TY - JOUR
T1 - Immune-related generalised oedema – A new category of adverse events with immune checkpoint inhibitors
AU - Velev, Maud
AU - Baroudjian, Barouyr
AU - Pruvost, Roxane
AU - De Martin, Eleonora
AU - Laparra, Ariane
AU - Babai, Samy
AU - Teysseire, Sandra
AU - Danlos, François Xavier
AU - Albiges, Laurence
AU - Bernigaud, Charlotte
AU - Benderra, Marc Antoine
AU - Pradère, Pauline
AU - Zaidan, Mohamad
AU - Decroisette, Chantal
AU - Fallah, Fatma
AU - Matergia, Gaelle
AU - Lavaud, Pernelle
AU - Jantzem, Hélène
AU - Atzenhoffer, Marina
AU - Buyse, Véronique
AU - Ammari, Samy
AU - Robert, Caroline
AU - Champiat, Stéphane
AU - Messayke, Sabine
AU - Marabelle, Aurélien
AU - Guettier, Catherine
AU - Lebbe, Céleste
AU - Lambotte, Olivier
AU - Michot, Jean Marie
N1 - Publisher Copyright:
© 2022 Elsevier Ltd
PY - 2023/1/1
Y1 - 2023/1/1
N2 - Background: Generalised oedema was occasionally reported associated with immune checkpoint inhibitors (ICPIs). The purpose of this study is to investigate immune-related generalised oedema (ir-GE) drug related to ICPI, through frequency, clinical and pathological characteristics, and patient's outcome. Patients and methods: Objectives of the study were to report on ir-GE associated with ICPI to define frequency, associated signs and symptoms, pathological characteristics, severity, and response to corticosteroids. To be included in the study, adult patients had to have ir-GE related to ICPI with certain or likely link, without any other known causes of generalised oedema. The study design was observational, over the period 2014–2020, from pharmacovigilance databases in France, including the prospective Registre des Effets Indésirables Sévères des Anticorps Monoclonaux Immunomodulateurs en Cancérologie (REISAMIC) registry. Calculation of the frequency of ir-GE was restricted to the prospective REISAMIC registry. Results: Over 6633 screened patients, 20 had ir-GE confirmed drug related to ICPI. Based on the prospective REISAMIC registry, the frequency of ir-GE was 0.19% of ICPI-treated patients (3 cases out of 1598 screened patients). The 20 patients with ir-GE had a median (range) age of 62 (26–81) years, most frequent tumour types were melanoma (n = 9; 45%) and lung cancer (n = 6; 30%). The most frequent localisations of oedema were peripheral (n = 17; 85%), pleural (n = 13; 65%), and peritoneal (n = 10; 50%). Polyserositis was observed in 11 (55%) patients. The median (range) weight gain per patient was 9 (2–30) kg. Associated signs and symptoms met criteria for capillary leak syndrome (n = 4; 20%), sinusoidal obstruction syndrome/veno-occlusive disease (SOS/VOD) (n = 3; 15%), or subcutaneous autoimmune syndrome (n = 2; 10%). Corticosteroids were administered to 15 patients; of them, 10 (67%) improved clinically after corticosteroids. Based on CTCAEV5.0, the highest severity of ir-GE was grade ≥4 in 11 (55%) patients and four (20%) patients died due to ir-GE. Conclusions: Generalised immune system-related oedema is a new category of adverse event with immune checkpoint inhibitors and is often associated with a life-threatening condition. The pathophysiology may in some cases be related to endothelial dysfunctions, such as SOS/VOD or capillary leak syndrome.
AB - Background: Generalised oedema was occasionally reported associated with immune checkpoint inhibitors (ICPIs). The purpose of this study is to investigate immune-related generalised oedema (ir-GE) drug related to ICPI, through frequency, clinical and pathological characteristics, and patient's outcome. Patients and methods: Objectives of the study were to report on ir-GE associated with ICPI to define frequency, associated signs and symptoms, pathological characteristics, severity, and response to corticosteroids. To be included in the study, adult patients had to have ir-GE related to ICPI with certain or likely link, without any other known causes of generalised oedema. The study design was observational, over the period 2014–2020, from pharmacovigilance databases in France, including the prospective Registre des Effets Indésirables Sévères des Anticorps Monoclonaux Immunomodulateurs en Cancérologie (REISAMIC) registry. Calculation of the frequency of ir-GE was restricted to the prospective REISAMIC registry. Results: Over 6633 screened patients, 20 had ir-GE confirmed drug related to ICPI. Based on the prospective REISAMIC registry, the frequency of ir-GE was 0.19% of ICPI-treated patients (3 cases out of 1598 screened patients). The 20 patients with ir-GE had a median (range) age of 62 (26–81) years, most frequent tumour types were melanoma (n = 9; 45%) and lung cancer (n = 6; 30%). The most frequent localisations of oedema were peripheral (n = 17; 85%), pleural (n = 13; 65%), and peritoneal (n = 10; 50%). Polyserositis was observed in 11 (55%) patients. The median (range) weight gain per patient was 9 (2–30) kg. Associated signs and symptoms met criteria for capillary leak syndrome (n = 4; 20%), sinusoidal obstruction syndrome/veno-occlusive disease (SOS/VOD) (n = 3; 15%), or subcutaneous autoimmune syndrome (n = 2; 10%). Corticosteroids were administered to 15 patients; of them, 10 (67%) improved clinically after corticosteroids. Based on CTCAEV5.0, the highest severity of ir-GE was grade ≥4 in 11 (55%) patients and four (20%) patients died due to ir-GE. Conclusions: Generalised immune system-related oedema is a new category of adverse event with immune checkpoint inhibitors and is often associated with a life-threatening condition. The pathophysiology may in some cases be related to endothelial dysfunctions, such as SOS/VOD or capillary leak syndrome.
KW - Capillary leak syndrome
KW - Endothelial syndrome
KW - Generalised oedema
KW - Immune checkpoint inhibitor
KW - Immunotherapy
KW - Pharmacovigilance
KW - Polyserositis
KW - Sinusoidal obstruction syndrome
UR - http://www.scopus.com/inward/record.url?scp=85143142075&partnerID=8YFLogxK
U2 - 10.1016/j.ejca.2022.11.001
DO - 10.1016/j.ejca.2022.11.001
M3 - Article
C2 - 36473326
AN - SCOPUS:85143142075
SN - 0959-8049
VL - 179
SP - 28
EP - 47
JO - European Journal of Cancer
JF - European Journal of Cancer
ER -