{"classes":[{"categories":[{"measurements":[{"groupId":"OG000","lowerLimit":"14.4","upperLimit":"54.6","value":"22.1"},{"groupId":"OG001","lowerLimit":"31.7","upperLimit":"58.1","value":"43.4"},{"groupId":"OG002","lowerLimit":"23.3","upperLimit":"104.0","value":"37.9"},{"groupId":"OG003","lowerLimit":"8.4","upperLimit":"73.6","value":"24.6"},{"groupId":"OG004","lowerLimit":"47.4","upperLimit":"117.0","value":"82.4"},{"comment":"NA indicates that upper limit of CI was not estimable due to insufficient number of participants with events at study closure.","groupId":"OG005","lowerLimit":"63.0","upperLimit":"NA","value":"111.4"},{"comment":"NA indicates that upper limit of CI was not estimable due to insufficient number of participants with events at study closure.","groupId":"OG006","lowerLimit":"32.9","upperLimit":"NA","value":"77.7"},{"comment":"NA indicates that upper limit of CI was not estimable due to insufficient number of participants with events at study closure.","groupId":"OG007","lowerLimit":"19.3","upperLimit":"NA","value":"49.6"}]}]}],"denoms":[{"counts":[{"groupId":"OG000","value":"32"},{"groupId":"OG001","value":"33"},{"groupId":"OG002","value":"32"},{"groupId":"OG003","value":"14"},{"groupId":"OG004","value":"62"},{"groupId":"OG005","value":"69"},{"groupId":"OG006","value":"18"},{"groupId":"OG007","value":"7"}],"units":"Participants"}],"description":"OS was defined as the interval of time between the date of the first dose of study treatment and the date of death due to any cause.","dispersionType":"95% Confidence Interval","groups":[{"description":"Participants with rhabdoid tumors (MRT, RTK, ATRT, and selected tumors with rhabdoid features, including SCCOHT, also known as MRTO) received tazemetostat 800 mg BID orally in continuous 28-day cycles until disease progression, development of an unacceptable toxicity, withdrawal of consent, or termination of the study.","id":"OG000","title":"Rhabdoid Tumors: Cohort 1"},{"description":"Participants with relapsed or refractory synovial sarcoma with SS18-SSX rearrangement received tazemetostat 800 mg BID orally in continuous 28-day cycles until disease progression, development of an unacceptable toxicity, withdrawal of consent, or termination of the study.","id":"OG001","title":"Synovial Sarcoma: Cohort 2"},{"description":"Participants with other INI-1-negative tumors or any solid tumor with EZH2 GOF mutation, including EMPNST, EMC, myoepithelial carcinoma, other INI-1-negative malignant tumors with sponsor approval, any solid tumor with EZH2 GOF mutation including but not limited to Ewing's sarcoma and melanoma received tazemetostat 800 mg BID orally in continuous 28-day cycles until disease progression, development of an unacceptable toxicity, withdrawal of consent, or termination of the study.","id":"OG002","title":"Other INI1-negative: Cohort 3"},{"description":"Participants with RMC received tazemetostat 800 mg BID orally in continuous 28-day cycles until disease progression, development of an unacceptable toxicity, withdrawal of consent, or termination of the study.","id":"OG003","title":"RMC: Cohort 4"},{"description":"Participants with ES received tazemetostat 800 mg BID orally in continuous 28-day cycles until disease progression, development of an unacceptable toxicity, withdrawal of consent, or termination of the study.","id":"OG004","title":"ES: Cohort 5"},{"description":"Participants with ES undergoing optional tumour biopsy received tazemetostat 800 mg BID orally in continuous 28-day cycles until disease progression, development of an unacceptable toxicity, withdrawal of consent, or termination of the study.","id":"OG005","title":"ES Paired Biopsy: Cohort 6"},{"description":"Participants with poorly differentiated chordoma (or other chordoma with sponsor approval) received tazemetostat 800 mg BID orally in continuous 28-day cycles until disease progression, development of an unacceptable toxicity, withdrawal of consent, or termination of the study.","id":"OG006","title":"Chordoma: Cohort 7"},{"description":"Participants with ES received tazemetostat 1600 mg QD orally in continuous 28-day cycles until disease progression, development of an unacceptable toxicity, withdrawal of consent, or termination of the study.","id":"OG007","title":"ES 1600 mg: Cohort 8"}],"paramType":"MEDIAN","populationDescription":"ITT population included all participants who received at least 1 dose of tazemetostat.","reportingStatus":"POSTED","timeFrame":"Tumor assessment performed at screening and every 8 weeks beginning at Cycle 3 Day 1, until disease progression or the start of subsequent anti-cancer therapy, whichever occurred first, up to 5.75 years (cycle duration: 28 days)","title":"All Cohorts: Overall Survival (OS)","type":"SECONDARY","unitOfMeasure":"Weeks"}