Surrogate End Points for Overall Survival in Metastatic, Locally Advanced, or Unresectable Pancreatic Cancer: A Systematic Review and Meta-Analysis of 24 Randomized Controlled Trials

2017 ◽  
Vol 24 (8) ◽  
pp. 2371-2378 ◽  
Author(s):  
Eleftherios A. Makris ◽  
Regina MacBarb ◽  
Danielle J. Harvey ◽  
George A. Poultsides
Nutrients ◽  
2020 ◽  
Vol 12 (9) ◽  
pp. 2798
Author(s):  
Fu-An Yang ◽  
Yang-Ching Chen ◽  
Cheng Tiong

Immunonutrition is administered to improve the outcome of patients with pancreatic cancer undergoing surgery. However, its effect and mechanism of action remain unclear. Therefore, we conducted this systematic review and meta-analysis to assess its effects on postoperative outcome and the immune system. Randomized controlled trials (RCTs) were identified and data extracted by two reviewers independently from electronic databases from their inception to 31 October 2019. The result was expressed as the risk ratio (RR) for categorical variables and mean difference (MD) for continuous variables with 95% confidence intervals (CIs). Six RCTs published from 1999 and 2016, with a total of 368 patients, were included. The results revealed that immunonutrition significantly decreased the rate of infectious complications (RR = 0.47, 95% CI (0.23, 0.94), p = 0.03) and the length of hospital stay (MD = −1.90, 95% CI (−3.78, −0.02), p = 0.05) by modulating the immune system, especially in preoperative group in subgroup analysis. We therefore recommend that patients with pancreatic cancer undergoing surgery could take the advantage of immunonutrition, especially in the preoperative period.


2021 ◽  
Vol 39 (15_suppl) ◽  
pp. e21139-e21139
Author(s):  
Yi Hu ◽  
Xiaochen Zhao ◽  
Yuezong Bai ◽  
Longgang Cui ◽  
Fan Zhang

e21139 Background: Several therapies based on immune checkpoint inhibitors (ICIs) have been approved as the 1L standard of care for PD-L1≥ 50% advanced non-small cell lung cancer (NSCLC). However, little is known about the difference in efficacy between different strategies. We conducted a systematic review and meta-analysis to help clinicians choose more reasonable treatment options. Methods: We searched PubMed, Cochrane library, Embase and major conference proceedings from January 2010 to December 2020 for randomized controlled trials that had available subgroup hazard ratios (HRs) for overall survival according to PD-L1≥ 50%. Only drugs met primary outcome or approved by FDA were included for analysis. The primary outcome was the difference in overall survival (OS). HRs and 95% CI were calculated for the pooled OS using a random-effects model. p<0.05 was considered as statistical difference. Results: A total of 10 randomized controlled trials were included for this meta-analysis. The pooled HR and 95% CI for monotherapy, ICI plus chemotherapy and ICI plus ICI were 0.64 (0.55, 0.74), 0.64 (0.51, 0.79) and 0.70 (0.55, 0.90), respectively. There was no statistical differences between ICI monotherapy and ICI plus chemotherapy (HR 1.00, 95% CI 0.77- 1.30), between ICI monotherapy and ICI plus ICI (HR 0.91, 95% CI 0.69- 1.22) or between ICI plus chemotherapy and ICI plus ICI (HR 0.91, 95% CI 0.66- 1.27). Conclusions: For PD-L1≥ 50% NSCLC patients, active ICI monotherapies showed no different efficacy when compared with ICI combination therapies.


2019 ◽  
Vol 37 (15_suppl) ◽  
pp. e14168-e14168
Author(s):  
Jianchun Duan ◽  
Longgang Cui ◽  
Zhengyi Zhao ◽  
Guoqiang Wang ◽  
Shiqing Chen ◽  
...  

e14168 Background: Immunotherapy has revolutionized the treatment of cancer, however, little is known about the effect of patients’ age on the efficacy of immune checkpoint inhibitors. We did a systematic review and meta-analysis to assess the heterogeneity of immune checkpoint inhibitor efficacy between young and elder patients in pan cancer. Methods: We systematically searched PubMed, Cochrane library, and Embase from January 2000 to November 2018 for randomized controlled trials that had available hazard ratios (HRs) for death according to patients’ age. We also reviewed abstracts and presentations from all major conference proceedings. Retrospective studies and trials that compared anti-PD-1/PD-L1 with other immunotherapies were excluded. The primary outcome was the difference in overall survival (OS). We calculated the pooled overall survival HR and 95% CI in young and elder patients using a random-effects model. Results: A total of 3365 publications were retrieved through initial literature search, 19 randomized controlled trials involving 12276 patients with solid tumors were included for this meta-analysis. PD-1 inhibitors exhibited significantly improved OS over PD-L1 inhibitors in younger patient population (HR 0.67, 95% CI 0.53-0.85), while no differences have been observed in elder population (HR 0.89, 95% CI 0.70-1.13). Subgroup analysis showed that PD-L1 inhibitors plus chemotherapies led to significantly improved overall survival (OS) in elder population (> = 65 years old) over that in younger population (< 65 years old) (HR 1.29, 95% CI 1.01-1.64). However, the opposite tendency was observed with PD-1 inhibitors plus chemotherapies, showing that the younger population obtained better OS benefit compared to the elder population (HR 0.69, 95% CI 0.47-1.01). Conclusions: In general, PD-1 inhibitors exhibited better clinical performance for survival outcome over PD-L1 inhibitors in younger patients. When combined with chemotherapies, PD-1 inhibitors and PD-L1 inhibitors showed distinct efficacy tendency across different age groups, indicating that age should be taken into account when making decisions about treatment strategies. Future studies and explorations of the underlying mechanisms are needed for the further optimization of treatment strategies in clinical practice.


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