HER2 低轉移性乳癌市場:Tumor Deck
年間契約型資訊服務
商品編碼
1349829

HER2 低轉移性乳癌市場:Tumor Deck

HER2-Low Metastatic Breast Cancer - Tumour Deck

出版日期: 年間契約型資訊服務 | 出版商: Mellalta Meets LLP | 英文 300 Pages

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簡介目錄

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。

目錄

第 1 章執行摘要

第2章 HER2低表現轉移性乳癌概述

  • HER2低表達轉移性乳癌的定義、症狀、病因和發病機制
  • HER2-低狀態的臨床意義

第3章 HER2低表現轉移性乳癌的定義與診斷

第 4 章 HER2 低表現轉移性乳癌的流行病學

  • 按國家/地區劃分的盛行率

第5章HER2低表現轉移性乳癌的治療實務

  • 目前的治療方法
  • 處理演算法
  • 用於快速核准的可接受端點

第 6 章核准的 HER2 低表達轉移性乳癌標靶治療

  • 已核准的治療方法摘要

第7章管道臨床試驗

  • HER2低表達轉移性乳癌管線狀況概述與分析
  • HER2低表現轉移性乳癌的競爭格局
  • 關鍵分子及臨床試驗結果
  • 主要藥物核准與上市的時間表

第8章三期資產

  • 臨床試驗和結果

第9章二期資產

  • 臨床試驗和結果

第10章第一期資產

  • 臨床試驗和結果

第 11 章 HER2 低表現轉移性乳癌管線中的非臨床分子

第12章醫生/KOL的看法

  • 來自美國、歐盟和日本 4 位 KOL 的見解

第13章HER2低表現轉移性乳癌的主要事件

  • 擴大已核准的標靶治療
  • 訂定新的可行目標

第 14 章 HER2 低表現轉移性乳癌市場預測 - 2033 年

  • 主要藥物的市場預測與病患份額

第15章附錄

簡介目錄
Product Code: MM20230024

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).

Mellalta Meets HER2-Low Expression in Breast Cancer: Evaluating the Evidence, Challenges, and Opportunities for Expanding Treatment Benefit to More Patients

Mellalta's HER2-Low Metastatic Breast Cancer Deck: Current Treatment Landscape

Currently the mainstay of treatment for HER2-Low Metastatic Breast Cancer consist of combination of different therapeutic approaches like chemotherapy, endocrine therapies, targeted therapies.

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."

Mellalta's HER2-Low Metastatic Breast Cancer Deck: Current Unmet Needs

  • Need for a clear and universally accepted definition of HER2-low, as the current classification is still evolving and there is ongoing research to determine the minimum threshold of HER2 expression required for treatment efficacy.
  • HER2-low breast cancer (BC) has a poor prognosis, making the development of more suitable treatment an unmet clinical need.
  • Need for standardized diagnostic criteria and guidelines for HER2-low tumors.
  • Limited options for combination therapies that can enhance the efficacy of HER2-targeted treatments in HER2-low tumours.

"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."

Mellalta's HER2-Low Metastatic Breast Cancer Deck: Key Takeaways

  • Human epidermal growth factor receptor 2 (HER2) breast cancer, especially in the unresected, metastatic setting, is no longer considered solely binary as positive or negative.
  • There is a new generation of approved antibody drug conjugate (ADC) like Trastuzumab deruxtecan (T-DXd) that have a higher drug-to-antibody ratio (DAR) and can deliver the toxin in a more effective manner for advanced unresectable, metastatic breast cancer.
  • The 2023 National Comprehensive Cancer Network (NCCN) guidelines for the use of trastuzumab deruxtecan (T-DXd) reflect the clinical trial eligibility for DESTINY-Breast04. This allows health care professionals to use other ADCs approved for hormone receptor (HR)-positive and triple negative disease, irrespective of HER2 status.
  • A traditional immunohistochemical (IHC) assay and scoring system have been used in testing to identify HER2-low tumors and the tumors with an IHC score of more than 0, less than 1+. New technologies may help to better identify patients with this subtype of tumor.
  • The recently presented data of the DAISY trial suggested meaningful activity of T-DXd even in patients with HER2-0 metastatic breast cancer

Mellalta's HER2-Low Metastatic Breast Cancer Deck: Questions Answered:

  • Potential challenges and opportunities in implementing targeted therapies for HER2-low breast cancer
  • What is the size of clinically and commercially relevant drug-treatable HER2 low BC populations, and how will drug-treatment rates change over time?
  • What is the expected market impact of recent drug approval such as Enhertu in treatment landscape of HER2-low metastatic BC?
  • What are the most promising agents in the pipeline, and how will they shape the future of this therapy market?
  • What key drivers and constraints will affect the HER2 low metastatic breast cancer therapy market over the forecast period?

Table of Content

1. Executive Summary

  • 1.1. Summary of future trends
  • 1.2. Potential opportunities to explore.
  • 1.3. Drivers/barriers for entry
  • 1.4. Unmet needs
  • 1.5. What's new in HER2-Low Metastatic Breast Cancer?

2. HER2-Low Metastatic Breast Cancer Overview

  • 2.1. HER2-Low Metastatic Breast Cancer definition, symptoms, etiology, Pathogenesis
  • 2.2. Clinical Significance of HER2-Low Status

3. HER2-Low Metastatic Breast Cancer Definition & Diagnosis

  • 3.1. Diagnostic Algorithm
  • 3.2. HER2 Assessment with Immunohistochemistry (IHC) and In Situ Hybridization (ISH) (ASCO/CAP Guidelines)
  • 3.3. AI-assisted interpretation of HER2 Status in HER2-Low Metastatic Breast Cancer

4. HER2-Low Metastatic Breast Cancer Epidemiology

  • 4.1. Incidence rates by countries

5. HER2-Low Metastatic Breast Cancer Treatment Practices

  • 5.1. Current treatment practices
  • 5.2. Treatment algorithms
  • 5.3. Acceptable endpoints for accelerated approval?

6. HER2-Low Metastatic Breast Cancer Approved Targeted Treatments

  • 6.1. Quick overview of approved therapy

7. Pipeline clinical trials

  • 7.1. HER2-Low Metastatic Breast Cancer pipeline landscape overview and analysis
  • 7.2. Competitive Landscape of HER2-Low Metastatic Breast Cancer
  • 7.3. Key molecules in clinical trials and results
  • 7.4. Timeline of key drug approvals and launches.

8. Phase III Assets

  • 8.1. Clinical trials and results

9. Phase II Assets

  • 9.1. Clinical trials and results

10. Phase I Assets

  • 10.1. Clinical trials and results

11. HER2-Low Metastatic Breast Cancer Pipeline Non-Clinical Molecules

  • 11.1. Pre-clinical molecules
  • 11.2. Mechanism of action, catalyst dates, and events

12. Physicians/KOLs Input

  • 12.1. Insights from 4 KOLs in the US, EU, and Japan

13. Key Catalyst Events in HER2-Low Metastatic Breast Cancer

  • 13.1. Expansion of approved targeted therapies
  • 13.2. Creation of new actionable targets

14. HER2-Low Metastatic Breast Cancer Market Forecast -2033

  • 14.1. Market Forecast and patient share by key drugs

15. Appendix