Vismodegib + Erlotinib (+/- Gemcitabine) for Pancreatic Cancer
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests a combination of cancer drugs to determine the best dose and monitor side effects in patients with metastatic pancreatic cancer or inoperable solid tumors. The drugs under study—Vismodegib (GDC-0449), Erlotinib Hydrochloride, and Gemcitabine Hydrochloride—aim to kill cancer cells or inhibit their growth. Participants must have a type of pancreatic cancer or solid tumor unsuitable for surgery or other standard treatments. This trial targets those who have declined standard treatment or exhausted other options. As a Phase 1 trial, the research focuses on understanding how the treatment works in people, offering participants a chance to receive potentially groundbreaking therapy.
Will I have to stop taking my current medications?
The trial protocol does not specify if you must stop taking your current medications, but it does exclude participants who are currently on a CYP3A4 inhibitor or inducer. It's best to discuss your current medications with the trial team to see if they might affect your eligibility.
Is there any evidence suggesting that this trial's treatments are likely to be safe?
Research has shown that the combination of vismodegib and erlotinib is generally manageable for patients. In earlier studies, patients taking these drugs together often experienced stable cancer for a few treatment cycles, indicating the drugs helped prevent the cancer from worsening temporarily. Although some patients did not see significant changes in their overall condition, most did not experience severe side effects.
Some patients in the study also took gemcitabine, a well-known cancer treatment with established safety. When all three drugs were used together, the combination remained manageable for patients.
Overall, while the drugs may not dramatically alter the disease for everyone, they have been shown to be safe enough for use in clinical trials, suggesting the treatment is unlikely to cause serious harm for most people.12345Why are researchers excited about this trial's treatments?
Unlike the standard treatments for pancreatic cancer, which typically involve chemotherapy drugs like gemcitabine, the investigational treatment with Vismodegib and Erlotinib offers a unique mechanism of action. Researchers are excited about these treatments because Vismodegib targets the Hedgehog signaling pathway, which is thought to play a role in the growth of cancer cells. Erlotinib adds another layer by inhibiting EGFR, a protein that helps cancer cells grow and divide. This combination could potentially offer a more comprehensive attack on cancer cells, making it a promising option for patients who may not respond well to existing therapies.
What evidence suggests that this trial's treatments could be effective for pancreatic cancer?
Research has shown that a combination of three drugs—vismodegib, erlotinib, and gemcitabine—might help destroy more cancer cells in pancreatic cancer. In this trial, some participants will receive vismodegib and erlotinib, while others will also receive gemcitabine. Erlotinib blocks certain proteins that cancer cells need to grow. Studies indicate that this drug combination is generally well-tolerated, but it hasn't yet significantly impacted patients with advanced pancreatic cancer. However, some patients have experienced stable disease for several treatment cycles. These early results are promising, but more research is needed to confirm the treatment's effectiveness.12346
Who Is on the Research Team?
Charles Erlichman
Principal Investigator
Mayo Clinic
Are You a Good Fit for This Trial?
This trial is for adults with metastatic pancreatic cancer or solid tumors that can't be surgically removed. They must not have curative standard therapy options, agree to use effective contraception, abstain from smoking, and be able to take oral medication. Excluded are those who've had certain recent treatments, uncontrolled illnesses, CNS metastases unless stable, pregnant/nursing women, or inadequate organ function.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive Hedgehog antagonist GDC-0449 and erlotinib hydrochloride orally once daily on days 1-28. Some patients also receive gemcitabine hydrochloride intravenously on days 1, 8, and 15. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.
Follow-up
Participants are monitored for safety and effectiveness after treatment completion, including adverse events and response assessment.
What Are the Treatments Tested in This Trial?
Interventions
- Erlotinib Hydrochloride
- GDC-0449
- Gemcitabine Hydrochloride
Find a Clinic Near You
Who Is Running the Clinical Trial?
National Cancer Institute (NCI)
Lead Sponsor