Guillain-Barré syndrome after adoptive cell therapy with tumor-infiltrating lymphocytes.
adoptive
immunotherapy
lymphocytes
melanoma
tumor-infiltrating
Journal
Journal for immunotherapy of cancer
ISSN: 2051-1426
Titre abrégé: J Immunother Cancer
Pays: England
ID NLM: 101620585
Informations de publication
Date de publication:
08 2020
08 2020
Historique:
accepted:
24
07
2020
entrez:
28
8
2020
pubmed:
28
8
2020
medline:
16
9
2021
Statut:
ppublish
Résumé
Adoptive cell therapy (ACT) using tumor-infiltrating lymphocytes (TILs) is a promising experimental immunotherapy that has shown high objective responses in patients with melanoma. Current protocols use a lymphodepletive chemotherapy before infusion of ex vivo expanded TILs, followed by high-dose interleukin-2 (IL-2). Treatment-related toxicities are mainly attributable to the chemotherapy regimen and to the high-dose IL-2 and are generally reversible. Neurological side effects have rarely been described. Nevertheless, due to improvements in cell production techniques and due to combinations with other immunomodulating molecules, side effects not previously described may be encountered. We report the case of a 53-year-old heavily pretreated patient with melanoma who developed Guillain-Barré syndrome (GBS) 19 days after ACT using autologous TILs, given in the context of a phase I trial. He presented with dorsal back pain, unsteady gait and numbness in hands and feet. Lumbar puncture showed albuminocytological dissociation, and nerve conduction studies revealed prolonged distal motor latencies in median, ulnar, tibial and peroneal nerves, compatible with a GBS. The patient was treated with intravenous immunoglobulins and intensive neurological rehabilitation, with progressive and full recovery at 21 months post-TIL-ACT. Concomitant to the onset of GBS, a cytomegalovirus reactivation on immunosuppression was detected and considered as the most plausible cause of this neurological side effect. We describe for the first time a case of GBS occurring shortly after TIL-ACT for melanoma, even though we could not identify with certainty the triggering agent. The report of such rare cases is of extreme importance to build on the knowledge of immune cellular therapies and their specific spectrum of toxicities.
Sections du résumé
BACKGROUND
Adoptive cell therapy (ACT) using tumor-infiltrating lymphocytes (TILs) is a promising experimental immunotherapy that has shown high objective responses in patients with melanoma. Current protocols use a lymphodepletive chemotherapy before infusion of ex vivo expanded TILs, followed by high-dose interleukin-2 (IL-2). Treatment-related toxicities are mainly attributable to the chemotherapy regimen and to the high-dose IL-2 and are generally reversible. Neurological side effects have rarely been described. Nevertheless, due to improvements in cell production techniques and due to combinations with other immunomodulating molecules, side effects not previously described may be encountered.
CASE PRESENTATION
We report the case of a 53-year-old heavily pretreated patient with melanoma who developed Guillain-Barré syndrome (GBS) 19 days after ACT using autologous TILs, given in the context of a phase I trial. He presented with dorsal back pain, unsteady gait and numbness in hands and feet. Lumbar puncture showed albuminocytological dissociation, and nerve conduction studies revealed prolonged distal motor latencies in median, ulnar, tibial and peroneal nerves, compatible with a GBS. The patient was treated with intravenous immunoglobulins and intensive neurological rehabilitation, with progressive and full recovery at 21 months post-TIL-ACT. Concomitant to the onset of GBS, a cytomegalovirus reactivation on immunosuppression was detected and considered as the most plausible cause of this neurological side effect.
CONCLUSION
We describe for the first time a case of GBS occurring shortly after TIL-ACT for melanoma, even though we could not identify with certainty the triggering agent. The report of such rare cases is of extreme importance to build on the knowledge of immune cellular therapies and their specific spectrum of toxicities.
Identifiants
pubmed: 32847987
pii: jitc-2020-001155
doi: 10.1136/jitc-2020-001155
pmc: PMC7451492
pii:
doi:
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.
Déclaration de conflit d'intérêts
Competing interests: GC has received grants or research support from or is coinvestigator in clinical trials by BMS, Celgene, Boehringer Ingelheim, Roche, Iovance and Kite, and has received honoraria for consultations or presentations by Roche, Genentech, BMS, AstraZeneca, Sanofi-Aventis, Nextcure and GeneosTx. SZ reports travel grants by AstraZeneca in the last 12 months.
Références
Trends Immunol. 2013 Sep;34(9):453-9
pubmed: 23770405
Neurology. 1996 Sep;47(3):668-73
pubmed: 8797462
J Neuroimmunol. 2007 Jan;182(1-2):135-52
pubmed: 17126916
J Clin Neuromuscul Dis. 2017 Dec;19(2):80-83
pubmed: 29189553
Clin Infect Dis. 2011 Apr 1;52(7):837-44
pubmed: 21427390
J Neurol Sci. 1993 Jun;116(2):185-92
pubmed: 8336165
J Immunother Cancer. 2016 Sep 20;4:52
pubmed: 27660706
J Immunother Cancer. 2019 Nov 8;7(1):296
pubmed: 31703609
Brain. 2003 Sep;126(Pt 9):2034-42
pubmed: 12847075
J Clin Oncol. 1999 Jul;17(7):2105-16
pubmed: 10561265
J Clin Oncol. 2015 Jun 20;33(18):2092-9
pubmed: 25918278
Int J Mol Sci. 2019 Apr 23;20(8):
pubmed: 31018546
Clin Infect Dis. 2013 Nov;57(9):1369-70
pubmed: 23899686
Neurology. 1998 Oct;51(4):1110-5
pubmed: 9781538
Trends Immunol. 2005 Feb;26(2):111-7
pubmed: 15668127
J Clin Oncol. 1986 Jan;4(1):74-9
pubmed: 2416889
J Neurol Neurosurg Psychiatry. 2008 Jun;79(6):664-71
pubmed: 17717020
Transpl Infect Dis. 2019 Feb;21(1):e13021
pubmed: 30403433
Brain. 2014 Jan;137(Pt 1):33-43
pubmed: 24163275
Transplantation. 2001 May 15;71(9):1311-6
pubmed: 11397969
Clin Cancer Res. 2011 Jul 1;17(13):4550-7
pubmed: 21498393
Ann Oncol. 2019 Dec 1;30(12):1902-1913
pubmed: 31566658
J Immunother. 2001 Jul-Aug;24(4):287-93
pubmed: 11565830
Drug Saf. 2019 Feb;42(2):315-334
pubmed: 30649750
Lancet. 2016 Aug 13;388(10045):717-27
pubmed: 26948435