Biologics

New Hope for Lung Cancer Patients as Breakthrough Treatment Approved in Europe

Published April. 3. 2024

In a significant development for lung cancer treatment, the European Commission has granted approval for KEYTRUDA, an innovative therapy developed by Merck, for the treatment of resectable non-small cell lung cancer (NSCLC). This milestone marks a breakthrough in the fight against the leading cause of cancer death globally.

The approval comes on the heels of compelling results from the Phase 3 KEYNOTE-671 trial, where KEYTRUDA, when combined with platinum-containing chemotherapy, demonstrated remarkable efficacy in improving overall survival in patients with resectable stage II, IIIA, or IIIB NSCLC. Notably, this combination therapy not only prolonged patients’ lives but also substantially reduced the risk of disease recurrence or progression.

Dr. Solange Peters, a prominent figure in oncology, underscored the significance of this approval for individuals diagnosed with resectable NSCLC, emphasizing the potential to extend their survival and improve outcomes.

Marjorie Green, representing Merck Research Laboratories, expressed optimism about advancing treatments for lung cancer, particularly in earlier stages, and reiterated the company’s commitment to seeking additional approvals worldwide.

Lung cancer remains a formidable health challenge, claiming millions of lives annually. With this approval, patients in Europe now have access to a promising new treatment option that offers renewed hope in their battle against lung cancer.

In addition to its efficacy, KEYTRUDA’s safety profile is also noteworthy. The therapy can cause immune-mediated adverse reactions, including colitis, hepatitis, and adrenal insufficiency. These potential side effects underscore the importance of close monitoring and prompt management by healthcare providers to ensure the safety and well-being of patients undergoing treatment.

Despite these considerations, the approval of KEYTRUDA represents a significant advancement in the field of oncology, offering new possibilities for patients facing the daunting diagnosis of lung cancer. With continued research and innovation, the medical community aims to further improve outcomes and quality of life for individuals affected by this devastating disease.

Join us at the 13th Edition of Biologics Manufacturing Korea 2024, Korea’s premier bioprocessing-focused conference. Discover cutting-edge manufacturing technologies, collaborate with industry leaders, and gain insights from success stories of Korea’s leading biopharmas and international companies. With sessions covering upstream and downstream processing, analytics, automation, and more, this event offers a comprehensive platform for knowledge exchange and collaboration in biologics manufacturing. Don’t miss out on August 13th-14th, 2024, at Songdo Convensia, Incheon, South Korea.

 

Source: https://www.merck.com/news/european-commission-approves-mercks-keytruda-pembrolizumab-plus-chemotherapy-as-neoadjuvant-treatment-then-continued-as-monotherapy-as-adjuvant-treatment-for-resectable-non-small-ce/

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