Radiation + Chemotherapy for Salivary Gland Cancer
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial aims to determine whether combining radiation therapy with chemotherapy is more effective than radiation alone for treating surgically removed salivary gland tumors. The treatments under investigation include 3-dimensional conformal radiation therapy, intensity-modulated radiation therapy, and the chemotherapy drug cisplatin. Suitable candidates have undergone surgery for high-risk salivary gland tumors and show no remaining cancer, but require further treatment to prevent recurrence. As a Phase 2 trial, this research focuses on assessing the treatment's effectiveness in an initial, smaller group of participants.
Will I have to stop taking my current medications?
The trial information does not specify if you need to stop taking your current medications. However, it does mention that you cannot have prior systemic chemotherapy or radiation therapy for salivary gland cancer and cannot use certain growth factors or stimulating agents during radiotherapy.
Is there any evidence suggesting that this trial's treatments are likely to be safe?
A previous study demonstrated promising safety results for intensity-modulated radiation therapy (IMRT). Only about 11% of patients experienced cancer recurrence, and side effects like skin irritation were manageable. Another study found that 3-dimensional conformal radiotherapy (3D-CRT) caused side effects that appeared later, but these were similar to those from standard treatments.
Cisplatin, a chemotherapy drug, has been used safely in other cancer treatments. Research has shown that combining cisplatin with another drug was effective and generally safe for patients with salivary gland cancer. However, about 15% of patients experienced a return of cancer in some form.
Overall, these treatments are in advanced testing stages, suggesting they are relatively well-tolerated. However, like all treatments, there is a chance of side effects. Participants should consider this and discuss any concerns with their healthcare provider.12345Why are researchers excited about this trial's treatments?
Most treatments for salivary gland cancer typically involve surgery followed by radiation therapy, sometimes combined with chemotherapy to manage the disease. However, researchers are excited about combining 3-dimensional conformal radiation therapy (3D-CRT) and intensity-modulated radiation therapy (IMRT) with chemotherapy because these advanced radiation techniques can more precisely target tumors. This precision spares healthy tissues and reduces side effects, potentially improving patient outcomes. Additionally, the integration of cisplatin, a chemotherapy drug, during radiation therapy may enhance the effectiveness of the treatment by sensitizing cancer cells to radiation, offering a promising approach over traditional methods.
What evidence suggests that this trial's treatments could be effective for salivary gland cancer?
This trial compares two types of radiation therapy, 3-dimensional conformal radiation therapy (3D-CRT) and intensity-modulated radiation therapy (IMRT), for treating salivary gland tumors. Research has shown that 3D-CRT can reduce dry mouth and protect the parotid glands, which are crucial for saliva production. IMRT has demonstrated better cancer control than 3D-CRT, particularly in more advanced cases. In Arm I of this trial, patients will receive either 3D-CRT or IMRT along with the chemotherapy drug cisplatin, which has about an 18% success rate in treating advanced salivary gland cancer. Although this rate is not very high, cisplatin can help manage the disease when combined with radiation. Arm II involves patients receiving only 3D-CRT or IMRT. Overall, combining these treatments aims to improve survival and control tumor growth after surgery.24678
Who Is on the Research Team?
Cristina P. Rodriguez, MD
Principal Investigator
OHSU Knight Cancer Institute
Are You a Good Fit for This Trial?
This trial is for patients with high-risk malignant salivary gland tumors removed by surgery. Eligible participants must have certain types of these tumors, no macroscopic disease post-surgery, and be free of distant metastases. They should not have had prior chemo or radiation for this cancer and must meet specific blood count and organ function criteria.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants undergo 3-dimensional conformal radiotherapy (3D-CRT) or intensity-modulated radiotherapy (IMRT) 5 days a week for 6-6.5 weeks. In Arm I, patients also receive cisplatin IV over 60 minutes on specified days during radiotherapy.
Follow-up
Participants are monitored for safety and effectiveness after treatment. Follow-up visits occur at 3, 6, 9, 12, and 24 months, every 6 months for 2 years, and then annually thereafter.
What Are the Treatments Tested in This Trial?
Interventions
- 3-dimensional conformal radiation therapy
- Cisplatin
- Intensity-modulated radiation therapy
Find a Clinic Near You
Who Is Running the Clinical Trial?
Radiation Therapy Oncology Group
Lead Sponsor
National Cancer Institute (NCI)
Collaborator
NRG Oncology
Collaborator