This review summarizes clinically relevant trials in metastatic breast cancer (MBC) presented at the 2018 San Antonio Breast Cancer Symposium (SABCS). At the meeting updates of two large phase III studies were presented: (1) the biomarker analysis of IMpassion130, trying to define the target population for the checkpoint inhibitor atezolizumab in triple-negative MBC and (2) a subgroup analysis of SOLAR-1, where the efficacy and safety of the alpha-specific Phosphoinositide 3(PI3)-kinase inhibitor alpelisib in combination with fulvestrant was investigated in patients with hormone receptor positive (HR+), human epidermal growth factor receptor 2 negative (HER2−) MBC. Furthermore, we review the results of a randomized phase II trial (CCTG MA38) comparing a continuous daily dosing of palbociclib to the standard treatment dose, and the phase 1b data of the B-cell lymphoma 2 (BCL-2) inhibitor venetoclax in combination with tamoxifen as a novel drug combination in patients with HR+/HER2−MBC.
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At the 2018 San Antonio Breast Cancer Symposium (SABCS), no new data from large phase III clinical studies in metastatic breast cancer (MBC) were presented. In this short review we instead focus on a number of interesting smaller trials, ranging from early drug development to quality of life studies and supportive treatment trials. Those study results might have direct influence on daily practice or show strong signals for successful future drug development. In detail, we summarize updated results of two phase III trials (IMpassion130 and SOLAR-1) as well as two smaller trials in hormone-receptor (HR) positive, human epidermal growth factor receptor 2 (HER2)-negative MBC investigating two different dosing schedules of the cyclin-dependent kinase 4/6 (CDK4/6) inhibitor palbociclib and a the combination of the BCL-2 inhibitor venetoclax with tamoxifen, respectively.
The IMpassion130 study was a phase III trial that evaluated atezolizumab, an anti-PD-L1 antibody, in combination with nab-paclitaxel as first-line treatment for metastatic triple negative breast cancer (TNBC) . In total, 902 patients were randomized 1:1 to nab-paclitaxel 100 mg/m2 i.v. (on days 1, 8 and 15 of a 28-day cycle) plus atezolizumab 840 mg i.v. every 2 weeks or nab-paclitaxel plus placebo.
The primary analysis was already presented at the ESMO congress 2018 and was published in the New England Journal of Medicine . The study showed a significantly longer progression-free survival (PFS) by the addition of atezolizumab in the intention-to-treat (ITT) population (hazard ratio [HR] 0.80; 95% confidence interval [CI] 0.69–0.92; P = 0.002). In patients with PD-L1 expression in at least 1% of tumor-infiltrating immune cells (PD-L1 IC+) the influence on PFS was more pronounced (HR 0.62; 95%CI 0.49–0.78; P < 0.001). At this time point, the interim overall survival (OS) analysis showed no statistical difference in the ITT population between the two study arms. Therefore, according to the protocol, no statistical analysis of OS in the PD-L1 IC+ subgroup was allowed. Nevertheless, the PD-L1 IC+ subgroup showed an absolute survival difference of almost 10 months between the two study arms (25.0 months vs. 15.5 months; HR 0.62; 95%CI 0.45–0.86).
At SABC 2018 a more detailed biomarker-analysis beyond PD-L1 was presented. First of all, in this TNBC cohort, a much higher prevalence of PD-L1 expression on immune cells was observed compared to PD-L1 expression on tumor cells (41% vs. 9%). In addition, these two subgroups were largely overlapping. Staining of PD-L1 was done by using the VENTANA SP142 IHC assay, which was approved by the FDA as companion diagnostic required for assessment of PD-L1 status in TBNC. A number of pathologists believe this biomarker evaluation to be of questionable value. The known weak staining capacity of SP142 for tumor cells opens the discussion if not other antibodies, more established for PD-L1 determination in other tumor entities, could be used as well .
For the PD-L1 IC-negative subgroup, absolutely no benefit by the addition of atezolizumab to nab-paclitaxel was shown both regarding PFS and OS. Within the PD-L1 positive subgroup, however, no difference between low (IC1; PFS HR 0.59; 95%CI 0.44–0.78) and intermediate or strong staining (IC2/3; PFS HR 0.64; 95%CI 0.43–0.97) was observed.
Beyond PD-L1 on immune cells, stromal tumor-infiltrating lymphocytes (sTILs) and tumor-infiltrating cytotoxic T cells (CD8+) were investigated as potential predictive markers. These markers by themselves, however, predicted clinical benefit with atezolizumab + nab-paclitaxel only if the infiltrating immune cells were also PD-L1 positive. Importantly, the efficacy of the combination treatment in PD-L1 IC+ patients was independent of their BRCA 1/2 mutation status.
Based on the study, atezolizumab received accelerated approval by the FDA in combination with nab-paclitaxel for the treatment of patients with triple-negative MBC with PD-L1 positivity on tumor-infiltrating immune cells (≥1%).
A subgroup analysis of the SOLAR-1 data was performed by Juric et al. . Phosphatidylinositol-3-kinase (PI3K) mutations are present in approximately 40% of patients with HR+/HER2− breast cancer leading to hyperactivation of the PI3K pathway and estrogen independent tumor growth [5, 6].
SOLAR-1 was a randomized, double-blind phase 3 study that investigated the efficacy and safety of the alpha-specific PI3K inhibitor alpelisib in combination with fulvestrant in patients with HR+/HER2− MBC. Patients were randomly assigned to receive alpelisib (300 mg/day p.o.) or placebo both in combination with fulvestrant (500 mg every 28 days and on days 1 and 15 of the first cycle i.m.). The primary results were presented at the 2018 ESMO congress. The study met its primary endpoint by nearly doubling median PFS in the PIK3CA-mutated subgroup (11 months vs 5.7 months; HR 0.65; 95%CI 0.50–0.85; P < 0.001). No benefit was seen in the PI3K-nonmutant cohort.
Three important subgroup analyses were presented in San Antonio: (1) Patients with prior CDK4/6 inhibitor therapy seemed to benefit in the same way from the PI3K inhibitor; however the subgroup was very small (18 patients) and the median duration of PFS in this subpopulation was short (5.5 vs 1.8 months; HR 0.48; 95%CI 0.17–1.36). (2) The benefit with alpelisib was consistent in first- (HR 0.71) and second-line (HR 0.61). (3) PIK3CA mutation status assessed in plasma circulating tumor DNA (ctDNA) was of predictive value, similar or even better than the tumor tissue mutation status (HR 0.55; 95%CI 0.39–0.79). However, the frequency of PIK3CA mutations in the plasma was much lower than in the tumor (34% vs. 60%), reflecting the detection limits of this technique.
OS data were still immature since only 92 deaths had occurred (52% of the planned analysis): 40 in the alpelisib plus fulvestrant arm and 52 in the placebo plus fulvestrant arm (HR 0.73; 95%CI 0.48–1.10; P = 0.06).
With 76% of patients having a grade 3/4 adverse event, the treatment with alpelisib requires careful management of side effects. Most frequent all-grade adverse events were hyperglycemia (65% vs 9%), diarrhea (54% vs 11%), nausea (46% vs 20%) and rash (40% vs 6%). Hyperglycemia is a reversible, on-target effect of PI3K inhibition, which is easily detectable and usually well manageable [7, 8]. However, in SOLAR-1, 44% of patients with hyperglycemia had dose reductions and 87% received anti-diabetic medication (76% with metformin). The risk for hyperglycemia was higher in patients who were prediabetic at baseline.
In conclusion, the combination of alpelisib and fulvestrant is a potential new treatment option for PIK3CA mutant HR+/HER2− MBC after progression on prior endocrine therapy. Given the challenging toxicity profile and the fact that the combination of everolimus and exemestane showed very similar results in BOLERO-2, irrespective of PI3K mutation status (HR 0.45; 95% 0.38–0.54; P < 0.001), the integration of this new treatment option in the therapeutic algorithm is not yet clear.
The CDK 4/6 inhibitor palbociclib is approved by EMA and FDA at a standard dose of 125 mg p.o. daily, 3 weeks on followed by one week off. Although this regimen is feasible for many patients, the on–off regimen might facilitate overdosing or non-adherence.
The Canadian Cancer Trials Group (CCTG) led a randomized phase II trial comparing the efficacy and tolerability of a continuous daily dose of 100 mg p.o. daily (CDD) to 125 mg p.o. daily 3 weeks on/1 week off (STD) . Patients with HR+/HER2− MBC after progression on first-line endocrine therapy were included. The primary endpoint was PFS, secondary endpoints included OS, safety and quality of life. In total 180 patients were enrolled. Palbociclib was found active in either 100 mg CDD or 125 mg STD schedule: PFS in CDD was 9.3 months (90%CI 6.93–13.9) compared to STD 11.3 months (90%CI 8.08–13.83). However, while non-hematological toxicity profiles were comparable between both arms, more hematological adverse events were seen in the CDD arm. The rate of dose modification in CDD vs STD due to neutropenia was 70% vs 40%, grade 3/4 neutropenia 69% vs 53%. The rate of febrile neutropenia was not different between the two arms. However, the higher rates of neutropenia and dose modifications do not favor CDD over STD in its current form and should therefore not be used in routine practice.
The B‑cell lymphoma protein 2 (BCL-2) is an estrogen-responsive gene that is overexpressed in 80% of ER-positive breast cancers and associated with good prognosis in luminal A tumors [11‐13]. Venetoclax is a potent inhibitor of BCL-2, routinely used in the treatment of chronic lymphatic leukemia (CLL). Its value in the treatment of solid tumors is yet to be evaluated. Preclinical data using xenograft models from ER+ breast cancer suggest that venetoclax shows a synergistic effect with tamoxifen to induce apoptosis . Based on these findings, a phase 1b 3 + 3 dose-escalation and expansion study was performed and presented in San Antonio . The primary aim was to determine the maximum tolerated dose (MTD), define dose-limiting toxicities (DLTs) and to identify the recommended phase 2 dose (RP2D).
Thirty-three patients with ER+ (>1%), BCL-2+ (>10%, 2‑3+ intensity), HER2− MBC received 200, 400, 600 or 800 mg/day of venetoclax together with tamoxifen 20 mg/day. The MTD was not reached and the treatment was well tolerated with no DLT or high grade 3/4 adverse events being observed. As a RP2D dose 800 mg/day were selected and the cohort expanded to include 24 patients (15 patients had received prior therapies for MBC, 30% of them tamoxifen, 61% of patients had visceral metastases).
The overall response rate for the RP2D cohort (n = 24) included 1 complete response (CR 4%) and 12 partial remissions (PR 50%). The clinical benefit rate (CBR) was 75%. The median duration of response were 42 weeks. Grade 3/4 adverse events included lymphopenia (6% G3), neutropenia (6% G3), anemia (6% G3), diarrhea (6% G3) and infections (9% G3).
Based on these promising results a randomized phase 2 trial examining the combination of fulvestrant ± venetoclax in patients with HR+/HER– disease after progression on CDK4/6 inhibitors was started (NCT03584009). Furthermore, the combination of venetoclax with palbociclib and letrozole is investigated in a phase Ib trial (PALVEN; NCT03900884).
Although no new large phase III clinical studies in MBC were presented at SABCS 2018, the shown data help to identify patients that might benefit most from potential or already established treatment options. Furthermore, some early phase studies, like the phase 1b study of the BCL-2 inhibitor venetoclax, paved the way for promising and maybe practice changing clinical trials.
Theresa Westphal: Speakers Honoraria: Novartis; Travel grants: Roche, Pfizer. Simon Peter Gampenrieder: Speakers Honoraria: Novartis, Roche, AstraZeneca; Advisory Boards: Roche, Novartis, Pfizer, AstraZeneca; Travel grants: Roche, Novartis, Pfizer; Research funding: Roche. Richard Greil: Speakers Honoraria: Novartis, Roche, AstraZeneca; Advisory Boards: Roche, Novartis, AstraZeneca; Travel grants: Roche, Novartis, AstraZeneca; Research funding: Novartis, Roche, AstraZeneca
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