Efficacy and safety of immune checkpoint inhibitors for patients with prostate cancer: a systematic review and meta-analysis

被引:3
|
作者
Noori, Maryam [1 ,2 ]
Azizi, Shadi [1 ]
Mahjoubfar, Aref [1 ]
Varaki, Farhan Abbasi [1 ]
Fayyaz, Farimah [3 ,4 ,5 ]
Mousavian, Amir-Hossein [2 ,6 ]
Bashash, Davood [7 ]
Parizi, Mehdi Kardoust [8 ,9 ]
Kasaeian, Amir [2 ,6 ,10 ]
机构
[1] Iran Univ Med Sci, Student Res Comm, Sch Med, Tehran, Iran
[2] Univ Tehran Med Sci, Res Inst Oncol Hematol & Cell Therapy, Hematol Oncol & Stem Cell Transplantat Res Ctr, Tehran, Iran
[3] Iran Univ Med Sci, Colorectal Res Ctr, Tehran, Iran
[4] Universal Sci Educ & Res Network USERN, Canc Immunol Project CIP, Tehran, Iran
[5] Universal Sci Educ & Res Network USERN, Network Immun Infect Malignancy & Autoimmun NIIMA, Tehran, Iran
[6] Univ Tehran Med Sci, Digest Dis Res Inst, Digest Dis Res Ctr, Tehran, Iran
[7] Shahid Beheshti Univ Med Sci, Sch Allied Med Sci, Dept Hematol & Blood Banking, Tehran, Iran
[8] Univ Tehran Med Sci, Shariati Hosp, Dept Urol, Tehran, Iran
[9] Med Univ Vienna, Dept Urol, Vienna, Austria
[10] Univ Tehran Med Sci, Shariati Hosp, Clin Res Dev Unit, Tehran, Iran
来源
FRONTIERS IN IMMUNOLOGY | 2023年 / 14卷
关键词
immune checkpoint inhibitors; prostate cancer; immunotherapy; PD-1; PDL; CTLA-4; NIVOLUMAB PLUS IPILIMUMAB; PHASE-II; DOUBLE-BLIND; CHEMOTHERAPY; IMMUNOTHERAPY; RADIOTHERAPY; ENZALUTAMIDE; MULTICENTER; COMBINATION; THERAPIES;
D O I
10.3389/fimmu.2023.1181051
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Immunotherapy has revolutionized the treatment paradigm of many cancers, however, its effectiveness in prostate cancer patients is still under question. In the present systematic review and meta-analysis, we sought for assessing the efficacy and safety of Immune checkpoint inhibitors (ICIs) in patients with prostate cancer. PubMed, Scopus, Web of Science, and EMBASE databases were searched on Aguste 19, 2022. Thirty five studies met the eligibility criteria. The median overall survival (mOS) of all treatments was 14.1 months, with the longest and shortest mOS was seen among patients who received anti-CTLA-4 monotherapy and anti-PD-1/PD-L1+anti-CTLA-4 regimen at 24.9 and 9.2 months, respectively. Noteworthy, all types of adverse events had the lowest incidence in the anti-PD-1/PD-L1 monotherapy group. Considering the ICI monotherapy regimens, we found that fatigue, diarrhea, and infusion reaction had the highest incidence rates. Future studies evaluating the efficacy and safety of novel combination therapies with ICIs are warranted.
引用
收藏
页数:16
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