{"description":"Adverse event reporting is collected routinely using case report forms. The SAE table reflects NCI Common Terminology Criteria for Adverse Events (CTCAEs) submitted by the institution, via expedited reporting (NCI AdEERs / CAeRs). The \"AE Other\" table reflects all CTCAEs collected excluding those that were reported as SAEs. Ineligible patients are excluded from reporting of adverse events. All-Cause Mortality includes all deaths collected on the study.","eventGroups":[{"deathsNumAffected":0,"deathsNumAtRisk":6,"description":"Part A1: Patients with relapsed/refractory solid tumors or anaplastic large cell lymphoma (ALCL) Part A2: Patients with recurrent/refractory malignancies who have confirmed ALK fusion proteins, ALK mutations, ALK amplification or evidence for MET mutation or amplification. Once Parts B and C are open to accrual, patients who are not eligible for either Part should enroll on Part A2, Part A3: Patients with recurrent/refractory neuroblastoma, who are not eligible for Part A1 or A2 or who cannot enroll on Part A1 because of stratum suspension or lack of available slots.","id":"EG000","otherNumAffected":6,"otherNumAtRisk":6,"seriousNumAffected":3,"seriousNumAtRisk":6,"title":"Phase 1: Part A: PF-02341066 100 mg/m²/Dose BID"},{"deathsNumAffected":0,"deathsNumAtRisk":8,"description":"Part A1: Patients with relapsed/refractory solid tumors or anaplastic large cell lymphoma (ALCL) Part A2: Patients with recurrent/refractory malignancies who have confirmed ALK fusion proteins, ALK mutations, ALK amplification or evidence for MET mutation or amplification. Once Parts B and C are open to accrual, patients who are not eligible for either Part should enroll on Part A2, Part A3: Patients with recurrent/refractory neuroblastoma, who are not eligible for Part A1 or A2 or who cannot enroll on Part A1 because of stratum suspension or lack of available slots.","id":"EG001","otherNumAffected":8,"otherNumAtRisk":8,"seriousNumAffected":6,"seriousNumAtRisk":8,"title":"Phase 1: Part A: PF-02341066 130 mg/m²/Dose BID"},{"deathsNumAffected":3,"deathsNumAtRisk":23,"description":"Part A1: Patients with relapsed/refractory solid tumors or anaplastic large cell lymphoma (ALCL) Part A2: Patients with recurrent/refractory malignancies who have confirmed ALK fusion proteins, ALK mutations, ALK amplification or evidence for MET mutation or amplification. Once Parts B and C are open to accrual, patients who are not eligible for either Part should enroll on Part A2, Part A3: Patients with recurrent/refractory neuroblastoma, who are not eligible for Part A1 or A2 or who cannot enroll on Part A1 because of stratum suspension or lack of available slots.","id":"EG002","otherNumAffected":23,"otherNumAtRisk":23,"seriousNumAffected":18,"seriousNumAtRisk":23,"title":"Phase 1: Part A: PF-02341066 165 mg/m²/Dose BID"},{"deathsNumAffected":2,"deathsNumAtRisk":12,"description":"Part A1: Patients with relapsed/refractory solid tumors or anaplastic large cell lymphoma (ALCL) Part A2: Patients with recurrent/refractory malignancies who have confirmed ALK fusion proteins, ALK mutations, ALK amplification or evidence for MET mutation or amplification. Once Parts B and C are open to accrual, patients who are not eligible for either Part should enroll on Part A2, Part A3: Patients with recurrent/refractory neuroblastoma, who are not eligible for Part A1 or A2 or who cannot enroll on Part A1 because of stratum suspension or lack of available slots.","id":"EG003","otherNumAffected":12,"otherNumAtRisk":12,"seriousNumAffected":10,"seriousNumAtRisk":12,"title":"Phase 1: Part A: PF-02341066 215 mg/m²/Dose BID"},{"deathsNumAffected":2,"deathsNumAtRisk":38,"description":"Part A1: Patients with relapsed/refractory solid tumors or anaplastic large cell lymphoma (ALCL) Part A2: Patients with recurrent/refractory malignancies who have confirmed ALK fusion proteins, ALK mutations, ALK amplification or evidence for MET mutation or amplification. Once Parts B and C are open to accrual, patients who are not eligible for either Part should enroll on Part A2, Part A3: Patients with recurrent/refractory neuroblastoma, who are not eligible for Part A1 or A2 or who cannot enroll on Part A1 because of stratum suspension or lack of available slots.","id":"EG004","otherNumAffected":38,"otherNumAtRisk":38,"seriousNumAffected":33,"seriousNumAtRisk":38,"title":"Phase 1: Part A: PF-02341066 280 mg/m2/Dose BID"},{"deathsNumAffected":1,"deathsNumAtRisk":11,"description":"Part A1: Patients with relapsed/refractory solid tumors or anaplastic large cell lymphoma (ALCL) Part A2: Patients with recurrent/refractory malignancies who have confirmed ALK fusion proteins, ALK mutations, ALK amplification or evidence for MET mutation or amplification. Once Parts B and C are open to accrual, patients who are not eligible for either Part should enroll on Part A2, Part A3: Patients with recurrent/refractory neuroblastoma, who are not eligible for Part A1 or A2 or who cannot enroll on Part A1 because of stratum suspension or lack of available slots.","id":"EG005","otherNumAffected":11,"otherNumAtRisk":11,"seriousNumAffected":11,"seriousNumAtRisk":11,"title":"Phase 1: Part A: PF-02341066 365 mg/m2/Dose BID"},{"deathsNumAffected":1,"deathsNumAtRisk":14,"description":"Part B: Patients with ALK+ relapsed/refractory neuroblastoma","id":"EG006","otherNumAffected":14,"otherNumAtRisk":14,"seriousNumAffected":13,"seriousNumAtRisk":14,"title":"Phase 2: Part B: PF-02341066 280 mg/m2/Dose BID"},{"deathsNumAffected":0,"deathsNumAtRisk":10,"description":"Part C: Patients with ALK+ relapsed/refractory ALCL","id":"EG007","otherNumAffected":10,"otherNumAtRisk":10,"seriousNumAffected":10,"seriousNumAtRisk":10,"title":"Phase 2: Part C: PF-02341066 280 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