Proton Therapy for Reoccurring Cancer After Radiation
Prospective Evaluation of Pencil Beam Scanning Proton Therapy for Previously Irradiated Tumors
Recruiting
N/AInterventional Study
CNS CancerHead and Neck CancerGI CancerGynecologic CancerProstate CancerThoracic CancerBreast Cancer
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
1,800 (estimated)
Sponsor
The New York Proton Center · Other
Who this trial is looking for
This trial is looking for adults who have had tumors treated with radiation before. Participants will receive a new type of radiation treatment called Proton Therapy to see if it helps treat their reoccurring cancer.
Are You a Good Fit for This Trial?
You may be able to join if
I am at least 18 years old.
I give my consent to take part in this study.
I have had a physical exam within the last 90 days.
I have an Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2 within the last 90 days.
You may not be able to join if
I have a serious non-cancer disease that prevents me from receiving treatment.
I have had a different type of cancer unless I have been free of it for at least 3 years.
I have an active connective tissue disorder, such as lupus or scleroderma.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
The goal of this clinical research trial is to study the use of differing investigational doses and scheduling for Proton Therapy for tumors previously treated with radiation therapy. Generally, when patients are first treated for cancer with radiation therapy, they are treated with traditional photon (or x-ray) radiation therapy, which uses high-energy waves to kill tumor cells. In some cases, th…
The goal of this clinical research trial is to study the use of differing investigational doses and scheduling for Proton Therapy for tumors previously treated with radiation therapy. Generally, when patients are first treated for cancer with radiation therapy, they are treated with traditional photon (or x-ray) radiation therapy, which uses high-energy waves to kill tumor cells. In some cases, the cancer either returns or a new tumor can present in a different part of the body. With the usual radiation treatment, the photon beams travel all the way through the body. As a result, healthy tissues in front of and behind the tumor are exposed to radiation. Physicians who treat these cases where the tumor has returned often use a much lower dose of radiation to prevent patients from experiencing serious and long-term side-effects. This dose is often not strong enough to destroy the cancerous tumor. Alternatively, they may also treat a smaller area than would be indicated for complete tumor eradication, again in an attempt to prevent serious and long-term toxicities, but at the cost of optimally treating the cancer. Proton therapy, however, may offer a chance to safely deliver a more effective dose and volume of radiation as it is more targeted and can spare healthy tissues surrounding the tumor.
The reason we are conducting this research study is to look at whether Proton therapy can be a better way to treat reoccurring tumors in patients who have previously received radiation therapy to the same area, compared to treatment approaches used to date.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Age 18 years
* Patient provides study specific informed consent prior to study entry.
* Documented history and physical exam within 90 days prior to registration.
* ECOG PS 0, 1, or 2 within 90 days prior to registration
Exclusion Criteria:
* Non malignant systemic disease t…
Inclusion Criteria:
* Age 18 years
* Patient provides study specific informed consent prior to study entry.
* Documented history and physical exam within 90 days prior to registration.
* ECOG PS 0, 1, or 2 within 90 days prior to registration
Exclusion Criteria:
* Non malignant systemic disease that would preclude the patient from receiving study treatment or would prevent required follow up.
* Prior invasive non study malignancy unless disease free for ≥ 3 years
* Non melanoma skin cancer, low risk prostate cancer, well differentiated thyroid cancers, in situ carcinomas of the oral cavity, cervix, and other organs, and tumors that are not thought to impact the life expectancy of the patient are permissible.
* History of active connective tissue disorder (i.e., systemic lupus erythematosus, scleroderma), dermatomyositis, xeroderma pigmentosum
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