Haematological immune-related adverse events with immune checkpoint inhibitors, how to manage?

被引:120
作者
Michot, J. M. [1 ,2 ]
Lazarovici, J. [3 ]
Tieu, A. [2 ]
Champiat, S. [1 ]
Voisin, A. L. [4 ]
Ebbo, M. [5 ]
Godeau, B. [6 ]
Michel, M. [6 ]
Ribrag, V. [1 ,3 ]
Lambotte, O. [2 ,7 ,8 ,9 ]
机构
[1] Univ Paris Saclay, Gustave Roussy, Dept Innovat Therapeut & Essais Precoces, 114 Rue Edouard Vaillant, F-94805 Villejuif, France
[2] Hop Bicetre, AP HP, Med Interne & Immunol Clin, F-94275 Le Kremlin Bicetre, France
[3] Univ Paris Saclay, Gustave Roussy, Dept Hematol, F-94805 Villejuif, France
[4] Univ Paris Saclay, Gustave Roussy, Unite Pharmacovigilance, F-94805 Villejuif, France
[5] Hop La Timone, AP HM, Med Interne, F-13005 Marseille, France
[6] Univ Paris Est Creteil, Hop Henri Mondor, AP HP, Med Interne,Ctr Reference Cytopenies Autoimmunes, F-94010 Creteil, France
[7] INSERM, U1184, Immunol Viral Infect & Autoimmune Dis, F-94276 Le Kremlin Bicetre, France
[8] Univ Paris Sud, UMR 1184, F-94276 Le Kremlin Bicetre, France
[9] CEA, DSV, iMETI, IDMIT, F-92265 Fontenay Aux Roses, France
关键词
Immune thrombocytopenia; Aplastic anaemia; Neutropenia; Autoimmune haemolytic anaemia; Cytokine release syndrome; Haemophagocytic syndrome; Immune-related adverse event; Immune checkpoint inhibitor; Anti-programmed cell death 1; Anti-programmed cell death ligand 1; Anti-cytotoxic T-lymphocyte-associated protein 4; AUTOIMMUNE HEMOLYTIC-ANEMIA; IDIOPATHIC THROMBOCYTOPENIC PURPURA; IPILIMUMAB-INDUCED THROMBOCYTOPENIA; METASTATIC MELANOMA PATIENT; PROGRAMMED DEATH 1; RED-CELL APLASIA; NIVOLUMAB THERAPY; ANTI-PD-1; THERAPY; DOUBLE-BLIND; OPEN-LABEL;
D O I
10.1016/j.ejca.2019.07.014
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Immune checkpoint inhibitors (ICIs) are changing the treatments of many patients with cancer. These immunotherapies are generally better tolerated than chemotherapy, and their adverse events are immune-related mimicking autoimmune or inflammatory conditions. Although these immune-related adverse events mainly affect the skin, endocrine glands, digestive tract, joints, liver or lungs, all the organs can be theoretically affected, and the haematopoietic system is not spared. This review of the literature will focus on the haematological immune-related adverse events (Haem-irAEs). By reviewing the largest clinical trials of ICIs, we estimate the frequency of Haem-irAEs at 3.6% for all grades and 0.7% for grades III-IV. Frequency of Haem-irAEs of all grades was found to be higher with anti-programmed cell death 1 (4.1%) or anti-programmed cell death ligand 1 (4.7%) than with anti-cytotoxic T-lymphocyte-associated protein 4 (0.5%) (p < 0.0001). From the 63 cases with Haem-irAEs reported in the literature, the mean time to the onset was found to be 10 weeks after ICI initiation, and the large range for occurrence (1-84 weeks) and the regular incidence suggest that Haem-irAEs could occur at any time after ICI therapy. Among the 63 reported cases with Haem-irAEs, the distribution was immune thrombocytopenia (n = 18, 29%), pancytopenia or immune aplastic anaemia (n = 12, 19%), neutropenia (n = 11, 17%), haemolytic anaemia (n = 10, 16%), cytokine release syndrome with haemophagocytic syndrome (n = 7, 11%) and other Haem-irAEs including bicytopenia or pure red cell aplasia (n = 5, 8%). Haem-irAEs are generally highly severe adverse reactions with a mortality rate of Haem-irAEs reported to be 14% (9 deaths among the 63 cases reported). The more severe and life-threatening Haem-irAEs were both cytokine release syndrome with haemophagocytic syndrome and pancytopenia or aplastic anaemia. Haem-irAEs induced by ICIs are potentially life-threatening. By discussing their pathophysiological aspects and clinical picture, we propose in this review clinical guidelines for management. (C) 2019 Elsevier Ltd. All rights reserved.
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页码:72 / 90
页数:19
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