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Web Exclusives
Mixed Findings in Annual Cancer Statistics Report
By
Yvette Florio Lane
In the News
Web Exclusives
— January 21, 2020
On January 8, 2020, the American Cancer Society published details of their annual cancer statistics report, including the most recent data on population‐based findings for cancer incidence through 2016 and for mortality through 2017 (
CA Cancer J Clin
. 2020;70:7-30). The report revealed encouraging news as well as some sobering trends.
Read Article
FDA Grants Approval to Avapritinib for Patients with GIST
FDA Approvals, News & Updates
,
Gastrointestinal Cancers
,
In the News
Web Exclusives
— January 13, 2020
The FDA approval of avapritinib marks the first time a drug has been approved specifically for patients with GIST harboring
PDGFRA
exon 18 mutations, which are involved in approximately 10% of GIST cases.
Read Article
Recap of FDA Drug Approvals in 2019
By
Yvette Florio Lane
FDA Approvals, News & Updates
,
In the News
Web Exclusives
— January 7, 2020
The FDA has confirmed another strong year regarding the approval of innovative new drugs and biosimilars, including several agents used in the treatment of patients with cancer.
Read Article
FDA Will Require Early Assessment of New Targeted Agents That May Be Used in Pediatric Cancers
In the News
,
Pediatric Cancer
Web Exclusives
— December 16, 2019
On December 12, 2019, the FDA issued draft guidance to implement amendments to the Federal Food, Drug, and Cosmetic (FD&C) Act that will facilitate early assessment of studies of molecularly targeted oncology drugs that may be effective in the treatment of pediatric cancers.
Read Article
Regenerative Medicine Advanced Therapy Designation Granted to ADP-A2M4 for Synovial Sarcoma
By
Yvette Florio Lane
FDA Approvals, News & Updates
,
In the News
,
Synovial Sarcoma
Web Exclusives
— December 11, 2019
On December 3, 2019, the FDA granted Regenerative Medicine Advanced Therapy (RMAT) designation to the biopharmaceutical company Adaptimmune Therapeutics for ADP-A2M4 for the treatment of synovial sarcoma. Earlier this year, the FDA granted Orphan Drug Designation to the agent for the treatment of soft tissue sarcomas.
Read Article
FDA Grants Priority Review to Keytruda for Patients with High-Risk, Non–Muscle-Invasive Bladder Cancer
By
Yvette Florio Lane
Bladder Cancer
,
FDA Approvals, News & Updates
,
Immunotherapy
Web Exclusives
— December 2, 2019
On December 2, 2019, Merck announced that the FDA has granted priority review for its supplemental biologics license application for the anti–PD-1 agent pembrolizumab (Keytruda).
Read Article
November 25, 2019 – Oncology News & Updates
By
Yvette Florio Lane
FDA Approvals, News & Updates
,
In the News
,
Leukemia
,
Lung Cancer
,
Lymphoma
Web Exclusives
— November 25, 2019
Read Article
In This Article
Calquence Receives FDA Approval for the Treatment of Patients with Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma
Despite Some Positive Trends, Report Confirms Lung Cancer Remains the Deadliest Form of Cancer
November 18, 2019 — Oncology News & Updates
By
Yvette Florio Lane
FDA Approvals, News & Updates
,
Hepatocellular Carcinoma
,
In the News
,
Lymphoma
Web Exclusives
— November 18, 2019
Read Article
FDA Approves Adakveo to Reduce Vaso-Occlusive Crises in Patients with Sickle-Cell Disease
By
Yvette Florio Lane
FDA Approvals, News & Updates
,
In the News
Web Exclusives
— November 16, 2019
On November 15, 2019, the FDA approved crizanlizumab (Adakveo; Novartis) to reduce the frequency of vaso-occlusive crises (VOCs) in adults and pediatric patients aged ≥16 years with sickle-cell disease.
Read Article
November 11, 2019 — Oncology News & Updates
FDA Approvals, News & Updates
,
In the News
Web Exclusives
— November 11, 2019
Read Article
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