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Anti-PD-1/L1-associated immune-related adverse events as harbinger of favorable clinical outcome: systematic review and meta-analysis
PArk, R; Lopes, L; Saeed, A.
Afiliação
  • PArk, R; Tufts University School of Medicine. Department of Medicine. Framingham. USA
  • Lopes, L; Tufts University School of Medicine. Department of Medicine. Framingham. USA
  • Saeed, A; Kansas University Medical Center. Division of Medical Oncology. Kansas. USA
Clin. transl. oncol. (Print) ; 23(1): 100-109, ene. 2021. graf, ilus
Artigo em Inglês | IBECS | ID: ibc-220455
Biblioteca responsável: ES1.1
Localização: ES15.1 - BNCS
ABSTRACT
Background Recent studies have observed an association between immune-related adverse events (irAE) and favorable clinical outcomes in the setting of cancer treatment with immune checkpoint inhibitors (ICI). However, results have been variable and inconclusive. Therefore, we have conducted a pan-cancer meta-analysis evaluating the relationship between irAEs and clinical outcomes. Materials and Methods The search included studies published in PubMed, Embase, and Web of Science from conception to 12.28.2019 as well as abstracts published in the ASCO and ESMO meetings from 2015 to 2019. Studies were included if ICI was used in advanced or metastatic cancer settings and excluded if data contained only combination therapy regimens or contained anti-CTLA-4. Raw data for overall response rate (ORR), hazard ratios (HR), number of patients (n), and p values for overall survival (OS) and progression-free survival (PFS) were extracted. Pooled sensitivity (SN), specificity (SP), positive (PPV) and negative predictive values (NPV), and odds ratios (ORs) were calculated using the 2 × 2 table and logit transformed proportions; and summary receiver operating curve (sROC) was generated using the bivariate approach for ORR. Pooled HRs were calculated using the means weighted by inverse of the variance for OS and PFS. Heterogeneity was assumed and random effects model was used throughout the analyses. Results Final analysis included 32 studies, among which ORR data were available in 15 studies, OS in 17, and PFS in 16. 17 studies evaluated non-small cell lung cancer (NSCLC), two studies melanoma, one study gastric cancer, three studies renal cell carcinoma (RCC), seven studies various cancer types, two studies urothelial carcinoma, and one study head and neck cancer (HNSCC). With respect to ORR, pooled SN, SP, PPV and NPV, and OR were 0.522 [0.423–0.619], 0.810 [0.771–0.844], 0.516 [0.413–0.618], 0.819 [0.764–0.864], and 4.59 [3.24–6.50], respectively (AU)
Assuntos

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Coleções: Bases de dados nacionais / Espanha Base de dados: IBECS Assunto principal: Antígeno B7-H1 / Neoplasias Limite: Humanos Idioma: Inglês Revista: Clin. transl. oncol. (Print) Ano de publicação: 2021 Tipo de documento: Artigo Instituição/País de afiliação: Kansas University Medical Center/USA / Tufts University School of Medicine/USA
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Coleções: Bases de dados nacionais / Espanha Base de dados: IBECS Assunto principal: Antígeno B7-H1 / Neoplasias Limite: Humanos Idioma: Inglês Revista: Clin. transl. oncol. (Print) Ano de publicação: 2021 Tipo de documento: Artigo Instituição/País de afiliação: Kansas University Medical Center/USA / Tufts University School of Medicine/USA
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