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Search / Trial NCT05351294

Assessment of Early Radiation Oncology Involvement Alongside Standard Oncologic Care in the Managemet

Launched by RUTGERS, THE STATE UNIVERSITY OF NEW JERSEY · Apr 27, 2022

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Quality Of Life Palliative Care And Supportive Care

ClinConnect Summary

This clinical trial is studying whether early involvement of radiation therapy, along with standard cancer care, can improve the quality of life for patients with metastatic cancer. Quality of life is measured using a specific questionnaire that asks patients about their overall well-being. The aim is to see if starting radiation therapy sooner can make a positive difference for patients compared to those who receive only standard care.

To be eligible for this trial, participants must be at least 18 years old and have a confirmed diagnosis of metastatic cancer, meaning the cancer has spread and is no longer curable. They should also have a life expectancy of 6 to 24 months and be receiving or planning to receive other cancer treatments, like chemotherapy or immunotherapy. If you join the study, you will be randomly assigned to either the group receiving early radiation therapy or the group receiving standard care alone. Throughout the trial, your health and well-being will be monitored to see how you are coping with your treatment.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • The inclusion criteria for this study are as follows:
  • 1. Age ≥ 18 years
  • 2. Zubrod performance status 0-2
  • 3. Pathology-proven cancer, with primary site outside of the central nervous system
  • 4. Clinical (based on physical exam or imaging) or pathological diagnosis of metastatic disease, for which curative intent treatment is not feasible and treatment goals are palliative. Both patients with newly diagnosed metastatic disease, and those who have a metastatic relapse after prior curative-intent treatment for their malignancy, are eligible.
  • 5. Estimated life expectancy 6-24 months. Guidelines for estimating life expectancy will be based on best available evidence, based primarily on tumor type, systemic therapy used and its expected outcome, line of systemic therapy, and in some cases patients' initial response to systemic therapy, along with the enrolling medical oncologist's judgement.
  • 6. Either planned, or actively receiving, systemic therapy (chemotherapy, targeted/biologic therapy, immunotherapy, or hormonal therapy)
  • 7. Ability to understand and the willingness to sign a written informed consent document
  • 8. If a patient is actively participating in another clinical trial utilizing an investigation agent, they are still eligible for participation in this study unless radiation therapy is explicitly not allowed in that trial.
  • Exclusion Criteria:
  • The exclusion criteria for this study are as follows:
  • 1. Patients with metastatic solid tumors but life expectancy longer than 24 months will be excluded. This list includes (but is not limited to):
  • 1. Castrate-sensitive prostate cancer (castrate-resistant prostate cancer are eligible)
  • 2. Breast cancer responsive to hormonal therapy
  • 3. Endometrial cancer responsive to hormonal therapy
  • 4. Patients receiving first line systemic therapy, for whom median progression-free survival is greater than 6 months, and response to therapy has not been assessed yet.
  • 2. Patients considered metastatic only due to pleural or peritoneal metastases without metastases to any other organ are excluded since palliative radiation therapy is less commonly used in these cases.
  • 3. Patients with cancer considered incurable that is locally advanced but nonmetastatic.
  • 4. Patients with leukemia or primary central nervous system cancers will be excluded since these patients less commonly are treated with palliative radiation therapy. Patients with lymphoma and multiple myeloma are eligible if they meet the other eligibility criteria.
  • 5. Any patient for whom standard-of-care radiation oncology referral would be immediately indicated for palliative radiation therapy. The purpose of this is to ensure that patients in the control arm will not have a detriment in their care by not seeing a radiation oncologist at enrollment,
  • 6. In order to avoid bias from prior standard-of-care radiation oncology involvement, patients will also be excluded if they are undergoing active follow-up with a radiation oncologist after prior palliative radiation therapy.
  • 7. History of whole brain radiation therapy for brain metastases (patients who underwent one prior treatment with radiosurgery for brain metastases are eligible)
  • 8. Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, adrenal insufficiency, chronic liver disease, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
  • 9. Pregnant or breastfeeding women; Subjects who are pregnant are excluded from this study because radiation therapy has the potential for teratogenic or abortifacient effects.
  • 10. Cognitively impaired adults lacking decision-making capacity or unable to consent. -

About Rutgers, The State University Of New Jersey

Rutgers, The State University of New Jersey, is a prestigious public research university renowned for its commitment to advancing medical science and public health. As a leading clinical trial sponsor, Rutgers leverages its extensive academic resources, cutting-edge facilities, and a diverse team of experts to conduct innovative research that addresses critical health challenges. The university fosters collaboration across disciplines, engaging in partnerships with healthcare institutions and industry leaders to enhance the development of novel therapies and improve patient outcomes. With a strong emphasis on ethical standards and regulatory compliance, Rutgers is dedicated to advancing clinical knowledge while prioritizing participant safety and well-being in all of its research endeavors.

Locations

New Brunswick, New Jersey, United States

Somerset, New Jersey, United States

New Brunswick, New Jersey, United States

Newark, New Jersey, United States

Newark, New Jersey, United States

Jersey City, New Jersey, United States

Newark, New Jersey, United States

Toms River, New Jersey, United States

Jersey City, New Jersey, United States

Patients applied

0 patients applied

Trial Officials

Malcolm Mattes, MD

Principal Investigator

Rutgers Cancer Institute of New Jersey

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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