Level B· Emerging clinical evidence with positive signalsClinical TrialEurope PMC

Microfluidic models for adoptive cell-mediated cancer immunotherapies

Adriani G., Pavesi A., Tan AT., Bertoletti A., Thiery JP., Kamm RD.

Clinical Trial on Hip, published in Drug Discov Today (2016) — summary generated from the PubMed abstract.

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Level B· Emerging clinical evidence with positive signalsEvidence level of this study

Several human studies show positive signals, while research methods and sample sizes continue to develop.

  • Level A · Stronger Clinical Evidence
  • Level B · Emerging clinical evidence with positive signals
  • Level C · Early human research exploring benefits
  • Level D · Scientific groundwork from lab and animal studies
  • Emerging · Emerging topic under active research
Read the A–D evidence level guide

This page is generated from the PubMed record. The Thai description is an automated summary of bibliographic fields and the abstract, not a full translation, and is not medical advice.

Study type
Clinical Trial
Journal
Drug Discov Today (2016)
Reported sample size
—
Source database
Europe PMC
PMID
27185084
PMCID
PMC5035566
DOI
10.1016/j.drudis.2016.05.006
Citations
52

Abstract (original English)

Current adoptive T cell therapies have shown promising results in clinical trials but need further development as an effective cancer treatment. Here, we discuss how 3D microfluidic tumour models mimicking the tumour microenvironment could help in testing T cell immunotherapies by assessing engineered T cells and identifying combinatorial therapy to improve therapeutic efficacy. We propose that 3D microfluidic systems can be used to screen different patient-specific treatments, thereby reducing the burden of in vivo testing and facilitating the rapid translation of successful T cell cancer immunotherapies to the clinic.

What this study does not prove

  • • This study does not prove SVF is an approved treatment or a replacement for standard care.

Evidence level

Several human studies show positive signals, while research methods and sample sizes continue to develop.

How we grade evidence
T-LymphocytesAnimalsHumansNeoplasmsImmunotherapy, AdoptiveLab-On-A-Chip Devices

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