In the open-label, multicentre, phase 2 NIMBUS trial (NCT03789110), the efficacy and safety of dual checkpoint inhibition with nivolumab plus low-dose ipilimumab was evaluated in patients with hyper-mutated breast cancer with a TMB≥9 mutations/megabase (mut/Mb). Dr Romualdo Barroso-Sousa (Hospital Sírio-Libanês, Brazil) presented the results [1].
The NIMBUS study included 30 patients with HER2-negative metastatic breast cancer (70% HR-positive, 30% triple-negative breast cancer) and a TMB of at least 9 mut/Mb (median 10.9 mut/Mb). The median number of prior chemotherapy lines was 1.5 and the maximum was 3. Patients received nivolumab (3 mg/kg every 2 weeks) plus ipilimumab (1 mg/kg every 6 weeks) until disease progression, unacceptable toxicity, or up to 24 months.
During a median 9.7 months of follow-up, there were 5 (16.7%) confirmed objective responses, all of which were partial. A further 6 (20%) patients had stable disease during follow-up. Median duration of response was 12.1 months, while median progression-free survival and overall survival were a respective 1.4 and 19.3 months. Exploratory analyses revealed that in patients with a high TMB (≥14 mut/Mb) the overall response rate was 60% versus 8% in the 25 patients with a TMB of 9–13 mut/Mb. Median progression-free survival and median overall survival was 9.5 months and not reached in patients with a TMB≥14 mut/Mb versus 1.4 months and 8.8 months in patients with a TMB of 9–13 mut/Mb.
Based on these results, Dr Barrosso-Sousa concluded that: “this study supports the use of checkpoint inhibitors among patients with HER2-negative metastatic breast cancer and TMB. However, the study does not answer the question whether dual checkpoint inhibition is better than pembrolizumab monotherapy.”
- Barroso-Sousa R, et al. Nimbus: A phase 2 trial of nivolumab plus ipilimumab for patients with hypermutated her2-negative metastatic breast cancer (MBC). GS2-10, SABCS 2021 Virtual Meeting, 7–10 December.
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Table of Contents: SABCS 2021
Featured articles
Early-Stage Breast Cancer
Aromatase inhibitors outperform tamoxifen in premenopausal women
Concurrent taxane plus anthracycline most beneficial in reducing risk of breast cancer
Reduced risk of recurrence with ovarian suppression plus tamoxifen/exemestane
Metformin does not improve outcomes in patients with early-stage breast cancer
Omitting sentinel lymph node biopsy improves arm symptoms
HR-positive/HER2-negative Breast Cancer
Addition of palbociclib to standard endocrine therapy does not improve outcome in adjuvant treatment
The SERD elacestrant improves outcomes for patients unresponsive to endocrine therapy
Consistent overall survival benefit of ribociclib in advanced breast cancer
Premenopausal women benefit from adjuvant chemotherapy next to endocrine therapy
Promising anti-tumour activity of the CDK7-inhibitor samuraciclib plus fulvestrant
ctDNA is prognostic and predictive for response to ribociclib plus letrozole
Early switch to fulvestrant plus palbociclib beneficial for patients with ESR1 mutation
Triple-Negative Breast Cancer
Single-cell spatial analysis can predict response to neoadjuvant immunotherapy
Neoadjuvant pembrolizumab plus chemotherapy benefits event-free survival in TNBC
Early use of ctDNA testing can identify likelihood of relapse in TNBC
Pembrolizumab plus chemotherapy benefits patients with combined positive score ≥10
Neratinib plus trastuzumab plus fulvestrant shows encouraging clinical activity
Phase 1–3 Trials
Datopotamab deruxtecan shows promising anti-tumour activity
Trastuzumab deruxtecan outperforms trastuzumab emtansine
Nivolumab plus ipilimumab serve promising dual checkpoint inhibition
Entinostat plus exemestane improves progression-free survival in Chinese patients
Efficacy of pyrotinib plus capecitabine confirmed in previously treated patients
Basic and Translational Research
Using genomics to match treatments improves outcomes
Loss of ASXL1 tumour suppressor promotes resistance to CDK4/6 inhibitors
Inducers of ferroptosis are potential drugs to target p53-mutated TNBC cells
MAPK-pathway alterations are associated with resistance to anti-HER2 therapy
Genomic signatures of DCIS define biology and correlate with clinical outcomes
BRCA2 linked to inferior outcomes with CDK4/6 inhibitors plus endocrine therapy
Miscellaneous
Olaparib is well tolerated as an additional treatment
Race effects the likelihood to develop lymphoedema following breast cancer treatment
Sentinel lymph node staging is non-inferior to complete axillary lymph node dissection
One in 7 breast cancers detected during screening are overdiagnosed
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