﻿WEBVTT

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<v ->So my name is Renee Donahue.</v>

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I'm a staff scientist at the National Cancer Institute

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at the National Institutes of Health in Bethesda, Maryland.

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I work in the laboratory of Tumor Immunology and Biology,

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which is a translational research program,

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composed of seven pre-clinical groups,

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and we work very closely with the Clinical Trials group.

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I lead one of those seven groups,

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and my team, especially, works very close

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with the Clinical Trials team.

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We're looking to, basically,

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examine the immune responses of patients

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that are enrolled in our clinical trials

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at the NCI.

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And we're looking, basically,

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for correlates or things that associate

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with clinical responses of patients

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or things that associate with the development

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of adverse events in these patients.

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I like to be in the lab as much as I can,

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but I have to rely heavily on my team

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to sort of move things along.

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So, day in and day out I'm designing experiments,

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analyzing data with my team,

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putting together presentations, writing papers.

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There's a lot of meetings with our oncologists

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where we're sort of looking to

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design and refine protocols that are planned

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in the future.

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One of the really cool things

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that we get to do in the lab is

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we do a lot of first in human studies.

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So these are trials where agents

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that have only been tested pre-clinically

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and have never been in people are actually put in patients.

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For example, the Phase 1 study of Avelumab,

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which is an anti-PD-L1 antibody

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that's capable of mediating ADCC,

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and there was a lot of concern raised about that

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because there was concern that we might deplete immune cells

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that express this target.

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So my lab was involved in sort of

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looking extensively at the immune responses

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of patients enrolled in this trial and was able to show

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that we did not deplete PD-L1 expressing subsets.

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And that's really exciting for us

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because this agent has since gone on

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to be approved by the FDA for two indications.

