Home Lung Cancer Treatment Enters a New Era: Janssen's Rybrevant® (Amivantamab Injection) Approved in China

Lung Cancer Treatment Enters a New Era: Janssen's Rybrevant® (Amivantamab Injection) Approved in China

Feb 11, 2025 15:37 CST Updated 15:37
Johnson & Johnson

Healthcare Product Manufacturers, Health Service Providers

On February 11, 2025, Johnson & Johnson announced that its innovative therapeutic drug Rykif (Amivantamab Injection) has been officially approved by the National Medical Products Administration (NMPA) for use in combination with carboplatin and pemetrexed for the first-line treatment of adult patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) whose tumors have epidermal growth factor receptor (EGFR) exon 20 insertion mutations as detected by a validated test. This approval marks Johnson & Johnson's official entry into the lung cancer treatment field in China, with the potential to redefine treatment standards and usher in a new era of lung cancer therapy.


The approval of Amivantamab is based on the results of the randomized, open-label, PAPILLON Phase III clinical trial. The study demonstrated that, compared to chemotherapy alone, the combination of Amivantamab and chemotherapy reduced the risk of disease progression or death by 61%. Based on the results of the PAPILLON clinical trial, the National Comprehensive Cancer Network (NCCN) "NCCN Clinical Practice Guidelines" recommend Amivantamab in combination with chemotherapy as the preferred first-line treatment for patients with EGFR exon 20 insertion-mutated non-small cell lung cancer.


Lung cancer ranks first in both incidence and mortality among all malignant tumors in China. According to statistics, there are over 1 million new cases of lung cancer each year in China, accounting for more than one-third of the total number of lung cancer patients worldwide. Non-small cell lung cancer (NSCLC) is the most common type of lung cancer, making up approximately 85% of all lung cancer cases. Among these, EGFR gene mutations are the most common driver gene mutations in non-small cell lung cancer, with about 40% of patients in China carrying this mutation type. Currently, 25%-40% of patients with EGFR mutations cannot proceed to second-line treatment due to severe disease progression. EGFR exon 20 insertion mutations are the third most common mutation type. Typically, non-small cell lung cancer driven by this mutation has a poorer prognosis and shorter survival compared to lung cancer driven by common EGFR mutations. Research shows that NSCLC patients with EGFR exon 20 insertion mutations have limited efficacy with currently approved third-generation EGFR-TKI targeted drugs and chemotherapy, leading to generally poor prognoses and facing dual challenges in survival time and quality of life. Therefore, providing more effective treatment options for patients during the first-line treatment phase is crucial.
Cherry Huang, President of Johnson & Johnson Innovative Pharmaceuticals China, stated: "With a patient-centered approach, Johnson & Johnson has been committed to helping patients achieve higher treatment goals throughout its over 30-year dedication to the oncology field, aiming to make cancer a manageable and treatable chronic disease while leading the exploration for a potential cure. In China, lung cancer is the leading type of cancer, with significant unmet treatment needs that urgently require more effective therapies. The recent approval of Rykertin brings greater survival hope to patients with EGFR-mutated non-small cell lung cancer, with the potential to further reshape the treatment landscape for non-small cell lung cancer in China. This also marks Johnson & Johnson's official entry into the lung cancer field in China, representing a significant breakthrough in the area of precision medicine."


The most common adverse reactions (≥20%) to Amivantamab injection include rash, nail toxicity, oral mucositis, infusion-related reactions, fatigue, edema, constipation, decreased appetite, nausea, COVID-19, diarrhea, and vomiting. The most common (≥2%) grade 3-4 laboratory abnormalities are decreased albumin, increased alanine aminotransferase, increased gamma-glutamyl transferase, decreased serum sodium, decreased serum potassium, decreased serum magnesium, leukopenia, decreased hemoglobin, neutropenia, thrombocytopenia, and lymphopenia.