Chemotherapy +/− Temsirolimus for Muscle Cancer
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial explores whether adding temsirolimus (an mTOR inhibitor) to standard chemotherapy improves treatment for rhabdomyosarcoma, a cancer that forms in muscles and soft tissues. The trial compares outcomes between patients receiving only chemotherapy and those receiving chemotherapy plus temsirolimus. It targets patients with intermediate-risk rhabdomyosarcoma, indicating a moderate chance of cancer recurrence after initial treatment. Newly diagnosed individuals with certain types of rhabdomyosarcoma who have not received prior chemotherapy may qualify to participate. The research aims to determine if temsirolimus can more effectively stop tumor growth. As a Phase 3 trial, this study represents the final step before FDA approval, offering patients a chance to contribute to potentially groundbreaking treatment advancements.
Will I have to stop taking my current medications?
The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the trial coordinators or your doctor.
Is there any evidence suggesting that this trial's treatments are likely to be safe?
Research has shown that temsirolimus has been safely used in patients with kidney cancer. It is approved in the U.S. and other countries for this purpose, indicating a reasonable level of safety. However, earlier studies in patients with soft tissue sarcoma found that temsirolimus had moderate side effects. These studies provide insight into how the drug might affect patients with similar conditions.
The chemotherapy drugs involved in the trial, such as vincristine sulfate, dactinomycin, cyclophosphamide, and irinotecan hydrochloride, have long been used in cancer treatments. They are generally well-tolerated at the doses used in trials, though side effects like nausea, fatigue, and low blood counts can occur. Extensive research has provided a strong base of safety data for these treatments.
While specific safety data for the exact combination being tested in this trial is not available, the trial phase suggests some confidence in its safety. This indicates that the treatment has passed earlier testing stages and has shown enough safety to be tested on a larger scale.12345Why are researchers excited about this trial's treatments?
Researchers are excited about these treatments for muscle cancer because they combine traditional chemotherapy drugs with temsirolimus, potentially enhancing effectiveness. Temsirolimus, a newer addition, inhibits a specific protein pathway (mTOR), which could stop cancer cells from growing and dividing. This targeted action differentiates it from standard chemotherapy, which generally affects both healthy and cancerous cells. Combining these mechanisms could lead to improved outcomes and fewer side effects compared to current treatments.
What evidence suggests that this trial's treatments could be effective for rhabdomyosarcoma?
Research shows that adding temsirolimus to standard chemotherapy does not benefit patients with intermediate-risk rhabdomyosarcoma, a type of muscle cancer. In this trial, participants in Regimen B will receive chemotherapy drugs such as vincristine, dactinomycin, and cyclophosphamide, along with temsirolimus. Studies have found that these chemotherapy drugs effectively stop tumor growth by killing cancer cells or preventing their spread. However, including temsirolimus does not enhance the treatment's effectiveness. Previous trials showed no significant improvement in patient outcomes with temsirolimus. While the chemotherapy itself works well, temsirolimus does not enhance its efficacy for this specific condition.16789
Who Is on the Research Team?
Abha A Gupta
Principal Investigator
Children's Oncology Group
Are You a Good Fit for This Trial?
This trial is for patients under 40 with newly diagnosed Rhabdomyosarcoma (RMS), a type of muscle tissue cancer, who haven't had previous chemotherapy or radiation. They must have an acceptable level of blood cells and kidney function, and be able to perform daily activities at least half the time. Pregnant women, breastfeeding mothers, those with uncontrolled diabetes or cholesterol levels, and individuals not using effective contraception are excluded.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive combination chemotherapy with or without temsirolimus, including surgery and radiotherapy
Maintenance
Participants receive vinorelbine and cyclophosphamide for maintenance therapy
Follow-up
Participants are monitored for safety and effectiveness after treatment
What Are the Treatments Tested in This Trial?
Interventions
- Cyclophosphamide
- Dactinomycin
- Irinotecan Hydrochloride
- Radiation Therapy
- Temsirolimus
- Vincristine Sulfate
- Vinorelbine
Cyclophosphamide is already approved in United States, European Union, Canada, Japan for the following indications:
- Breast cancer
- Ovarian cancer
- Multiple myeloma
- Leukemia
- Lymphoma
- Rheumatoid arthritis
- Breast cancer
- Ovarian cancer
- Multiple myeloma
- Leukemia
- Lymphoma
- Rheumatoid arthritis
- Breast cancer
- Ovarian cancer
- Multiple myeloma
- Leukemia
- Lymphoma
- Rheumatoid arthritis
- Breast cancer
- Ovarian cancer
- Multiple myeloma
- Leukemia
- Lymphoma
Find a Clinic Near You
Who Is Running the Clinical Trial?
National Cancer Institute (NCI)
Lead Sponsor