Expired Study
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New York, New York 10065


Purpose:

To compare the volumetric response achieved using semi-automated computer techniques with the uni-dimensional (RECIST) and bi-dimensional (WHO) criteria as part of clinical trials running at MSKCC, testing new agents for different types of solid tumors.


Study summary:

To compare the volumetric response achieved using semi-automated computer techniques with the uni-dimensional (RECIST) and bi-dimensional (WHO) criteria as part of clinical trials running at MSKCC, testing new agents for different types of solid tumors.


Criteria:

Inclusion Criteria: - Registered and being treated on one of the following therapeutic protocols: 06-043, 07-052, 07-057, 07-112, 07-116, 08-093, and 08-054 - Have at least one measurable lesion* as per RECIST criteria situated in lung, liver or lymph node meeting RECIST criteria noted on a baseline CT scan. - Baseline** and at least one follow-up CT scan to likely to be obtained at an MSKCC facility - All patients must be > or = to 18 years old - The measurable lesions are metastatic in the liver, lung and lymph nodes. The algorithms do not distinguish between primary and metastatic disease, therefore, in selected cases, a primary lesion such as in the liver or lung may also be assessed. - Baseline CT are prefer but if not able to obtain for volumetric reconstructions follow up studies will still be use for other objectives if the study. Exclusion Criteria: - Pregnant or lactating women


NCT ID:

NCT00582751


Primary Contact:

Principal Investigator
Robert Lefkowitz, MD
Memorial Sloan-Kettering Cancer Center


Backup Contact:

N/A


Location Contact:

New York, New York 10065
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: January 20, 2018

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