Introduction
Eribulin mesylate (Halaven
®, INNM: eribulin mesilate, E7389), a non-taxane microtubule dynamics inhibitor, is a structurally simplified, synthetic analog of the natural product Halichondrin B, isolated from the marine sponge
Halichondria okadai [
1,
2]. By predominantly binding to high affinity sites on the growing plus (+) ends of microtubules, eribulin inhibits microtubule polymerization without affecting depolymerization, which in turn induces irreversible mitotic block at G
2-M phase and apoptosis [
1‐
6]. This mechanism of action is distinct from most other tubulin-targeting chemotherapeutic agents currently in clinical use, including taxanes, vinorelbine, and epothilones [
3,
5].
In the randomized Phase III Eisai Metastatic Breast Cancer Study Assessing Physician’s Choice Versus E7389 (EMBRACE) trial, which involved patients with heavily pre-treated locally recurrent or metastatic breast cancer (MBC), eribulin was compared with treatment of physician’s choice (TPC) [
7]. Patients had received a median of four previous chemotherapy regimens including an anthracycline and a taxane. Patients who received eribulin mesylate (1.4 mg/m
2, days 1 and 8 of a 21-day cycle) exhibited a significant improvement in median overall survival (OS) compared with TPC (13.1 vs. 10.6 months; hazard ratio [HR] 0.81; 95 % confidence interval [CI] 0.66–0.99;
p = 0.041). An updated analysis of OS requested by regulatory authorities confirmed the significant increase in OS for eribulin compared with TPC (13.2 vs. 10.5 months; HR 0.81; 95 % CI 0.67–0.96; nominal
p = 0.014). This was the first Phase III monotherapy study to meet its primary endpoint of prolonged OS in this patient population. These results contributed in part to the Food and Drug Administration’s approval of eribulin mesylate for treatment of patients with MBC who have previously received at least two chemotherapies for the treatment of metastatic disease and an anthracycline and a taxane in either the adjuvant or metastatic setting [
8].
Peripheral neuropathy (PN) is a common toxicity associated with chemotherapy agents which target microtubules. It can also be a treatment-limiting factor for patients with heavily pre-treated MBC [
9], and have a significant impact on patients’ routine activities, functions, and behavior [
10]. In EMBRACE, 35 % of patients treated with eribulin experienced PN (all grades), with 8 % and <1 % reporting Grade 3 and 4 PN, respectively [
7]. For patients in the TPC arm, total incidence of PN was 16 % (Grade 3, 2 %; no Grade 4 events) [
7]. In two Phase II studies of eribulin in patients who had previously received an anthracycline and a taxane [
11] or an anthracycline, a taxane, and capecitabine [
12], incidences of PN were 26 % (Grade 1/2) and 5–7 % (Grade 3), with no Grade 4 events reported in either study.
Ixabepilone is an epothilone B analog, which induces microtubule stabilization [
13]. It is indicated for treatment of locally advanced or MBC after failure of an anthracycline, a taxane, and capecitabine, or combined with capecitabine following anthracycline and taxane failure [
14]. Ixabeplione has been investigated in three Phase II monotherapy studies [
15‐
17] and included as a comparator in a Phase III study [
18] involving patients with MBC. In two of the Phase II studies (ixabepilone in patients with MBC resistant to either a taxane [
15] or an anthracycline, a taxane, and capecitabine [
16]), 60–63 % of patients reported sensory PN (all grades); motor neuropathy was reported by 2–10 % of patients and Grade 3/4 events reported by 12–13 % of patients [
15,
16]. In the third Phase II study, ixabepilone was administered as first-line therapy in taxane-naïve patients with MBC previously treated with an adjuvant anthracycline. Treatment with ixabepilone was associated with an incidence of sensory PN of 71 % (all grades) and 20 % (Grade 3; no Grade 4), and of motor neuropathy of 6 % (5 % Grade 3; no Grade 4) [
17]. In the Phase III study comparing paclitaxel, nanoparticle albumin-bound paclitaxel, and ixabepilone, with or without bevacizumab, as first-line therapy for MBC, ≥Grade 2 sensory PN was reported for 44 % of patients treated with ixabepilone [
18].
While these reports highlight that incidences of chemotherapy-induced PN differs between conventional agents, the precise underlying cellular mechanisms are unclear. In preclinical studies using mouse models of neuropathy, paclitaxel and ixabepilone at their equivalent maximum tolerated doses produced deficits in nerve conduction parameters and caused degenerative pathological changes, whereas eribulin did not affect conduction and caused milder, less frequent effects on cell morphology [
19]. In in vitro studies, inhibition of microtubule-dependent axonal transport was reduced with eribulin compared with paclitaxel, ixabepilone, and vincristine [
20]. These results suggest that eribulin may have lesser clinical impact upon nerve function and morphology than other tubulin-targeting agents.
This Phase II, randomized study assessed the incidence and severity of neuropathy adverse events (AEs) in patients with locally recurrent or MBC after treatment with either eribulin or ixabepilone. Overall safety, tolerability, and efficacy profiles were also examined.
Methods
Study design
This Phase II, multicenter, randomized, open label study (Study E7389-G000-209; NCT00879086) recruited patients with locally recurrent or MBC who had received prior taxane therapy, at least one prior cytotoxic chemotherapy for advanced disease, and progressed during or after their last anti-cancer therapy. Patients were enrolled at 48 sites in the United States.
Patients were pre-stratified based on pre-existing neuropathy (National Cancer Institute Common Terminology Criteria for Adverse Events version 3.0 [CTCAE] Grade 0 or 1) and number of prior chemotherapies (≤3 or >3). Patients were then randomized (1:1) to eribulin or ixabepilone treatment groups in a consecutive sequence.
All patients provided written informed consent. The study was conducted in accordance with the International Conference on Harmonization Guidelines for Good Clinical Practice, the Declaration of Helsinki, and the institutional review board/ethics committee at each site.
Study objectives
The primary objective was to assess the incidence of neuropathy AEs in patients treated with eribulin or ixabepilone, graded using the CTCAE. Neuropathy was based on a broad list of preferred terms for neuropathy and the following additional preferred terms: neuropathy, hyperesthesia, painful response to normal stimuli, pallanesthesia, and allodynia. As a sensitivity analysis, analysis of neuropathy was also performed based on a narrow definition of PN (combined term), including the following preferred terms: neuropathy peripheral, peripheral motor neuropathy, polyneuropathy, peripheral sensory neuropathy, peripheral sensorimotor neuropathy, demyelinating polyneuropathy, and paresthesia. The secondary safety objectives included: comparison of severity of neuropathy AEs (defined as for the primary objective), patient-reported neurotoxicity questionnaire (PNQ), and vibration sensitivity (vibration perception threshold [VPT]); time to onset and resolution of neuropathy; and overall safety and tolerability. Secondary efficacy objectives were objective response rate (ORR), clinical benefit rate (CBR), progression-free survival (PFS), and disease control rate (DCR).
Patients
Key inclusion criteria were: women at least 18 years old with histologically or cytologically confirmed carcinoma of the breast (locally recurrent or metastatic); prior taxane therapy and at least one prior cytotoxic chemotherapy for locally recurrent or MBC; disease progression during or after last anti-cancer therapy; pre-existing neuropathy <Grade 2; Eastern Cooperative Oncology Group performance status of 0–2; adequate renal, liver, and bone marrow function. Patients must have shown resolution of all prior chemotherapy or radiation-related toxicities to Grade ≤1, except for alopecia, and the ability to complete the PNQ without assistance from study-site personnel.
Exclusion criteria included: prior ixabepilone or eribulin therapy; a history of diabetes mellitus concurrent diseases or conditions expected to interfere with neuropathy assessments; and significant cardiovascular impairment.
Treatment
Eribulin mesylate 1.4 mg/m
2 (equivalent to eribulin 1.23 mg/m
2 [expressed as free base]) was administered intravenously over 2–5 min on days 1 and 8 of each 21-day cycle, and ixabepilone (starting dose 32 or 40 mg/m
2 as per approved labeling) as a 3-h intravenous infusion on day 1 of each 21-day cycle. A reduced dose of ixabepilone at 32 or 20 mg/m
2 was allowed for patients with mild or moderate hepatic impairment, respectively, according to approved labeling [
14].
Treatment continued until unacceptable toxicity, progression of disease, or the investigator considered that discontinuation of therapy was in the patient’s best interest. Dose delays and modifications were permitted to manage toxicities.
Concomitant medication
Any medication considered necessary for the patient’s welfare that was not expected to interfere with the evaluation of either study drug was permitted at the investigator’s discretion. Palliative radiotherapy was permitted if the irradiated area involved <10 % of the bone marrow and was not to be used for tumor response assessment. Study treatment was delayed during palliative radiotherapy. Strong CYP3A4 inhibitors, other investigational drugs, and other anti-tumor therapies were prohibited during the study; mild or moderate CYP3A4 inhibitors, strong CYP3A4 inducers, and CYP3A4 substrates were administered with caution.
Safety
AEs were graded using CTCAE and coded according to the Medical Dictionary for Regulatory Activities. AEs reported here were considered treatment-emergent, i.e., they commenced on or after day 1 of cycle 1, and/or increased in severity during the trial, or had an onset date within 30 days after the last dose of study drug.
Neuropathy assessments (PNQ and VPT) were performed at baseline and on day 1 of cycles 2–6, at the beginning of every third cycle thereafter, and at the end of treatment and post-treatment follow-up visits (21 and 42 days after the last dose, respectively). PNQ consisted of three items (sensory, motor, and composite). VPT was measured on the ventral surface of the distal index finger (contralateral to the side of mastectomy or primary disease) and on the distal pad of the right and left great toes, using a Vibratron II device (Physitemp, Inc., Clifton, NJ, USA).
Time to onset of neuropathy was defined as number of weeks from first dose of study treatment to onset of the earliest neuropathy of CTCAE grade greater than baseline for that patient. Time to resolution of neuropathy was defined as number of weeks from last dose of study treatment to the earliest date of resolution of neuropathy (neuropathy that had stopped or resolved to either the level at baseline or lower, and after which there was no further onset).
Efficacy
Tumor assessments performed at screening/baseline and between days 15 and 21 of cycles 2, 4, and 6 included: computed tomography (CT) scans of the chest, abdomen, and pelvis; a bone scan and/or clinical assessments/photographs of skin lesions; and CT/magnetic resonance imaging scans. In the extension phase, tumor assessments were performed every three cycles until progressive disease (PD) developed.
Tumor response was assessed according to modified Response Evaluation Criteria in Solid Tumors version 1.0, and classified as complete response, partial response (PR), stable disease, or PD. PFS was defined as time from randomization until PD or death due to any cause.
Statistics
The intent-to-treat population consisted of all randomized patients, and the safety population comprised all patients who received at least one dose of study medication and had at least one post-dose safety assessment. A sample size of 49 patients per group was required to detect a significant difference in the incidence of neuropathy between treatments with 80 % power, at a proportion of 0.35 in the eribulin group to 0.63 in the ixabepilone group (odds ratio 0.316), at the 0.05 two-sided significance level.
The primary safety endpoint was analyzed using the Cochran–Mantel–Haenszel test, sensory and motor PNQ scores were analyzed separately using a generalized linear model, and hand and foot VPT data were evaluated by regression analysis. Other neuropathy-related endpoints were not tested for statistical significance. ORR, DCR, and CBR were analyzed using the Clopper-Pearson method, and PFS estimated using Kaplan–Meier analysis.
Discussion
This is the first clinical study to directly compare neuropathy, safety, and efficacy of eribulin and ixabepilone in patients with MBC. The overall incidences of neuropathy and PN were 33.3 versus 48.0 % and 31.4 versus 44.0 % for eribulin versus ixabepilone, respectively. Regardless of baseline pre-existing neuropathy (Grade 0 or 1) and the number of prior chemotherapies (≤3, >3), these differences were not significant. The original sample size calculation for the study, to detect a 28 % difference in neuropathy with a power of 80 %, was based on historical estimates on the incidence of neuropathy with the two treatments (incidence rates of CTCAE neuropathy events for eribulin [35 %] as per a previous Phase II study [
12], and the package insert for ixabepilone [63 %]). The aforementioned results should, therefore, be interpreted with consideration to the fact that the study was not sufficiently powered to detect the observed magnitude of difference between the two treatment arms.
The severity of neuropathy AEs according to grade supported the overall incidence results, with fewer eribulin-treated patients reporting Grade 3/4 neuropathy or PN. There were no significant between-group differences in post-baseline PNQ scores and baseline to worst post-baseline PNQ scores. Additionally, there was no significant effect of time (cycles 2 through 6 or overall) on the correlation between the maximum treatment-emergent motor neuropathy CTC grade and worst post-baseline motor PNQ score. Although the degree of on-study deterioration in sensory function was slightly higher with eribulin, these differences in the pattern of VPT findings across treatment groups were not clinically meaningful or significant. The findings in this study must be tempered by the small number of patients in each group, especially at cycle 6, and by the substantial variance in the calculated change in VPT scores across patients.
Eribulin was associated with a longer time to onset of neuropathy in this study. Resolution of neuropathy (in patients with existent neuropathy at the time of treatment discontinuation) tended to occur relatively sooner in patients receiving ixabepilone. However, patients receiving eribulin achieved a greater median number of treatment cycles and remained on treatment for longer than those receiving ixabepilone. This raises the possibility that the observed longer time to resolution of neuropathy in patients with ongoing neuropathy at the time of treatment discontinuation in the eribulin group could be attributed to treatment for a longer period than those receiving ixabepilone. A recent pooled analysis of five ixabepilone studies in patients with MBC suggested that PN associated with this agent is cumulative, as the incidence of Grade 3/4 events was shown to increase with median cumulative ixabepilone dose [
21]. In addition, PN associated with ixabepilone was shown in monotherapy studies to be generally reversible and often manageable with dose reduction [
15‐
17]. In one such trial, Grade 3/4 PN resolved in 76 % of patients, with a median time to resolution of 5.4 weeks [
16]. In EMBRACE, time to onset or resolution of neuropathy were not examined; however, patients with Grade 3/4 PN who continued eribulin treatment also showed improvement following dose modification [
7].
In the current study, both agents demonstrated manageable safety profiles. Eribulin exhibited fewer neuropathy-related treatment discontinuations than ixabepilone (3.9 vs. 18.0 %), which is in line with previously reported trials. In EMBRACE, treatment discontinuation due to PN occurred in 5 % of patients in the eribulin group [
7], whereas monotherapy studies of ixabepilone have reported discontinuations due to neuropathy ranging from 6 to 28 % of patients [
15‐
17]. Discontinuation from treatment due to any toxicity (including neuropathy) was also lower with eribulin than ixabepilone (11.8 vs. 32.0 %).
Due to the small sample size, formal statistical analyses were not planned in the study. In addition, a considerable proportion of patients being either censored or deemed “non evaluable” for efficacy assessments precluded any robust efficacy interpretations from the study. Eribulin, however, had a more favorable impact on ORR than ixabepilone (15.4 vs. 5.8 %, respectively) due to a higher proportion of patients exhibiting PRs. In the current study, tumor responses observed with eribulin are similar to those in three previous reports, each of which included patients who had received a median of four previous chemotherapies: in the two earlier Phase II studies of eribulin, ORRs were 9.3 % (95 % CI 6.1–13.4) and 11.5 % (95 % CI 5.7–20.1) [
11,
12]; and in EMBRACE, a significantly higher ORR was reported for eribulin (12 % [95 % CI 9.4–15.5]) compared with TPC (5 % [95 % CI 2.3–8.4];
p = 0.002) [
7]. With the median PFS being numerically similar in the eribulin group compared with the ixabepilone group (3.4 vs. 3.1 months, respectively), no clinically meaningful differences in PFS between eribulin and ixabepilone were observed.
In conclusion, differences in the overall incidence of neuropathy were not statistically significant even after controlling for baseline pre-existing neuropathy (Grade 0 or 1) and number of prior chemotherapies (≤3, >3). Small sample size and lack of power in the study to detect the observed magnitude of differences may explain why there was no significant numerical differences in the primary safety endpoint between eribulin and ixabepilone. Time to onset of neuropathy tended to occur later and resolve later with eribulin compared with ixabepilone, possibly because patients in the eribulin group received a greater number of treatment cycles and remained on treatment for longer than those in the ixabepilone group. Compared with ixabepilone, fewer patients receiving eribulin discontinued treatment due to neuropathy or AEs in general. Additional studies may be required to confirm whether patients may derive significant benefits with eribulin over ixabepilone with respect to the neuropathy profile.
Acknowledgments
We thank all the patients and investigators who participated in these studies. Editorial support was provided by Haley Bennett, PhD, of Complete Medical Communications and was funded by Eisai Inc. This study was funded by Eisai Inc.