- Research article
- Open Access
- Open Peer Review
Data mining of digitized health records in a resource-constrained setting reveals that timely immunophenotyping is associated with improved breast cancer outcomes
- Arturo López-Pineda†1Email authorView ORCID ID profile,
- Mario F Rodríguez-Moran†2View ORCID ID profile,
- Cleto Álvarez-Aguilar2, 3View ORCID ID profile,
- Sarah M Fuentes Valle4View ORCID ID profile,
- Román Acosta-Rosales5,
- Ami S Bhatt6, 7View ORCID ID profile,
- Shruti N Sheth8 and
- Carlos D Bustamante1, 6View ORCID ID profile
© The Author(s). 2018
- Received: 25 February 2018
- Accepted: 18 September 2018
- Published: 27 September 2018
Organizations that issue guidance on breast cancer recommend the use of immunohistochemistry (IHC) for providing appropriate and precise care. However, little focus has been directed to the identification of maximum allowable turnaround times for IHC, which is necessary given the diversity of hospital settings in the world. Much less effort has been committed to the development of digital tools that allow hospital administrators to monitor service utilization histories of their patients.
In this retrospective cohort study, we reviewed electronic and paper medical records of all suspected breast cancer patients treated at one secondary-care hospital of the Mexican Institute of Social Security (IMSS), located in western Mexico. We then followed three years of medical history of those patients with IHC testing.
In 2014, there were 402 breast cancer patients, of which 30 (7.4% of total) were tested for some IHC biomarker (ER, PR, HER2). The subtyping allowed doctors to adjust (56.7%) or confirm (43.3%) the initial therapeutic regimen. The average turnaround time was 56 days. Opportune IHC testing was found to be beneficial when it was available before or during the first rounds of chemotherapy.
The use of data mining tools applied to health record data revealed that there is an association between timely immunohistochemistry and improved outcomes in breast cancer patients. Based on this finding, inclusion of turnaround time in clinical guidelines is recommended. As much of the health data in the country becomes digitized, our visualization tools allow a digital dashboard of the hospital service utilization histories.
- Breast neoplasms
- Tumor biomarkers
- Medical records
- Clinical coding
- Data mining
In breast cancer, immunohistochemistry (IHC) is a critical part of the accepted standard of care for determining prognosis and response to therapy. A panel of three IHC markers—estrogen receptor (ER), progesterone receptor (PR), and human epidermal growth factor receptor 2 (HER2)—are the most commonly used due to its predictive value for chemotherapy response in breast cancer . Despite the existence of other IHC markers (e.g. Ki67, p53) , and the development of several commercial multi-gene tests that improve prognosis and treatment selection , the availability and expense of these tests remain largely prohibitive for constrain-resourced hospital settings, regardless of country income.
Mexico is an emerging country with an upper-middle income economy (as considered by the World Bank), where the healthcare system still has challenges procuring enough resources. The Mexican consensus  and clinical practice guidelines for breast cancer [5–7], the main working documents for oncologists in the country, recommend routine use of a 3-marker panel (ER, PR, HER2) to guide management and treatment for patients. In Mexico, estimating the nationwide frequencies of molecular status is a challenging task due to the absence of cancer registries. However, two recent cohort studies in Mexico City [8, 9] showed that 56–64% of tumors had positive hormone receptor (ER, PR) status; 16–20% had HER2 positive status; and 23–26% had triple negative status. While these frequencies mirror those of other high and middle income countries, there is a troubling onset of disease among younger patients in Mexico (aged < 40), with a high prevalence of triple-negative breast cancers . Furthermore, there is an increased mortality trend associated with breast cancer in the country . Timely testing for these IHC biomarkers needs to be fully recognized in clinical guidelines and hospital policies, and the testing must account for the wide diversity of patient trajectories and hospital settings .
The Breast Health Global Initiative (BHGI) guideline for breast cancer healthcare in low-income and middle-income countries  offers four levels of guidance: basic (hormone receptor status by empiric assessment or response to treatment); limited (determination of ER status by IHC); enhanced (determination of PR status by IHC and measurement of HER2 overexpression); and maximal (gene profiling testing).
The National Comprehensive Cancer Network (NCCN) framework for oncology care resource-stratification  offers four levels of guidance equivalent to those in the BHGI guideline.
The American Society for Clinical Oncology (ASCO) offers a resource-stratified guideline for cervical cancer , which can be used to illustrate the need for a similar guideline for breast cancer.
The World Health Organization (WHO)  offers guidance to countries on three resource scenarios (low, medium, high) with differential actions in the national cancer control programs, but has not yet offered a breast cancer specific resource-stratified guideline.
In this study, we aimed to quantify the potential effect that timely IHC testing has in improving patient outcomes. We hypothesized that with the use of data mining on digitized hospital records it is possible to facilitate the quantification of IHC testing as well as other services offered to breast cancer patients. At the same time, this study provided hospital administrators with a visual monitoring tool that facilitates the burden of human-intensive labor to quantify critical procedures in resource-constrained hospitals (including IHC testing).
The Mexican Institute of Social Security is a hybrid single-payer system with an integrated network of hospitals nationwide. In Michoacan (a state located in western Mexico), the General Regional Hospital No. 1 (HGR1) is the designated secondary-care facility for the IMSS-insured population, estimated at 1,288,695 people (28% of the state’s population), according to the 2015 census ; of these, 202,547 are women with ages between 40 to 69 years, which correspond to the target group for mammography screening for breast cancer. While there is a lot of heterogeneity between states in Mexico, it is important to highlight that the state of Michoacan ranks 29 out of 32 states in terms of competitiveness, governmental efficiency, and overall wealth .
The HGR1 hospital is located in a suburban community adjacent to Morelia (the capital of Michoacan). HGR1 is the secondary-care facility that serves as reference for seven General Zone Hospitals and 45 Family Medicine Units within the state of Michoacan. HGR1 has an oncology unit with a full complement of fixed staff and facilities available to all patients. It also offers pathology services, diagnostic imaging, and therapeutic capabilities with access to all approved drugs. Patients with breast cancer who require chemotherapy are sent to the outpatient medical unit, and patients with breast cancer who require radiation therapy are provided the service through an outsourced private service in the same city. The personnel include gynecologists, medical oncologists, surgical oncologists with significant breast cancer training, adequate numbers of nursing and pharmacy staff, surgeons with significant training, and cancer pathologists.
The study population for this research was all cumulative breast cancer patients seen in 2014 by medical staff at HGR1, as reported by the institution’s breast cancer census in the absence of a cancer registry. To avoid selection bias in our study, we did not restrict the selection of patients to members of the female sex or any age group.
The general process at IMSS for breast cancer diagnosis is as follows. A patient with suspected breast cancer is referred from a primary-care facility to HGR1 after being examined by his/her family physician. If the physician suspects the existence of a breast lesion, the patient undergoes an imaging assessment using the breast imaging-reporting and data system (BIRADS) score. Upon arriving at HGR1, the patient is either seen by the breast cancer clinic (patients with BIRADS score 0 and 3) for further imaging studies and/or fine-needle biopsy assessments, or directly referred to the medical oncology service (patients with BIRADS score 4, 5 and 6), at which point they undergo surgical biopsies for pathology analysis. The gold-standard diagnosis of breast cancer is then provided by a board-certified pathologist, who assigns one of the C50 codes (malignant neoplasms of breast) from the international classification of diseases version 10 (ICD 10).
The final inclusion criteria were those whose biopsies had been tested with IHC to detect ER, PR, HER2 antibodies; then. We reviewed the medical records (both electronic and paper) of all breast cancer patients at HGR1, selected only those with IHC testing, and followed their medical histories, ending with March 2017, making note of multiple medical visits to the breast cancer clinic, medical oncology service, and/or surgical oncology service. From their medical records, we extracted information about IHC testing (antibody ordered, date of ordering, date of results being obtained), chemotherapy and hormonal drugs administered, and radiation sessions and surgical procedures undertaken.
This was a retrospective hospital-based cohort study, using medical records collected routinely as part of clinical care. The objective was to understand the therapeutic impact on breast cancer patients of the time taken to test immunohistochemistry biomarkers in a resource-constrained hospital in western Mexico. We built a digital monitoring tool to report the frequency of treatment selection or treatment adjustment frequencies depending on breast cancer subtyping and the turnaround times for immunohistochemistry biomarker testing. The STROBE checklist is provided in Additional file 1. All analyses were performed in R version 3.3.2.
Patient trajectory monitoring
List of medical events with UMLS codes and descriptions in English and Spanish
Description in Spanish
Atención inicial en la unidad de medicina familiar (primer nivel de atención).
Visit for: gynecological exam
Atención inicial en la consulta de ginecología (segundo nivel de atención).
Oncology; primary focus of visit; work-up, evaluation, or staging at the time of cancer diagnosis or recurrence
Atención inicial en la consulta de oncología médica.
Oncology; primary focus of visit; expectant management of patient with evidence of cancer for whom no cancer- directed therapy is being administered or arranged at present
Atención subsecuente en la consulta de oncología médica.
Request lab results from pathology
Solicitud de estudios de patología.
Request lab results from hematology
Solicitud de estudios básicos de laboratorio clínico.
Request lab results from x-ray
Solicitud de estudios de imagen (tele de tórax, ultrasonido, mastografía).
Request lab results from CT
Realización de estudios especiales de imagen (tomografía).
Request lab results from MRI
Realización de estudios especiales de imagen (resonancia magnética).
Biopsy / Pathology
Needle biopsy of breast
Realización de biopsia con aguja fina o gruesa.
Surgical biopsy of breast
Realización de biopsia por escisión quirúrgica.
Reporte de estudio histopatológico.
Selection for Treatment
Selección de tipo de tratamiento (quimioterapia, radioterapia, cirugía).
Inicio de quimioterapia.
Surgery / Radiation
Inicio de radioterapia.
Realización de mastectomía radical.
Lumpectomy of breast
Realización de lumpectomía
Quantitative HER2 immunohistochemistry (IHC) evaluation of breast cancer consistent with the scoring system defined in the ASCO/CAP guidelines (PATH)
Solicitud de estudios de inmunohistoquímica (Receptor de HER2).
Quantitative non-HER2 immunohistochemistry (IHC) evaluation of breast cancer (eg, testing for estrogen or progesterone receptors [ER/PR]) performed (PATH)
Solicitud de estudios de inmunohistoquímica (Receptores de estrógeno y progesterona).
Treatment adjusted per protocol
Ajuste de tratamiento de primera línea (posterior al primer ciclo de quimioterapia).
Hormone replacement therapy started
Inicio de tratamiento de reemplazo hormonal.
Complicación de proceso oncológico (internamiento a causa de cáncer)
Local recurrence of malignant tumor of breast
Recaída de proceso oncológico (mismo sitio tumor primario). Recidiva local de tumor maligno de mama.
Metastasis from malignant neoplasm of breast
Reconocimiento de metástasis (tumor secundario).
Fallecimiento / Muerte
Evolución favorable de paciente, mejoría clínica; remisión.
Missing data was assumed to be non-missing at random (NMAR), and the events from Table 1 were considered missing for a specific reason. For example, if the code C2186775 (request lab result from MRI) was missing from a patient’s medical record, we left that value unassigned, since it was assumed that an MRI was not requested for that patient. There is a small chance that this assumption might be violated (and introduce some bias) if the physician did request the exam/procedure but forgot to write it down in the medical record. However, we did not impute any missing data, since that might be a larger source of bias for this EHR-based data.
We assessed the time-to-event distribution for each event in Table 1, and reported the distribution of the patient cohort in violin plots that included: the median turnaround time, the interquartile probability density estimation, and the 95% confidence interval (whiskers). Outliers were identified using the 1.5 interquartile rule, but were not removed from the downstream analysis due to scarcity of data.
We searched for groups of patients that had similar journeys in their hospital care. More technical details about the hierarchical clustering method are shown in Additional file 2. The input was a matrix of the number of days when events from Table 1 occurred for every patient, relative to their initial day of diagnosis in the hospital (day 0). Given that missing events were considered to be not missing at random (NMAR), they were filled with a large negative value (− 1000 for this cohort). Then, a patient similarity distance was calculated using Euclidean distance between these time-to-event values for every pair of patients. An agglomerative hierarchical clustering was constructed using complete linkage, the distance between the two furthest points in two clusters. The selection of the appropriate number of clusters was done through cluster stability analysis.
Clinical characteristics of the cohort and receptor status for patients with IHC testing
With IHC testing (%)
N = 402
N = 30
Age at diagnosis
Patients without IHC testing
Patients with IHC testing
Additional IHC testing
Subtype according to the Mexican Consensus 
not enough information to assign
In Mexico, breast cancer continues to be a public health concern, even though more and more research is being done on its genomic changes and characteristics. Although our study investigated a small cohort of patients, the epidemiological characteristics among our cohort is similar to what has previously been estimated for the country (in regards to age group and staging) . Our study further investigates the use of digital health mining tools for evaluating the timeliness of IHC testing, and the percentage of patients being tested. This tool can then be used to inform hospital administrators and public health officials.
On the therapeutic value of IHC testing
Despite the small number of patients with IHC, the results suggest usefulness of the IHC in therapeutic decision-making and in determining the prognosis of the patient. In the hospital included in this study, therapeutic decisions are made based on clinical, surgical and histological results such as physical appearance, tumor size, lymphatic invasion, tumor necrosis, histological type, degree of differentiation and the number of affected lymph nodes. This study supports the therapeutic importance of immunophenotyping (the use of IHC testing for subtyping of cancer patients), as has been demonstrated broadly in other studies focusing on populations in high income settings. These results should be carefully considered and addressed in treatment plans created by the multidisciplinary care team. With the incorporation of information about receptor status, the traditional (FEC) chemotherapy regimen recommended by the IMSS protocol, composed by 5-fluorouracil, epirubicin, and cyclophosphamide, can be adjusted to improve treatment outcomes.
Patients with estrogen positive (ER+) and/or progesterone positive (PR+) could benefit from anti-hormone or endocrine therapy to prevent recurrence, either aromatase inhibitors to block estrogen production (e.g. anastrozole, letrozole, or exemestane), or the selective estrogen receptor modulators (SERMs), which interfere with the ability of estrogen to stimulate the growth of breast cells (e.g. tamoxifene or toremifene).
Additionally, patients with HER2 positive (HER2+), in which tumors tend to grow and spread more aggressively, could benefit from a targeted therapy that could block HER2 (e.g. trastuzumab or pertuzumab). The use of in situ hybridization (ISH), instead of IHC, can be used to determine HER2 status with an overall concordance with IHC, and it may be more beneficial to use both . Furthermore, HER2 status has been successfully incorporated into medical practice to guide treatment decisions for breast cancer patients. In fact, the American Society of Clinical Oncology/College of American Pathologists (ASCO/CAP) updated their 2013 guidelines to designate more patients as eligible for trastuzumab therapy, in accordance with ISH and IHC testing . Also, the BHGI resource stratified guidelines recommend the use of trastuzumab at the enhanced level due to the high cost of the drug, as well as for the availability for testing. The IMSS’s medications chart  reports trastuzumab as an available drug for any HER+ positive patient in the country.
On the timeliness of IHC testing
Opportune IHC testing, understood as the availability of IHC results before the beginning of any treatment, is of critical importance. For the IMSS hospital in this study, IHC results were typically not timely opportune, but whenever they were available they triggered a response from the clinical oncology team to adjust patient treatments. The wide dispersion of time to request and turnaround time demonstrates the lack of standardization of this process. Many factors could have contributed to the delay in IHC testing, including: patient non-adherence to appointments; hospital overflow, resulting in delayed appointments; logistical problems between IMSS and the external laboratory service; and administrative problems within the hospital resulting in inadequate tracking of tests and results.
It is important to establish an appropriate timeline for opportune IHC testing. For example, In the United States, the College of American Pathologists’ (CAP) guideline on turnaround time for biopsy testing is around two days for 90% of cases . In fact, the joint guideline on HER2 testing from the American Society of Clinical Oncology (ASCO) and CAP recommends informing the patients about the expected turnaround time . In Australia, a study revealed that the average turnaround time was between 4 and 5 days . In Saudi Arabia, a study showed that 24% of cases fall outside the recommended CAP turnaround time . The European Society for Medical Oncology (ESMO) published a survey on 24 European countries were the turnaround time was 10 days or less for 89% of laboratories . In the United Kingdom, the Royal College of Pathologists recommend the use of key performance indicators to have a histopathology diagnosis within seven days of biopsy in 90% of cases .
Given their resource-available settings, clinical guidelines in developed countries do not have a recommendation regarding the maximum turnaround time that could be effective in a patient’s treatment trajectory. More importantly, they do not address the time between initial diagnosis, molecular testing, and the selection of treatment. In Mexico, clinical guidelines for breast cancer recommend testing for ER, PR, and HER2 as part of the histopathology study, but fail to provide guidance regarding turnaround time. IMSS maintains a medical procedures manual, which includes ten key indicators for breast cancer screening, diagnosis, and treatment . This manual measures time-to-diagnosis in a 30-day period, including imaging through mammography and results of histopathology report. In addition, the institution also measures time-to-treatment measured from the date of diagnosis, which should be achieved within a 21-day period. Recognizing the resource constraints of IMSS, the implementation of a key indicator policy related to IHC testing might significantly reduce turnaround times.
On the need to monitor the percentage of patients being tested
The monitor shown in Fig. 1 quickly provides a patient history overview of hospital care, while Fig. 2 shows the detailed information for turnaround time. With more work on the user interface, we envision a tool that could eventually represent a valuable visual aid for hospital administrators, providing a quick overview of the patients seen in their hospital, which could be used as a decision-making tool, with the proper validation.
The low percentage (7.4%) of patients observed to be tested requires special attention. A common concern of retrospective chart review studies is underreporting. The amount of recorded information in the hospital included in our study can be improved by providing training to the clinical and administrative staff about the importance of requesting and reporting IHC testing. In the absence of a cancer registry, our best estimate of the disease is the institutional census, which does not record IHC testing results. As the hospitals in Mexico, and elsewhere, continue to become more and more electronic, there is a need to develop better software tools to facilitate recording and analyzing clinical information, including medical natural language processing and machine learning applications.
Adverse events in the trajectory of an oncological patient, which might include hospitalization related to cancer, recurrence of tumor, or metastasis, are extremely costly for the healthcare system. The use of IHC testing was shown in our study to help with the selection of precise treatment for patients (either by adjusting the treatment or confirming it). The time in which IHC testing is performed is of critical importance if we want to influence improved prognosis.
We have revealed in this cohort that the use of opportune IHC testing is associated with beneficial therapeutic effects on breast cancer patients. The aims of any healthcare system should be the identification of earlier events that can have an impact on downstream events in the trajectory of an oncological patient’s treatment. In resource-constrained settings, it is important not only to consider alternatives to more costly diagnostics (e.g. genomic testing), but also to incorporate the regulatory and logistical aspects of implementing these tests.
IMSS must face the important challenge of continuing to improve their turnaround times, which should have a positive impact on the prognosis of their patients. As the Mexican healthcare system continues to transition from reactive to preventative care, the need for more IHC testing in breast cancer and other diseases will certainly allow for the further development of digital patient monitoring.
The authors wish to acknowledge Katie Kanagawa, PhD, for her valuable support in editing this manuscript.
Research reported in this publication was partially supported via institutional funds from each individual researcher institution, either the Mexican Institute of Social Security (IMSS) or Stanford University. In addition, ALP and CDB were partially supported by the following grants: U01 HG007436–04 from the National Human Genome Research Institute (NHGRI)‘s Clinically Relevant Genome Variation Database; and U01 FD004979 from the Food and Drug Administration (FDA)‘s joint Center of Excellence in Regulatory Science and Innovation (CERSI) at the University of California, San Francisco and Stanford University. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Availability of data and materials
Data belongs to the Mexican Institute of Social Security (IMSS), through its state Delegation of Michoacan. IMSS’s Coordination of Health Research may grant access to this data on a case-by-case basis to researchers who obtain the necessary approvals from IMSS’s National Scientific Research Committee and National Bioethics Committee.
ALP designed the study. MFRM reviewed medical notes. MFRM and ALP performed the analysis of the data. ASB, SNS, RAR, CAA, SMFV and CDB provided interpretation of the results. Translations. The present manuscript was translated into Spanish by bilingual co-author ALP. The translated manuscript is provided in Additional file 3. ALP drafted the manuscript, and all authors contributed critically, read, revised and approved the final version.
Ethics approval and consent to participate
This research was reviewed and approved by the Mexican Institute of Social Security (IMSS)‘s National Scientific Research Committee and its National Bioethics Committee, under protocol number R-2017-785-010, and locally by IMSS’ Local Research and Ethics Committee, under specific protocol number R-2017-1602-14 HGR1 Charo, Michoacan. Stanford’s Institutional Review Board provided a non-human subject determination under eProtocol: 40704. Researchers only received access to non-identifiable data under the considerations of the applicable Mexican bylaws on health research, patient privacy, and electronic medical records. Consent was not required.
Consent for publication
RAR declares to be IMSS’s state delegate in Michoacan, overseeing the hospital mentioned in this study. The authors declare that they have no competing interests.
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