Abstract

BackgroundProgrammed cell death 1 (PD-1) and programmed cell death-ligand 1(PD-L1) inhibitors have captured our attention as new therapeutic options for several tumor types. Nonetheless, the differences in efficacy between PD-1/PD-L1 inhibitors and conventional treatments (chemotherapy or targeted therapy) in pretreated advanced cancer patients remain unclear.Materials and MethodsA systematic literature search was conducted to identify phase III randomized controlled trials (RCTs)-based investigations of PD-1(nivolumab, pembrolizumab)/PD-L1 inhibitors (atezolizumab) against pretreated advanced cancer. We evaluated these trials for inclusion, assessed each study’s risk of bias and selected relevant data for analysis.ResultsThe eligibility criteria were met by 5,093 patients from 8 phase III RCTs. PD-1/PD-L1 inhibitors significantly extended overall survival relative to the conventional treatment, expressed as hazard ratio [HR] (0.72, 95% CI, 0.66 to 0.77, P < 0.001) and median month difference (2.83 months, 95% CI, 1.87 to 3.78, P < 0.001). The progression-free survival HRs favored PD-1/PD-L1 inhibitors over conventional treatment (0.88; 95% CI, 0.82 to 0.95, P = 0.002), whereas median month difference was just the opposite (−0.69 months, 95% CI, −1.14 to −0.24, P < 0.001).ConclusionsAmong selected patients with pretreated advanced cancer, PD-1/PD-L1 inhibitors, compared with conventional treatments (chemotherapy or targeted therapy), were associated with improvement in overall survival (2.83 months) but not progression-free survival. These findings will be important in considering PD-1/PD-L1 inhibitors in the treatment of pretreated advanced cancer and have implications for future study design.

Highlights

  • Cancer, especially advanced cancer, is still a pressing worldwide health issue [1]

  • Programmed cell death 1 (PD-1)/programmed cell death ligand 1 (PD-L1) inhibitors significantly extended overall survival relative to the conventional treatment, expressed as hazard ratio [HR] (0.72, 95% CI, 0.66 to 0.77, P < 0.001) and median month difference (2.83 months, 95% CI, 1.87 to 3.78, P < 0.001)

  • The progression-free survival HRs favored PD-1/PD-L1 inhibitors over conventional treatment (0.88; 95% CI, 0.82 to 0.95, P = 0.002), whereas median month difference was just the opposite (-0.69 months, 95% CI, -1.14 to -0.24, P < 0.001)

Read more

Summary

Introduction

Chemotherapy and radiation therapy have significantly improved overall clinical outcomes for localized cancer patients, advanced cancer patients present therapeutic challenges [2]. Especially programmed cell death 1(PD-1) and programmed cell death-ligand 1(PD-L1) have captured our attention as new therapeutic options for patients with selected advanced cancer for which no effective treatment yet existed [7]. Based on the initial trial findings, PD-1/ PD-L1 inhibitors have shown clinical efficacies against many different solid and hematologic malignancies, including NSCLC, melanoma, renal cell cancer and others [9,10,11,12]. Programmed cell death 1 (PD-1) and programmed cell deathligand 1(PD-L1) inhibitors have captured our attention as new therapeutic options for several tumor types. The differences in efficacy between PD-1/PDL1 inhibitors and conventional treatments (chemotherapy or targeted therapy) in pretreated advanced cancer patients remain unclear

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call