A Study of Reduced-dose Radiation in People With Metastatic Tumors With a Genetic Change

  • STATUS
    Recruiting
  • End date
    Aug 1, 2024
  • participants needed
    58
  • sponsor
    Memorial Sloan Kettering Cancer Center
Updated on 1 October 2021

Summary

This study will test whether reduced-dose radiotherapy is an effective treatment for metastatic tumors with an ATM mutation. The researchers want to find the lowest dose of radiation that would still be effective to treat these tumors.

Details
Condition Liver Metastases, Brain Metastases, metastasized, Bone Metastases, Cancer, Metastatic, metastases, secondaries, Neoplasm Metastasis, cancers metastatic, secondary cancer, Metastasis, Metastatic Cancer, metastatic disease, metastatic tumor
Treatment Palliative radiotherapy
Clinical Study IdentifierNCT05010031
SponsorMemorial Sloan Kettering Cancer Center
Last Modified on1 October 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Histologically confirmed malignancy with at least one metastatic lesion referred for palliative radiotherapy
Pathogenic mutation in ATM (somatic and germline allowed)
ECOG performance status 0-2
Age 18 years
Able to provide informed consent
Patients at reproductive potential must agree to practice an effective contraceptive method during radiation treatments
Expected life expectancy of at least 6 months

Exclusion Criteria

Previous radiotherapy to the intended treatment site that precludes developing a treatment plan that respects normal tissue tolerances
Serious medical co-morbidities precluding radiotherapy
Pregnant or breast-feeding women
Concomitant pathogenic mutation in p53
Lesions excluded from de-escalation include regions in which the risk of local disease progression is unacceptably high, including CNS disease and cord compression, and areas in which re-irradiation would not be feasible, including spinal cord overlap
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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