Understanding Evidence-Based Practice Patterns in Advanced NSCLC: An Educational/Research Initiative in Mid-Atlantic States

Non-small cell lung cancer (NSCLC) accounts for about 25% of all cancer deaths and is by far the leading cause of cancer death among both men and women. Each year, more people die of lung cancer than of colon, breast, and prostate cancers combined. NSCLC mainly occurs in older adults. About two out of three people diagnosed with lung cancer are 65 or older; the average age at the time of diagnosis is 70 years. Despite the many advances over the past few decades related to surgery, radiation therapy and chemotherapy, death rates attributable to lung cancer have remained relatively unchanged. Most patients are diagnosed with distant disease and have a 5 -year survival of only 4%. Today, however, there is renewed optimism that these trends have started to change as recent research advances have led to an explosion in lung cancer genetic and biologic knowledge among NSCLC scientists and expert clinicians. A major focus of recent lung cancer research has been the development and subsequent approval of several immunotherapy and molecular-targeted agents and the identification of related biomarkers to help guide treatment selection for those individuals who harbor specific oncogenic alterations.

Improvements in advanced NSCLC outcomes have been achieved by the discovery of predictive molecular markers that identify subgroups of patients that may derive benefit from targeted treatment. Multiple molecular markers have been found to have clinical value in advanced NSCLC: EGFR mutations, ALK rearrangements, as well as HER2, MET, B-RAF, RET, and ROS1. In addition, the classification for lung adenocarcinoma was recently revised and now requires morphology, immunohistochemical, and molecular studies, including EGFR and ALK status, as well as ROS1, BRAF, HER2, MET, RET. It is thus important that proper biopsy technique accommodate these crucial tests, that the correct tests are ordered for specific patient populations, and that the results of testing are accurately interpreted to individualize care for patients with targeted agents such as erlotinib, afatinib, crizotinib, and osimertinib. Molecular testing for NSCLC is not ordered routinely due to insufficient knowledge by the multidisciplinary team (medical, surgical, and radiation oncologists) or lack of reimbursement. Several studies have quantified this failure: De Souza et al (2012) showed that no testing for EGFR mutations was observed in 23.5% of patients administered erlotinib, and Pan et al (2013) demonstrated that EGFR testing rates were only 2.3% before 2010, 15.2% in 2010, and still only 32.0% in 2011. Similarly, Spicer et al (2015) demonstrated that 23% of oncologists do not consider EGFR mutation subtypes in making treatment decisions and EGFR mutation testing is not performed in up to 25% of patients. A survey of 133 US medical oncologists found that most (74%) are not very familiar with using biomarkers to tailor therapy. In addition, lung cancer test panels often do not include next generation sequencing, which can greatly streamline the process. Biopsies are often too small or too low quality for adequate testing, necessitating rebiopsy. For example, Ost et al (2013) found that only 21% of patients had a diagnostic evaluation consistent with guidelines.

National guidelines on molecular testing in NSCLC are available from the NCCN, ASCO, College of American Pathologists, International Association for the Study of Lung Cancer, Association for Molecular Pathology, and others. These guidelines make evidence-based recommendations to better align the latest clinical research with patient care in practice. For example, the NCCN notes that there is a significant association between EGFR mutations-especially exon 19 deletion and exon 21 (L858R, L861) and exon 18 (G719X, G719) mutations-and sensitivity to TKIs, and that the exon 20 insertion mutation may predict resistance to clinically achievable levels of TKIs. The prevalence of EGFR mutations in adenocarcinomas is 10% of Western and up to 50% of Asian patients, with higher EGFR mutation frequency in non-smokers, women, and non-mucinous cancers. KRAS mutations are most common in non-Asians, smokers, and in mucinous adenocarcinoma. In addition, primary resistance to TKI therapy may be associated with KRAS mutation, so KRAS gene sequencing could be useful for the selection of patients as candidates for TKI therapy. ALK fusions have been identified in a subset of patients with NSCLC and represent a unique subset of NSCLC patients for whom ALK inhibitors may represent a very effective therapeutic strategy.

The current treatment of advanced NSCLC is based on the evaluation of genetic mutations that can guide the personalization of treatment with molecularly targeted agents. The most common genetic variant is the gene that encodes the epidermal growth factor receptor (EGFR) and is found in approximately 15% of Caucasian and more than 50% of Asian patients. Patients harboring EGFR mutations are usually treated with tyrosine kinase inhibitors (TKI), such as gefitinib, erlotinib or afatinib. Similarly, a gain of function of anaplastic lymphoma kinase (ALK) due to a rearrangement with the echinoderm microtubule-associated protein-like 4 (EML4) represents a predictive biomarker of the efficacy of ALK-TKI inhibitors such as crizotinib. However, clinicians may not be adequately informed about newly approved and emerging TKIs.

It is nearly impossible for the modern-day oncologist to remain current regarding the clinical tsunami of research to personalize NSCLC treatment. This is evidenced by the fact that only 55% -75% of NSCLC patients within the United States are receiving evidence-based care. The tremendous pressures cancer centers and their oncology providers face in quantifiably demonstrating value in the care delivered compounds this problem. Almost instantly, government and commercial payers are demanding a change from pay for quantity to pay for value. In April 2016, CMMI implemented the Oncology Care Model (OCM). The new OCM program is complementary to other value-based payment initiatives in which oncologists may participate, including the Bundled Payment for Care Initiative, Chronic Care Management Program, Transforming Clinical Practices Initiative, Transitional Care Management Program, ACO/Medicare Shared Savings Program, and Medicare Care Choice Model, and others rapidly being introduced by commercial payers. These payment programs are transforming oncology care so that it is more pro-active, coordinated, vigilant and patient focused. At the center of this payment reform is the patient, as the ultimate consumer of health care services. Until recently, patients have been relatively blind to the actual cost and quality of the care they receive. Now, out-of-pocket costs are rising steeply and patients have instant access to a trove of health information as they are forced to become better-educated consumers regarding the costs and likely outcomes of their treatment. A recent JAMA Op-Ed piece receiving significant attention highlights that delivering value-based care requires an understanding of what the patient values. To that end, all the current cancer valued-based models require that oncology providers document their patient's goals of care and that the treatment course is evidence-based and commensurate with patient goals.