Guillain-Barré syndrome after adoptive cell therapy with tumor-infiltrating lymphocytes.


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
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.

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Auteurs

Angela Orcurto (A)

Immuno-oncology Service, Department of Oncology, CHUV, Lausanne, Vaud, Switzerland angela.orcurto@chuv.ch.

Andreas Hottinger (A)

Oncology Service, Department of Oncology, CHUV, Lausanne, Vaud, Switzerland.
Service of Neurology, Department of Clinical Neurosciences, CHUV, Lausanne, Vaud, Switzerland.

Benita Wolf (B)

Oncology Service, Department of Oncology, CHUV, Lausanne, Vaud, Switzerland.

Blanca Navarro Rodrigo (B)

Immuno-oncology Service, Department of Oncology, CHUV, Lausanne, Vaud, Switzerland.
Ludwig Institute for Cancer Research, Lausanne Branch, University of Lausanne, Epalinges, Vaud, Switzerland.

Maria Ochoa de Olza (M)

Immuno-oncology Service, Department of Oncology, CHUV, Lausanne, Vaud, Switzerland.
Ludwig Institute for Cancer Research, Lausanne Branch, University of Lausanne, Epalinges, Vaud, Switzerland.

Aymeric Auger (A)

Ludwig Institute for Cancer Research, Lausanne Branch, University of Lausanne, Epalinges, Vaud, Switzerland.
Center of Experimental Therapeutics, Department of Oncology, CHUV, Lausanne, Vaud, Switzerland.

Thierry Kuntzer (T)

Service of Neurology, Department of Clinical Neurosciences, CHUV, Lausanne, Vaud, Switzerland.

Denis Comte (D)

Service of Immunology and Allergy, Department of Medicine, CHUV, Lausanne, Vaud, Switzerland.

Virginie Zimmer (V)

Center of Experimental Therapeutics, Department of Oncology, CHUV, Lausanne, Vaud, Switzerland.

Philippe Gannon (P)

Center of Experimental Therapeutics, Department of Oncology, CHUV, Lausanne, Vaud, Switzerland.

Lana Kandalaft (L)

Ludwig Institute for Cancer Research, Lausanne Branch, University of Lausanne, Epalinges, Vaud, Switzerland.
Center of Experimental Therapeutics, Department of Oncology, CHUV, Lausanne, Vaud, Switzerland.

Olivier Michielin (O)

Oncology Service, Department of Oncology, CHUV, Lausanne, Vaud, Switzerland.

Stefan Zimmermann (S)

Immuno-oncology Service, Department of Oncology, CHUV, Lausanne, Vaud, Switzerland.

Alexandre Harari (A)

Ludwig Institute for Cancer Research, Lausanne Branch, University of Lausanne, Epalinges, Vaud, Switzerland.
Center of Experimental Therapeutics, Department of Oncology, CHUV, Lausanne, Vaud, Switzerland.

Lionel Trueb (L)

Immuno-oncology Service, Department of Oncology, CHUV, Lausanne, Vaud, Switzerland.

George Coukos (G)

Immuno-oncology Service, Department of Oncology, CHUV, Lausanne, Vaud, Switzerland.
Ludwig Institute for Cancer Research, Lausanne Branch, University of Lausanne, Epalinges, Vaud, Switzerland.

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