RecruitingPhase 2ACTRN12605000509662
Gemcitabine and carboplatin induction chemotherapy followed by concurrent cisplatin and IMRT for locally advanced nasopharyngeal cancer
Sponsor
Peter MacCallum Cancer Centre
Enrollment
30 participants
Start Date
Jul 1, 2004
Study Type
Interventional
Conditions
Eligibility
Sex: Both males and females
Plain Language Summary
Simplified for easier understanding
This study is testing a treatment approach for locally advanced nasopharyngeal cancer — a type of cancer that develops in the back of the nose and throat. The treatment combines two chemotherapy drugs (gemcitabine and carboplatin) given first to shrink the cancer, followed by radiation therapy with a precision technique called IMRT given at the same time as another chemotherapy drug (cisplatin). This combination approach aims to improve control of the cancer while limiting damage to surrounding tissues.
You may be eligible if:
- You have been diagnosed with WHO Type 2 or Type 3 nasopharyngeal cancer
- Your cancer is at an advanced local stage (T3–T4) or has spread to nearby lymph nodes (N1 > 3 cm, N2–N3)
- You have not had any prior cancer treatment
- You have no prior chemotherapy or radiation therapy
You may NOT be eligible if:
- There are no additional exclusion criteria listed for this study
Talk to your doctor about whether this trial might be right for you.
This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.
Interested in this trial?
Get notified about updates and connect with the research team.
Interventions
Induction chemotherapy for 9 weeks followed by concurrent chemoradiation for 7 weeks.
Induction chemotherapy for 9 weeks followed by concurrent chemoradiation for 7 weeks.
Locations(1)
View Full Details on ANZCTR
For the most up-to-date information, visit the official listing.
ACTRN12605000509662