scholarly journals Undetectable Tumor Cell-Free DNA in a Patient With Metastatic Breast Cancer With Complete Response and Long-Term Remission

2020 ◽  
Vol 18 (4) ◽  
pp. 375-379
Author(s):  
Natasha Hunter ◽  
Sarah Croessmann ◽  
Karen Cravero ◽  
Daniel Shinn ◽  
Paula J. Hurley ◽  
...  

The ability to serially monitor tumor-derived cell-free DNA (cfDNA) brings with it the potential to measure response to anticancer therapies and detect minimal residual disease (MRD). This report describes a patient with HER2-positive metastatic breast cancer with an exceptional response to trastuzumab and nab-paclitaxel who remains in complete remission several years after cessation of therapy. Next-generation sequencing of the patient’s primary tumor tissue showed several mutations, including an oncogenic hotspot PIK3CA mutation. A sample of cfDNA was collected 6 years after her last therapy and then analyzed for mutant PIK3CA using digital PCR. No detectable mutations associated with the primary tumor were found despite assaying >10,000 genome equivalents, suggesting that the patient had achieved a molecular remission. Results of this case study suggest that serial monitoring of MRD using liquid biopsies could provide a useful method for individualizing treatment plans for patients with metastatic disease with extreme responses to therapy. However, large-scale clinical studies are needed to validate and implement these techniques for patient care.

2019 ◽  
Vol 37 (29) ◽  
pp. 2601-2609 ◽  
Author(s):  
Jame Abraham ◽  
Albert J. Montero ◽  
Rachel C. Jankowitz ◽  
Mohamad Adham Salkeni ◽  
Jan H. Beumer ◽  
...  

PURPOSE Patients with human epidermal growth factor receptor 2 (HER2)–positive metastatic breast cancer eventually develop resistance to dual-antibody therapy with trastuzumab plus pertuzumab. Mechanisms of resistance have not been well elucidated. We evaluated the safety, tolerability, and efficacy of ado-trastuzumab emtansine (T-DM1) plus neratinib in patients who progressed on trastuzumab plus pertuzumab. PATIENTS AND METHODS In this 3 + 3 dose-escalation study, patients with metastatic breast cancer who progressed on trastuzumab, pertuzumab, and a taxane were treated with T-DM1 at 3.6 mg/kg intravenously every 3 weeks and dose-escalating neratinib at 120, 160, 200, or 240 mg/d orally. RESULTS Twenty-seven patients were treated across four dose-levels of neratinib. Dose-limiting toxicity in cycle 1 was grade 3 diarrhea in six patients and grade 3 nausea in one; no patient experienced grade 4 diarrhea, and there were no grade 5 toxicities. Other grade 3 to 4 toxicities included nausea (11%), dehydration (11%), electrolyte abnormality (19%), thrombocytopenia (15%), elevated transaminase levels (7%), and fatigue (7%). Twelve (63%) of 19 evaluable patients had an objective response. Responses occurred at all neratinib doses. Plasma cell–free DNA at baseline showed ERBB2 (HER2) amplification in 10 of 27 patients. Deep and more durable responses occurred in patients with cell-free DNA ERBB2 amplification. Two complete responders had high expression of total HER2 and p95HER2 in baseline tissue. CONCLUSION We report the recommended phase II dose of T-DM1 3.6 mg/kg and neratinib 160 mg/d for this combination. Possible resistance mechanisms to HER2 antibodies may be loss of the HER2 receptor and high expression of p95HER2. These data provide the basis for an ongoing phase II study to better define the activity of this regimen.


The Breast ◽  
2020 ◽  
Vol 53 ◽  
pp. 111-118
Author(s):  
Hongnan Mo ◽  
Xiaobing Wang ◽  
Fei Ma ◽  
Ziliang Qian ◽  
Xiaoying Sun ◽  
...  

2018 ◽  
Vol 44 ◽  
pp. S42-S43
Author(s):  
Daniel Fernandez Garcia ◽  
Allison Hills ◽  
David Guttery ◽  
Karen Page ◽  
Katherine Goddard ◽  
...  

2016 ◽  
Vol 34 (15_suppl) ◽  
pp. 519-519 ◽  
Author(s):  
Mary Ellen Moynahan ◽  
Patricia Sung ◽  
David Chen ◽  
Wei He ◽  
Aliaksandra Samoila ◽  
...  

2017 ◽  
Vol 164 (3) ◽  
pp. 627-638 ◽  
Author(s):  
Kara N. Maxwell ◽  
Danielle Soucier-Ernst ◽  
Emin Tahirovic ◽  
Andrea B. Troxel ◽  
Candace Clark ◽  
...  

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