NCT00132704

Brief Summary

Doctors will take some tissue from the tissue removed during surgery in order to study how the blood vessels of the tumor respond to radiation therapy. The tissue obtained will be used to determine how these tumor blood vessels respond to radiation therapy delivered to the tumor, after it has been removed. This radiation is delivered in the research lab. This research is being conducted in order to develop new methods to treat tumors by radiation therapy. No additional surgery will be performed to obtain these samples, and only materials that remain after all diagnostic testing has been completed will be used.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
149

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Aug 2004

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 1, 2004

Completed
1 year until next milestone

First Submitted

Initial submission to the registry

August 18, 2005

Completed
4 days until next milestone

First Posted

Study publicly available on registry

August 22, 2005

Completed
8.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2014

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2014

Completed
Last Updated

July 24, 2014

Status Verified

July 1, 2014

Enrollment Period

9.9 years

First QC Date

August 18, 2005

Last Update Submit

July 23, 2014

Conditions

Keywords

Lung cancer metastases to the CNS (adenocarcinomas)Melanoma metastases to the CNSBreast cancer metastases to the CNS (ductal carcinomas)Central nervous system gliomasColorectal cancers (adenocarcinomas)Ovarian cancers (papillary serous carcinomas)Endometrial cancers (endometrioid carcinomas)Cervical cancers (squamous cell carcinomas)Sarcomas (liposarcomas and leiomyosarcomas)Thoracic mesotheliomasColorectal cancers metastatic to the liverPrimary adenocarcinomas of the lungPrimary squamous cell carcinomas of the lungPancreatic Cancers-adenocarcinoma

Outcome Measures

Primary Outcomes (1)

  • apoptotic response

    The peak apoptotic radiation response will be obtained for each of the tumor type and the result compared to that of the mouse experiments in Garcia-Barros (no formal testing only qualitative statements).

    2 years

Study Arms (2)

A

The experiments in Group A will be conducted in order to determine if human tumor microvascular endothelium displays similar dose parameters as mouse tumor endothelium, and if the microvascular endothelium of tumors of different types behaves in a similar fashion in its response to IR.

Radiation: Ionizing radiation (IR) therapy

B

The experiments in Group B will be conducted in order to determine if tumor endothelium isolated to near homogeneity demonstrates dose parameters similar to those used in single dose radiotherapy of brain tumors.

Radiation: Ionizing radiation (IR)

Interventions

Tumors will be sliced into 0.5cm fragments, incubated in culture medium and then irradiated to evaluate the kinetics and dose-dependencies of the endothelial apoptotic response. We will irradiate tumor fragments ex vivo at 0, 7, 13, 15, 17, and 25 Gy.

A

Tissue fragments of a total quantity of at least a 4x4x4 cm3 will be required. For each tumor a paraffin block will also be made for routine staining and IHC. Endothelial cell populations (at least 500 cells) will then be exposed to radiation at 0, 7, 11, 13, 15, 17, and 25 Gy and harvested at 4, 5 and 8 hours post IR.

B

Eligibility Criteria

Age19 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

undergoing surgery on the Neurosurgery, Hepatobiliary, Colorectal, Urology, Head and Neck, Gynecology, GMT and Thoracic Services at Memorial Sloan- Kettering Cancer Center.

You may qualify if:

  • Patients who are felt to have adequate tumor volume for these studies, at least a 2 x 2 x 2 cm3 tumor by physical exam, imaging studies or colonoscopy reports
  • Primary or recurrent tumors are eligible
  • Patients must be suitable candidates for surgery
  • Patients who have signed the informed consent

You may not qualify if:

  • Patients who are not considered suitable candidates for surgery
  • Patients who have received prior radiation therapy to the tumor being removed
  • Patients who have received chemotherapy within 6 months of tumor removal
  • Patients who are pregnant
  • Patients may choose to be excluded at any time
  • Minors are excluded from this study because there are expected to be very few minors with the tumor types which the investigators are evaluating in this study

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Memorial Sloan-Kettering Cancer Center

New York, New York, 10065, United States

Location

Related Links

Biospecimen

Retention: SAMPLES WITH DNA

tissue

MeSH Terms

Conditions

Ovarian NeoplasmsColorectal NeoplasmsMelanomaSmall Cell Lung CarcinomaLiposarcomaAdenocarcinomaCarcinoma, DuctalEndometrial NeoplasmsCarcinoma, EndometrioidUterine Cervical NeoplasmsCarcinoma, Squamous CellSarcomaLeiomyosarcoma

Interventions

Radiation, IonizingTherapeutics

Condition Hierarchy (Ancestors)

Endocrine Gland NeoplasmsNeoplasms by SiteNeoplasmsOvarian DiseasesAdnexal DiseasesGenital Diseases, FemaleFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesGenital Neoplasms, FemaleUrogenital NeoplasmsGenital DiseasesEndocrine System DiseasesGonadal DisordersIntestinal NeoplasmsGastrointestinal NeoplasmsDigestive System NeoplasmsDigestive System DiseasesGastrointestinal DiseasesColonic DiseasesIntestinal DiseasesRectal DiseasesNeuroendocrine TumorsNeuroectodermal TumorsNeoplasms, Germ Cell and EmbryonalNeoplasms by Histologic TypeNeoplasms, Nerve TissueNevi and MelanomasSkin NeoplasmsSkin DiseasesSkin and Connective Tissue DiseasesCarcinoma, BronchogenicBronchial NeoplasmsLung NeoplasmsRespiratory Tract NeoplasmsThoracic NeoplasmsLung DiseasesRespiratory Tract DiseasesNeoplasms, Adipose TissueNeoplasms, Connective and Soft TissueCarcinomaNeoplasms, Glandular and EpithelialNeoplasms, Ductal, Lobular, and MedullaryUterine NeoplasmsUterine DiseasesUterine Cervical DiseasesNeoplasms, Squamous CellNeoplasms, Muscle Tissue

Intervention Hierarchy (Ancestors)

RadiationPhysical Phenomena

Study Officials

  • Michael Zelefsky, M.D.

    Memorial Sloan Kettering Cancer Center

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 18, 2005

First Posted

August 22, 2005

Study Start

August 1, 2004

Primary Completion

July 1, 2014

Study Completion

July 1, 2014

Last Updated

July 24, 2014

Record last verified: 2014-07

Locations