her2
No description yet: the sentence for this tag has not been written. 12 records carry it: 8 biomarkers, 4 people.
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12 records
| Cancers | Other tags | ||||
|---|---|---|---|---|---|
Cristina Saura Head of the Breast Cancer Unit, Vall d'Hebron University Hospital and VHIO · Vall d'Hebron University Hospital / VHIO Spanish breast oncologist leading DESTINY-Breast09, which moved trastuzumab deruxtecan into first-line HER2-positive disease. | HER2-positive breast cancer | none | breast, adc | ||
Helena Earl Emeritus Professor of Clinical Cancer Medicine, University of Cambridge · Cancer Research UK Cambridge Centre / CRUK Cambridge Institute Led PERSEPHONE, which showed six months of trastuzumab is nearly as good as twelve for most patients. | HER2-positive breast cancer | none | breast, de-escalation | ||
HER2 (ERBB2) activating mutation ERBB2 A HER2 mutation is a change in the gene's kinase domain, most often an exon 20 insertion, found in about 2 to 3 percent of lung adenocarcinomas. It is a different thing from HER2 amplification or overexpression, and it selects trastuzumab deruxtecan and, since 2025, zongertinib in lung cancer. | Non-small-cell lung cancer | none | biomarker | ||
HER2 IHC 0 (HER2-negative, including ultralow) ERBB2 IHC 0 is no HER2 staining, or faint staining in 10 percent or fewer cells. It is HER2-negative, but the label now separates true zero from 'IHC 0 with membrane staining', the ultralow group that trastuzumab deruxtecan can treat in hormone-receptor-positive breast cancer. | Breast cancer, HER2-low and HER2-ultralow metastatic breast cancer, HR-positive / HER2-negative breast cancer | none | biomarker | ||
HER2 IHC 1+ ERBB2 IHC 1+ is faint, incomplete HER2 staining. It was called HER2-negative for twenty years; since 2022 it is the larger half of HER2-low, which trastuzumab deruxtecan treats in breast cancer. | Breast cancer, HER2-low and HER2-ultralow metastatic breast cancer, HR-positive / HER2-negative breast cancer | none | biomarker | ||
HER2 IHC 2+ (equivocal, reflex to ISH) ERBB2 IHC 2+ is the in-between HER2 result: moderate staining that cannot be called positive or negative by eye, so the laboratory runs an ISH gene test. 2+ with amplification is HER2-positive; 2+ without it is HER2-low. | Breast cancer, HER2-low and HER2-ultralow metastatic breast cancer, HER2-positive gastric cancer | none | biomarker | ||
HER2 IHC 3+ (HER2-positive by immunohistochemistry) ERBB2 IHC 3+ means strong, complete membrane staining for HER2 in more than 10 percent of tumour cells. It is HER2-positive without needing a gene test and is the gate for trastuzumab, its combinations and antibody-drug conjugates in breast, stomach, biliary and, since 2024, any solid tumour. | HER2-positive breast cancer, Early HER2-positive breast cancer, HER2-positive gastric cancer | none | biomarker | ||
HER2 ISH amplified (ERBB2 gene amplification) ERBB2 ISH counts copies of the HER2 gene in each tumour cell. A ratio of 2 or more against the chromosome 17 control, or 6 or more copies per cell, is amplified and HER2-positive whatever the protein stain showed. | HER2-positive breast cancer, HER2-positive gastric cancer, Early HER2-positive breast cancer | none | biomarker | ||
HER2-low (IHC 1+ or IHC 2+/ISH-negative) ERBB2 HER2-low is not a new stain but a new reading of the old one: 1+ or 2+ without gene amplification. It covers about half of breast cancers and makes them eligible for trastuzumab deruxtecan. | HER2-low and HER2-ultralow metastatic breast cancer, HR-positive / HER2-negative breast cancer, Metastatic triple-negative breast cancer | none | biomarker | ||
HER2-ultralow (IHC 0 with membrane staining) ERBB2 HER2-ultralow is an IHC 0 result with a trace of membrane staining in a few cells. Since 2025, in hormone-receptor-positive breast cancer that has stopped responding to hormone therapy, it is enough for trastuzumab deruxtecan. | HER2-low and HER2-ultralow metastatic breast cancer, HR-positive / HER2-negative breast cancer | none | biomarker | ||
Ian E. Krop Associate Cancer Center Director for Clinical Research, Yale Cancer Center · Yale Cancer Center / Smilow Cancer Hospital Breast oncologist who took T-DM1 and then trastuzumab deruxtecan from first-in-human studies to approval. | HER2-positive breast cancer | none | breast, adc | ||
Sandra M. Swain Professor of Medicine and Associate Dean for Research Development, Georgetown University Medical Center · Georgetown Lombardi Comprehensive Cancer Center Led CLEOPATRA, which showed dual HER2 blockade with pertuzumab gives an unprecedented 16-month survival gain in metastatic disease. | HER2-positive breast cancer | none | breast, trialist |
