2019
DOI: 10.1007/s10549-019-05427-1
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Radiological complete remission in HER2-positive metastatic breast cancer patients: what to do with trastuzumab?

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Cited by 15 publications
(13 citation statements)
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“…We included patients with HER2-positive MBC who received > 1 cycle of trastuzumab-based treatment in one of eight participating Dutch hospitals between January 2000 and December 2014, as described before [12]. Patients were identified using the Netherlands Cancer Registry.…”
Section: Patients and Data Collectionmentioning
confidence: 99%
“…We included patients with HER2-positive MBC who received > 1 cycle of trastuzumab-based treatment in one of eight participating Dutch hospitals between January 2000 and December 2014, as described before [12]. Patients were identified using the Netherlands Cancer Registry.…”
Section: Patients and Data Collectionmentioning
confidence: 99%
“…47 For HER2positive MBC with minimal disease burden and an extended period of stability, we consider holding therapy with surveillance for progression every 3-6 months. 65,66 To decrease frequent visits for those receiving H 6 P, we offer extending the dosing interval from 3 weeks to 4 weeks, especially if receiving other treatments every 4 weeks. 67 We advise caution in the use of therapies with high risk of pulmonary toxicity, such as immunotherapy for metastatic TNBC 68 or trastuzumab deruxtecan for HER2-positive MBC.…”
Section: Metastatic Breast Cancermentioning
confidence: 99%
“…The final CLEOPATRA results after 8 years of follow‐up show a sustained response to first‐line treatment with taxane, trastuzumab, and pertuzumab, with a median OS of 37% for the combined taxane, trastuzumab, and pertuzumab group compared with 23% in the combined taxane, trastuzumab, and placebo group, with a similar long‐term toxicity profile 24 . Given these results, the question of when to discontinue HER2‐directed therapy in the setting of a sustained radiologic complete response to therapy is a pertinent question 71 ; further research is needed to identify patients in whom trastuzumab may safely be discontinued. T‐DM1 was FDA approved on the basis of the EMILIA trial and is typically administered in the second‐line metastatic setting 23 .…”
Section: Therapeutic Advances and Challenges In The Treatment Of Advamentioning
confidence: 99%