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China Approval of Avastin′s New Indication

  • 分類:最新消息
  • 作者:華訊知識產權
  • 來源:
  • 發布時間:2020-09-28 13:44
  • 訪問量:

【概要描述】As the world's first anti-tumor angiogenesis treatment drug, Avastin was approved in China for the treatment of colorectal cancer and non-small cell lung cancer(NSCLC) indications. On September 21, Roche announced that Avastin has been approved by the National Medical Products Administration (NMPA) of China for the treatment of adult patients with recurrent glioblastoma (GBM). Avastin is a humanized monoclonal antibody lgG1 developed by Roche. Avastin can bind to tumor Vascular Endothelial Growth Factor (VEGF) so that it cannot stimulate the growth of blood vessels. The blood, oxygen, and other nutrients required for tumor growth are blocked, preventing their growth or spreading to other parts of the body, and ultimately achieving anti-cancer effects. Glioblastoma (GBM) is the most common and deadly primary brain tumor in adults. In the West, the annual incidence or number of new diagnoses is 2 to 3 per 100,000 people. GBM accounts for 12% to 15% of all intracranial tumors and 50% to 60% of astrocytoma. GBM can invade and infiltrate the normal surrounding brain tissue extensively, making complete resection impossible. Even with comprehensive treatments such as surgery, radiotherapy and chemotherapy, GBM patients are still very prone to relapse and die of tumors quickly. GBM is considered to be one of the most difficult tumors in the field of neurosurgery. The approval of this new indication is mainly based on a multi-center, open-label, randomized controlled, pivotal phase III clinical trial EORTC 26101. The results of this study confirmed that compared with chemotherapy alone, Avastin-based treatment prolonged the time to progression-free survival or the time to death (median PFS: 4.2 months vs. 1.5 months, HR=0.52, 95%CI: 0.41-0.64), the risk of disease progression can be reduced by 51%. During the progression-free survival period, patients in remission showed more stable global health scores and cognitive functions than non-remission patients. This means that Avastin will bring new treatment options for Chinese GBM patients. The approval of Avastin this time fills up the gap in the field of GBM treatment in China. It is of great significance to improving the level of GBM diagnosis and treatment in China, and will bring good news to patients who lack effective treatment options.

China Approval of Avastin′s New Indication

【概要描述】As the world's first anti-tumor angiogenesis treatment drug, Avastin was approved in China for the treatment of colorectal cancer and non-small cell lung cancer(NSCLC) indications. On September 21, Roche announced that Avastin has been approved by the National Medical Products Administration (NMPA) of China for the treatment of adult patients with recurrent glioblastoma (GBM).



Avastin is a humanized monoclonal antibody lgG1 developed by Roche. Avastin can bind to tumor Vascular Endothelial Growth Factor (VEGF) so that it cannot stimulate the growth of blood vessels. The blood, oxygen, and other nutrients required for tumor growth are blocked, preventing their growth or spreading to other parts of the body, and ultimately achieving anti-cancer effects.

Glioblastoma (GBM) is the most common and deadly primary brain tumor in adults. In the West, the annual incidence or number of new diagnoses is 2 to 3 per 100,000 people. GBM accounts for 12% to 15% of all intracranial tumors and 50% to 60% of astrocytoma. GBM can invade and infiltrate the normal surrounding brain tissue extensively, making complete resection impossible. Even with comprehensive treatments such as surgery, radiotherapy and chemotherapy, GBM patients are still very prone to relapse and die of tumors quickly. GBM is considered to be one of the most difficult tumors in the field of neurosurgery.



The approval of this new indication is mainly based on a multi-center, open-label, randomized controlled, pivotal phase III clinical trial EORTC 26101. The results of this study confirmed that compared with chemotherapy alone, Avastin-based treatment prolonged the time to progression-free survival or the time to death (median PFS: 4.2 months vs. 1.5 months, HR=0.52, 95%CI: 0.41-0.64), the risk of disease progression can be reduced by 51%. During the progression-free survival period, patients in remission showed more stable global health scores and cognitive functions than non-remission patients. This means that Avastin will bring new treatment options for Chinese GBM patients.

The approval of Avastin this time fills up the gap in the field of GBM treatment in China. It is of great significance to improving the level of GBM diagnosis and treatment in China, and will bring good news to patients who lack effective treatment options.

  • 分類:最新消息
  • 作者:華訊知識產權
  • 來源:
  • 發布時間:2020-09-28 13:44
  • 訪問量:
詳情

As the world's first anti-tumor angiogenesis treatment drug, Avastin was approved in China for the treatment of colorectal cancer and non-small cell lung cancerNSCLCindications. On September 21, Roche announced that Avastin has been approved by the National Medical Products Administration (NMPA) of China for the treatment of adult patients with recurrent glioblastoma (GBM).

Avastin is a humanized monoclonal antibody lgG1 developed by Roche. Avastin can bind to tumor Vascular Endothelial Growth Factor (VEGF) so that it cannot stimulate the growth of blood vessels. The blood, oxygen, and other nutrients required for tumor growth are blocked, preventing their growth or spreading to other parts of the body, and ultimately achieving anti-cancer effects.

Glioblastoma (GBM) is the most common and deadly primary brain tumor in adults. In the West, the annual incidence or number of new diagnoses is 2 to 3 per 100,000 people. GBM accounts for 12% to 15% of all intracranial tumors and 50% to 60% of astrocytoma. GBM can invade and infiltrate the normal surrounding brain tissue extensively, making complete resection impossible. Even with comprehensive treatments such as surgery, radiotherapy and chemotherapy, GBM patients are still very prone to relapse and die of tumors quickly. GBM is considered to be one of the most difficult tumors in the field of neurosurgery.

The approval of this new indication is mainly based on a multi-center, open-label, randomized controlled, pivotal phase III clinical trial EORTC 26101. The results of this study confirmed that compared with chemotherapy alone, Avastin-based treatment prolonged the time to progression-free survival or the time to death (median PFS: 4.2 months vs. 1.5 months, HR=0.52, 95%CI: 0.41-0.64), the risk of disease progression can be reduced by 51%. During the progression-free survival period, patients in remission showed more stable global health scores and cognitive functions than non-remission patients. This means that Avastin will bring new treatment options for Chinese GBM patients.

The approval of Avastin this time fills up the gap in the field of GBM treatment in China. It is of great significance to improving the level of GBM diagnosis and treatment in China, and will bring good news to patients who lack effective treatment options.

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