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Operational Pathways for Molecular Testing in NSCLC

As the role of molecular testing in the diagnosis and treatment planning for non-small cell lung cancer continues to expand, the efficiency and timeliness of molecular testing processes are an increasing concern for cancer care programs and providers. Guideline-concordant molecular testing for patients with non-small cell lung cancer informs the subtype of lung cancer, development of the treatment plan, and prognosis. Lack of clarity on operational and care pathways for molecular testing may contribute to inefficiencies and delays that can affect treatment initiation or act as a barrier to patient access to testing, and in turn impact the potential benefits from precision medicine treatments requiring companion diagnostic tests.

Consideration of operational pathways for molecular testing in non-small cell lung cancer is a potential avenue to improve the standardization of institutional, care team, and provider processes for molecular testing; increase timeliness of care; and reduce overall costs. When multidisciplinary teams have a greater understanding of the guideline recommendations and testing available, there is improved consistency in the utilization of molecular testing results, which can inform treatment planning and shared decision-making. Improved consistency also allows for the development of processes for ongoing evaluation of molecular testing protocols and institutional care pathways.

Through this educational program, ACCC will identify and disseminate examples of effective practices and tools for developing, implementing, and assessing operational pathways for molecular testing for eligible patients with non-small cell lung cancer.

For more information on this project, please contact the ACCC Provider Education department.

 

Biomarker Testing Implementation Roadmap for Advanced NSCLC

This innovative learning tool can help multidisciplinary cancer care teams obtain the knowledge they need to implement, expand, and sustain biomarker testing for patients with advanced NSCLC.

Amy Jo Pixley"Deciding how best to develop and implement a new process requires a vision, a strategic plan, and a team devoted to the success of the project. By designing a concise visual representation of biomarker testing, this Biomarker Testing Implementation Roadmap will arm oncology practices and programs with access to a preemptive blueprint detailing the action steps and resources necessary to carry the initiative from vision to reality."

Amy Jo Pixley, MSN, RN, OCN, ONN-CG(T)
Oncology Nurse Navigator
Ann B. Barshinger Cancer Institute at Penn Medicine Lancaster General
Lancaster, PA
View Roadmap

Operational Pathways for Biomarker Testing in NSCLC Environmental Scan

operational-pathways-nsclc-environmental-scan ThumbnailThis environmental scan provides an overview of the current landscape of biomarker testing at cancer programs, challenges or barriers to implementing testing recommendations, efforts by ACCC and others to-date, and possible solutions toward creating operational efficiencies in testing.
Download Environmental Scan

 

From the ACCCBuzz Blog

Barriers to Liquid Biopsy


October 14, 2021
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Liquid biopsy, a genetic test that can eliminate some of the most serious potential drawbacks of traditional tissue biopsy, is gaining more traction in cancer care. But there remain significant barriers to its widespread use.  

What Is a Liquid Biopsy? 

An essential element of cancer care, tumor tissue biopsies can confirm a cancer diagnosis, identify the cell type of a tumor, and determine whether a patient’s tumor contains specific genetic alterations that may make them candidates for targeted therapies. However, tumor tissue biopsies require invasive procedures (including surgery), and some patients may not be candidates due to poor health or a tumor’s specific location in the body.  

To overcome these barriers, researchers have developed technologies for capturing and analyzing DNA and other types of genetic material released by patients’ tumor cells into their blood. The removal of blood or other bodily fluids to detect cancerous cells or cancerous DNA is called liquid biopsy. Liquid biopsies have the benefit of being non-invasive, which means they can be done more frequently to better track tumors and mutations over time. They may also be used to validate the efficacy of a cancer treatment or monitor patients for potential relapse. And they can be a less costly alternative to the genomic analysis of tissue biopsies.

On June 1, 2016, the Food and Drug Administration approved the first liquid biopsy test for use in cancer. The test detects key mutations that make patients with advanced non-small cell lung cancer candidates for treatment with the targeted therapy erlotinib (Tarceva®). The FDA previously approved this test for this indication using tumor specimens; the new approval is for the detection of the same mutation using blood samples. 

But barriers to using biomarker testing are common. Respondents to ACCC’s Trending Now in Cancer Care survey indicate that insufficient insurance coverage, reimbursement, and protocols are among the issues working against the widespread implementation of biomarker testing in oncology practices. Accordingly, the adoption of biomarker testing has been slow.

A study presented at the 2021 American Society of Clinical Oncology (ASCO) Annual Meeting found that of nearly 3,500 patients with advanced NSCLC, 90% had been given at least one biomarker test. However, only 46% of these patients had been given all five of the biomarker tests commonly used for NSCLC. There is also evidence of significant disparities in the use of biomarker testing among different racial groups. Another study presented at the same ASCO meeting revealed that 39% of Black patients with metastatic NSCLC underwent next-generation sequencing, compared to 50% of their White counterparts.

Cost & Coverage Barriers 

The process of paying for expensive molecular tests and for the expertise of the multiple professionals required to interpret test results and formulate treatment plans is inconsistent and complex. This is especially the case with newer technologies such as liquid biopsy, which can come with higher price tags. Physicians, pathologists, and patients often do not know the costs of molecular testing services until they are reimbursed or billed. The confusion that results is distressing for both patients and providers.  

Payers also structure their policies for biomarker coverage in multiple ways, making them difficult to understand. While some reimburse for many types of tests, others reimburse for only the most basic tests, or for tests for very specific clinical conditions and genes. This wide variation often increases the challenge of assessing and tracking numerous coverage policies.

To learn more about the status of liquid biopsies in community cancer centers, listen to the ACCC CANCER BUZZ podcast, What You Need to Know About Liquid Biopsy. There, J. Nicholas Bodor, MD, PhD, MPH—assistant professor in the Department of Hematology/Oncology at Fox Chase Cancer Center—and Kathryn A. Phillips, PhD—professor of health economics and health services research and director of the Center for Translational and Policy Research on Personalized Medicine at the University of California San Francisco—address the feasibility of offering liquid biopsies in community cancer centers and the pros and cons of doing so.

Additional ACCC resources:

 

 

 

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Our Supporter

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This project is sponsored by Amgen.