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ASCO 2015
ASCO 2015 Highlights
Real-World Healthcare Utilization and Costs Support Broader Use of CAR T-Cell Therapy
By
Phoebe Starr
Economics & Value
,
Value-Based Care
February 2020, Vol 11, No 1 | Payers’ Perspectives In Oncology | Including ASH 2019 Highlights
Orlando, FL—Chimeric antigen receptor (CAR) T-cell therapy is now approved as third-line treatment for patients with B-cell lymphomas and leukemias. For some patients, CAR T-cell therapy is a miracle therapy, extending survival and, in some cases, as a bridge to a potentially curative transplant.
Read Article
Surgery for Cholangiocarcinoma
Cholangiocarcinoma
,
Personalized Medicine
February 2020, Vol 11, No 1 | Payers’ Perspectives In Oncology | Including ASH 2019 Highlights
At the First Annual Cholangiocarcinoma Summit, presenters discussed recent advances in the management of patients with cholangiocarcinoma (CCA).
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Advances in Cellular Therapies for Hematologic Malignancies Highlighted at ASH 2019
By
Wayne Kuznar
ASH Highlights
February 2020, Vol 11, No 1 | Payers’ Perspectives In Oncology | Including ASH 2019 Highlights
Orlando, FL—The emergence of cellular immunotherapy for a broad array of hematologic malignancies was featured prominently at ASH 2019. The development of adoptive therapy with T-cells that target oncologic malignancies was the subject of the E. Donnall Thomas Lecture “The Long Road to Develop Adoptive Therapy with T Cells That Can Effectively Target Acute Myeloid Leukemia (AML) and Other Malignancies,” delivered by Philip Greenberg, MD, Head, Program in Immunology, Fred Hutchinson Cancer Research Center, Seattle, WA.
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Managing CCA Patients While Waiting for Molecular Biomarker Testing Results
By
Angela Lamarca, MD, PhD, MSc
;
Vaibhav Sahai, MBBS, MS
;
Milind M. Javle, MD
Interview with the Innovators
,
Cholangiocarcinoma
Videos
Dr Vaibhav Sahai and Dr Angela Lamarca consider options for managing patients with CCA while awaiting results from biomarker testing, which can take 3 to 6 weeks. They discuss starting these patients on first-line chemotherapy and then switching appropriate patients to second-line targeted therapy, and also speak to the increased utility of next-generation sequencing in CCA.
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AVBCC: The Prime Venue for Candid Conversations About Value in Cancer Care
By
Barry D. Brooks, MD
Videos
AVBCC Co-Chair Barry Brooks describes how the AVBCC Summit is a premier opportunity to discuss the future of cancer care with some of the most knowledgable industry leaders, practitioners, pharmacists, payers, policymakers, and C-suite executives.
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AVBCC Provides Real-World Discussions for All Cancer Care Stakeholders
By
William McGivney, PhD
Videos
AVBCC Co-Chair William McGivney talks about what attendees can expect to gain from the AVBCC Summit, and why the value equation in cancer care is an issue that affects all stakeholders in the oncology space.
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Why Invest in the AVBCC Summit?
By
Burt Zweigenhaft, PhD, D.Litt
Videos
Watch AVBCC Co-Founder and Chairman Burt Zweigenhaft as he explains what differentiates the AVBCC Summit from other oncology meetings and why you can't afford to miss out on this unique gathering of stakeholders from all facets of the cancer care spectrum.
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FDA Grants Priority Review to New Drug Application for the RET Kinase Inhibitor Selpercatinib
By
Yvette Florio Lane
FDA Approvals, News & Updates
,
In the News
,
Lung Cancer
,
Personalized Medicine
,
Thyroid Cancer
Web Exclusives
On January 29, 2020, Eli Lilly announced that the FDA granted priority review to their New Drug Application for selpercatinib (LOXO-292) for the treatment of patients with advanced
RET
fusion-positive non–small-cell lung cancer,
RET
-mutant medullary thyroid cancer, and
RET
fusion-positive thyroid cancer.
Read Article
The Use of Molecular Biomarker Testing in Patients with CCA
By
Vaibhav Sahai, MBBS, MS
;
Milind M. Javle, MD
Interview with the Innovators
,
Cholangiocarcinoma
Videos
Dr Vaibhav Sahai discusses different approaches to molecular biomarker testing, including when to order the tests in the course of the disease, use of institutional and commercial testing facilities, and what platforms exist for testing.
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Tazverik Receives FDA Approval as First Treatment Specifically for Metastatic or Locally Advanced Epithelioid Sarcoma
By
Yvette Florio Lane
FDA Approvals, News & Updates
,
In the News
Web Exclusives
On January 23, 2020, the FDA granted accelerated approval to tazemetostat (Tazverik; Epizyme), a methyltransferase inhibitor, for the treatment of metastatic or locally advanced epithelioid sarcoma in adults and pediatric patients aged ≥16 years who are not eligible for complete resection.
Read Article
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Ashley Gamble, PhD
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Home
Issues
Online First
Issue Archive
Special Issues
Browse By Topic
Personalized Medicine
Economics & Value
FDA Approvals, News & Updates
COVID-19
Cholangiocarcinoma
View All Topics ›
Conference Correspondent
ESMO 2025 - Wrap-Up: Triple-Negative Breast Cancer
ASCO 2025 - Wrap-Up: Triple-Negative Breast Cancer
Web Exclusives
Web Exclusive Articles
Videos
Interview with the Innovators
Webinars
Quick Quiz
Press Releases
Association for Value-Based Cancer Care
Value-Based Care in Myeloma