Advancing the Science

Mayo Clinic Medical Science Blog – an eclectic collection of research- and research education-related stories: feature stories, mini news bites, learning opportunities, profiles and more from Mayo Clinic.

Share this:
July 25, 2018

Advances in lung cancer immunotherapy and management of immune-mediated adverse events

By Advancing the Science contributor

Malignancies before and after immunotherapy (click image for comparison)

Over the last few years, immunotherapy using immune checkpoint inhibitors targeting programmed cell death receptor 1 (PD-1) or programmed cell death receptor ligand 1 (PD-L1) has revolutionized the therapeutic approach to advanced-stage non-small cell lung cancer and numerous other malignancies.

Monotherapy, using the anti-PD-1 antibody pembrolizumab, is now Food and Drug Administration (FDA) approved for patients with stage IV non-small cell lung cancer without a driver mutation and 50 percent or greater tumor cell PD-L1 expression by immunohistochemistry staining. Moreover, the combination of systemic platinum-based chemotherapy and pembrolizumab was also recently approved for first line therapy of metastatic nonsquamous non-small cell lung cancer independent of PD-L1 status.

Nivolumab (anti-PD-1) and atezolizumab (anti-PD-L1) also are FDA approved for second line therapy of stage IV lung cancer. For this indication, with the exception of pembrolizumab, which requires 1 percent or greater PD-L1 expression, no PD-L1 expression level is required to initiate therapy.

On average, objective response rates to immunotherapy range around 20 to 30 percent and sustained long-term responses have been observed. However, since the majority of patients do not benefit from second line immunotherapy, many efforts are being made to improve durable responses. The newest addition is a Mayo Clinic investigator-initiated study, the Trial of Measles Virotherapy in Combination With Atezolizumab in Patients With Metastatic Non-Small Cell Lung Cancer, which explores the combination of the intratumoral administration of the measles virus with systemic PD-L1 targeted immunotherapy using atezolizumab for second line therapy of non-small cell lung cancer.

Immune-mediated adverse events

PD-1/PD-L1 targeted immunotherapy is generally well-tolerated and has fewer acute side effects compared with standard cytotoxic chemotherapies. However, these new therapeutic agents have been linked to a growing number of immune-mediated adverse events (imAEs).

Immune-mediated adverse events (click image for examples)

ImAEs are observed in 70 percent of patients and include autoimmune colitis, thyroiditis, hypophysitis, dermatitis and pneumonitis. The severity of imAEs ranges from asymptomatic to life-threatening presentations, while the time course can be either transient or chronic and relapsing.

Mayo Clinic's true multidisciplinary team approach includes experts in medical oncology, rheumatology, pulmonary medicine, gastroenterology, endocrinology and neurology to optimally manage patients with imAEs. Besides stopping immunotherapy, patients are most commonly treated with immunosuppression (most commonly corticosteroids).

The pathogenesis, risk factors, diagnostic criteria and individualized management of patients experiencing immunotherapy-related imAEs outside of controlled clinical trials, however, remains unclear. A diagnosis of an imAE, published in Melanoma Research in 2016, represents a diagnosis of exclusion and depends on the active elimination of alternative diagnosis.

For more information

Vyriad. Trial of Measles Virotherapy in Combination With Atezolizumab in Patients With Metastatic Non-Small Cell Lung Cancer. ClinicalTrials.gov.

Kottschade L, et al. A multidisciplinary approach to toxicity management of modern immune checkpoint inhibitors in cancer therapy. Melanoma Research. 2016;26:469.

This article was originally published in Mayo Clinic's Clinical Updates for Medical Professionals newsletter.

Related links:

Tags: immunotherapy, Innovations, lung cancer, Mayo Clinic Cancer Center

COMMENT

Please login or register to post a comment.
Contact Us · Privacy Policy