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Participants who experienced investigator-reported DP but were benefitting from study treatment were permitted to continue GSK2118436 treatment upon approval of the GlaxoSmithKline Medical Monitor.","id":"EG000","otherNumAffected":181,"otherNumAtRisk":187,"seriousNumAffected":64,"seriousNumAtRisk":187,"title":"GSK2118436 150 mg BID"},{"deathsNumAffected":0,"deathsNumAtRisk":59,"description":"In the RP, participants received IV DTIC 1000 mg/m\\^2 every 3 weeks. Dose reductions were permitted based on the severity of the hematological toxicity. Stopping recommendations for study treatment were also provided for cases of reoccurring skin toxicity, cardiovascular complication or abnormalities, and liver abnormalities. Participants continued on treatment until DP, death, the occurrence of an unacceptable AE, or withdrawal from the study.","id":"EG001","otherNumAffected":51,"otherNumAtRisk":59,"seriousNumAffected":14,"seriousNumAtRisk":59,"title":"DTIC 1000 mg/m^2 in RP"},{"deathsNumAffected":1,"deathsNumAtRisk":37,"description":"Participants who received DTIC in the RP and experienced DP had the option, at the discretion of the Investigator, of receiving GSK2118436 150 mg BID in the Crossover Phase. Participants who permanently discontinued DTIC treatment due to an AE, withdrawal of consent, or for any reason other than DP were not eligible for crossover to GSK2118436. Crossover participants continued on GSK2118436 until further DP was noted. After DP on GSK2118436, participants were followed for response, progression, survival, and further anti-cancer therapy.","id":"EG002","otherNumAffected":37,"otherNumAtRisk":37,"seriousNumAffected":9,"seriousNumAtRisk":37,"title":"GSK25118436 in the Crossover Phase"}],"frequencyThreshold":"5","otherEvents":[{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"19.0","stats":[{"groupId":"EG000","numAffected":10,"numAtRisk":187,"numEvents":14},{"groupId":"EG001","numAffected":7,"numAtRisk":59,"numEvents":9},{"groupId":"EG002","numAffected":3,"numAtRisk":37,"numEvents":5}],"term":"Anaemia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system 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