Sara M. Tolaney, MD, MPH
Trastuzumab (Herceptin) remains a standard of care in the neoadjuvant and adjuvant treatment settings for patients with HER2-positive breast cancer. Sara M. Tolaney, MD, is trying to determine whether combination regimens with additional HER2-directed therapies or alternative therapies could improve responses in this patient population without added toxicities.
Tolaney, associate director of clinical research, Breast Oncology, Susan F. Smith Center for Women’s Cancers, Dana-Farber Cancer Institute, and assistant professor of medicine, Harvard Medical School, explained the state of HER2-directed therapies for patients with HER2-positive breast cancer during the 16th Annual International Congress on the Future of Breast Cancer, hosted by Physicians’ Education Resource®
, LLC (PER®
In the multi-arm BCIRG-006 study assessing the benefit of adding anthracyclines to chemotherapy for early stage HER2-positive breast cancer, patients in both trastuzumab-containing arms performed significantly better than patients who were not treated with trastuzumab.1
Both trastuzumab-containing regimens showed an increased disease-free survival (DFS) rate compared with chemotherapy alone at 10.3 years follow-up. The DFS rate was 74.6% with doxorubicin (Adriamycin)/cyclophosphamide/docetaxel plus trastuzumab (AC-TH) and 73.0% with docetaxel/carboplatin plus trastuzumab (TCH). DFS was 67.9% for patients treated with doxorubicin/cyclophosphamide/docetaxel (AC-T) without added trastuzumab.
Tolaney pointed out that only 10 DFS events separated the 2 trastuzumab-containing regimens.
Treatment-related outcomes in patients with higher-risk lymph-node positive disease mimicked results of the overall population, and again, investigators observed no significant difference between the 2 trastuzumab-containing arms. The DFS was 69.6% with AC-TH compared with 68.4% with TCH. DFS with AC-T was 62.2%, and Tolaney suggested that this could indicate that there is still an advantage for anthracycline-based therapy, even in the higher-risk population.
However, trastuzumab is known to have cardiotoxicity risks. There was a 2% incidence of grade 3/4 congestive heart failure in the AC-TH arm in the BCIRG-006 trial, and a 0.4% incidence rate with TCH.
“One approach I have taken is to use TCH in patients with cardiac risk factors and AC-TH in most other patients,” she said.
Trastuzumab in Combination
“While outcomes for HER2-positive disease have dramatically improved with the addition of trastuzumab, approximately 15% of women with early stage HER2-positive disease still recur, so there is a need to do better,” Tolaney said.
Several combination regimens are being explored adding to trastuzumab in order to improve responses in these patients. One common approach is dual HER2-targeted therapy. Several studies have looked at the addition of lapatinib (Tykerb) to trastuzumab in the neoadjuvant setting. Patients treated with the combination have higher rates of pathologic complete response (pCR) compared with trastuzumab or lapatinib alone.
“These favorable pCR rates achieved with lapatinib and trastuzumab led many to think that dual inhibition may improve survival outcomes in the adjuvant setting,” she noted.
To test this hypothesis, the phase III ALTTO trial explored the combination of trastuzumab and lapatinib in the adjuvant setting in patients with early stage disease, yet no significant role was found when lapatinib was added in this setting.2
Patients were assigned to single-agent trastuzumab, single-agent lapatinib, lapatinib plus trastuzumab, or trastuzumab followed by lapatinib. At 6 years, the DFS rate with lapatinib and trastuzumab was 85%, compared with 84% for trastuzumab followed by lapatinib, and 82% in patients treated with trastuzumab alone.
Moreover, lapatinib monotherapy and the combination of lapatinib plus trastuzumab were associated with a much higher rate of adverse events (AEs). Nearly all (93%) of patients treated with the combination and 90% of those treated with lapatinib alone experienced treatment-related AEs compared with 64% among those treated with trastuzumab monotherapy.
Researchers have also actively explored pertuzumab (Perjeta) in combination with trastuzumab in breast cancer. In 2013, the FDA granted an accelerated approval to pertuzumab in combination with trastuzumab and docetaxel in the neoadjuvant setting for patients with HER2-positive breast cancer based on results of the NeoSphere and TRYPHAENA trials.
Results from APHINITY evaluating the role of pertuzumab in the adjuvant setting, were presented at the 2017 ASCO Annual Meeting. Adding pertuzumab to trastuzumab and chemotherapy resulted a slight improvement in 4-year invasive DFS rate compared with trastuzumab and chemotherapy alone, 92.3% versus 90.6% (HR, 0.81; P
= .045) The absolute benefit was 1.7%.3
Tolaney said the only real difference between the 2 arms was the higher rate of grade ≥3 diarrhea in the pertuzumab arm (9.8% vs 3.7% with trastuzumab and chemotherapy alone), but there was no great difference in the rate of cardiotoxicity with added pertuzumab.
Patients with node-positive and hormone receptor (HR)–negative disease appeared to derive a greater benefit from the addition of pertuzumab in subset analyses. Therefore, Tolane said, this combination should potentially be reserved for patients with high-risk disease, such as those with node-positive or HR-negative disease. She noted that the additional toxicity was small, but the financial cost was high, amounting to an extra $100,000 per patient for 1 year of added pertuzumab therapy.
The antibody drug conjugate trastuzumab emtansine (T-DM1) has shown similar affinity to trastuzumab in binding to HER2. In the KRISTINE study, researchers explored T-DM1 in the neoadjuvant setting in combination with pertuzumab (T-DM1+P) compared with docetaxel, carboplatin, trastuzumab, and pertuzumab (TCH+P).4
The pCR rate was greater in the TCH+P arm (56% vs 44% in the T-DM1+P arm), but patients suffered significantly more serious AEs in the TCH+P arm (29%) compared with the T-DM1+P arm (5%). For high-risk patients, Tolaney said, T-DM1 may not be as effective as multi-agent chemotherapy with trastuzumab and pertuzumab.
The phase III KAITLIN and KATHERINE studies are exploring further the role of T-DM1. KAITLIN evaluates T-DM1 as a replacement for trastuzumab alone in the treatment regimen in the adjuvant setting. Tolaney noted that this study has completed accruing patients and the results are pending.
The KATHERINE study compares T-DM1 with trastuzumab in patients with residual disease following surgery.
In the phase III ExteNET trial, researchers investigated Neratinib (Nerlynx), an irreversible pan-HER inhibitor, versus placebo in patients with early stage HER2-positive breast cancer.5
Results of this study led to the FDA approval of neratinib on July 17, 2017 for extended adjuvant treatment.
At 5 years, invasive DFS was 90.2% for patients assigned to neratinib compared with 87.7% for placebo (HR, 0.73; 95% CI, 0.57-0.92; 2-sided P
= .008) for a survival difference of 2.5%. Researchers also noted a 4.4% survival difference (HR, 0.60; 95% CI, 0.43-0.83; 2-sided P
= .002) in the HR-positive patient population, but not in the HR-negative subgroup (HR, 0.95; 95% CI, 0.66-1.35; 2-sided P
However, neratinib comes with toxicity concerns, said Tolaney. There was a 40% incidence rate of grade 3 diarrhea with neratinib in ExteNET. However, she added that these results should be interpreted with caution as the trial did not include the use of prophylactic loperamide, which decreases the rates of diarrhea.
Prophylactic use of antidiarrheal agents reduced rates of grade 3 diarrhea in the phase II CONTROL study.6
Loperamide reduced the rate the grade 3 rate diarrhea to 31%. The combination of colestipol and loperamide cut the rate to 8% and 46% of patients experienced no diarrhea.
There is currently no data assessing the benefit of neratinib in patients who have been exposed to prior pertuzumab therapy, but the use of neratinib should certainly be considered in patients with high-risk HR-positive, node-positive disease, Tolaney said.
- Slamon DJ, Eiermann W, Robert NJ, et al: Ten-year follow-up of BCIRG-006 comparing doxorubicin plus cyclophosphamide followed by docetaxel with doxorubicin plus cyclophosphamide followed by docetaxel and trastuzumab with docetaxel, carboplatin and trastuzumab in HER2-positive early breast cancer patients. Abstract presented at: 2015 San Antonio Breast Cancer Symposium; December 8-12, 2015; San Antonio, TX. Abstract S5-04.
- Moreno-Aspitia A, Holmes EM, Jackisch C, et al. Updated results from the phase III ALTTO trial (BIG 2-06; NCCTG (Alliance) N063D) comparing one year of anti-HER2 therapy with lapatinib alone (L), trastuzumab alone (T), their sequence (T→L) or their combination (L+T) in the adjuvant treatment of HER2-positive early breast cancer [ASCO abstract 502]. J Clin Oncol. 2017;35(suppl). abstracts.asco.org/199/AbstView_199_191859.html.
- Von Minckwitz G, Procter MJ, De Azambuja E, et al. APHINITY trial (BIG 4-11): A randomized comparison of chemotherapy (C) plus trastuzumab (T) plus placebo (Pla) versus chemotherapy plus trastuzumab (T) plus pertuzumab (P) as adjuvant therapy in patients (pts) with HER2-positive early breast cancer (EBC) [ASCO abstract LBA500]. J Clin Oncol. 2017;35(suppl). abstracts.asco.org/199/AbstView_199_189357.html.
- Hurvitz SA, Martin M, Symmans WF, et al. Pathologic complete response rates after neoadjuvant trastuzumab emtansine (T-DM1) + pertuzumab vs. docetaxel + carboplatin + trastuzumab + pertuzumab (TCH+P) treatment in patients with HER2-positive (HER2+) early breast cancer(KRISTINE/TRIO-021). J Clin Oncol. 2016;34(suppl; abstr 500).
- Study evaluating the effects of neratinib after adjuvant trastuzumab in women with early stage breast cancer (ExteNET). clinicaltrials.gov/ct2/show/NCT00878709. Updated June 27, 2017. Accessed July 21, 2017.
- Ibrahim E, Tripathy D, Wilkinson M, et al. Effects of adding budesonide or colestipol to loperamide prophylaxis on neratinib-associated diarrhea in patients with HER2+ early-stage breast cancer: the CONTROL trial. Poster presented at: 2017 AACR Annual Congress; April 1-5, 2017; Washington, DC. Abstract CT128.