年間契約型資訊服務
商品編碼
1349829
HER2 低轉移性乳癌市場:Tumor DeckHER2-Low Metastatic Breast Cancer - Tumour Deck |
HER2 表現量低(定義為 HER2 IHC 評分 1+ 或 2+)且未檢測到 ERBB2 擴增的腫瘤被歸類為 HER2 低轉移性乳癌類別。 這是新定義的 HER2 陰性 BC 子集,其 HER2 免疫組織化學 (IHC) 評分為 1+ 或評分 2+/原位雜交 (ISH) 陰性表型。 IHC/ISH 是目前用於定義 HER2 表達的唯一標準技術。
針對 HER2 低表達的轉移性乳癌的治療正在迅速發展。 最近的臨床試驗表明,CDK4/6 抑制劑與內分泌治療聯合作為標準一線治療是有效的。 此外,PI3K抑制劑和AKT抑制劑的使用也在臨床試驗中進行研究,可能在不久的將來提供進一步的治療選擇。
HER2低表達轉移性乳癌是一種新的乳癌亞型,約佔新診斷乳癌病例的50%至60%。 這顯示HER2低表現的轉移性乳癌是一種相對常見的亞型。 HER2 表達低的乳癌通常被視為 HER2 陰性,即使它們表達 HER2。 儘管 HER2 低表達在 HR+ 乳癌中更為常見,但研究表明,在 HR 陰性乳癌中也觀察到這種情況。
目前,HER2低表達轉移性乳癌的主要治療方法是化療、內分泌治療、標靶治療等不同治療方法的結合。
近年來,標靶治療在臨床試驗中顯示出前景,並被視為替代療法。 由於標靶治療的最新進展,目前 HER2 低轉移性乳癌的護理標準正在迅速發展。 最近的臨床試驗表明,新型 HER2 導向的抗體藥物偶聯物 (ADC) 在治療 HER2 低腫瘤中具有顯著的臨床益處。 其中一種核准的 ADC 曲妥珠單抗 deruxtecan (T-Dxd) 在 HER2 低表達乳癌中顯示出有希望的結果。
除了標靶治療外,內分泌治療也是HER2低表現乳癌的重要治療選擇,尤其是荷爾蒙受體陽性患者。 合併治療,例如CDK4/6抑制劑和內分泌治療的合併治療,也有望改善HER2低表現乳癌患者的預後。
本報告調查了全球 HER2 低轉移性乳癌市場,並提供了市場現狀、病例量趨勢、患者趨勢、競爭產品市場定位和市場機會。
The current clinical definition of HER2-low Breast Cancer (HER2-Low BC) used in clinical practice and ongoing clinical trials relies on the standard IHC and ISH approach; thus, tumors with low level of HER2 expression (defined as a HER2 IHC score of 1+ or 2+) and no detectable ERBB2 amplification fall into this category. It is a newly defined subset of HER2-negative BC that has HER2 immunohistochemical (IHC) score of 1+ or score of 2+/in situ hybridization (ISH) negative phenotype. IHC/ISH is the only standard technique currently applied to define HER2 expression.
"The treatment armamentarium for HER2-low metastatic breast cancer is rapidly evolving. Recent clinical trials have demonstrated the efficacy of CDK4/6 inhibitors in combination with endocrine therapy as a standard first-line treatment option. Additionally, the use of PI3K inhibitors and AKT inhibitors is being explored in clinical trials and may provide further treatment options in the near future."
HER2 low metastatic breast cancer is a new subtype of breast cancer which accounts for approximately 50%-60% of newly diagnosed breast cancer cases. This indicates that HER2 low breast cancer is a relatively common subtype of the disease. Even though HER2-low breast cancer has some HER2 expression, it is generally considered and treated as HER2 negative. Studies have shown that HER2-low expression is more common in HR+ breast cancer, but it can also be found in HR negative breast cancer (Won et al., 2021; Tan et al., 2021).
In recent years, targeted therapies have shown promise in clinical trials and are being explored as alternative treatment options. The current standard of care for HER2-low metastatic breast cancer is rapidly evolving due to recent advancements in targeted therapies. Recent clinical trials have demonstrated significant clinical benefits of novel HER2-directed antibody-drug conjugates (ADCs) in treating HER2-low tumors. One such approved ADC is trastuzumab deruxtecan (T-Dxd), which has shown promising results in HER2-low breast cancer.
In addition to targeted therapies, endocrine therapy is also an important treatment option for HER2-low breast cancer, particularly in patients with hormone receptor-positive disease. Combination therapies, such as CDK4/6 inhibitors in combination with endocrine therapy, have also shown promise in improving outcomes for patients with HER2-low breast cancer.
"It is exciting that we have been able to now translate HER2-targeted therapy to a broader group of patients with HER2-low-expressing breast cancer. Overall, promising responses to T-DXd offer newfound treatment possibilities for a substantial number of patients, many of whom were previously considered to have limited therapeutic options. The recognition of HER2-low status also signals an opportunity to develop more precise, individualized therapeutic approaches through future research."
"We are facing real challenges in terms of [HER2] identification in the clinic, and I would contend that we are in a state of flux in terms of the identification."