Resolution of Melanoma to Programmed Death-1 Blockade but Simultaneous Rapid Progression of Concomitant Chronic Lymphocytic Leukemia.
Humans
CTLA-4 Antigen
/ antagonists & inhibitors
Disease Progression
Leukemia, Lymphocytic, Chronic, B-Cell
/ drug therapy
Melanoma
/ drug therapy
Programmed Cell Death 1 Receptor
/ antagonists & inhibitors
Skin Neoplasms
/ drug therapy
B7-H1 Antigen
Immune Checkpoint Inhibitors
/ immunology
Antineoplastic Agents
/ immunology
CLL
Immune-checkpoint blockade
Metastatic melanoma
Journal
Acta haematologica
ISSN: 1421-9662
Titre abrégé: Acta Haematol
Pays: Switzerland
ID NLM: 0141053
Informations de publication
Date de publication:
2023
2023
Historique:
received:
24
06
2022
accepted:
10
10
2022
medline:
28
3
2023
pubmed:
24
10
2022
entrez:
23
10
2022
Statut:
ppublish
Résumé
Here, we present a novel case of a patient with chronic lymphocytic leukemia (CLL) who received CTLA-4 and then PD-1 immune-checkpoint blockade (ICB) as treatment for concomitant metastatic melanoma. Whereas the metastatic melanoma was responsive to ICB, the CLL rapidly progressed (but responded to ICB cessation and ibrutinib). There were no new genetic mutational drivers to explain the altered clinical course. PD-1/PD-L1/PD-L2 and CTLA-4/CD80/CD86 expression was not increased in CLL B cells, CD8+ or CD4+ T-cell subsets, or monocytes. The patient's CLL B cells demonstrated strikingly prolonged in vitro survival during PD-1 blockade, which was not observed in samples taken before or after ICB, or with other patients. To our knowledge, a discordant clinical course to ICB coupled with these biological features has not been reported in a patient with dual malignancies.
Identifiants
pubmed: 36273464
pii: 000527631
doi: 10.1159/000527631
doi:
Substances chimiques
CTLA-4 Antigen
0
Programmed Cell Death 1 Receptor
0
B7-H1 Antigen
0
PDCD1 protein, human
0
Immune Checkpoint Inhibitors
0
ibrutinib
1X70OSD4VX
Antineoplastic Agents
0
Types de publication
Case Reports
Langues
eng
Sous-ensembles de citation
IM
Pagination
166-171Informations de copyright
© 2022 The Author(s). Published by S. Karger AG, Basel.