Response durability after cessation of immune checkpoint inhibitors in patients with metastatic Merkel cell carcinoma: a retrospective multicenter DeCOG study.


Journal

Cancer immunology, immunotherapy : CII
ISSN: 1432-0851
Titre abrégé: Cancer Immunol Immunother
Pays: Germany
ID NLM: 8605732

Informations de publication

Date de publication:
Nov 2021
Historique:
received: 30 09 2020
accepted: 23 03 2021
pubmed: 20 4 2021
medline: 16 10 2021
entrez: 19 4 2021
Statut: ppublish

Résumé

Immune checkpoint inhibitors (ICI) have led to a prolongation of progression-free and overall survival in patients with metastatic Merkel cell carcinoma (MCC). However, immune-mediated adverse events due to ICI therapy are common and often lead to treatment discontinuation. The response duration after cessation of ICI treatment is unknown. Hence, this study aimed to investigate the time to relapse after discontinuation of ICI in MCC patients. We analyzed 20 patients with metastatic MCC who have been retrospectively enrolled at eleven skin cancer centers in Germany. These patients have received ICI therapy and showed as best overall response (BOR) at least a stable disease (SD) upon ICI therapy. All patients have discontinued ICI therapy for other reasons than disease progression. Data on treatment duration, tumor response, treatment cessation, response durability, and tumor relapse were recorded. Overall, 12 of 20 patients (60%) with MCC relapsed after discontinuation of ICI. The median response durability was 10.0 months. Complete response (CR) as BOR to ICI-treatment was observed in six patients, partial response (PR) in eleven, and SD in three patients. Disease progression was less frequent in patients with CR (2/6 patients relapsed) as compared to patients with PR (7/11) and SD (3/3), albeit the effect of initial BOR on the response durability was below statistical significance. The median duration of ICI therapy was 10.0 months. Our results did not show a correlation between treatment duration and the risk of relapse after treatment withdrawal. Major reasons for discontinuation of ICI therapy were CR (20%), adverse events (35%), fatigue (20%), or patient decision (25%). Discontinuation of ICI due to adverse events resulted in progressive disease (PD) in 71% of patients regardless of the initial response. A re-induction of ICI was initiated in 8 patients upon tumor progression. We observed a renewed tumor response in 4 of these 8 patients. Notably, all 4 patients showed an initial BOR of at least PR. Our results from this contemporary cohort of patients with metastatic MCC indicate that MCC patients are at higher risk of relapse after discontinuation of ICI as compared to melanoma patients. Notably, the risk of disease progression after discontinuation of ICI treatment is lower in patients with initial CR (33%) as compared to patients with initial PR (66%) or SD (100%). Upon tumor progression, re-induction of ICI is a feasible option. Our data suggest that the BOR to initial ICI therapy might be a potential predictive clinical marker for a successful re-induction.

Sections du résumé

BACKGROUND BACKGROUND
Immune checkpoint inhibitors (ICI) have led to a prolongation of progression-free and overall survival in patients with metastatic Merkel cell carcinoma (MCC). However, immune-mediated adverse events due to ICI therapy are common and often lead to treatment discontinuation. The response duration after cessation of ICI treatment is unknown. Hence, this study aimed to investigate the time to relapse after discontinuation of ICI in MCC patients.
METHODS METHODS
We analyzed 20 patients with metastatic MCC who have been retrospectively enrolled at eleven skin cancer centers in Germany. These patients have received ICI therapy and showed as best overall response (BOR) at least a stable disease (SD) upon ICI therapy. All patients have discontinued ICI therapy for other reasons than disease progression. Data on treatment duration, tumor response, treatment cessation, response durability, and tumor relapse were recorded.
RESULTS RESULTS
Overall, 12 of 20 patients (60%) with MCC relapsed after discontinuation of ICI. The median response durability was 10.0 months. Complete response (CR) as BOR to ICI-treatment was observed in six patients, partial response (PR) in eleven, and SD in three patients. Disease progression was less frequent in patients with CR (2/6 patients relapsed) as compared to patients with PR (7/11) and SD (3/3), albeit the effect of initial BOR on the response durability was below statistical significance. The median duration of ICI therapy was 10.0 months. Our results did not show a correlation between treatment duration and the risk of relapse after treatment withdrawal. Major reasons for discontinuation of ICI therapy were CR (20%), adverse events (35%), fatigue (20%), or patient decision (25%). Discontinuation of ICI due to adverse events resulted in progressive disease (PD) in 71% of patients regardless of the initial response. A re-induction of ICI was initiated in 8 patients upon tumor progression. We observed a renewed tumor response in 4 of these 8 patients. Notably, all 4 patients showed an initial BOR of at least PR.
CONCLUSION CONCLUSIONS
Our results from this contemporary cohort of patients with metastatic MCC indicate that MCC patients are at higher risk of relapse after discontinuation of ICI as compared to melanoma patients. Notably, the risk of disease progression after discontinuation of ICI treatment is lower in patients with initial CR (33%) as compared to patients with initial PR (66%) or SD (100%). Upon tumor progression, re-induction of ICI is a feasible option. Our data suggest that the BOR to initial ICI therapy might be a potential predictive clinical marker for a successful re-induction.

Identifiants

pubmed: 33870464
doi: 10.1007/s00262-021-02925-4
pii: 10.1007/s00262-021-02925-4
pmc: PMC8505278
doi:

Substances chimiques

Immune Checkpoint Inhibitors 0

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

3313-3322

Informations de copyright

© 2021. The Author(s).

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Auteurs

H M Stege (HM)

Department of Dermatology, University Medical Center of the Johannes Gutenberg University, Mainz, Germany. henner.stege@unimedizin-mainz.de.

M Haist (M)

Department of Dermatology, University Medical Center of the Johannes Gutenberg University, Mainz, Germany.

S Schultheis (S)

Department of Dermatology, University Medical Center of the Johannes Gutenberg University, Mainz, Germany.

M I Fleischer (MI)

Department of Dermatology, University Medical Center of the Johannes Gutenberg University, Mainz, Germany.

P Mohr (P)

Department of Dermatology, Elbe-Kliniken Buxtehude, Buxtehude, Germany.

S Ugurel (S)

Department of Dermatology, University Medical Center Essen, Essen, Germany.

P Terheyden (P)

Department of Dermatology, Allergology and Venerology, University Lübeck, Lübeck, Germany.

A Thiem (A)

Department of Dermatology, University Medical Center Würzburg, Würzburg, Germany.
Department of Dermatology, University Medical Center Rostock, Rostock, Germany.

F Kiecker (F)

Department of Dermatology and Allergology at the Charité, University Medical Center Berlin, Berlin, Germany.

U Leiter (U)

Dermato-Oncology, Department of Dermatology, University Medical Center Tübingen, Tübingen, Germany.

J C Becker (JC)

Department of Dermatology, University Medical Center Essen, Essen, Germany.
German Consortium for Translational Oncology (DKTK) and German Cancer Research Center (DKFZ), Heidelberg, Germany.

M Meissner (M)

Department of Dermatology, University Medical Center Frankfurt, Frankfurt, Germany.

J Kleeman (J)

Department of Dermatology, University Medical Center Frankfurt, Frankfurt, Germany.

C Pföhler (C)

Department of Dermatology, University Medical Center Homburg, Homburg, Germany.

J Hassel (J)

Department of Dermatology, University Medical Center Heidelberg, Heidelberg, Germany.

S Grabbe (S)

Department of Dermatology, University Medical Center of the Johannes Gutenberg University, Mainz, Germany.

C Loquai (C)

Department of Dermatology, University Medical Center of the Johannes Gutenberg University, Mainz, Germany.

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