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Tag: Cancer: Breast

The U.S. Food and Drug Administration has given its blessing to the first immunotherapy regimen for breast cancer.

FDA Approves First Immunotherapy Drug for Breast Cancer

Combo of Tecentriq and chemo given accelerated approval for triple-negative breast cancer
Genetic testing should be made available to all patients with a history of breast cancer

Genetic Testing Recommended for All Patients With Breast Cancer

All with personal history of breast cancer should be offered testing; updated testing recommended
Digital breast tomosynthesis is associated with lower recall and higher cancer detection rates than digital mammography

Recall Down, Cancer Detection Up With Digital Breast Tomosynthesis

Breast cancers detected by DBT less often classified as having poor prognosis than those identified by DM
Both low- and high-income women who are switched to high-deductible health plans experience delays in breast cancer diagnosis and treatment

Breast Cancer Diagnosis Delays Seen With High-Deductible Health Plans

Delays observed in first breast imaging, biopsy, incident early-stage breast cancer diagnosis, chemo
Performance improvements after adoption of digital breast tomosynthesis (DBT) relative to digital mammography performance have been sustained

Performance Improvement Sustained After DBT Adoption

Early improvement after adoption of digital breast tomosynthesis seen regardless of DBT volume
The use of robotically assisted surgical devices for breast removal and other cancer-related surgeries is not approved by the U.S. Food and Drug Administration because there is no proof of its safety or effectiveness in such cases

Robotically Assisted Devices Not Approved for Cancer Surgery

FDA aware that surgeons have been using the devices for uses not granted marketing authorization
Despite claims to the contrary

FDA: Thermography No Substitute for Mammograms

Agency is taking action to stop false advertising about thermography
One-third of primary care providers report participating in breast cancer treatment decisions

One-Third of PCPs Discuss Breast Cancer Treatments With Patients

However, many report feeling uncomfortable or believing they lack the necessary knowledge
An antibody-drug conjugate

Sacituzumab Govitecan Promising in Triple-Negative Breast Cancer

Response rate of 33.3 percent, median response duration of 7.7 months observed in 108 patients
The multigene expression test Oncotype DX is not cost-effective for women with breast cancer who are at low risk for recurrence

Oncotype DX Not Cost-Effective for Low-Risk Breast Cancer

Incremental cost-effectiveness ratio varies across clinical risk groups, sensitive to patient age