{"description":"All patients included in mortality assessment; only patients that received treatment included in adverse event reporting","eventGroups":[{"deathsNumAffected":31,"deathsNumAtRisk":355,"description":"Patients receive oxaliplatin IV over 2 hours and leucovorin calcium IV over 2 hours on day 1, and fluorouracil IV as a bolus on day 1, then continuously over 46 hours on days 1-3 of each cycle. Treatment repeats every 14 days for up to 12 cycles in the absence of disease progression or unacceptable toxicity. Patients also receive atezolizumab IV over 30-60 minutes on day 1 of each cycle, beginning in cycle 1 or 2. Treatment repeats every 14 days for up to 25 cycles in the absence of disease progression or unacceptable toxicity. Patients undergo CT or MRI every 6 months for the first 2 years, then for years 3-5 or until evidence of relapse, whichever comes first. Patients may also undergo blood sample collection throughout the trial. \\> \\> Atezolizumab: Given IV \\>\n\n* Biospecimen Collection: Undergo blood sample collection \\>\n* Computed Tomography: Undergo CT \\>\n* Fluorouracil: Given IV \\>\n* Leucovorin Calcium: Given IV \\>\n* Magnetic Resonance Imaging: Undergo MRI \\>\n* Oxaliplatin: Given IV \\>\n* Quality-of-Life Assessment: Ancillary studies","id":"EG000","otherNumAffected":346,"otherNumAtRisk":346,"seriousNumAffected":197,"seriousNumAtRisk":346,"title":"Arm I (Combination Chemotherapy, Atezolizumab)"},{"deathsNumAffected":33,"deathsNumAtRisk":357,"description":"Patients receive oxaliplatin IV over 2 hours and leucovorin calcium IV over 2 hours on day 1, and fluorouracil IV as a bolus on day 1, then continuously over 46 hours on days 1-3 of each cycle. Treatment repeats every 14 days for up to 12 cycles in the absence of disease progression or unacceptable toxicity. Patients undergo CT or MRI every 6 months for the first 2 years, then for years 3-5 or until evidence of relapse, whichever comes first. Patients may also undergo blood sample collection throughout the trial. \\>\n\n* Biospecimen Collection: Undergo blood sample collection \\>\n* Computed Tomography: Undergo CT \\>\n* Fluorouracil: Given IV \\>\n* Leucovorin Calcium: Given IV \\>\n* Magnetic Resonance Imaging: Undergo MRI \\>\n* Oxaliplatin: Given IV \\>\n* Quality-of-Life Assessment: Ancillary studies","id":"EG001","otherNumAffected":324,"otherNumAtRisk":334,"seriousNumAffected":138,"seriousNumAtRisk":334,"title":"Arm II (Combination Chemotherapy)"}],"frequencyThreshold":"0","otherEvents":[{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 12.1","stats":[{"groupId":"EG000","numAffected":161,"numAtRisk":346,"numEvents":1549},{"groupId":"EG001","numAffected":148,"numAtRisk":334,"numEvents":1051}],"term":"Anemia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 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