Real World Experience of Long Term Treatment Outcome in Hormone Receptor-positive Metastatic Breast Cancer with or without Everolimus and Exemestane after Prior Aromatase Inhibitor
Background: Everolimus/exemestane has been shown to improve progression-free survival in patients with endocrine-resistant metastatic breast cancer. The regimen has been well-accepted despite lack of survival benefit. In real-life setting, patients were not well-selected and hence benefit of such treatment may not be as robust.
Method: This is a retrospective review of 143 hormone receptor (HR) positive, HER-2 negative MBC patients who progressed on nonsteroidal aromatase inhibitors. Patients who received everolimus/exemestane in any treatment lines (EE group) were compared to patients who never received everolimus (NE group). Primary end point was survival adjusted to prognostic factors.
Results: There were 52 patients in EE group and 91 in NE group with mean age of 58.6 years. Median follow-up time was 51 months. Unadjusted median OS was significantly longer in EE [33 vs 25 months, HR 0.66 (95%CI 0.44-0.998); p = 0.049]. In univariate analysis, factors affecting survival included numbers of metastatic sites, bone metastasis, EE treatment and numbers of treatment lines. Independent factors that remained significant in multivariate analysis were treatment lines [HR 0.71 (95%CI 0.63-0.79); p < 0.05] and numbers of metastatic sites. Median numbers of treatment line after NSAI failure was 5.2 vs 3.6 lines in EE and NE, respectively.
Conclusion: In this real-life practice data, pts with HR positive, HER-2 negative MBC who had progressed on NSAI, sequential use of multiple treatment regimens of endocrine and chemotherapy is essential to longer survival. Everolimus/exemestane may have contributed, to a lesser extent, to this improvement in survival.
Breast cancer is the most common female cancer in Thailand  and consisted of many different subtypes such as hormone receptor (HR) positive, amplified-human epidermal growth factor receptor type 2 (HER-2), or triple negative breast cancer.(2) Over two-thirds of breast cancer patients are HR positive disease . Metastatic breast cancer (MBC) is so far incurable. The goal of treatment at this stage is to control tumor growth, improve quality of life and prolong survival . The treatment strategies of HR positive and HER-2 non-amplified MBC included endocrine and chemotherapy [2,5]. Patient with asymptomatic, mildly symptomatic or non-visceral crisis may be treated upfront by endocrine therapy which carries less side effects and provides better quality of life compared to chemotherapy-based therapy [6-7]. Multiple classes of endocrine therapy agents are available, included selective estrogen receptor modulator (SERM) such as tamoxifen, selective estrogen receptor down regulator (SERD) such as fulvestrant, non-steroidal aromatase inhibitor (AI) (anastrozole and letrozole) and steroidal AI (exemestane) . In postmenopausal women, AI are more effective than tamoxifen [8-11], while non-steroidal AI (NSAI) are equally effective to steroidal AI [12-13]. More recently, CDK4/6 inhibitors have emerged as a highly effective treatment option in combination with the aforementioned agents [14-19]. Sequential use of these agents provides meaningful disease control period before chemotherapy initiation [20-23].
Everolimus is a sirolimus derivative that inhibits mTOR through allosteric binding to mTOR complex 1 . Activation of phosphatidylinositol-3-kinase (PI3K)-protein kinase B (AKT)-mammalian Target of Rapamycin (mTOR) pathways has been proposed as one mechanism of endocrine resistance [25-28], in which everolimus has been shown to reverse such occurrence. The drug has been approved for advance ER positive, HER2 negative breast cancer that has progressed on NSAI in several countries worldwide including Thailand since 2013. The approval was based on the positive results from 2 randomized control trials, a phase 2 TAMRAD study
 and phase 3 BOLERO-2 trial [30-33]. Both studies showed a remarkable improvement in progression free survival (PFS) with HR of 0.54 and 0.45, respectively. However, upon longer follow-up, a survival benefit could not be demonstrated so far . In addition, in a more recent phase 2 trial, BOLERO-6 study , the effectiveness of this combination compared to capecitabine, a commonly used single agent chemotherapy in MBC remained inconclusive.
Due to CDK4/6 inhibitors is a novel and expensive drug in Thailand which only few people who can access it. And CDK4/6 inhibitor has just been launched in Thailand since middle year of 2018 while PI3K inhibitors is likely to be launched in late 2020, therefore data of CDK4/6 inhibitor including PI3K inhibitors in a real-world practice especially low to middle income regions like in Thailand is very limited. Compare to CDK4/6 inhibitors and PI3K inhibitors, everolimus is more widely accessible in Thailand.
Due to the high cost of everolimus in Thailand together with its toxicity, notwithstanding the lack of survival advantage, called for a cautious use of the agent. In spite of the fact that the population in BOLERO-2 trial were not heavily pretreated, in real life practice in Thailand, this was not a common practice pattern and many patients had received several lines of systemic therapy before being treated with everolimus-exemestane combination in later lines. There has been limited data on its efficacy and optimal timing in routine clinical practice in Thai patients. So, this study was conducted to evaluate the efficacy of combination of everolimus and exemestane in a broader population i.e. in any line of treatment compared with everolimus-free regimen using survival as a primary endpoint in HR positive, HER-2 negative MBC that had progressed on previous NSAI in a single academic center.
Materials and Methods
Patients were eligible to be included in the study if they were postmenopausal with histological or cytological confirmation of HR positive and HER-2 nonamplified MBC without visceral crisis, whose disease was refractory to previous letrozole or anastrozole therapy. NSAI-refractory was defined as recurrence while on, or within 12 months of adjuvant therapy with letrozole or anastrozole, or progression during treatment, or within one month of treatment with NSAI for locally advanced or MBC. Other previous anticancer endocrine treatments and/or chemotherapy regimen for metastatic disease were allowed. Exclusion criteria were age of 17 years or younger, use of mTOR inhibitor prior to NSAI, lack of detailed clinical data and HER2 amplified MBC. All patients were diagnosed with NSAI resistance during January 1, 2013 to August 31, 2017 and received treatment at Ramathibodi hospital, a tertiary care, referral hospital in Bangkok, Thailand.
Study Design and Treatment
We retrospectively collected data of NSAI refractory MBC patients from Ramathibodi Cancer Registry from January 1, 2013 to August 31, 2017. All patients who were diagnosed with NSAI refractory were categorized according to the subsequent treatment they received into 2 groups: 1) patients who received everolimus and exemestane combination in any line were defined as everolimus-exemestane (EE) group and 2) those who had never been treated with everolimus in any line of treatment [defined as non-everolimus (NE) group]. Treatment assignments were based on treating physicians’ decision. The primary end point of the study was overall survival (OS), defined as time at NSAI refractory to death from any causes. Secondary end points included OS in subgroup of patients treated with EE in various sequence, i.e., immediately or subsequently after NSAI failure; progression-free survival (PFS) and response rate of EE combination therapy compared with others systemic therapy as first subsequent line of treatment after NSAI failure. PFS was defined by time at start of treatment to time of progression on the basis of radiographic study assessed by investigators or death. The study was approved by institutional review board of Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
OS and PFS were estimated with the use of the Kaplan-Meier method and comparison between groups, using log rank test. A cox-proportional hazard model was used to estimate the hazard ratios (HR). Patient’s baseline characteristics were reported using descriptive statistics. All qualitative variables were compared with the chi-square test or Fisher’s test. All quantitative variables were compared with the student’s t-test. Univariate and multivariate cox regression analysis were used to analyze prognostic factors affecting survival of endocrine refractory, HER-2 negative MBC patients. A p-value of < 0.05 was considered to be statistically significant. All analyses were performed with the use STATA, version 15.
A total of 143 women who fulfilled the eligibility criteria were identified from Ramathibodi Cancer Registry database between January 1, 2013 and August 31, 2017. There were 52 patients in EE group and 91 patients in the NE group. Baseline characteristics were summarized in Table 1.
|Characteristic||Everolimus-exemestane (N=52)||Non-everolimus (N=91)||p-value|
|Age of endocrine refractory||0.81|
|Year, mean +SD||58.3 +11.3||58.8 +11.7|
|0||9 (17.3%)||17 (18.7%)|
|1||37 (71.1%)||66 (72.5%)|
|2 or more||6 (11.5%)||8 (8.8%)|
|No. of metastatic site(s)||0.28|
|1||15 (28.8%)||38 (41.8%)|
|2||22 (42.3%)||34 (37.4%)|
|3 or more||15 (28.8%)||19 (20.9%)|
|Visceral metastasis (lung or liver or pleural or lymphangitis)||41 (78.8%)||61 (67.4%)||0.13|
|Lung||25 (48.1%)||39 (42.9%)||0.55|
|Liver||21 (40.4%)||25 (27.5%)||0.11|
|Bone||36 (69.2%)||55 (60.4%)||0.29|
|Brain||2 (3.8%)||7 (7.7%)||0.49|
|Bone only disease||7 (13.5%)||19 (20.9%)||0.27|
|Previous endocrine treatment for metastasis before NSAI||0.84|
|Tamoxifen||7 (13.5%)||15 (16.5%)|
|Others||1 (1.9%)||2 (2.2%)|
|Previous treatment with letrozole or anastrozole|
|Adjuvant therapy only†||12 (23.1%)||21 (23.1%)||0.88|
|Metastatic disease (with or without adjuvant NSAI)||40 (76.9%)||70 (76.9%)||>0.05|
|Neoadjuvant or adjuvant therapy only||28 (58.3%)||42 (47.7%)||0.24|
|Treatment of metastatic disease (with or without prior neoadjuvant or adjuvant chemotherapy)||17 (32.7%)||29 (31.9%)||0.92|
|No. of lines of chemotherapy for metastatic disease before NSAI||(N=17)||(N=29)|
|1||12 (70.6%)||14 (48.3%)|
|2||4 (23.5%)||13 (44.8%)|
|3||1 (5.9%)||2 (6.9%)|
|No. of previous systemic therapy before NSAI in metastatic setting||0.56|
|0#||35 (67.3%)||53 (58.2%)|
|1||9 (17.3%)||21 (23.1%)|
|2 or more||8 (15.4%)||17 (18.7%)|
†Number of patients who progressed on adjuvant letrozole or anastrozole; # 0, patients who received NSAI as first-line treatment of MBC
The mean age in both groups was 58 years. Nearly all of them had Eastern Cooperative Oncology Group (ECOG) score of 0 to 1. There were numerically higher numbers of metastatic sites and visceral metastasis in EE group without statistical difference. Twenty-three percent each had tumor progression while on adjuvant endocrine therapy. NSAI was the first line treatment of MBC in 67.3% in EE group and 58% in NE group (p=0.56). No significant difference in numbers of systemic therapy (chemotherapy / endocrine therapy) received prior to NSAI were seen. Approximately one-third in both arms had received chemotherapy in metastatic setting before NSAI and most had received less than 3 chemotherapy regimens prior to NSAI. For patients in EE group (n=52), 13 patients (25%) and 39 patients (75%), the starting dose of everolimus was 5 mg per day and 10 mg per day, respectively. Of those who received 10 mg daily dose, 44% of them required a dose reduction during treatment.
Efficacy End Points
Data was censored on 31 August 2018, with median follow-up time of 51 months (59 months in EE and 36 months in NE). Among 143 patients, 100 patients had died (70%) (EE: 40 patients, NE: 60 patients). Median OS of EE and NE group were 33 and 25 months, respectively. (HR of death, 0.66; 95% confidence interval (CI) 0.44- 0.998; p=0.049) (Figure 1, Table 2).
|Variable||Everolimus+exemestane (n=52)||Non-everolimus (n=91)||p-value||Hazard ratio (95%CI)|
|Overall survival||0.04||0.66 (0.44-0.998)|
|Event-Death,||40 (76.9)||60 (65.9)|
|Duration, months (Median, IQR†)||33 (18-48)||25 (10-38)|
CI denotes confidence interval; † IQR denotes interquartile range
Of 52 patients in EE group, 14 patients (27%) received everolimus as first subsequent treatment following NSAI failure, while 18 patients (35%) and 20 patients (38%) received everolimus as a second and later line following progression on NSAI. Median numbers of prior chemotherapy and endocrine therapy before receiving EE was 3 lines (range 1-7), i.e. EE was given as 4th line of treatment. In both groups, the 4 most commonly used agents after NSAI failure (aside from everolimus in EE group) were capecitabine, paclitaxel, fulvestrant and exemestane, with no difference in frequency between the 2 groups (Table 3).
|Everolimus-Exemestane Arm (n=52)||Non-Everolimus Arm (n=91)||p-value|
|Paclitaxel||35 (67.3%)||49 (53.8%)||0.12|
|Capecitabine||34 (65.4%)||52 (57.1%)||0.33|
|Fulvestrant||30 (57.7%)||45 (49.5%)||0.34|
|Eribulin||23 (44.2%)||18 (19.8%)||0.002**|
|Exemestane||17 (32.7%)||37 (40.7%)||0.34|
|Docetaxel||17 (32.7%)||23 (25.3%)||0.34|
|Tamoxifen||14 (26.9%)||29 (31.9%)||0.54|
|AC||6 (11.5%)||9 (9.9%)||0.76|
|Megestrol||5 (9.6%)||14 (15.4%)||0.33|
|Gemcitabine||4 (7.7%)||9 (9.9%)||0.66|
|Nab-Paclitaxel||1 (1.9%)||1 (1.1%)||>0.05|
|Lipo-doxorubicin||1 (1.9%)||1 (1.1%)||>0.05|
|Vinorelbine||1 (1.9%)||3 (3.3%)||>0.05|
p< 0.05 indicates statistically significant; AC denotes anthracycline-cyclophosphamide; CMF denotes cyclophosphamide-methotrexate fluorouracil
However, significantly more patients in EE group received eribulin (44% vs 20%, p=0.002). Patients in EE group received more lines of systemic treatment in metastatic setting after NSAI refractory with mean (+ 2SD) of 5.19 (+ 2.51) lines compared to 3.62 (+ 2.19) lines in NE group(p<0.05). Due to the imbalance in the total treatment received between the 2 groups, this factor was incorporated into factor analysis for survival together with other baseline variables known to be prognostic. A univariate analysis for prognostic factors to survival (Table 4) indicated EE treatment, number of metastatic sites, bone metastasis and number of total lines of treatment after NSAI refractory were significant factors. In multivariate analysis (Table 4), 2 factors that remained as independent factors for survival were number of total lines of treatment after NSAI refractory [HR per one line increase 0.71 (95%CI0.64-0.79); p<0.05], and numbers of metastatic site [HR per one site increase 1.35 (95%CI 1.05-1.73); p = 0.02].
|Factors||Univariate analysis||Multivariate analysis|
|Hazard Ratio (95%CI)||P-value||Hazard Ratio (95%CI)||p-value|
|Everolimus-exemestane treatment||0.66 (0.437-0.998)||0.049**||0.74 (0.48-1.14)||0.17|
|Age of endocrine refractory (per 1 year)||1.00 (0.98-1.02)||0.959|
|ECOG (per one ECOG status)||1.31 (0.92-1.86)||0.14|
|Number of metastatic sites||1.28 (1.02-1.61)||0.03**||1.35 (1.05-1.73)||0.02**|
|Visceral (lung or liver or pleural or lymphangitis) metastasis||1.08 (0.69-1.696)||0.74|
|Bone||1.61 (1.05-2.47)||0.03**||1.34 (0.86-2.1)||0.19|
|Bone only disease||0.93 (0.55-1.59)||0.8|
|Previous endocrine treatment for metastasis before NSAI (compared to without)|
|Previous treatment with letrozole or anastrozole|
|Progressed on Adjuvant therapy||0.77 (0.48-1.24)||0.29|
|Metastatic disease (with or without adjuvant NSAI)||1.29 (0.8-2.08)||0.295|
|Neoadjuvant or adjuvant therapy||1.05 (0.695-1.58)||0.83|
|Neoadjuvant or adjuvant therapy||0.9 (0.59-1.39)||0.65|
|for metastatic disease|
|No. of previous systemic therapy prior to refractory to NSAI (per one line)||1.04 (0.83-1.29)||0.75|
|No. of lines treatment after NSAI refractory (per one line)||0.71 (0.64-0.79)||<0.05**||0.71(0.63-0.79)||<0.05**|
CI denotes confident interval; ** P< 0.05 indicates statistically significant
Treatment with everolimus-exemestane was no longer significant in multivariate analysis [HR 0.74 (0.48-1.14); p = 0.17]. Subgroup analysis of survival showed benefits in all subgroups of patients who received EE except for patients who have had chemotherapy before NSAI and those who were heavily pretreated with chemotherapy. However, the confidence intervals were very wide (Figure 2).
Timing of Everolimus and Outcome
Median OS in patients treated with EE as first, second and third subsequent line after refractory to NSAI were 23, 21 and 38 months, respectively (Table 5).
|Median Duration of Treatment with EE (95%CI), months||Median Overall Survival (95%CI), months||Hazard Ratio of Death†||P-value Overall by Log Rank Test|
|First line (n=14)||9 (6.6-11.4)||23 (17.2-28.8)||0.91||0.16|
|Second line (n=18)||4 (2.6-5.4)||21 (15.8-26.2)||0.74|
|Later line (n=20)||3 (1.6-4.4)||38 (29.3-46.8)||0.499|
|Non-everolimus group (n=91)||25 (16.3-33.7)|
†Hazard ratio of death of 1st, 2nd, Later line of treatment compared with non-everolimus group; p< 0.05 indicates statistically significant; CI denotes confidence interval
The corresponding OS in NE group was 25 months. Comparison between groups with different timing of treatment and control revealed a non-significant difference in OS (log-rank p 0.16). HR of death in patients treated with EE in first, second and third/ subsequent line after refractory to NSAI were not statistically different (HR 0.91, 0.74 and 0.499; p=0.16 by log rank test) (Table 5). Within the EE group, there were 32 patients (62%) who had received < 1 line of chemotherapy before EE, which was one of the inclusion criteria of BOLERO-2 trial . OS of this subgroup was 28 months (16.35-39.65) (Table 6).
|EE group (n=32)||NE group (n=91)||Hazard ratio (95%CI), p-value|
|Median OS (months) (95%CI)||28 (16.35-39.65)||25 (16.26-33.74)||0.7 (0.43-1.14), p=1.56|
EE denotes everolimus-exemestane, NE denotes non-everolimus; PFS denotes progression free survival, OS denotes overall survival, CI denotes confidence interval
Median duration of treatment with EE was 4 months (95%CI 2.2-5.8), time on treatment was noted to be longer with earlier use of EE (Table 5).
Progression-Free Survival and Response Rate after AI Failure
Overall PFS of the entire EE group was 8 months (95% CI 5.3-10.7). In order to evaluate anti-tumor activity of EE, we explored the PFS of patients treated with EE immediately after NSAI (n=14) compared to those treated with other agents listed in Table 7.
|Number of patients||Median PFS (months)||95%CI||HR of EE compared with other agents||p-value|
PFS denotes progression free survival, HR denotes hazard ratio, CI denotes confidence interval; p< 0.05 indicates statistically significant
Early use of EE gave a superior trend in median PFS of 10 months, whereas with the commonly used single agent chemotherapy or non-everolimus-based endocrine therapy, PFS ranged from 4-7 months. Fulvestrant seemed to provide the longest PFS among others.
Objective responses, on the basis of radiographic studies assessed by local investigators, in first subsequent treatment after NSAI refractory with EE and other agents were summarized in Table 8.
|PR||5 (35.7%)||4 (33.3%)||1 (5.6%)||3 (9.4%)||0(0%)||12 (37.5%)||7 (53.8%)|
|SD||7 (50%)||4 (33.3%)||11 (61.1%)||19 (59.4%)||9 (75%)||16 (50%)||4 (30.8%)|
|PD||2 (14.3%)||4 (33.3%)||6 (33.3%)||9 (28.1%)||2 (16.7%)||4 (12.5%)||2 (15.4%)|
|p-value (compared with EE)||0.53||0.11||0.15||0.09||>0.05||0.6|
CR denotes complete response, PR denotes partial response, SD denotes stable disease, PD denotes progressive disease, N/A denotes non-available; p< 0.05 indicates statistically significant; †CBR, clinical benefit response (CR+PR+SD)
There was no complete response (CR) except for one unconfirmed CR with tamoxifen. The overall clinical benefit response (CR+PR+SD) was numerically higher in patients received EE, paclitaxel and docetaxel, as compared to others.
We described a retrospective cohort study of patients with advanced ER positive breast cancer after failure from NSAI whose subsequent therapy contained or devoided of everolimus-exemestane in a real-life practice. As of this study, CDK4 / 6 inhibitors and PI3K inhibitors were not included due to a financial incompatibility and an inaccessibility of these drugs in Thailand. Patients in both comparison groups were well-balanced in baseline characteristics including prior therapy before NSAI. Our study explored the use of EE in a much broader population than in the pivotal BOLERO-2 study, which is much more representative of the real-world situation. The result showed that the use of everolimus-exemestane combination, although exerted some therapeutic benefit, did not translate to overall survival when adjusted for an imbalance in subsequent therapy. The more important factor for survival of these patients in our study was the ability to receive as many lines of treatment as possible. This finding, in fact, is in line with the final analysis of survival in BOLERO-2.
In this study, we chose overall survival as a primary endpoint as it is a more solid outcome than progression-free survival in retrospective database. To our knowledge, it is the study with the second longest follow-up time next to Italian cohort . The median follow-up time was 51 months compared to 29 months in BOLERO-2 and 5 to 67 months in other phase IIIb expanded studies [32, 35-39] Hence, we are confident that the result represented a reasonably mature outcome. In addition, none of those expanded access reports and other real-world setting retrospective data have focused on overall survival; they mainly explored the response and safety aspects of EE.
Patients in our study, in some aspects, were different from BOLERO-2. They carried more visceral metastasis (79% vs 56%) and more liver metastasis (40% vs 33%). Despite high numbers of visceral metastasis, 58-67% of our patients received NSAI as their first line treatment for MBC, in accordance with the current recommendation of endocrine therapy in non-visceral crisis population. In BOLERO-2, the protocol had limited the number of prior chemotherapies in advanced disease to < 1. Therefore, in BOLERO-2, only 26% of patients had received 1 regimen of chemotherapy for metastasis, while in our EE cohort, 28% (15 patients) and 38% (20 patients) received one and > 2 lines of chemotherapy in metastatic setting before receiving EE, respectively.
The optimal timing of EE in the treatment sequence also remained inconclusive. In BOLERO-2, 74% received EE immediately after NSAI and hence the recommendation to consider treatment earlier in the course of their disease. However, in our study, only 27% received EE as an immediate subsequent therapy after NSAI and 50% of our patients received EE as their 4th line of treatment. But even with more disease burden and late line use of EE, OS of our cohort compared well to that in BOLERO-2 (BOLERO-2: 31 months (EE) and 27 months (placebo), current study: 33 months (EE) and 25 months (NE)). When considering only 32 patients who received < 1 line of chemotherapy similar to inclusion criteria of BOLERO-2, OS was 28 months. In BOLERO-6 trial, patients who received everolimus after NSAI failure, OS was only 23 months compared to 25.6 months with capecitabine alone . We found that patients who received EE in later line after NSAI refractory had longer survival (38 months) compared to earlier use although time on treatment was shorter. Because survival in this study was calculated from time of NSAI failure, it is plausible that the patients who received late-line EE were already pre-selected (able to have received several lines of systemic treatment before EE). Other large post-marketing observational studies of everolimus, most of which were also in more heavily pretreated patients similar to ours, could not confirm the adverse effect of prior chemotherapy on outcomes of patients receiving everolimus [32, 36-39]. Moreover, they also demonstrated comparable PFS to BOLERO-2. These data, including ours, thus suggested that EE could be considered at any line of treatment in ER+, HER2 – MBC, with preserved clinical activity.
As stated earlier, the initial unadjusted overall survival was in favor of EE treatment, which could be a result of differences in post-progression therapy. None of the patients in NE group received subsequent everolimus, mainly due to re-imbursement issue. On the contrary, we noted that more patients in EE group also significantly received eribulin compared to NE group. Eribulin has been shown in EMBRACE trial  to improve survival compared with physician’s treatment choice in patients who had been exposed to multiple systemic therapy. In addition to eribulin use, patients in EE did receive more total lines of systemic treatment than in control arm (5.2 vs 3.6 lines, p < 0.05). When these factors were included into Cox-regression multivariate analysis, numbers of line of treatment was confirmed to be a strong parameter for survival benefit whereas the effect of EE and eribulin use were no longer seen. This finding thus implied that access to multiple treatment lines in MBC is vital for good outcome and everolimus-combination was merely a surrogate marker of access to more sequential treatment, at least in our population with limited healthcare resources. Everolimus/exemestane including CDK4/6 inhibitors and PI3K inhibitors were not included in Thailand’s basic cancer protocol of universal coverage health care scheme. Therefore, this finding may have an impact on the policy change to allow access to more lines of therapy that is less costly than EE as currently only 3 lines of chemotherapy are covered for these patients.
Although we have highlighted above some of the interesting observations, this study did have limitations. As might be expected based on a retrospective nature of the non-randomized trial, selection bias was likely to exist. Patients in no-everolimus arm could have been pre-selected not to receive everolimus-exemestane if their disease were rapidly progressing and might result in poorer survival in that arm and thus over-estimated the benefit of everolimus-exemestane. To this aspect, the effect was partially adjusted by Cox-regression analysis. Secondly, our study, compared to other real-world data, was relatively small but yet, with mature data on survival. Thirdly, caution should be noted on PFS and response rate in this study as they were based on local investigator radiographic assessments, which again, could also have been biased. And lastly, our study lacked the information on side effects, dose modification of everolimus and patients’ quality of life.
With these limitations in mind, however, we felt that our data provided some valuable perspective for practicing oncologists. In summary, our study based on routine clinical practice, revealed that patients with HR +ve, HER-2 –ve advanced breast cancer that had progressed on NSAI, the sequential use of multiple treatment options for metastatic breast cancer led to increased survival. Everolimus combined with exemestane could be added into the armamentarium of such treatment with preserved clinical activity in heavily pretreated patients.
The authors would like to thank Ramathibodi Cancer Registry Unit of Ramathibodi Comprehensive Cancer Center for the support of clinical data.
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