Summary
In the areas of chemotherapy, targeted therapy and immunotherapy, several interesting and clinically relevant data were presented at the 2017 San Antonio Breast Cancer Symposium (SABCS). This short review focuses on dose-dense and/or sequential administration of adjuvant chemotherapy, provides an update on targeted therapies for HER2-positive and triple-negative breast cancer and summarizes new results in the field of immunotherapy.
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Introduction
Results of several clinically relevant studies were presented at the 2017 San Antonio Breast Cancer Symposium (SABCS). This short review provides an update on novel data in the fields of chemotherapy, targeted therapy and immunotherapy.
Dose-dense and/or sequential chemotherapy
The term dose-dense chemotherapy refers to the application of chemotherapeutic drugs at standard dose in shorter intervals (i.e., every two weeks instead of once every three weeks). Based upon a Gompertzian model of tumour-growth, dose-dense strategies increase the log-kill of tumour cells, thereby effectively preventing cancer regrowth [1]. Sequential as opposed to concurrent administration of chemotherapy is another attractive way of increasing the activity of adjuvant treatment; this approach allows for the administration of each drug at the maximum tolerated dose [2]. In order to further elucidate the role of dose-dense and sequential chemotherapy, the Early Breast Cancer Trialists’ Collaborative Group (EBCTCG) conducted a meta-analysis of prospective randomised phase III trials comparing dose-dense and/or sequential regimens with conventional adjuvant chemotherapy.
In total, individual data of 34,122 patients included into 25 trials were available [3]. Dose-dense and/or sequential administration of chemotherapy resulted in a consistent reduction of recurrence risk and breast cancer-specific mortality. Furthermore, a pooled analysis including all 25 studies reported a similar reduction of all-cause mortality (RR [relative risk] 0.87; 95% CI 0.82–0.91; 10-year gain 3.0%).
In summary, these data indicate a relevant benefit for dose-dense and/or sequential chemotherapy regimens compared with conventionally dosed treatment in terms of recurrence risk and mortality; superiority was seen in all subgroups and independent of hormone-receptor status. In addition, no increased risk of alternative mortality (due to increased toxicity of more intense adjuvant treatment) was observed as shown by the sustained effect on all-cause mortality and no increase of rates of death without recurrence. Despite these clear-cut data, it needs to be stressed that the use of three-weekly paclitaxel in the control groups of several studies investigating dose-dense regimens may have influenced this outcome as it is well known that three-weekly paclitaxel is a suboptimal way of taxane administration. In addition, no advantage of dose-dense administration was shown for docetaxel to date [4]. Therefore, dose-dense and/or sequential chemotherapy is a potential adjuvant treatment standard but should not be regarded as the only appropriate way to administer adjuvant chemotherapy in early stage breast cancer.
GeparSepto
The neoadjuvant German Breast Group (GBG) GeparSepto trial investigated the substitution of solvent-based paclitaxel by nanoparticle albumin-bound (nab) paclitaxel as a component of neoadjuvant treatment. As already published, nab-paclitaxel increased pathologic complete response (pCR) rates in the overall population with the largest benefit observed in triple-negative breast cancer (TNBC; [5]). Of note, pCR predicts improved long-term outcome on an individual patient level in high-risk breast cancer subtypes; still, a correlation of pCR with long-term outcome has not yet been convincingly demonstrated on a trial level [6]. At the 2017 SABCS, disease-free survival (DFS) data of GeparSepto were presented [7]. At a median follow-up of 49 months, nab-paclitaxel significantly reduced breast cancer recurrence risk by an absolute 6.4% (HR [hazard ratio] 0.69; 0.54–0.89). This effect was observed in all of the predefined subgroups and surprisingly most pronounced in tumours with low proliferation rate. The DFS associated with nab-paclitaxel was in the range expected from the pCR increase in TNBC (and the results therefore indicate a correlation of pCR and DFS) while a residual effect beyond pCR must be assumed in luminal breast cancer where only a small pCR delta was observed. In addition, these data suggest that luminal breast cancer patients should not be excluded from neoadjuvant chemotherapy studies per se.
HER2-positive breast cancer
The phase III SOLD study was the fourth trial to compare short-term trastuzumab administration with the current standard of one year of adjuvant treatment [8]. The intent-to-treat population consisted of 2174 patients; at a median follow-up of 5.2 years, non-inferiority of 9 weeks of weekly trastuzumab could not be established (DFS HR 1.39; 95% CI 1.12–1.72). These results again indicate that one year of adjuvant immunotherapy remains the standard of care.
The German GAIN-2 trial included a substudy conducted in HER2-positive patients comparing trastuzumab bioavailability of two different places of subcutaneous application [9]. Administration into the thigh according to standard practice resulted in a 30% higher bioavailability of trastuzumab as compared to administration into the abdominal wall. While no cross-over design was included and the clinical relevance of these findings remain unclear, results from the GAIN-2 HER2-substudy indicate that the thigh remains the preferred place of subcutaneous trastuzumab administration.
A central review of the HER2-status in North American adjuvant trastuzumab studies suggested that a benefit for trastuzumab may exist in patients with HER2 low-expressing tumours [10]. This led to the phase III NSABP B‑47 trial comparing an additional one-year of adjuvant trastuzumab after standard chemotherapy with no immunotherapy in patients with HER2 1+ or 2+ (ISH negative) breast cancer [11]. Disappointingly, no difference between the two arms was observed (HR 0.98; 95% CI 0.77–1.26) indicating that trastuzumab should be reserved for HER2-positive tumours as defined by HER2 overexpression and/or HER2/neu gene amplification.
The phase Ib/II PANACEA trial (KEYNOTE-014) evaluated the combination of trastuzumab with the immune-checkpoint inhibitor pembrolizumab in metastatic breast cancer patients progressing on prior HER2-directed therapy [12]. The study was based upon preclinical data suggesting that this combination may offer the chance to overcome trastuzumab resistance [13]; safety and efficacy of trastuzumab plus pembrolizumab in HER2-positive metastatic breast cancer patients with PD-L1 expressing tumours was defined as the primary study endpoint. A second, smaller, PD-L1 negative cohort was included as well. Overall, 58 patients were accrued; all had received prior trastuzumab-containing therapy and 51 additional anti-HER2 therapy as well (including pertuzumab and T‑DM1). Overall response rate (ORR) in the PD-L1 positive cohort was 15% (90% CI 7–29) and an encouraging disease-control rate (DCR; CR + PR + SD ≥ 6 months) of 25% (90% CI 14–49) was reported, while no relevant activity was seen in PD-L1 negative subjects. Median progression-free survival (PFS) in the PD-L1 positive cohort was only 2.7 months but patients responding to treatment experienced prolonged disease control.
Update immunotherapy
Besides PANACEA, several other studies on the potential role of immunotherapy in breast cancer were presented. In the phase II trial KEYNOTE-086, patients with metastatic TNBC received single-agent pembrolizumab [14]. Two different patient cohorts were accrued. As already reported, activity of pembrolizumab in pretreated patients (cohort A; n = 170) was low with a response rate of 4.7%; in the first-line cohort, however (cohort B; n = 84), an encouraging response rate of 23% (95% CI 15–33%) was observed indicating relevant clinical activity.
Several combination trials of checkpoint inhibitors with other agents such as eribulin [15], abemaciclib [16], or olaparib [17] were presented as well. All of these trials suggested clinical activity and treatment was generally well tolerated with no overlapping toxicity observed. These studies, however, were limited by their non-randomized designs and the fact that activity was within the range expected from single-agent treatment. Therefore, randomized trials are required in order to fully assess the clinical potential of these strategies in metastatic breast cancer.
Sacituzumab govitecan (IMMU-132)
IMMU-132 is regarded as being one of the most promising agents for the treatment of TNBC. This antibody-drug conjugate (ADC) consists of a humanized antibody targeting Trop-2 (tumour-associated calcium signal transducer 2) linked to SN-38, the active metabolite of irinotecan [18]. Of note, Trop-2 is commonly overexpressed in epithelial cancers and >90% of TNBC have high Trop-2 expression.
In total, 110 patients with metastatic TNBC and ≥2 treatment lines were accrued to a single-arm phase II trial [19]. Confirmed ORR was 34% and DCR 46%; median PFS was 5.5 months. Treatment was overall well tolerated with the majority of ≥3 grade adverse events consisting of neutropenia (39%), leukopenia (14%), and anaemia (10%). In summary, these data suggest superior activity of IMMU-132 compared with conventional chemotherapy in this setting.
EMBARCA
The OlympiaD trial established that the PARP-inhibitor olaparib was superior to treatment by physician’s choice (TPC) in metastatic breast cancer patients harbouring germ-line (g) BRCA mutations [20]. The randomized phase III EMBARCA trial compared the novel PARP inhibitor talazoparib with TPC (capecitabine, eribulin, gemcitabine, vinorelbine) in 431 pretreated or previously untreated patients with metastatic breast cancer and gBRCA mutations [21]. Median PFS in the talazoparib group was 8.6 months as compared with 5.6 months in the TPC arm (HR 0.54; 95% CI 0.41–0.71; p < 0.0001). This benefit was observed in all predefined subgroups and even patients with brain metastases upon inclusion benefitted from PARP-inhibitor therapy. Taken together, data from EMRACA and OlympiAD suggests that PARP inhibitors when available in the clinical routine setting will have an important role in this patient subset.
Summary
Several clinically relevant studies were presented at the 2017 SABCS. Dose-dense and/or sequential administration of chemotherapy is a potential standard in the adjuvant treatment of early stage breast cancer patients. Immunotherapy, PARP inhibitors or ADCs such as sacituzumab govitecan may ultimately change the treatment strategies in metastatic breast cancer.
References
Norton L. Conceptual basis for advances in the systemic drug therapy of breast cancer. Semin Oncol. 1997;24(4 Suppl. 11):11–2–11–12.
Citron ML, Berry DA, Cirrincione C, et al. Randomized trial of dose-dense versus conventionally scheduled and sequential versus concurrent combination chemotherapy as postoperative adjuvant treatment of node-positive primary breast cancer. J Clin Oncol. 2003;21(8):1431–9. first report of Intergroup Trial C9741/Cancer and Leukemia Group B Trial 9741.
Gray R, Bradley R, Braybrooke J, et al. Increasing the dose density of adjuvant chemotherapy by shortening intervals between courses or by sequential drug administration significantly reduces both disease recurrence and breast cancer mortality. San Antonio Breast Cancer Symposium; 12.2017; San Antonio, Texas, USA. 2017. An EBCTCG meta-analysis of 21,000 women in 16 randomised trials. Abst. GS1–01.
Foukakis T, von Minckwitz G, Bengtsson NO, et al. Effect of tailored dose-dense chemotherapy vs standard 3‑weekly adjuvant chemotherapy on recurrence-free survival among women with high-risk early breast cancer: a randomized clinical trial. JAMA. 2016;316(18):1888–96.
Untch M, Jackisch C, Schneeweiss A, et al. Nab-paclitaxel versus solvent-based paclitaxel in neoadjuvant chemotherapy for early breast cancer (GeparSepto-GBG 69): a randomised, phase 3 trial. Lancet Oncol. 2016;17(3):345–56.
Cortazar P, Zhang L, Untch M, et al. Pathological complete response and long-term clinical benefit in breast cancer: the CTNeoBC pooled analysis. Lancet. 2014;384(9938):164–72.
Schneeweiss A, ackisch C, Schmatloch S, et al. Survival analysis of the prospectively randomized phase III GeparSepto trial comparing neoadjuvant chemotherapy with weekly nab-paclitaxel with solvent-based paclitaxel followed by anthracycline/cyclophosphamide for patients with early breast cancer—GBG69. San Antonio Breast Cancer Symposium; 12.2017; San Antonio, Texas, USA. 2017. Abst. GS3-05.
Joensuu H, Fraser J, Wildiers H, et al. A randomized phase III study of adjuvant trastuzumab for a duration of 9 weeks versus 1 year, combined with adjuvant taxane-anthracycline chemotherapy, for early HER2-positive breast cancer (the SOLD study). San Antonio Breast Cancer Symposium; 12.2017; San Antonio, Texas, USA. 2017. Abst. GS3-04.
Moebus V, Mahlberg R, Janni W, et al. Pharmacokinetic results of a subcutaneous injection of trastuzumab into the thigh versus into the abdominal wall in patients with HER2-positive primary breast cancer (BC) treated within the neo-/adjuvant GAIN-2 study. San Antonio Breast Cancer Symposium; 12.2017; San Antonio, Texas, USA. 2017. Abst. P5-20-09.
Perez EA, Reinholz MM, Hillman DW, et al. HER2 and chromosome 17 effect on patient outcome in the N9831 adjuvant trastuzumab trial. J Clin Oncol. 2010;28(28):4307–15.
Fehrenbacher L, Cecchini RS, Geyer CE, et al. NSABP B‑47 (NRG oncology): Phase III randomized trial comparing adjuvant chemotherapy with adriamycin (A) and cyclophosphamide (C) → weekly paclitaxel (WP), or docetaxel (T) and C with or without a year of trastuzumab (H). San Antonio Breast Cancer Symposium; 12.2017; San Antonio, Texas, USA. 2017. in women with node-positive or high-risk node-negative invasive breast cancer (IBC) expressing HER2 staining intensity of IHC 1+ or 2+ with negative FISH (HER2-Low IBC). Abst. GS1-02.
Loi S, Giobbe-Hurder A, Gombos A, et al. Phase Ib/II study evaluating safety and efficacy of pembrolizumab and trastuzumab in patients with trastuzumab-resistant HER2-positive metastatic breast cancer: Results from the PANACEA (IBCSG 45-13/KEYNOTE-014) study. San Antonio Breast Cancer Symposium; 12.2017; San Antonio, Texas, USA. 2017. Abst. GS2-06.
Stagg J, Loi S, Divisekera U, et al. Anti-ErbB-2 mAb therapy requires type I and II interferons and synergizes with anti-PD-1 or anti-CD137 mAb therapy. Proc Natl Acad Sci USA. 2011;108(17):7142–7.
Adams S, Loi S, Toppmeyer DL, et al. KEYNOTE-086 cohort B: pembrolizumab monotherapy for PD-L1–positive, previously untreated, metastatic triple-negative breast cancer (mTNBC). San Antonio Breast Cancer Symposium; 12.2017; San Antonio, Texas, USA. 2017. Abst. PD6-10.
Tolaney SM, Kalinsky K, Kaklamani V, et al. Phase 1b/2 study to evaluate eribulin mesylate in combination with pembrolizumab in patients with metastatic triple-negative breast cancer. San Antonio Breast Cancer Symposium; 12.2017; San Antonio, Texas, USA. 2017. Abst. PD6-13.
Rugo HS, Kabos P, Dickler MN, et al. A phase 1b study of Abemaciclib plus Pembrolizumab for patients with hormone receptor-positive (HR+), human epidermal growth factor receptor 2‑negative (HER2-) metastatic breast cancer (MBC). San Antonio Breast Cancer Symposium; 12.2017; San Antonio, Texas, USA. 2017. Abst. P1-09-01.
Domchek SM, Postel-Vinay S, Bang Y‑J, et al. An open-label, multitumor, phase II basket study of olaparib and durvalumab (MEDIOLA): results in germline BRCA-mutated (gBRCAm) HER2-negative metastatic breast cancer (MBC). San Antonio Breast Cancer Symposium; 12.2017; San Antonio, Texas, USA. 2017. Abst. PD6-11.
Bardia A, Mayer IA, Diamond JR, et al. Efficacy and safety of anti-trop-2 antibody drug conjugate Sacituzumab Govitecan (IMMU-132) in heavily pretreated patients with metastatic triple-negative breast cancer. J Clin Oncol. 2017;35(19):2141–8.
Bardia A, Vahdat LT, Diamond J, et al. Sacituzumab govitecan (IMMU-132), an anti-Trop-2-SN-38 antibody-drug conjugate, as ≥3rd-line therapeutic option for patients with relapsed/refractory metastatic triple-negative breast cancer (mTNBC): efficacy results. San Antonio Breast Cancer Symposium; 12.2017; San Antonio, Texas, USA. 2017. Abst. GS1-07.
Robson M, Im SA, Senkus E, et al. Olaparib for metastatic breast cancer in patients with a Germline BRCA mutation. N Engl J Med. 2017;377(6):523–33.
Litton JK, Rugo HS, Ettl J, et al. EMBRACA: A phase 3 trial comparing talazoparib, an oral PARP inhibitor, to physician’s choice of therapy in patients with advanced breast cancer and a germline BRCA mutation. San Antonio Breast Cancer Symposium; 12.2017; San Antonio, Texas, USA. 2017. Abst. GS6-07.
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R. Bartsch: advisory boards Novartis, Puma, Roche; lecture honoraria Novartis, Roche; research support Roche; travel support Roche. E. Bergen: travel support Roche.
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Bartsch, R., Bergen, E. SABCS 2017: update on chemotherapy, targeted therapy, and immunotherapy. memo 11, 204–207 (2018). https://doi.org/10.1007/s12254-018-0430-0
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DOI: https://doi.org/10.1007/s12254-018-0430-0