Risk of cutaneous adverse events in cancer patients treated with phosphatidylinositol-3-kinase inhibitors: A systematic review and meta-analysis of randomized controlled trials

被引:0
作者
Wang, Yushu [1 ,2 ]
Ma, Zhuo [1 ]
An, Zhuoling [1 ]
Zhang, Yi [1 ,2 ]
Feng, Xin [2 ]
Yu, Xiaojia [1 ]
机构
[1] Capital Med Univ, Beijing Chao Yang Hosp, Dept Pharm, 8 Gongtinan Rd, Beijing 100020, Peoples R China
[2] Capital Med Univ, Beijing Maternal & Child Hlth Care Hosp, Beijing Obstet & Gynecol Hosp, Dept Pharm, 17 Qi He Lou St, Beijing 100026, Peoples R China
来源
CANCER MEDICINE | 2023年 / 12卷 / 03期
关键词
cancer; cutaneous adverse events; PI3K inhibitors; randomized controlled trials; rash; CHRONIC LYMPHOCYTIC-LEUKEMIA; PI3K INHIBITORS; B-CELL; DOUBLE-BLIND; OPEN-LABEL; PHASE-III; IDELALISIB; P110-DELTA; RITUXIMAB; COPANLISIB;
D O I
10.1002/cam4.5153
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Cutaneous adverse effects (AEs) are common following the phosphoinositide-3-kinase (PI3K) inhibitors treatment. We aim to estimate the incidence and risk of PI3K inhibitor-related cutaneous AEs. Methods The protocol was submitted to the PROSPERO registry. We searched and international databases up to July 29, 2022. Meta-analysis was conducted by using risk ratios (RRs) with 95% confidence intervals (CIs). Results Fourteen randomized controlled trials (RCTs) comprising 3877 patients were analyzed in this study. Compared with control arms, PI3K inhibitors showed a significant increase in the risk of all-grade rash, high-grade rash, and serious rash events (RR 2.29, 95% CI 1.58-3.31, p < 0.00001; RR 9.34, 95% CI 4.21-20.69, p < 0.00001; RR 5.11, 95% CI 2.11-12.36, p = 0.0003). The overall incidences of all-grade rash and high-grade rash were 26.2% (592/2257) and 4.4% (66/1487). Subgroup analyses of all-grade rash according to cancer types and PI3K inhibitor assignations identified the significant associations. PI3K inhibitors also significantly increased the risk of pruritus and dry skin (RR 1.63, 95% CI 1.14-2.33, p = 0.007; RR 3.34, 95% CI 2.30-4.85, p < 0.00001), with incidences of 13.4% (284/2115) and 9.8% (141/1436) in the treatment group. Conclusion There is a significantly increased risk of some cutaneous AEs in patients using PI3K inhibitors. Advance intervention is recommended in case of severe and life-threatening events. Further research is required to investigate the risk factors and pathogenesis.
引用
收藏
页码:2227 / 2237
页数:11
相关论文
共 67 条
  • [1] Mutational spectra of PTEN/MMAC1 gene: a tumor suppressor with lipid phosphatase activity
    Ali, IU
    Schriml, LM
    Dean, M
    [J]. JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1999, 91 (22): : 1922 - 1932
  • [2] Inactivation of PI(3)K p110δ breaks regulatory T-cell-mediated immune tolerance to cancer
    Ali, Khaled
    Soond, Dalya R.
    Pineiro, Roberto
    Hagemann, Thorsten
    Pearce, Wayne
    Lim, Ee Lyn
    Bouabe, Hicham
    Scudamore, Cheryl L.
    Hancox, Timothy
    Maecker, Heather
    Friedman, Lori
    Turner, Martin
    Okkenhaug, Klaus
    Vanhaesebroeck, Bart
    [J]. NATURE, 2014, 510 (7505) : 407 - +
  • [3] ALIQOPA, 2017, PRESCR INF
  • [4] Balagula Yevgeniy, 2010, J Support Oncol, V8, P149
  • [5] Targeting PI3 kinase in cancer
    Bauer, Todd M.
    Patel, Manish R.
    Infante, Jeffrey R.
    [J]. PHARMACOLOGY & THERAPEUTICS, 2015, 146 : 53 - 60
  • [6] Phosphoinositide 3-kinase signaling to Akt promotes keratinocyte differentiation versus death
    Calautti, E
    Li, J
    Saoncella, S
    Brissette, JL
    Goetinck, PF
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (38) : 32856 - 32865
  • [7] The present and future of PI3K inhibitors for cancer therapy
    Castel, Pau
    Toska, Eneda
    Engelman, Jeffrey A.
    Scaltriti, Maurizio
    [J]. NATURE CANCER, 2021, 2 (06) : 587 - 597
  • [8] ClinicalTrials.gov, 2018, EFF SAF ID GS 1101 C
  • [9] ClinicalTrials.gov, Glossary of common site terms
  • [10] FAQs