical management, treatment patterns, and outcomes of advanced melanoma patients in both the adjuvant and unresectable setting. Early relapses in patients undergoing adjuvant treatment pose a particular challenge but these patients are generally excluded from first-line trials. The approved first-line metastatic treatments are highly effective in the real-world setting with 5-year OS rates around 50%. However, outcomes remain poor for patients with brain metastases or who fail first-line treatment.

Sections du résumé

BACKGROUND BACKGROUND
Immune checkpoint inhibitors (ICIs) and BRAF/MEK inhibitors (BRAF/MEKi) have drastically changed the outcomes of advanced melanoma patients in both the resectable/adjuvant and unresectable/metastatic setting. In this follow-up analysis of real-world data, we aimed to investigate the clinical management and outcomes of advanced melanoma patients in a tertiary referral center in Switzerland approximately a decade after the introduction of ICIs and BRAF/MEKi into clinical use. Moreover, we aimed to compare the results with seminal phase 3 trials and to identify areas of high unmet clinical need.
METHODS METHODS
This single-center retrospective cohort study analyzed the melanoma registry of the University Hospital Zurich, a tertiary cancer center in Switzerland, and included patients treated in the resectable/adjuvant (n = 331) or unresectable/metastatic setting (n = 375).
RESULTS RESULTS
In the resectable setting, adjuvant anti-PD1 or BRAF/MEKi showed a 3-year relapse-free survival (RFS) of 53% and 67.6%, respectively, and the overall median RFS was 50 months. Patients with lymph node plus in-transit metastases or with distant metastases prior to commencing adjuvant treatment had a significantly reduced overall survival (OS). In 10.9% of patients, the treatment was stopped due to toxicity, which did not affect RFS/OS, unless the duration of the treatment was <3 months. Following a relapse of the disease during the first adjuvant treatment, the median progression-free survival (PFS2) was only 6.6 months; outcomes were particularly poor for relapses that were unresectable (median PFS2 3.9 months) or occurred within the first 2 months (median PFS2 2.7 months). A second adjuvant treatment for patients with resectable relapses still showed efficacy (median RFS2 43.7 months). Elevated LDH levels in patients with an unresectable relapse was correlated with a strong reduction in OS2 (HR 9.84,
CONCLUSION CONCLUSIONS
Our study offers real-world insights into the clinical management, treatment patterns, and outcomes of advanced melanoma patients in both the adjuvant and unresectable setting. Early relapses in patients undergoing adjuvant treatment pose a particular challenge but these patients are generally excluded from first-line trials. The approved first-line metastatic treatments are highly effective in the real-world setting with 5-year OS rates around 50%. However, outcomes remain poor for patients with brain metastases or who fail first-line treatment.

Identifiants

pubmed: 38473216
pii: cancers16050854
doi: 10.3390/cancers16050854
pii:
doi:

Types de publication

Journal Article

Langues

eng

Auteurs

Ramon Staeger (R)

Faculty of Medicine, University of Zurich, 8006 Zurich, Switzerland.
Department of Dermatology, University Hospital Zurich, 8091 Zurich, Switzerland.

Julia M Martínez-Gómez (JM)

Faculty of Medicine, University of Zurich, 8006 Zurich, Switzerland.
Department of Dermatology, University Hospital Zurich, 8091 Zurich, Switzerland.

Patrick Turko (P)

Faculty of Medicine, University of Zurich, 8006 Zurich, Switzerland.
Department of Dermatology, University Hospital Zurich, 8091 Zurich, Switzerland.

Egle Ramelyte (E)

Faculty of Medicine, University of Zurich, 8006 Zurich, Switzerland.
Department of Dermatology, University Hospital Zurich, 8091 Zurich, Switzerland.

Lukas Kraehenbuehl (L)

Faculty of Medicine, University of Zurich, 8006 Zurich, Switzerland.
Department of Dermatology, University Hospital Zurich, 8091 Zurich, Switzerland.

Valerio Del Prete (V)

Faculty of Medicine, University of Zurich, 8006 Zurich, Switzerland.
Department of Dermatology, University Hospital Zurich, 8091 Zurich, Switzerland.

Omar Hasan Ali (O)

Faculty of Medicine, University of Zurich, 8006 Zurich, Switzerland.
Department of Dermatology, University Hospital Zurich, 8091 Zurich, Switzerland.

Mitchell P Levesque (MP)

Faculty of Medicine, University of Zurich, 8006 Zurich, Switzerland.
Department of Dermatology, University Hospital Zurich, 8091 Zurich, Switzerland.

Reinhard Dummer (R)

Faculty of Medicine, University of Zurich, 8006 Zurich, Switzerland.
Department of Dermatology, University Hospital Zurich, 8091 Zurich, Switzerland.

Mirjam C Nägeli (MC)

Faculty of Medicine, University of Zurich, 8006 Zurich, Switzerland.
Department of Dermatology, University Hospital Zurich, 8091 Zurich, Switzerland.

Joanna Mangana (J)

Faculty of Medicine, University of Zurich, 8006 Zurich, Switzerland.
Department of Dermatology, University Hospital Zurich, 8091 Zurich, Switzerland.

Classifications MeSH