System and method for outcome tracking and analysis

A computer implemented method for matching an oncology patient to clinical trials, comprising:

• (a) receiving, for a patient, a patient profile comprising one or more molecular findings derived from genomic testing and one or more clinical attributes including at least one of tumor type, affected gene or pathway, and treatment information;
• (b) maintaining access to information for a plurality of clinical trials, the information including descriptive trial information for each clinical trial;
• (c) comparing the patient profile with the clinical trial information to identify one or more clinical trials relevant to the patient;
• (d) generating, for each identified clinical trial, a match indication automatically based on the comparison, wherein the match reflects the relevance of the clinical trial to the patient profile;
• and
• (e) causing a user interface to present at least one identified clinical trial together with the match indication and additional trial information to support clinical decision making.

A system for oncology clinical trial matching, comprising:

• (a) one or more processors;
• and
• (b) a memory storing instructions that, when executed by the one or more processors, cause the system to:
• (i) maintain patient profiles comprising molecular findings and clinical attributes for a plurality of patients;
• (ii) maintain access to clinical trial information for a plurality of clinical trials;
• (iii) compare a selected patient profile with the clinical trial information to identify one or more relevant clinical trials;
• (iv) generate, automatically based on the comparison, a match indication for each identified clinical trial;
• and
• (v) output, to a user interface, at least one identified clinical trial together with the match indication and associated trial information.

A non transitory computer readable storage medium storing instructions that, when executed by one or more processors, cause a system to:

• (a) receive a patient profile comprising molecular findings and clinical attributes;
• (b) access descriptive information for a plurality of clinical trials;
• (c) compare the patient profile with the clinical trial information to identify one or more relevant clinical trials;
• (d) generate, automatically based on the comparison, a match indication for each identified clinical trial;
• and
• (e) generate a presentation for display in a user interface, the presentation comprising at least one identified clinical trial together with the match indication and associated trial information.