Rate and characteristics of inflammatory neuropathies associated with brentuximab vedotin therapy

Author:

Matthys Arthur12,Bardel Benjamin34ORCID,Le Bras Fabien5,Créange Alain14ORCID,Nordine Tarik34,Gounot Romain5,Ingen‐Housz‐Oro Saskia6,Carvalho Muriel7,Lefaucheur Jean‐Pascal34,Haioun Corinne5,Planté‐Bordeneuve Violaine14,Gendre Thierry14ORCID

Affiliation:

1. Department of Neurology AP‐HP, Henri Mondor University Hospital Créteil France

2. Center for Interdisciplinary Research in Biology, Collège de France, CNRS UMR 7241, INSERM U1050, Labex Memolife PSL Research University Paris France

3. Unit of Clinical Neurophysiology AP‐HP, Henri Mondor University Hospital Créteil France

4. Reference Center for Neuromuscular Diseases Nord/Est/Ile‐de‐France Paris France

5. Lymphoid Malignancies Unit AP‐HP, Henri Mondor University Hospital Créteil France

6. Department of Dermatology, Paris‐Est Créteil University EpiDermE AP‐HP, Henri Mondor University Hospital Créteil France

7. Department of Pharmacy AP‐HP, Henri Mondor University Hospital Créteil France

Abstract

AbstractBackground and purposePeripheral neuropathy is a frequent complication of brentuximab vedotin (BV), used in CD30+ lymphoma treatment. Classic BV‐induced neuropathy (BV‐CN) is a mild distal sensory axonal polyneuropathy. Severe BV‐induced inflammatory neuropathies (BV‐IN) have been described. BV‐IN contribute to lymphoma‐associated morbidity but might be immunotherapy‐responsive. Our primary objective was to evaluate the rate of BV‐IN. Our secondary objectives were to determine risk factors and warning signs.MethodsWe conducted a retrospective cohort study on all patients treated with BV at our center between April 2014 and September 2021. Clinical, biological, and electrophysiological data were collected. BV‐induced neuropathy was defined as the occurrence of neuropathy up to 3 months after BV discontinuation. BV‐IN was defined with criteria adapted from European Academy of Neurology/Peripheral Nerve Society 2021 electrodiagnostic criteria for chronic inflammatory demyelinating polyradiculoneuropathy. Other neuropathies were classified as BV‐CN.ResultsAmong 83 patients, 41 (49%) developed neuropathy: 35 BV‐CN and 6 BV‐IN. Thus, the rate of BV‐IN was 7.2%. Compared to patients with BV‐CN, no predisposing factor was identified. However, patients with BV‐IN more frequently presented muscle weakness (67% vs. 5.7%, p < 0.05), gait disorders (83% vs. 20%, p < 0.05), or acute or subacute onset (67% vs. 14%, p < 0.05). BV‐IN was frequently more severe (Common Terminology Criteria for Adverse Events grade ≥3; 50% vs. 0%, p < 0.05). Four patients were treated with immunotherapy.ConclusionsBrentuximab vedotin‐induced neuropathy is an overlooked complication. Based on four easily identifiable “red flags”, we provide an algorithm to help non‐neurologist physicians that care for BV‐treated patients to detect BV‐IN. The aim of the algorithm is to decrease the diagnostic and management delay of this disabling neuropathy.

Publisher

Wiley

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Is there a role for capsaicin in Cancer pain management?;Current Opinion in Supportive & Palliative Care;2024-09-12

2. Brentuximab-vedotin;Reactions Weekly;2024-07-13

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