Severe infections in patients with chronic lymphocytic leukemia included in trials investigating BTK and BCL2 inhibitors

被引:0
|
作者
Mauro, Francesca R. [1 ]
Frustaci, Anna Maria [2 ]
Visentin, Andrea [3 ]
Vitale, Candida [4 ,5 ]
Bartoletti, Michele [6 ,7 ]
Oltolini, Chiara [8 ]
Zappulo, Emanuela [9 ]
Mikulska, Malgorzata [10 ,11 ]
机构
[1] Sapienza Univ, Dept Translat & Precis Med, Hematol, Via Benevento 6, I-00161 Rome, Italy
[2] ASST Grande Osped Metropolitano Niguarda, Milan, Italy
[3] Univ Padua, Dept Med, Hematol & Clin Immunol Unit, Padua, Italy
[4] AOU Citta Salute & Sci Torino, Div Hematol, Turin, Italy
[5] Univ Turin, Dept Mol Biotechnol & Hlth Sci, Turin, Italy
[6] Humanitas Univ, Dept Biomed Sci, Via Rita Levi Montalcini 4, I-20090 Pieve Emanuele Milan, Italy
[7] IRCCS Humanitas Res Hosp, Infect Dis Unit, Via Manzoni 56, I-20089 Milan, Italy
[8] Univ Vita Salute San Raffaele, San Raffaele Sci Inst, Clin Infect Dis, Milan, Italy
[9] Univ Federico II Naples, Dept Clin Med & Surg, Naples, Italy
[10] Univ Genoa, Dept Hlth Sci DISSAL, Genoa, Italy
[11] IRCCS Osped Policlin San Martino Genoa, Infect Dis Unit, Genoa, Italy
关键词
Chronic lymphocytic leukemia; Treatment; Infections; BTK inhibitors; BCL2; inhibitors; IBRUTINIB PLUS VENETOCLAX; MINIMAL RESIDUAL DISEASE; BRUTONS TYROSINE KINASE; ATRIAL-FIBRILLATION; 1ST-LINE TREATMENT; INTERIM ANALYSIS; OPEN-LABEL; FOLLOW-UP; RITUXIMAB; CLL;
D O I
10.1016/j.critrevonc.2024.104408
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Bruton tyrosine kinase inhibitors (BTKi) and the BCL-2 inhibitor venetoclax have significantly improved the prognosis of patients with chronic lymphocytic leukemia (CLL). However, the incidence of severe infections in patients receiving these agents needs to be better understood. Our review aimed to provide an overview of grade >= 3 infections in patients with CLL who received BTKi and venetoclax-based therapy in prospective trials. Infection rates were influenced by the age of patients and the duration of follow-up. For treatment-naive (TN) patients receiving BTKi, infection rates ranged between 11.4 % and 27.4 % and were close to 30 % in relapsed/ refractory (R/R) patients. TN and R/R patients receiving fixed-duration venetoclax-based treatments showed variable rates, with maximum values around 20 %. Opportunistic and fatal infections were uncommon. In conclusion, infections remain a concern in patients with CLL receiving targeted agents. A better definition of factors increasing infection vulnerability could help identify those patients who require infection prophylaxis.
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页数:11
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