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| Home > Publications database > Trastuzumab Emtansine for Residual Invasive HER2-Positive Breast Cancer. > print |
| Home > Publications database > Trastuzumab Emtansine for Residual Invasive HER2-Positive Breast Cancer. > print |
| 001 | 142997 | ||
| 005 | 20240229112538.0 | ||
| 024 | 7 | _ | |a 10.1056/NEJMoa1814017 |2 doi |
| 024 | 7 | _ | |a pmid:30516102 |2 pmid |
| 024 | 7 | _ | |a 0028-4793 |2 ISSN |
| 024 | 7 | _ | |a 1533-4406 |2 ISSN |
| 024 | 7 | _ | |a altmetric:52223136 |2 altmetric |
| 037 | _ | _ | |a DKFZ-2019-00622 |
| 041 | _ | _ | |a eng |
| 082 | _ | _ | |a 610 |
| 100 | 1 | _ | |a von Minckwitz, Gunter |b 0 |
| 245 | _ | _ | |a Trastuzumab Emtansine for Residual Invasive HER2-Positive Breast Cancer. |
| 260 | _ | _ | |a Waltham, Mass. |c 2019 |b MMS |
| 336 | 7 | _ | |a article |2 DRIVER |
| 336 | 7 | _ | |a Output Types/Journal article |2 DataCite |
| 336 | 7 | _ | |a Journal Article |b journal |m journal |0 PUB:(DE-HGF)16 |s 1551857678_15264 |2 PUB:(DE-HGF) |
| 336 | 7 | _ | |a ARTICLE |2 BibTeX |
| 336 | 7 | _ | |a JOURNAL_ARTICLE |2 ORCID |
| 336 | 7 | _ | |a Journal Article |0 0 |2 EndNote |
| 520 | _ | _ | |a Patients who have residual invasive breast cancer after receiving neoadjuvant chemotherapy plus human epidermal growth factor receptor 2 (HER2)-targeted therapy have a worse prognosis than those who have no residual cancer. Trastuzumab emtansine (T-DM1), an antibody-drug conjugate of trastuzumab and the cytotoxic agent emtansine (DM1), a maytansine derivative and microtubule inhibitor, provides benefit in patients with metastatic breast cancer that was previously treated with chemotherapy plus HER2-targeted therapy.We conducted a phase 3, open-label trial involving patients with HER2-positive early breast cancer who were found to have residual invasive disease in the breast or axilla at surgery after receiving neoadjuvant therapy containing a taxane (with or without anthracycline) and trastuzumab. Patients were randomly assigned to receive adjuvant T-DM1 or trastuzumab for 14 cycles. The primary end point was invasive disease-free survival (defined as freedom from ipsilateral invasive breast tumor recurrence, ipsilateral locoregional invasive breast cancer recurrence, contralateral invasive breast cancer, distant recurrence, or death from any cause).At the interim analysis, among 1486 randomly assigned patients (743 in the T-DM1 group and 743 in the trastuzumab group), invasive disease or death had occurred in 91 patients in the T-DM1 group (12.2%) and 165 patients in the trastuzumab group (22.2%). The estimated percentage of patients who were free of invasive disease at 3 years was 88.3% in the T-DM1 group and 77.0% in the trastuzumab group. Invasive disease-free survival was significantly higher in the T-DM1 group than in the trastuzumab group (hazard ratio for invasive disease or death, 0.50; 95% confidence interval, 0.39 to 0.64; P<0.001). Distant recurrence as the first invasive-disease event occurred in 10.5% of patients in the T-DM1 group and 15.9% of those in the trastuzumab group. The safety data were consistent with the known safety profile of T-DM1, with more adverse events associated with T-DM1 than with trastuzumab alone.Among patients with HER2-positive early breast cancer who had residual invasive disease after completion of neoadjuvant therapy, the risk of recurrence of invasive breast cancer or death was 50% lower with adjuvant T-DM1 than with trastuzumab alone. (Funded by F. Hoffmann-La Roche/Genentech; KATHERINE ClinicalTrials.gov number, NCT01772472 .). |
| 536 | _ | _ | |a 313 - Cancer risk factors and prevention (POF3-313) |0 G:(DE-HGF)POF3-313 |c POF3-313 |f POF III |x 0 |
| 588 | _ | _ | |a Dataset connected to CrossRef, PubMed, |
| 650 | _ | 7 | |a Antineoplastic Agents, Immunological |2 NLM Chemicals |
| 650 | _ | 7 | |a Maytansine |0 14083FR882 |2 NLM Chemicals |
| 650 | _ | 7 | |a ERBB2 protein, human |0 EC 2.7.10.1 |2 NLM Chemicals |
| 650 | _ | 7 | |a Receptor, ErbB-2 |0 EC 2.7.10.1 |2 NLM Chemicals |
| 650 | _ | 7 | |a Trastuzumab |0 P188ANX8CK |2 NLM Chemicals |
| 650 | _ | 7 | |a ado-trastuzumab emtansine |0 SE2KH7T06F |2 NLM Chemicals |
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| 700 | 1 | _ | |a Loibl, Sibylle |b 3 |
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| 700 | 1 | _ | |a Singel, Stina M |b 27 |
| 700 | 1 | _ | |a Geyer, Charles E |b 28 |
| 700 | 1 | _ | |a Investigators, KATHERINE |b 29 |e Collaboration Author |
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| 700 | 1 | _ | |a Rimawi, M. |b 328 |
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| 700 | 1 | _ | |a Shalaby, I. |b 335 |
| 700 | 1 | _ | |a Sinclair, S. |b 336 |
| 700 | 1 | _ | |a Steen, P. |b 337 |
| 700 | 1 | _ | |a Sturtz, K. |b 338 |
| 700 | 1 | _ | |a Tamkus, D. |b 339 |
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| 700 | 1 | _ | |a Valero, V. |b 345 |
| 700 | 1 | _ | |a Vaughn, C. |b 346 |
| 700 | 1 | _ | |a Wahl, T. |b 347 |
| 700 | 1 | _ | |a Waisman, J. |b 348 |
| 700 | 1 | _ | |a Wapnir, I. |b 349 |
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| 700 | 1 | _ | |a Zera, R. |b 355 |
| 700 | 1 | _ | |a Zhang, W. |b 356 |
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