Four cycles of adriamycin and cyclophosphamide followed by four cycles of docetaxel (NSABP-B27) with concomitant trastuzumab as neoadjuvant therapy for high-risk, early-stage, HER2-positive breast cancer patients

Abstract

Background

The majority of breast cancer patients in Jordan are diagnosed at a young age and present with metastatic or locally advanced disease. The National Surgical Adjuvant Breast and Bowel Project Protocol B27 (NSABP-B27) (four cycles of adriamycin and cyclophosphamide [AC] followed by four cycles of docetaxel) is a standard neoadjuvant regimen in our institution. In this study, we report the efficacy of adding trastuzumab to docetaxel in this regimen for high-risk human epidermal growth factor receptor 2 (HER2)-positive early-stage disease.

Patients and methods

Consecutive HER2-positive breast cancer patients treated with this regimen were included. Treatment was given at standard doses and schedules as reported in NSABP-B27. Trastuzumab was given with docetaxel and then continued for 1 year.

Results

A total of 121 patients (mean age 45.4 years) were included. The majority had high-risk features including large tumor size, positive axillary lymph nodes, and grade III disease. Three patients did not complete the planned cycles of AC due to a lack of response. Eight (6.6%) patients missed at least one cycle of docetaxel. Following neoadjuvant therapy, 119 patients underwent surgery, of whom 59 (49.6%) patients achieved pathological complete response. The response was higher in node-negative patients (64.0 vs 45.7%; P=0.03) and in hormone receptor-negative disease patients (69.7 vs 41.9%; P=0.018). Breast-conserving surgery was performed in 21.5% of the patients. The median disease-free survival (DFS) for the whole group was not reached while the 3- and 5-year DFS rates were 84.2 and 74.1%, respectively.

Conclusion

Trastuzumab added to the NSABP-B27 regimen is a unique combination. When used in high-risk patients, as in our study, outcomes similar to reported data were achieved without unexpected toxicities.

Introduction

Breast cancer is the most common cancer among Jordanian females. The majority of patients are young and present with locally advanced disease. Neoadjuvant therapy, also known as primary systemic treatment, was initially introduced for the treatment of inoperable locally advanced or inflammatory breast cancer. Increasingly, neoadjuvant chemotherapy is now considered for women with large but operable tumors as well. The rationale of this approach is to provide early chemotherapy that allows down-staging of the tumor, higher rates of breast-conserving surgeries (BCSs), and in vivo testing of chemosensitivity of the tumor.^1–5

The National Surgical Adjuvant Breast and Bowel Project Protocol B27 (NSABP-B27) trial⁶ utilized four cycles of adriamycin and cyclophosphamide (AC) with or without four cycles of docetaxel. Surgery was performed before or after docetaxel. Preoperative AC followed by docetaxel was associated with better clinical complete response rate (63.6%) compared to 40.1% (P=0.001) in the group that received AC alone. The overall clinical response rate (90.7 vs 85.5%; P=0.001), the pathological complete response (pCR) rate (26.1 vs 13.7%; P=0.001), and the proportion of patients with negative nodes at time of surgery (58.2 vs 50.8%; P=0.001) were also higher in the docetaxel arm.⁶ Similar results were also achieved in the Aberdeen trial, which utilized a different docetaxel-based neoadjuvant chemotherapy regimen.⁷ Similar results have been repeatedly demonstrated, thus establishing the role of taxanes in the neoadjuvant setting for breast cancer patients.

Approximately 20–25% of patients with breast cancer demonstrate over-amplification of the human epidermal growth factor receptor 2 (HER2) gene, resulting in an over-expression of the HER2 receptor, a transmembrane tyrosine kinase receptor. The activation of this receptor is known to result in an increased activity of a variety of molecular pathways associated with tumor growth and progression.⁸ Published data clearly demonstrate that patients with cancers overexpressing HER2 have a relatively worse prognosis independent of other clinical and pathological variables, such as tumor size and nodal status.^9–11

Trastuzumab, a monoclonal antibody against the HER2 receptor, was extensively studied in different combinations and schedules in neoadjuvant settings. Despite the various definitions of pCR in many of these trials, the addition of trastuzumab resulted in a significant improvement in pCR rate.^12–14 pCR is increasingly used as a surrogate marker for better disease outcome. The correlation of pCR with improved disease-free survival (DFS) and overall survival (OS) has already been demonstrated in several studies that included HER2-positive patients treated with trastuzumab.^15–17

The NSABP-B27 regimen is the standard neoadjuvant regimen at our institution.¹⁸ In this study, we report the efficacy and safety of adding trastuzumab to docetaxel following AC in the neoadjuvant therapy of patients with high-risk, HER2-positive, early-stage disease.

Patients and methods

Patients’ medical records and the hospital’s database were searched for all consecutive HER2-positive breast cancer patients treated at our institution between October 2008 and September 2015 using the neoadjuvant NSABP-B27 chemotherapy regimen along with trastuzumab. Patients included were those with primary breast cancer diagnosed by core needle biopsy.

Clinical and pathological data collected included patients’ age, histopathological type and grade, lymphovascular invasion, hormone receptors and HER2 status, clinical tumor size, lymph nodes’ status, number of chemotherapy cycles received, type of surgery performed following chemotherapy, clinical and pathological responses, and disease status at last follow-up visit.

Chemotherapy was given at the standard doses and schedules as originally reported in the NSABP-B27 study.^6,19 Four cycles of AC (adriamycin [60 mg/m²] and cyclophosphamide [600 mg/m²]) followed by four cycles of docetaxel (100 mg/m²) were given; all were delivered on the first day of a 3-week cycle. Dexamethasone 8 mg was given orally every 12 hours, starting the day before docetaxel, and continued for a total of 3 days. In addition, patients received ondansetron at a dose of 8 mg every 12 hours for 3 days and granulocyte-colony stimulating factor support starting on day 2 of docetaxel for 5 days.

Trastuzumab was given concomitantly with docetaxel at a dose of 8 mg/kg intravenously on the first day of the first treatment cycle, administered over 90 minutes. Subsequent doses were administered at a dose of 6 mg/kg over 30 minutes for three cycles and then continued for a total of one full year. Ejection fraction was followed by echocardiogram every 3 months.

The type of surgery intended (BCS or mastectomy) vs the performed surgery was reviewed. Following surgery, radiation therapy was given as per standard international guidelines. Hormonal therapy in the form of tamoxifen or an aromatase inhibitor (AI) was used following the completion of the planned chemotherapy for all hormone receptor-positive patients and was continued for 5 years. High-risk, node-positive postmenopausal patients were offered an additional 5 years of AI following the completion of the planned first 5 years of hormonal therapy as per the published MA-17 trial.²⁰

Disease responses were analyzed and reported based on NSABP-B27 criteria. pCR was defined as no evidence of invasive carcinoma in the breast at the time of surgery. Clinical tumor response was defined as complete if there was no palpable tumor in the breast or axillary lymph nodes at the time of surgery. Clinical partial response was defined as >50% clinical improvement in total tumor size while disease progression (PD) was defined as >50% increase in the size of the tumor. Tumors that did not meet the criteria for partial response or PD were considered to represent stable disease. All patients with either progressive or stable disease were considered nonresponders.

Patients were seen in the medical oncology clinic prior to each cycle of chemotherapy for response evaluation and follow-up for any possible side effects or complications. Echocardiogram was done before starting adriamycin for high-risk patients and then prior to starting trastuzumab as a baseline and followed once every 12 weeks thereafter.

Statistical methods

Patient characteristics were tabulated and described. Descriptive statistics was performed for all variables. Results for continuous variables are expressed as median (interquartile range). Categorical variables are expressed as number (percentage). A significance level of P≤0.05 was used in the analysis. All statistical analyses were carried out using the SAS software (version 9.4; SAS Institute Inc., Cary, NC, USA).

Ethical approval

All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Declaration of Helsinki and its later amendments or comparable ethical standards. Given the retrospective nature of our study and the absence of any patient identity, our Institutional Review Board (IRB) granted an exemption from full board review. Additionally, patients’ consent to review their medical records was not required by our IRB.

Results

A total of 137 patients diagnosed with early-stage or locally advanced, HER2-positive breast cancer treated with neo-adjuvant chemotherapy with the NSABP-B27 regimen and trastuzumab were retrospectively analyzed. All patients were females, and the median age at diagnosis was 45 (range 24–78) years. Sixteen (11.7%) patients had inflammatory breast cancer and were excluded from further analysis.

The majority of the patients had high-risk pathological features. The mean tumor size was 5.5 cm; 59 (48.8%) patients had T3 disease, 19 (15.7%) patients had T4 disease, and only two patients had T1 disease. Axillary lymph nodes were involved in 95 (78.5%) patients, and 69 (57.0%) patients had grade III disease. Hormone receptors (estrogen receptor and/or progesterone receptor) were positive in 88 (72.7%) patients; details of patient’s characteristics are summarized in Table 1.

Table 1.

Patients’ characteristics

	Number	%
Age group (years), median: 45 (range 24–78) years
<50	82	67.8
50–59	23	19.0
≥60	16	13.2
Histology
Infiltrating ductal	117	96.7
Infiltrating lobular	3	2.5
Clinical tumor size (cm), mean: 5.5 cm
≤2	6	5.0
2.1–4	39	32.2
>4	76	62.8
Gradea
I	2	1.7
II	47	38.8
III	69	57.0
Node status
Negative	27	22.3
Positive	94	77.7
Hormone receptors
ER positive	82	67.8
PR positive	75	62.0
ER and/or PR positive	88	72.7
ER and PR negative	33	27.2
Type of surgeryb
Mastectomy	93	76.9
BCS	26	21.5

Note:

^aThree patients had unknown tumor grade;

^btwo patients did not undergo surgery.

Abbreviations: BCS, breast-conserving surgery; ER, estrogen receptor; PR, progesterone receptor.

The planned four cycles of AC were completed and tolerated in all patients, but in three (2.5%) patients, treatment was stopped due to the lack of response. All planned AC cycles were given at full dose with no delay.

Eight (6.6%) patients missed at least one cycle of docetaxel; three of them refused to complete the planned treatment, two of whom achieved complete clinical responses before completing planned docetaxel. Two patients died during treatment: the first was a diabetic patient who developed severe necrotizing fasciitis and the other died due to sudden pulmonary embolism. The remaining three patients had no significant clinical response, so chemotherapy was stopped by the treating physician. All patients received all planned concomitant trastuzumab with the docetaxel cycles with no significant adverse events.

Response to treatment

Following the four cycles of AC, 108 (89.3%) patients had clinical responses; 10 (8.3%) patients achieved a complete clinical response, and 98 (81.0%) patients had a partial response. Thirteen (10.7%) patients had stable disease. Clinical response was further improved following the docetaxel and trastuzumab treatment; complete clinical response documented at the end of the docetaxel treatment was achieved in 58 (47.9%) patients.

Surgery was performed in 119 patients. In an intention to treat analysis, pCR, as defined by the original NSABP-B27 (ypT0N0 or ypTisN0) trial, was achieved in 59 (48.8%) patients. However, 27 (22.3%) patients had a residual noninvasive tumor (ductal carcinoma in situ [ypTis]). As such, 32 (26.4%) patients of the whole group had no invasive or noninvasive tumor in the breast or axillary lymph nodes (ypT0N0). For the remainder of the discussion, the original NSABP-B27 definition of pCR will be used.

pCR (ypT0, Tis) was higher in hormone receptor-negative disease compared to hormone receptor-positive disease (23 [69.7%] of the 33 patients vs 36 [41.9%] of the 86 patients, respectively; P=0.018). pCR was also slightly higher, although not statistically significant, in smaller tumors, achieved in 26 (54.2%) of the 48 patients with tumors <5.0 cm compared to 33 of the 71 patients (46.5%) with tumors ≥5.0 cm (P=0.119). Patients with no axillary lymph node involvement had a higher pCR rate, achieved in 16 (64.0%) of the 25 patients with negative axilla at diagnosis compared to 43 (45.7%) of the 94 patients with positive axilla at time of diagnosis (P=0.03) (Figure 1). Of the patients who underwent surgery, BCS was performed in 26 (21.8%) patients, 12 (46.2%) of whom were found to have a pCR.

Figure 1.

pCR rate according to pretreatment characteristics.

Abbreviations: HR, hormone receptor; pCR, pathological complete response.

The median DFS for the whole group was not reached. The 3- and 5-year DFS rates were 84.2 and 74.1%, respectively (Figure 2A). The 5-year DFS was 84.7% for those who achieved a pCR in both the breast and axilla (pT0N0) compared to 70.7% for those who did not (P=0.433, Figure 2B).

Figure 2.

(A) Disease-free survival for all patients. (B) Disease-free survival by pCR.

Abbreviation: pCR, pathological complete response.

Similarly, the median OS for the whole group was not reached. The 3- and 5-year OS rates were 87.2 and 83.4%, respectively (Figure 3A). Patients who achieved a pCR both in the breast and axilla had an improved 5-year survival rate (96.0%) compared to those who did not (80.0%). However, the difference was not statistically significant (P=0.220, Figure 3B).

Figure 3.

(A) Overall survival for all patients. (B) Overall survival by pCR.

Abbreviation: pCR, pathological complete response.

Cardiac toxicity was not reported in any of the 121 patients who received trastuzumab, and there were no additional toxicities related to trastuzumab use.

Discussion

To our knowledge, this is the first study to report on the efficacy and safety of trastuzumab when added to the neo-adjuvant NSABP-B27 regimen. The use of trastuzumab in the neoadjuvant setting was assessed in many large clinical trials in patients with newly diagnosed locally advanced breast cancer.

The Neoadjuvant Herceptin (NOAH) trial used a complex combination of doxorubicin with paclitaxel followed by paclitaxel single agent, then cyclophosphamide, methotrexate, and 5-fluorouracil with or without concomitant trastuzumab in patients with newly diagnosed locally advanced breast cancer. Patients who received trastuzumab had a better pCR rate in breast tissue (43 vs 22%; P=0.0007) compared with those who received chemotherapy alone.^12,13

The German Breast Group/Gynecologic Oncology Study Group (GeparQuattro) trial was also designed to evaluate the effect of trastuzumab on pCR rates in a group of breast cancer patients with locally advanced (T3 or T4), lymph node-positive tumors. All patients were scheduled to receive four cycles of epirubicin and cyclophosphamide (EC) and were then randomly assigned to one of the three treatment arms; the first arm received four cycles of docetaxel (EC-D), the second arm received four cycles of docetaxel and capecitabine (EC-DX), and the third arm received four cycles of docetaxel followed by four cycles of capecitabine on days 1–14 (EC-D-X). Patients with HER2-positive disease, in all three arms, received trastuzumab started at the time of EC initiation and continued for 52 weeks. pCR rate, defined as no invasive or in situ residual tumors in the breast (ypT0), was achieved in 31.7% of the patients who had received neoadjuvant trastuzumab with chemotherapy and was not significantly different in any of the three arms.²¹

Another study, the TECHNO trial, included 217 patients with HER2-positive breast cancer and utilized a chemotherapy regimen closer to the NSABP-B27 regimen with four cycles of EC followed by four cycles of paclitaxel and trastuzumab; all given every 3 weeks before surgery. Trastuzumab was continued after surgery to complete 1 year of treatment. pCR, defined as no residual invasive tumor in breast and lymphatic tissue, was obtained in 39% of patients.¹⁴

In our group of patients, breast conservation was done in only 21.5% of the patients, mostly related to the advanced nature of the disease at time of initial diagnosis. Almost two-thirds of patients presented with T3 or T4 disease (64.5%), and the majority had lymph node involvement at time of presentation (78.5%). This was much higher than rates reported in the previously mentioned TECHNO study in which less than a third (29%) of the patients had T3 or T4 disease.¹⁴

The 3-year DFS and OS results (84.2 and 87.2%, respectively) for our group of patients were similar to those that had been previously published in large clinical trials. At a median follow-up of 3.2 years, the 3-year event-free survival and OS in the previously mentioned NOAH trial were 71 and 87%, respectively.¹² The German group also reported similar results in the TECHNO trial with the 3-year DFS and OS rates of 77.9 and 89.4%, respectively, at a median follow-up of 41 months.¹⁴

Our data showed that patients who achieved a pCR had better DFS and OS rates. This difference, however, was not statistically significant, likely due to the small number of patients included.

Conclusion

Trastuzumab added to the NSABP-B27 regimen is a unique combination. Our patient population had higher risk and worse prognostic features than previously reported studies. Despite the limitations related to relatively small number of patients included and the retrospective nature of the study, the high pCR rate achieved in our patient population supports our conclusion that this treatment regimen is effective. Larger clinical trials are needed to confirm our findings.