Natural Language Processing to Identify Cancer Treatments With Electronic Medical Records

Author:

Zeng Jiaming1ORCID,Banerjee Imon2ORCID,Henry A. Solomon3ORCID,Wood Douglas J.3,Shachter Ross D.4ORCID,Gensheimer Michael F.5ORCID,Rubin Daniel L.6ORCID

Affiliation:

1. Department of Management Science and Engineering, Huang Engineering Center, Stanford, CA

2. Department of Biomedical Informatics, Department of Radiology, Emory University School of Medicine, Atlanta, GA

3. Research Informatics Center, Stanford University, Stanford, CA

4. Department of Management Science and Engineering, Stanford University School of Engineering, Stanford, CA

5. Department of Radiation Oncology, Stanford University School of Medicine, Stanford, CA

6. Department of Biomedical Data Science, Radiology, and Medicine (Biomedical Informatics), Stanford University School of Medicine, Stanford, CA

Abstract

PURPOSE Knowing the treatments administered to patients with cancer is important for treatment planning and correlating treatment patterns with outcomes for personalized medicine study. However, existing methods to identify treatments are often lacking. We develop a natural language processing approach with structured electronic medical records and unstructured clinical notes to identify the initial treatment administered to patients with cancer. METHODS We used a total number of 4,412 patients with 483,782 clinical notes from the Stanford Cancer Institute Research Database containing patients with nonmetastatic prostate, oropharynx, and esophagus cancer. We trained treatment identification models for each cancer type separately and compared performance of using only structured, only unstructured ( bag-of-words, doc2vec, fasttext), and combinations of both ( structured + bow, structured + doc2vec, structured + fasttext). We optimized the identification model among five machine learning methods (logistic regression, multilayer perceptrons, random forest, support vector machines, and stochastic gradient boosting). The treatment information recorded in the cancer registry is the gold standard and compares our methods to an identification baseline with billing codes. RESULTS For prostate cancer, we achieved an f1-score of 0.99 (95% CI, 0.97 to 1.00) for radiation and 1.00 (95% CI, 0.99 to 1.00) for surgery using structured + doc2vec. For oropharynx cancer, we achieved an f1-score of 0.78 (95% CI, 0.58 to 0.93) for chemoradiation and 0.83 (95% CI, 0.69 to 0.95) for surgery using doc2vec. For esophagus cancer, we achieved an f1-score of 1.0 (95% CI, 1.0 to 1.0) for both chemoradiation and surgery using all combinations of structured and unstructured data. We found that employing the free-text clinical notes outperforms using the billing codes or only structured data for all three cancer types. CONCLUSION Our results show that treatment identification using free-text clinical notes greatly improves upon the performance using billing codes and simple structured data. The approach can be used for treatment cohort identification and adapted for longitudinal cancer treatment identification.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

General Medicine

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