# Early therapeutic monitoring of response to therapy with serial ultrasound in metastatic RCC

> **NIH NIH R03** · STANFORD UNIVERSITY · 2020 · $157,700

## Abstract

Project Summary
We propose a pilot study to detect therapeutic response as early as 3 weeks after initiating therapy,
using Doppler ultrasound to measure changes in tumor vascularity in patients with metastatic renal cell
carcinoma (mRCC). Biomarkers to rapidly detect response to RCC therapy are urgently needed, because not
all patients respond to first line treatment with anti-angiogenesis tyrosine kinase inhibitor (axitinib), plus anti-PD-
1 immune checkpoint inhibitor (pembrolizumab). Yet all patients endure the side effects of this combination
treatment (fatigue, nausea, diarrhea, and/or liver inflammation) while awaiting standard of care computed
tomography (CT) imaging. Currently, 12 weeks is required to assess response by measuring decreases in tumor
diameters with CT because tumor size does not typically change before 12 weeks of therapy. Rapid detection
of response to RCC therapy would minimize use of ineffective drugs and allow patients to discontinue ineffective
therapies and continue only effective therapy. Because RCC treatments target angiogenesis, we have found that
imaging-based measurements of tumor vascularity, such as perfusion CT scans, or novel PET agent F18-
FPPRGD2 that binds blood vessels, can detect early response to therapy in mRCC. But these require
intravenous injections and visits to the radiology department. We have developed highly sensitive, non-contrast,
vascular imaging using advanced power Doppler ultrasound that can be performed at bedside in the oncology
clinic to image vessels as small as 1mm in diameter. Now, we propose to use advanced power Doppler
ultrasound for a pilot study to assess changes in tumor vascularity, during routine oncology clinic visits for
patients receiving combined therapy. We hypothesize that changes in tumor vascularity measured by
ultrasound, can detect response to treatment earlier than changes in tumor diameters. We will enroll 20
patients with mRCC, to be evaluated with power Doppler ultrasound before treatment and after 3 weeks and 6
weeks of combined axitinib and pembrolizumab therapy. Our pilot study aims to determine if 1) power Doppler
ultrasound can detect changes as early as 3 and/or 6 weeks after initiating therapy with pembrolizumab and
axitinib; 2) if changes detected by ultrasound correlate with response measured by standard of care CT scan
after 12 weeks of therapy; and 3) if ultrasound at 3 weeks or 6 weeks has better correlation with standard 12
week results. We will use power Doppler ultrasound imaging to accelerate detection of response to
combined axitinib + pembrolizumab. If successful, we can apply our approach to additional tumors and
drugs, as changes in tumor vascularity are a key mechanism of response to most cancer therapies.

## Key facts

- **NIH application ID:** 10046819
- **Project number:** 1R03CA252776-01
- **Recipient organization:** STANFORD UNIVERSITY
- **Principal Investigator:** Jeremy Dahl
- **Activity code:** R03 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2020
- **Award amount:** $157,700
- **Award type:** 1
- **Project period:** 2020-08-14 → 2023-07-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10046819

## Citation

> US National Institutes of Health, RePORTER application 10046819, Early therapeutic monitoring of response to therapy with serial ultrasound in metastatic RCC (1R03CA252776-01). Retrieved via AI Analytics 2026-05-24 from https://api.ai-analytics.org/grant/nih/10046819. Licensed CC0.

---

*[NIH grants dataset](/datasets/nih-grants) · CC0 1.0*
