BREAST CANCER Capivasertib, an AKT Kinase Inhibitor, as Monotherapy or in Combination with Fulvestrant in Patients with AKT1E17K-Mutant, ER-Positive Metastatic Breast Cancer
Purpose: The activating mutation AKT1E17K occurs in approximately 7% of estrogen receptor–positive (ER+) metastatic breast cancer (MBC). We report, from a multipart, first-in-human, phase I study (NCT01226316), tolerability and activity of capivasertib, an oral AKT inhibitor, as monotherapy or combined with fulvestrant in expansion cohorts of patients with AKT1E17K-mutant ER+ MBC.
Patients and Methods: Patients with an AKT1E17K mutation, detected by local (next-generation sequencing) or central (plasma-based BEAMing) testing, received capivasertib 480 mg twice daily, 4 days on, 3 days off, weekly or 400 mg twice daily combined with fulvestrant at the labeled dose. Study endpoints included safety, objective response rate (ORR; RECIST v1.1), progression-free survival (PFS), and clinical benefit rate at 24 weeks (CBR24). Biomarker analyses were conducted in the combination cohort.
Results: From October 2013 to August 2018, 63 heavily pretreated patients received capivasertib (20 monotherapy, 43 combination). ORR was 20% with monotherapy, and within the combination cohort was 36% in fulvestrant-pretreated and 20% in fulvestrant-naïve patients, although the latter group may have had more aggressive disease at baseline. AKT1E17K mutations were detectable in plasma by BEAMing (95%, 41/43), droplet digital PCR (80%, 33/41), and next-generation sequencing (76%, 31/41). A ≥50% decrease in AKT1E17K at cycle 2 day 1 was associated with improved PFS. Combination therapy appeared more tolerable than monotherapy [most frequent grade ≥3 adverse events: rash (9% vs. 20%), hyperglycemia (5% vs. 30%), diarrhea (5% vs. 10%)].
Conclusions: Capivasertib demonstrated clinically meaningful activity in heavily pretreated patients with AKT1E17K-mutant ER+ MBC, including those with prior disease progression on fulvestrant. Tolerability and activity appeared improved by the combination.
Early identification of the AKT1E17K genomic biomarker, coupled with a novel targeted and nonmyeloablative agent, could enhance treatment options in AKT1E17K-mutant estrogen receptor–positive (ER+) metastatic breast cancer. In this first-in-human, multipart, phase I expansion study, capivasertib alone or in combination with fulvestrant was well tolerated and showed promising anticancer activity in such a patient population, including those with prior disease progression on fulvestrant. Tolerability and efficacy appeared marginally better with combination therapy, suggesting that combination AKT and ER inhibition is an effective targeted therapy approach for AKT1E17K-mutant ER+ metastatic breast cancer. Furthermore, our data provide a rationale for incorporating potentially actionable alterations in breast cancer into diagnostic testing algorithms for the early identification of these alterations in the metastatic disease course.
Estrogen receptor–positive (ER+), HER2-negative (HER2–) breast cancer is the most common subtype of metastatic breast cancer (MBC), accounting for >400,000 deaths worldwide every year (1, 2). The incorporation of inhibitors of mTOR and CDK4/6 into endocrine therapy has led to substantial improvements in patient outcomes (3–8). However, once endocrine therapy–refractory disease inevitably develops, chemotherapy remains the only approved option, and little progress has been made for this phase of illness. Given the successes of genomically selected therapy in other solid tumors harboring driver alterations (9, 10), widescale efforts to identify therapeutically actionable genomic subsets of breast cancer have been undertaken (11–15).
The PI3K pathway is one of the most commonly activated signaling pathways in ER+ breast cancer (16). The efficacy of an isoform-selective PI3K inhibitor in PIK3CA-mutant ER+ HER2– MBC was recently demonstrated in a phase III study (17), providing proof of concept that this pathway is therapeutically targetable in this clinical context. While PIK3CA mutations represent the most common mechanism of PI3K pathway activation, in an estimated 7% of ER+ breast cancers, pathway activation can occur through mutation in AKT1 (15), predominantly AKT1E17K (∼80%). In such cases, signaling is constitutively activated through pathologic localization of AKT1 to the plasma membrane (18–20). Although, in the largest comparative analysis of matched patients with AKT1-mutant and wild-type ER+ MBC, there did not appear to be significant differences in terms of overall survival or duration on endocrine and CDK4/6 inhibitor therapy; patients with AKT1-mutant disease were, however, noted to have significantly longer durations on mTOR inhibitor therapy (21), indicative of the potential therapeutic relevance of this alteration in breast cancer. Moreover, AKT1E17K-mutant tumors may not be amenable to PI3K inhibitors owing to their PI3K-independent mechanism of AKT activation (15, 22–27). As such, patients harboring AKT1E17K mutations represent a genomic subset of ER+ MBC in need of unique therapeutic approaches.
Capivasertib (AZD5363) is an oral, potent, selective ATP-competitive pan-AKT kinase inhibitor (28). We previously explored the efficacy of capivasertib monotherapy in patients with advanced solid tumors harboring an AKT1E17K mutation, including 20 patients with ER+ MBC, whereby the objective response rate (ORR) was 20% and median progression-free survival (PFS) was 5.5 months (29). Consistent with this observation, similar capivasertib monotherapy efficacy was recently reported in the AKT1-mutant arm of the NCI-MATCH study in multiple solid tumors, including ER+ MBC (30).
As observed with isoform-selective PI3K inhibitors, preclinical data with capivasertib suggests that efficacy in ER+ breast cancer may be limited in part by a compensatory increase in ER-dependent gene transcription, suggesting that combination strategies may be required to maximize therapeutic efficacy in this subtype (31–33). Accordingly, preclinical models suggest synergistic efficacy when capivasertib is combined with fulvestrant, an ER antagonist and degrader approved for the treatment of ER+ MBC (32). Therefore, to clinically explore the hypothesis that simultaneous inhibition of AKT and ER would enhance antitumor efficacy in AKT1E17K-mutant ER+ breast cancer, we amended the prior phase I study to include a multicohort expansion of the combination of capivasertib and fulvestrant.
Here we present the safety, efficacy, and biomarker analysis for the combination of capivasertib and fulvestrant in ER+, AKT1E17K-mutant MBC. To provide additional clinical context, final results for capivasertib monotherapy in ER+, AKT1E17K-mutant MBC are also presented.
Patients and Methods
Study design and participants
The protocol started as the first-in-human, multipart, phase I, dose- and schedule-finding study of capivasertib. Following identification of a recommended phase II dose, the safety and efficacy of capivasertib was further explored in multiple molecularly and histologically defined phase I expansion cohorts recruited at study centers worldwide. Results of the initial dose escalation, pharmacodynamic cohort, and monotherapy efficacy in patients with advanced solid tumors, as well as those with activating PIK3CA or AKT1 mutations, have previously been reported (29, 34). The study start date was December 2010 and the estimated completion date is December 2019 (ClinicalTrials.gov, NCT01226316).
Here we report the results of capivasertib plus fulvestrant in patients with advanced ER+ breast cancer with AKT1E17K mutations, including patients without prior fulvestrant therapy (fulvestrant-naïve cohort) and those who received prior fulvestrant (fulvestrant-pretreated cohort; Fig. 1). Updated and final efficacy data of capivasertib monotherapy in ER+ AKT1E17K-mutant breast cancer are also included.
Eligible patients had histologically confirmed ER+, HER2– MBC with progressive measurable disease [according to Response Evaluation Criteria in Solid Tumors (RECIST) v1.1] that was refractory to standard therapies or for which no standard therapies exist, and they harbored an AKT1E17K tumor mutation. Qualifying AKT1E17K mutations were identified either through local testing, as routinely obtained at participating sites, or via a central plasma-based analysis using the OncoBEAM BEAMing (beads, emulsification, amplification, and magnetics) assay with previously described methods (11). Specifically, local testing employed various next-generation sequencing (NGS)-based assays, in accordance with local standard practice without any threshold for positivity mandated by AstraZeneca for enrollment. Central plasma-based BEAMing analysis with the OncoBEAM assay used a 0.02% threshold of analyzed AKT1 copies containing the E17K mutation for positivity (35). Further inclusion criteria included age 18 years or older and an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1. Key exclusion criteria included active central nervous system metastases, prior treatment with catalytic AKT inhibitors (prior exposure to all other agents in the PI3K/AKT/mTOR pathway, including allosteric AKT inhibitors, was allowed), and clinically significant abnormalities of glucose metabolism, defined by any of the following criteria: (i) diagnosis of diabetes mellitus type I or II (irrespective of management); (ii) baseline fasting glucose value of ≥7 mmol/L (fasting is defined as no calorific intake for at least 8 hours); and (iii) glycated hemoglobin (HbA1c) >8% (>64 mmol/mol).
All patients provided written informed consent, and the study was performed in accordance with the Declaration of Helsinki, Good Clinical Practice, and the AstraZeneca policy on bioethics (36).
Monotherapy patients were treated with capivasertib at the previously determined recommended phase II monotherapy dose of 480 mg (34), administered orally, twice daily for 4 days on followed by 3 days off, repeated weekly. A treatment cycle was defined as 3 weeks. In the combination cohorts, capivasertib was administered at the previously determined recommended phase II combination therapy dose of 400 mg twice daily, 4 days on, 3 days off, repeated weekly, in addition to fulvestrant at the labeled dose (37).
Response assessments were performed by CT or MRI every two cycles for 24 weeks, then every 12 weeks until disease progression, death, or withdrawal. Safety was assessed throughout the study period and until day 28 after discontinuation of study treatment according to the National Cancer Institute's Common Terminology Criteria for Adverse Events (CTCAE) v4.0. Adverse events were coded with the Medical Dictionary for Regulatory Activities (MedDRA) v19.1.
Blood was collected at every study visit for analysis of tumor-derived, cell-free DNA (cfDNA). AKT1E17K mutation status was assessed in tumor tissue by local testing and/or in cfDNA by central testing using BEAMing (OncoBEAM, Sysmex Inostics; ref. 38) and droplet digital PCR technology (ddPCR) with an allele-specific assay for both the mutant and the wild-type allele (39). Central NGS was performed retrospectively on tumor tissue when available, by FoundationOne (40), and on cfDNA using a hybrid capture–based panel covering 300 genes (AZ300).
The primary study endpoint was safety and tolerability of capivasertib in combination with fulvestrant. Secondary endpoints included: ORR, defined as a confirmed partial response (PR) or complete response (CR); duration of response (DOR), defined as the time from confirmed objective response to disease progression or death; PFS, defined as the time from the first day of treatment to disease progression or death; and clinical benefit rate at 24 weeks (CBR24), defined as disease response (PR or CR) or stabilization for ≥24 weeks. Responses were investigator assessed according to RECIST v1.1 and required confirmation. Patients who discontinued prior to their first response assessment were considered nonevaluable for best overall response and nonresponders by intent-to-treat analysis.
All analyses were conducted according to the protocol and statistical analysis plan (and were as previously reported for the monotherapy cohort; ref. 29). Although the primary endpoint throughout this multipart phase I study remained safety and tolerability, the sample size of the expansion cohort reported here was determined with the aim of detecting a signal of efficacy, should one exist, using CBR24. The capivasertib and fulvestrant combination cohorts underwent protocol-specified analyses, conducted independently for each (fulvestrant-naïve and fulvestrant-pretreated) cohort, when 12 patients (at interim analysis) and 24 (at final analysis) per cohort were evaluable for CBR24 (Fig. 1). The sample size was determined on the basis of prespecified target values for CBR24 of 65% and 40% for fulvestrant-naïve and fulvestrant-pretreated patients, respectively (with 24 patients per cohort, there would be a 90% chance of at least 13 and 7 clinical benefit responses, respectively). At interim analysis, enrollment to the fulvestrant-naïve cohort halted, while the fulvestrant-pretreated cohort continued and completed accrual. Eight subsequent patients who were being screened at the time of closing each cohort were permitted to enroll, leading to a total of 16 and 28 patients in the fulvestrant-naïve and fulvestrant-pretreated cohorts, respectively. Final analysis occurred on August 7, 2018, when all 44 patients had the opportunity to reach 24 weeks of treatment. All patients who received at least one dose of capivasertib (n = 44) were evaluable for safety. Efficacy data are reported for 43 AKT1E17K-mutant patients and exclude one patient enrolled with a non-E17K mutation (AKT1E40K).
DOR and PFS were estimated using the Kaplan–Meier method. Patients without a progression event as of the analysis date were censored at the last known assessment. Post hoc analyses of endocrine-sensitive and -pretreated subpopulations and of patients treated with ≤2 or ≥3 prior lines of chemotherapy for MBC were performed. Patients were defined as sensitive to prior endocrine therapy if they had ≥24 months of endocrine therapy before recurrence in the adjuvant setting and/or a response or stabilization for ≥6 months of endocrine therapy for advanced disease. Exploratory biomarker analyses investigated the association between cfDNA response, defined as >50% decrease in AKT1E17K-mutant copies/mL plasma from baseline to cycle 2 day 1, and radiographic response. All analyses were done with SAS v9.04.
Data sharing statement
Data underlying the findings described in this manuscript may be obtained in accordance with AstraZeneca's data sharing policy described at https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure.
Sixty-three AKT1E17K-mutant ER+ MBC patients received capivasertib either as monotherapy (n = 20) or in combination with fulvestrant (n = 43; Table 1). The majority of combination therapy patients were enrolled on the basis of AKT1E17K mutation detection by local laboratory testing of tumor tissue (77%, 33/43), with the remaining (n = 10) patients enrolled through central laboratory plasma testing. Among patients who received the combination, 28 were previously fulvestrant pretreated and 15 were fulvestrant naïve. Median age was 57 years (range: 38–76). Most patients had visceral disease at enrollment (87%) and were heavily pretreated. Overall, 91% of patients had received prior chemotherapy, 35% mTOR inhibitors, and 24% CDK4/6 inhibitors for metastatic disease. Only 54% of patients exhibited sensitivity to prior endocrine therapy, defined by at least 24 months of endocrine therapy before recurrence in the adjuvant setting and/or a response or stabilization for at least 6 months of endocrine therapy for advanced disease. However, caution should be exercised in interpreting this seemingly low rate of endocrine therapy sensitivity compared with rates of approximately 80% reported in pivotal phase III trials conducted in patients with ER+ MBC (5, 41), given the retrospective and exploratory nature of this analysis. In combining both monotherapy and combination therapy cohorts, certain differentiating baseline characteristics were apparent between the fulvestrant-naïve (n = 21) and fulvestrant-pretreated (n = 42) patients. Specifically, a high proportion of fulvestrant-naïve patients were treated with first-line chemotherapy in the metastatic setting (38% vs. 12%, respectively) and had received fewer total lines of endocrine therapy (median 2 vs. 4, respectively).
Adverse events (AEs) causally linked to study treatment by the investigator are shown in Table 2. The most common all-grade AEs for the monotherapy cohort were diarrhea (65%), nausea (50%), hyperglycemia (45%), and vomiting (45%). Similarly, for the combination cohort, the most common AEs were diarrhea (59%), nausea (30%), maculopapular rash (21%), fatigue (18%), and hyperglycemia (18%). Grade ≥3 AEs attributed to study treatments were observed in 50% of patients in the monotherapy cohort, most commonly hyperglycemia (30%) and maculopapular rash (20%), and 21% of patients in the combination cohort, most commonly maculopapular rash (9%). AEs irrespective of causality are shown in Supplementary Table S1. No new safety signals were identified with the combination with fulvestrant.
Median duration of capivasertib exposure in the monotherapy cohort and combination cohort was 166 days (mean daily dose 870 mg) and 123 days (775 mg), respectively. In the monotherapy cohort, 13 (65%) patients required dose interruption, 7 (35%) dose reduction, and 1 (5%) discontinuation as a result of a treatment-related AE (confusion). In the combination cohort, 19 (43%) patients required dose interruption, 4 (9%) dose reduction, and 5 (11%) discontinuation because of an AE (Supplementary Table S2), three of which were treatment related (eosinophilic pneumonia, fatigue, and rash). There were no treatment-related or AE-attributable deaths in either cohort.
At the time of data cutoff, 7 patients remained on therapy, the majority having discontinued because of disease progression (Supplementary Fig. S1). Median follow-up (time to event) for all capivasertib-treated patients who were censored at the time of primary analysis was 8.1 months (range: 0–27.5). Efficacy in the monotherapy cohort and combination cohorts (overall and by prior fulvestrant therapy exposure) is shown in Table 3 and Figs. 2 and 3. Among patients receiving combination therapy, ORR was 36% (95% CI: 19–56) in fulvestrant-pretreated patients and 20% (95% CI: 4–48) in fulvestrant-naïve patients. ORR in the monotherapy cohort was 20% (95% CI: 8–58). Across both monotherapy and combination cohorts (n = 63), ORR was 33% (95% CI: 20–50) in fulvestrant-pretreated patients and 14% (95% CI: 3–36) in fulvestrant-naïve patients. Despite the numerically higher ORRs observed in the fulvestrant-pretreated patients, CBR24 was broadly similar across groups. Specifically, in the combination cohort, CBR24 was 50% (95% CI: 31–69) in fulvestrant-pretreated and 47% (95% CI: 21–73) in fulvestrant-naïve patients. Across both monotherapy and combination cohorts, CBR24 was 50% (95% CI: 34–66) in fulvestrant-pretreated and 43% (95% CI: 22–66) in fulvestrant-naïve patients.
To determine whether additional patient and treatment characteristics could further enrich for patients who experienced benefit from capivasertib, several exploratory post hoc subgroup analyses were conducted. Across monotherapy and combination therapy patients, ORR and CBR24 were numerically higher in patients who had received ≤2 prior lines of chemotherapy (35% and 62%, respectively) compared with those who had received ≥3 prior lines (22% and 38%, respectively; Supplementary Table S3). Analyses classifying patients based on prior endocrine therapy sensitivity were also conducted but did not clearly predict benefit of capivasertib-based therapy.
Exploratory biomarker analyses
Central biomarker assessments in the combination cohort utilized a variety of assays. Central tissue NGS was performed in 42% (18/43) of patients. BEAMing was used for mutation detection in plasma cfDNA collected at screening and detected the AKT1E17K mutation in 95% (41/43) of patients. ddPCR and broader NGS profiling were performed on plasma cfDNA collected on the first day of treatment (cycle 1 day 1), detecting the AKT1E17K mutation in 80% (33/41) and 76% (31/41) of patients tested, respectively (Fig. 3). These data demonstrate that plasma-based analyses offer an additional diagnostic opportunity for AKT1E17K mutation testing (35). In this cohort, a ≥50% decrease from baseline at cycle 2 day 1 was associated with improved PFS (Supplementary Fig. S2), similar to that previously demonstrated in the monotherapy cohort (29).
In 41 patients tested, the broader genetic profiling of plasma samples by NGS identified cooccurring alterations in ESR1 (n = 10, almost all in fulvestrant-pretreated patients and all in those with a detectable AKT1E17K mutation by plasma NGS), TP53 (n = 8, predominantly in fulvestrant-naïve patients), MAP3K1 (n = 4), PIK3CA (n = 4), and FGFR1 (n = 2; Fig. 3). In one of the PIK3CA-mutant cases, despite an AKT1E17K mutation being detected by BEAMing at a very low mutant allele fraction (MAF), the AKT1E17K mutation was not in fact detectable by NGS, indicative of the subclonality of the alteration in this patient (Supplementary Fig. S3). Evidence of a subclonal AKT1E17K mutation could also be found in another patient, in whom the AKT1E17K mutation was detected by BEAMing and ddPCR but not by the NGS analysis that detected other somatic mutations in this patient. While 8 (20%) patients did not shed sufficient circulating tumor DNA for mutation detection by NGS (i.e., low shedders), in all other (31; 94%) patients, the AKT1E17K mutation was detected at a level around or above the median MAF indicative of the predominantly clonal nature of this alteration (Fig. 3; Supplementary Fig. S3). In this limited sample set, no obvious pattern in AKT1E17K clonality or coincident tumor mutations was associated with clinical outcome, although, potentially of interest, 6 of the 8 (75%) cases identified as low shedders by NGS had an objective response, and none of the patients whose tumors harbored a TP53 mutation achieved an objective response. While the sample size was small, the observed higher frequency of TP53 mutations in the fulvestrant-naïve compared with the fulvestrant-pretreated cohort (33% vs. 12%, respectively) potentially supports the observation that this group had more aggressive disease biology (42). Equally, the identified TP53 mutations could be related to the greater degree of cytotoxic chemotherapy exposure in this cohort (43, 44). An integrated analysis of efficacy and genomic data is shown in Fig. 3.
In this multicohort phase I study, we sequentially explored the safety and efficacy of the pan-AKT inhibitor capivasertib, initially alone and later in combination with fulvestrant, in patients with ER+ AKT1E17K-mutant MBC. The safety profile was similar to that in prior reports (29, 34, 45), although combination therapy appeared better tolerated, likely because of the lower dose of capivasertib (400 mg twice daily, 4 days on, 3 days off) administered with fulvestrant compared with the monotherapy dose of capivasertib (480 mg twice daily, 4 days on, 3 days off), as suggested by the dose–response relationship observed for key capivasertib-related toxicities such as hyperglycemia (46).
Although the study was not designed to directly compare activity across groups, and noting that the fulvestrant-naïve (n = 21) patients treated in this study may have had a more aggressive disease profile at baseline than those who were fulvestrant pretreated (n = 42), optimal efficacy was nonetheless observed with combination therapy, specifically in fulvestrant-pretreated patients (ORR 36%; CBR24 50%). Taken together, these findings are encouraging, particularly given the heavily pretreated nature of the study population. There is also reason to believe that our data compare favorably with prior reports on molecular therapy in the clinic. For example, BELLE-3 evaluated fulvestrant, with or without the pan-PI3K inhibitor buparlisib, in mTOR inhibitor–exposed patients, reporting, respectively, an ORR of 8% versus 2% and CBR24 of 25% versus 15% (47). This provides a useful benchmark for fulvestrant monotherapy following mTOR inhibitor exposure in a notably less pretreated (no more than one line of chemotherapy and no prior fulvestrant were permitted) population. Similarly, our data compare favorably with expected chemotherapy outcomes in endocrine-resistant patients (48).
The benefit of adding capivasertib to hormone therapy in AKT1E17K-mutant patients is consistent with preclinical data (32). More broadly, the role for cotargeting ER and PI3K pathway alterations has been demonstrated in multiple randomized, phase III studies of PI3K inhibitors (17, 49). Furthermore, in the recently reported randomized phase II FAKTION study, the addition of capivasertib to fulvestrant showed a significant improvement in PFS in a molecularly unselected, aromatase inhibitor–pretreated but fulvestrant-naïve ER+ MBC population (37). Given the increasing genomic complexity of breast cancer as it advances through multiple lines of therapy, this recent trial report supports our observation and hypothesis, and others', that earlier introduction of targeted therapies to a less clonally diverse disease is likely to be necessary to garner significant improvements in outcome in patients harboring these driver oncogenic alterations (14).
Acknowledging that only 24% of enrolled patients in this study received prior CDK4/6 inhibitors, agents that are now standard of care in combination with an aromatase inhibitor or fulvestrant in the first- or second-line setting, these data remain of interest. Outcomes of targeted therapy following CDK4/6 inhibitor exposure in ER+ MBC are largely unknown. However, preclinical models with acquired resistance to CDK4/6 inhibitors do indicate retained sensitivity to PI3K pathway inhibition combined with endocrine therapy (50, 51). Indeed, in SOLAR-1, the small subset of patients with prior CDK4/6 inhibitor exposure did still appear to derive benefit from the addition of apelisib to fulvestrant (17). In addition, of interest, recent preclinical data have implicated PTEN loss as a potential mechanism of resistance to CDK4/6 inhibitors, via increased AKT activation in vitro and in vivo (52), a hypothesis since observed in the clinic, where enrichment of PTEN loss-of-function alterations has been described in tumor samples obtained after CDK4/6 inhibitor therapy (53). Intriguingly, in this context (PTEN-null models resistant to CDK4/6 inhibitors), AKT inhibition may in fact be superior to PI3K inhibition (52). It is also clear from preclinical work that constitutively active AKT induces resistance to PI3K inhibition in breast cancer cell lines, and, interestingly, increased AKT1 expression was identified in a very small cohort of biopsies collected post-treatment with alpelisib (54). Clinical data demonstrating a role for AKT1 mutations mediating resistance to antiestrogens or CDK4/6 inhibitors are limited. A recent clinical series (n = 57) noted an over-representation of PI3K pathway mutations (PIK3CA, AKT1, TSC2, and/or loss or truncation mutations of PTEN) among patients with a poor response to neoadjuvant letrozole [Preoperative Endocrine Prognostic Index (PEPI) >4 and/or recurrence], although this was unlikely to be driven by AKT1, as none of the three AKT1-mutant cases in this report experienced a recurrence and two of the three were actually categorized in the responder group (PEPI < 4 and no recurrence; ref. 55). In addition, an endocrine therapy–exposed ER+ breast cancer dataset did not identify AKT1 mutations in tumors intrinsically resistant to letrozole; rather, AKT1 mutations were detected in those sensitive to the therapy (56, 57). In agreement with this, genomic profiling of a large (n = 1,501) cohort of endocrine therapy–naïve versus endocrine therapy–exposed ER+ breast cancers did not show any evidence of AKT1 mutations being associated with resistance to hormonal therapy (15). Finally, findings from a recent institutional dataset (n = 58) have proposed activating events in AKT1 as a possible mechanism of resistance to therapy containing CDK4/6 inhibitors, along with in vitro data showing overexpression of AKT1 as conferring resistance to CDK4/6 inhibitors (37), although, thus far, this has not been observed in genomic analysis from the registration studies of these agents (58, 59). Moreover, genomic analysis of 348 ER+ breast cancers treated with CDK4/6 inhibitors, as well as comparative analysis of tumors before (n = 838) versus after (n = 221) CDK4/6 inhibitor therapy, along with paired analysis of tumors before versus after CDK4/6 inhibitor therapy (n = 210), has not identified an association between AKT1 mutations and therapeutic resistance to CDK4/6 inhibitors (53, 60).
Our study has several important limitations. First, this trial was not formally powered to compare efficacy across treatment groups. Second, although efficacy appeared most robust in fulvestrant-pretreated patients, it is noteworthy that the fulvestrant-naïve patients enrolled here appeared to be a subgroup with poorer prognosis. Given this, we cannot rule out the role that demographic imbalance between the groups driven by adverse patient selection factors may have played in the apparent difference in treatment outcomes. Third, we do not know the extent to which the presence of an AKT1E17K mutation may influence the natural history or response to standard therapy for MBC. Despite this, recent analyses suggest that prognoses of patients with AKT1E17K-mutant and wild-type MBC appear largely comparable, somewhat mitigating this concern (21). Finally, despite opening this study at 16 sites internationally, the rarity of this biomarker led to slow accrual (22 months to enroll 44 patients in the combination cohort), despite having central screening by BEAMing in plasma implemented, in addition to local testing.
In conclusion, this study demonstrates that AKT1E17K is a clinically relevant, valid target in ER+ breast cancer and that the AKT inhibitor capivasertib is tolerable and active as both monotherapy and in combination with fulvestrant, including in patients with prior fulvestrant resistance. We confirm that the majority of enrolled patients had detectable AKT1E17K in plasma at baseline and demonstrate the feasibility of enrollment based on centralized plasma screening for this rare genomic biomarker (35). With other genomic biomarkers such as PIK3CA mutations expected to become part of routine management paradigms over the coming years in breast cancer, these data have the prospect of becoming part of a rationale to incorporate other potentially actionable alterations in breast cancer, including ERBB2 and AKT1, into diagnostic testing algorithms and for the early identification of these alterations in the metastatic disease course (61, 62). Finally, data from this study, along with the FAKTION study, have provided the basis for a confirmatory phase III study that will take into account populations with and without prior use of CDK4/6 inhibitors.