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De-escalation strategies in HER2positive early breast cancer (EBC): final analysis of the WSG-ADAPT HER2+/HR- phase II trial: efficacy, safety, and predictive markers for 12 weeks of neoadjuvant dual blockade with trastuzumab and pertuzumab +/- weekly paclitaxel
Although FDA does not currently clear or approve laboratory-developed tests in the U.S., certification of the laboratory is required under CLIA to ensure the quality and validity of the tests.
Temperature fluctuationssuch as leaving tirzepatide on the counter during preparation or in a warm carcan shorten its stability window
Accessed July 10, 2023
Clinical Epigenetics, 7(1), 14
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