Toxicity associated with PD-1 blockade after allogeneic haematopoietic cell transplantation.
Adult
Aged
Allografts
Antibodies, Monoclonal
/ adverse effects
Antineoplastic Agents
/ adverse effects
Carcinoma, Renal Cell
/ drug therapy
Female
Hematopoietic Stem Cell Transplantation
Hodgkin Disease
/ drug therapy
Humans
Immunologic Factors
/ therapeutic use
Male
Melanoma
/ drug therapy
Middle Aged
Nivolumab
Programmed Cell Death 1 Receptor
/ immunology
Retrospective Studies
Journal
Swiss medical weekly
ISSN: 1424-3997
Titre abrégé: Swiss Med Wkly
Pays: Switzerland
ID NLM: 100970884
Informations de publication
Date de publication:
04 11 2019
04 11 2019
Historique:
entrez:
11
11
2019
pubmed:
11
11
2019
medline:
12
5
2020
Statut:
epublish
Résumé
Cancer immunotherapy with immune checkpoint inhibitors (ICIs) such as programmed death ligand-1 (PD-L1) blockers offers pronounced clinical benefit with durable responses and a manageable safety profile. Patients with a high risk of immune-related adverse events are generally excluded from clinical trials testing ICI therapy. Thus, only a little information on the safety and clinical outcome of patients treated with an ICI after allogeneic haematopoietic cell transplantation (HCT) is currently available. Here, we report the characteristics and outcomes of six patients with, respectively, clear cell renal carcinoma, diffuse large cell B-cell lymphoma, Hodgkin lymphoma, a microsatellite instable colorectal cancer and melanoma who were treated with PD-1 blocking antibodies. All patients had previously undergone allogeneic HCT. Severe grade 3–5 immune-related adverse events were observed in three of five patients who received full-dose ICI therapy. One patient received a lower dose of PD-1 blocking antibody. Only one patient had an objective response, whereas all the other patients had progressive disease. The high toxicity of a full- dose anti-PD-1 treatment regimen suggests that other treatment approaches for patients after allogeneic HCT are needed outside of the context of relapsed Hodgkin disease. In cases where ICI therapy is the only treatment option, reduced dosing should be explored.
Identifiants
pubmed: 31707719
doi: 10.4414/smw.2019.20150
pii: Swiss Med Wkly. 2019;149:w20150
doi:
pii:
Substances chimiques
Antibodies, Monoclonal
0
Antineoplastic Agents
0
Immunologic Factors
0
Programmed Cell Death 1 Receptor
0
Nivolumab
31YO63LBSN
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM