{"denoms":[{"counts":[{"groupId":"OG000","value":"0"}],"units":"Participants"}],"description":"Tumor invasiveness and aggressiveness, determined by assessing the relationship between select indicators (including Ki67 nuclear labelling index, p53 expression, MGMT expression/methylation status, and additional tumor genetic profiling) with response to chemotherapy, time to progression, and tumor invasiveness (based on the Knosp criteria).","groups":[{"description":"All subjects will receive:\n\n1. Capecitabine (oral 5-Fluorouracil) 1500mg/m2 orally per day (divided into two doses with maximum daily dose of 2500mg) on days 1 through 14.\n2. Temozolomide (second generation alkylating agent) 150 to 200 mg/m2 orally on days 10 through 14.\n\nAfter completion of 6 cycles, patients achieving a complete or partial tumor response may continue to receive capecitabine temozolomide at the investigator's discretion in the absence of disease progression or unacceptable toxicity. Patients will be monitored for six months after they come off the study (either after completing 6 cycles or in setting of disease progression or unacceptable toxicity).\n\nCapecitabine: 1500mg/m2 orally per day (divided into two doses with maximum daily dose of 2500mg) on days 1 through 14.\n\nTemozolomide: 150 to 200 mg/m2 orally on days 10 through 14.","id":"OG000","title":"All Patients"}],"populationDescription":"Data was not collected in the specified time frame for this outcome measure.","reportingStatus":"POSTED","timeFrame":"6 months","title":"Tumor Invasiveness and Aggressiveness, Determined by Assessing the Relationship Between Select Indicators With Response to Chemotherapy, Time to Progression, and Tumor Invasiveness.","type":"SECONDARY"}