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市場調查報告書

惡性黑色素瘤:關鍵意見領袖(KOL)的考察

Malignant Melanoma: KOL Insight

出版商 FirstWord 商品編碼 317172
出版日期 內容資訊 英文
商品交期: 最快1-2個工作天內
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惡性黑色素瘤:關鍵意見領袖(KOL)的考察 Malignant Melanoma: KOL Insight
出版日期: 2015年11月01日 內容資訊: 英文
簡介

由於2011年的癌症的免疫療法的認證,癌症專門醫生使用作為惡性黑色素瘤的治療的藥物環境大幅變化。還有突變實驗的可用性也影響了治療選擇,尤其是標靶治療的選擇。Bristol-Myers Squibb的Opdivo和Amgen的T-VEC等,選項更擴大。

本報告提供惡性黑色素瘤的已上市藥概要,開發平台藥物概要與開發情形,關鍵意見領袖(KOL)的各種見解及考察等彙整資料。

近幾年上市的藥物、疫苗

  • Yervoy (ipilimumab)
  • Keytruda (pembrolizumab)
  • Opdivo (nivolumab)
  • Cotellic (cobimetinib)
  • Mekinist (trametinib)
  • Zelboraf (vemurafenib)
  • Tafinlar (dabrafenib)
  • M-Vax
  • Talimogene laherparepvec (T-VEC)

開發平台藥物、疫苗

  • Masitinib
  • Encorafenib
  • Binimetinib
  • Zastumotide
  • Seviprotimut-L (POL 103A)
  • Eltrapuldencel-T

調查課題

  • 依據有效性、毒性、患者簡介,選擇KOL作為第一選擇療法的組合是什麼?
  • 新的聯合治療的認證會帶給未來第一選擇療法選擇的影響嗎?在處方上積極的KOL是什麼?
  • c-KIT變異患者的實驗中資源上的實踐困難度比採用其他治療途徑的優點還要重大嗎?或是可以利基市場作為目標呢?
  • 治療的定序相關疑慮
  • 考慮KOL的免疫療法的替代法的利基市場是什麼?
  • 影響選擇的部分驚人的要素
    • 冷藏庫的可用性、注射的經驗、文件事務、投藥計劃等
  • 各藥物的最新的臨床試驗的彙整

本網頁內容可能與最新版本有所差異。詳細情況請與我們聯繫。

目錄
Product Code: 596200414

Malignant Melanoma: KOL Insight reveals the impact of immunotherapy on first-line treatment combination choices

The arrival of cancer immunotherapy in 2011 significantly changed the landscape for drugs used by oncologists for treating malignant melanoma . The availability of mutation testing is also impacting the choice of treatments, particularly for targeted therapies. With new approvals for Bristol-Myers Squibb's Opdivo and Amgen's T-VEC, the options available continue to grow

As the treatment landscape for malignant melanoma becomes more crowded , you need to understand how and why physicians are making complex decisions about their first-line drug choices. Find out what KOLs are saying about your brands, and the brands of your closest competitors.

Answering Key Questions

Recently marketed drugs and vaccines

  • Yervoy (ipilimumab) : Will the drug's adoption, gained from early approval, be threatened by new arrivals with better response rates and reduced toxicity?
  • Keytruda (pembrolizumab) : What role does dosing schedule play in driving preference for this drug?
  • Opdivo (nivolumab) : What concerns still underlie the positive reception of this recently approved therapy?
  • Cotellic (cobimetinib) : Does combination therapy offer a way forward, and will its use depend on side-effects or pricing?
  • Mekinist (trametinib) : For patients with BRAF mutations, what will be the driving factor for selection of combination therapy, and will safety concerns outweigh this in treatment decisions?
  • Zelboraf (vemurafenib) : What is the impact of not having an approved combination on its label in relation to its use as a first-line therapy?
  • Tafinlar (dabrafenib) : Does its side-effect profile give it an edge, or will it lose out if a cobimetinib and vemurafenib combination becomes available?
  • M-Vax : Has immunotherapy side-lined the role of vaccines in melanoma treatments because of the limited efficacy of vaccines? Or is it useful for a niche subset of patients?
  • Talimogene laherparepvec (T-VEC) : While some activity has been shown, and there is potential benefit for a niche patient group, is this enough to overcome the restrictions and challenges presented by this recently-approved vaccination?

Pipeline drugs and vaccines

  • Masitinib : Should trials concentrate on the Far East where there is a higher-rate of c-KIT mutated melanoma in order to speed up possible access to an on-label option?
  • Encorafenib : Is the safety profile going to be enough to get physicians to switch treatments in an already crowded field?
  • Binimetinib : Is this just another 'me-too' third-line drug or do KOLs, waiting on Phase III trial results, think it has potential for NRAS-mutated patients?
  • Zastumotide : The results of NSCLC data from an adjuvant setting is already colouring the view of this vaccine. Does it have any future as a malignant melanoma treatment?
  • Seviprotimut-L (POL 103A) : KOLs are still asking big questions about this vaccine - especially about potential results. Will it find a place in the treatment paradigm?
  • Eltrapuldencel-T : Will the complications of it as a treatment be a barrier to take-up if efficacy is proved?

Key Issues Explored

  • Which combinations are KOLs preferring to use as first-line treatments based on efficacy, toxicity and patient profiles?
  • How new drug combination approvals are likely to effect the first-line choice of treatments in future, and which KOLs are keen to be able to prescribe.
  • Whether the practical difficulties with resources for testing patients with c-KIT mutations will outweigh the benefits of using a different treatment pathway for relevant patients? Or does this targeting offer a real niche market?
  • What concerns exist about the sequencing of treatments?
  • Where KOLs think the alternatives to immunotherapy will find their niche with particular populations.
  • Some of the surprising factors that can influence choices - from availability of fridges and experience with injections, to paperwork and dosing schedules.
  • A round-up of the latest clinical trials for each drug included.

Contributors

Expert knowledge and insights

KOLs from North America

  • Dr Richard W. Joseph, MD. Assistant Professor of Oncology, Mayo Clinic Health System, Florida, USA.
  • Dr Igor Puzanov, MD, MSCI, FACP. Associate Professor of Medicine, Vanderbilt University, Nashville, TN, USA.
  • Dr Rene Gonzalez, MD. Professor of Medicine, Division of Medical Oncology, University of Colorado Denver, USA.
  • Prof. Bartosz Chmielowski, MD, Ph.D. Assistant Professor, Department of Medicine, UCLA, CA, USA.
  • Dr Anthony Olszanski, MD, RPh. Medical Oncologist, Fox Chase Cancer Center, Philadelphia, PA, USA.
  • Dr Stergios Moschos MD. University of North Carolina at Chapel Hill, School of Medicine, UNC Lineberger, Carolina, USA.

KOLs from Europe

  • Dr Nicolas Blin, MD. Consultant Physician at Nantes University Hospital, France.
  • Dr J Mayordomo, Ph.D. Medical Director, Translational Research Unit, Albacete University Hospital, Spain.
  • Dr Maria Elisabetta Fratto, MD. Oncologist, University Campus Bio Medico, Rome, Italy.
  • German KOL, Prof. Dr. A chief consultant, head of the Clinical Cooperation Unit Dermato-oncology in the Department of Dermatology, Venereology and Allergology at the University Hospital.
  • Prof. Ruth Plummer, MA, DPhil, BMBCh, MD, FRCP. Consultant Medical Oncologist, Newcastle Upon Tyne Hospitals, UK.
  • Dr Marianne Nicolson, MD, FRCP. Consultant, Aberdeen Royal Infirmary, Scotland, UK.

Ongoing Benefits

The world of pharma is ever changing and executives must always be up-to-date with new developments that could affect their own products, position and research. That is why FirstWord's guarantee to keep Therapy Trends clients up to date with Update Bulletins offers a real commercial advantage.

Update Bulletins include expert insight and analysis based on FirstWord analyst re-engagement with the KOLs after major events such as product approvals, key data releases and major conferences to deliver the most valuable insights with each update.

  • Your Therapy Trends Report purchase entitles you to receive three Update Bulletins, which are published approximately every three months for 12 months following the report's publication date, October 2014.
  • You will receive a copy of each Update Bulletin once available, which are issued each quarter after the publication date.
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