A Narrative Review of Repository Corticotropin Injection for the Treatment of Systemic Lupus Erythematosus.

Systemic lupus erythematosus (SLE) is a chronic autoimmune disorder that affects multiple organ systems. The most prevalent manifestations include constitutional symptoms, arthritis, and rash. An SLE flare is defined as a measurable increase in disease activity that may prompt a change in treatment. According to the European Alliance of Associations for Rheumatology guidance, SLE treatments should be aimed at reducing disease activity and flares, as well as preventing organ damage. Standard-of-care treatment of SLE includes glucocorticoids, but their long-term use is associated with damage accrual. Repository corticotropin injection (RCI; Acthar® Gel) is a naturally sourced complex mixture of adrenocorticotropic hormone analogs and other pituitary peptides that has anti-inflammatory and immunomodulatory effects beyond its steroidogenic effect, and has been US Food and Drug Administration-approved for the treatment of SLE flares and as a maintenance therapy. This review summarizes data from three clinical trials that evaluated the efficacy and safety of RCI in the treatment of patients with moderate-severe refractory SLE. These clinical trials confirmed that RCI improved global disease activity scores and some SLE clinical manifestations. Analysis of pooled data from these trials showed that RCI treatment significantly improved the British Isles Lupus Assessment Group 2004 (BILAG-2004) index scores after 8 weeks of treatment, and tender and swollen joint counts after 4 weeks. These clinical trials demonstrated an acceptable safety profile with few serious adverse events reported. The distinct mechanisms of action from standard-of-care therapies and the favorable safety and good efficacy profiles support the use of RCI as therapy for patients with refractory SLE.

Key Summary Points

Introduction

Systemic lupus erythematosus (SLE) is a chronic autoimmune disorder with an unpredictable course and the potential for affecting multiple organ systems [1, 2]. The most common manifestations of SLE are fatigue, arthritis, and rash [1, 3–6]. Like other autoimmune disorders, SLE has a relapsing–remitting or a chronic progressive course with fluctuating disease activity. SLE flares are measurable exacerbations of disease activity in one or more organ systems [7]. Most patients with SLE have recurrent disease flares [8]. Risk factors for repeated SLE flares include African American race, male sex, disease onset at ≤ 25 years of age, presence of neuropsychiatric symptoms, cytopenia, nephritis, vasculitis, and poor treatment adherence [8]. Triggers include sun exposure, medication changes, hormonal changes, and infections [2]. Preventing and reducing damage accrual is a primary goal of SLE treatment, and this is best achieved by reducing disease activity, preventing flares, and minimizing steroid use [8].

The pathophysiology of SLE is not entirely understood [1, 9]. Environmental, hormonal, and genetic factors lead to abnormal innate and adaptive immune responses, production of auto-antibodies, inflammation, tissue damage, and the clinical manifestations of SLE [1, 2]. Dysregulated and hyper-reactive B cells are central to the immune dysfunction in SLE [10, 11]. B cells serve as antigen-presenting cells (of self-antigens in SLE) and produce auto-antibodies, leading to overexpression of pro-inflammatory cytokines including tumor necrosis factor α (TNF-α), interleukin (IL)-6, IL-10, B cell activating factor (BAFF), and a proliferation-inducing ligand (APRIL) [11, 12].

This review summarizes the evidence supporting the use of repository corticotropin injection (RCI; Acthar® Gel) as a treatment option for SLE from studies published after 2010. This manuscript is based on previously performed and published studies and does not contain any new human participants or animal studies performed by any of the authors.

Steroids are a Standard Treatment Option for SLE

The selection of therapies for SLE is determined by the disease manifestations, their severity, and comorbidities [1]. In general, treatment of SLE is divided into two phases: induction of remission/low disease activity and maintenance. Based on the recent guidelines from the European Alliance of Associations for Rheumatology and others, treatment goals are to lower disease activity, achieve remission, and prevent flares in order to reduce cumulative organ damage, morbidity, and mortality [13-15]. These treatment guidelines recommend antimalarials and glucocorticoids as first-line therapies, whereas immunosuppressants and biologics are administered to those with disease that is more difficult to treat [13-15]. Suboptimal response rates and treatment side effects, especially those adverse events (AEs) caused by steroids, underscore the need for safer and more effective therapies [12]. Chronic glucocorticoid use may contribute to hypertension (> 30%), cataracts, osteoporosis (21–30%), hyperglycemia (fourfold increase), cardiovascular events (4%), Cushingoid appearance (4–70%), psychiatric manifestations, and/or avascular necrosis [16, 17]. It is estimated that approximately 80% of the damage that occurs in SLE can be attributed to steroid exposure [18]. Despite these substantial risks, steroids have been transformative in the care of patients with inflammatory diseases. However, many patients who receive treatment with maximized standard-of-care therapies, including glucocorticoids, may continue to experience SLE flares. Therefore, alternative treatments for refractory SLE are needed.

RCI for the Treatment of SLE

RCI is a naturally sourced complex mixture of adrenocorticotropic hormone analogs and other pituitary peptides that is US Food and Drug Administration–approved for the treatment of SLE flares and as a maintenance therapy [19]. As an agonist of all five melanocortin receptors (MCRs), RCI likely provides therapeutic efficacy in the treatment of SLE via multiple mechanisms of action. Preclinical studies have shown that RCI is a full agonist of MC1R, MC2R, MC3R, and MC4R and a partial agonist of MC5R [20]. The anti-inflammatory mechanism of action for RCI was originally thought to be via activation of MC2R on adrenocortical cells, which stimulates production of endogenous cortisol; however, recent evidence has shown that RCI has relatively low agonistic activity of MC2R [20, 21]. This is supported by studies in animals [20] and healthy human subjects [21, 22], which showed lower levels of endogenous corticosteroid production after administration of RCI compared to synthetic ACTH1–24 (Fig. 1).

Fig. 1

Baseline-corrected plasma free cortisol concentrations in healthy human subjects after RCI or synthetic ACTH1–24 depot administration on study day 1 (A) and day 4 (B); baseline-corrected free cortisol concentrations were calculated by subtracting the time-matched baseline (day−1) free cortisol concentrations from the respective day 1 and day 4 free cortisol concentrations for each study drug. The basal range of plasma free cortisol concentration (0.2–23.0 ng/mL) is shaded gray. ACTH1–24 first 24 amino acids of adrenocorticotropic hormone, RCI repository corticotropin injection, SEM standard error of the mean. Reproduced from Poola et al. [22] under the CC BY-NC-ND 4.0 open access license

In vitro and animal studies have demonstrated direct, steroidogenesis-independent, immunomodulatory effects of RCI [10, 22–26]. Studies of human B cells reported that RCI inhibits their activation and proliferation and reduces immunoglobulin G (IgG) production [23, 25]. In human monocyte-derived macrophages, RCI directly reduced inflammatory cytokine release, including TNF-α and IL-6 [26]. Mouse models of SLE have shown that RCI treatment significantly reduced levels of splenic follicular and germinal center B cells, as well as T helper and dendritic cells [10, 24]. Taken together, preclinical evidence supports that RCI functions through multiple, direct, non-steroidogenic mechanisms in different immune cell types (Fig. 2). Additional studies are needed to demonstrate a direct immunomodulatory effect of RCI in patients with SLE.

Fig. 2

Mechanisms of action for RCI. GC glucocorticoid, IgG immunoglobulin-G, IL-6 interleukin 6, MC1R melanocortin receptor 1, MC2R melanocortin receptor 2, RCI repository corticotropin injection, TNF tumor necrosis factor

To our knowledge, head-to-head mechanistic studies of RCI versus glucocorticoids have not been performed. While both have anti-inflammatory effects, the molecular mechanisms are different. Glucocorticoids activate the glucocorticoid receptor [27], and RCI activates MCRs [20], likely inducing different signaling mechanisms. How MCR versus glucocorticoid receptor signaling causes different immunomodulatory or anti-inflammatory responses is currently unclear. While RCI does stimulate glucocorticoid release from the adrenal cortex, the cortisol levels are relatively low (as shown in Fig. 1). Therefore, it has been hypothesized that the primary mechanism of action for RCI may be through direct modulation of immune cell activity, as most immune cells express MCRs [23, 25, 28].

Studies on the molecular and cellular mechanisms of RCI are sparse; however, clinical studies have supported that RCI has a unique mechanism of action that differs from glucocorticoids, since RCI has demonstrated efficacy in subjects with refractory inflammatory diseases despite receiving glucocorticoid treatment [29-31]. A recent systematic review comparing the safety of RCI with glucocorticoids in the treatment of rheumatoid arthritis demonstrated that RCI has a more favorable safety profile with fewer AEs compared to glucocorticoids, further suggesting that RCI has a unique mechanism of action beyond its steroidogenic effects [31].

As reported by three recent clinical trials, RCI demonstrated efficacy in patients with SLE that had not responded to standard-of-care therapies, including glucocorticoids (summarized in Table 1) [29, 32–35]. Additionally, two retrospective chart reviews found that RCI improved disease activity scores in patients with SLE that had not responded to standard SLE therapies [36, 37].

Table 1

Summary of recent clinical trials of RCI in the treatment of SLE

Clinical trial	Treatment duration	Treatment regimen	Primary outcomes	Key secondary outcomes	Common AEs in the RCI group (≥ 3% frequency)	SAEs
Askanase et al. [31]	24 weeks	1 mL (80 U) RCI or placebo every other day for 4 weeks, then twice weekly for 20 weeks	Improvement in the proportion of SRI-4 responders at week 16	Reduced CLASI-Activity (p = 0.04) and 28 SJC/TJC (p = 0.02) at week 16	Upper respiratory tract infection, insomnia, headache, hypertension, urinary tract infection, influenza, nasopharyngitis, injection site urticaria, bronchitis, drug hypersensitivity, and hyperglycemia	SLE flare, herpes zoster, and nephrotic syndrome
Fietchner et al. [27]	4 weeks	1 mL (80 U) RCI daily for 10 days, with optional 5-day extension; open label	SLEDAI-2K score significantly reduced from baseline (p < 0.01)	Improved PGA, PtGA, FACIT-Fatigue (p < 0.01) at day 28 Improved ESR and Lupus QoL (p ≤ 0.03) at day 28	Sinus infection and bilateral edema (resolved by end of trial)	None reported
Fietchner et al. [28]	24-week extension after 4 weeks	1 mL (80 U) RCI twice weekly for 6 months; open label	SLEDAI-2K score significantly reduced from baseline at month 3 (p = 0.04) and month 6 (p = 0.0007)	Improved TJC and SJC (p < 0.004) at month 6 BILAG scores all reduced to 0 at month 6, except 1 subject with mild alopecia All subjects discontinued prednisone by month 6	Hematuria at trial onset (resolved by next evaluation)	None reported
Furie et al. [29]	8 weeks	0.5 mL (40 U) RCI daily or 1 mL (80 U) RCI or placebo every other day for 8 weeks, with dose tapering to twice weekly during weeks 5–8	No significant difference between treatment groups in the proportion of RCI responders (defined as hSLEDAI and rash reduction with no BILAG score worsening) at week 4	Improvement in SRI-4 (p = 0.032), hSLEDAI (p = 0.008), BILAG (p = 0.001), CLASI-Activity (p < 0.05) in combined RCI groups at week 8	Weight gain, infections, abdominal pain, back pain, diarrhea, fatigue, fluid retention, irritability, mood swings, and oropharyngeal pain	Moderate chest discomfort/gastroesophageal reflux disease,a false-positive hepatitis C test results and subsequent death from Klebsiella sepsis, moderate hemorrhagic ovarian cyst, and viral infection
Furie et al. [30]	44-week extension after 8 weeks	0.2 mL (16 U), 0.5 mL (40 U), or 1 mL (80 U) RCI twice weekly for 44 weeks; open label	By week 52, 48% of subjects were RCI responders (defined as hSLEDAI and rash reduction with no BILAG score worsening)	Improvements in hSLEDAI, BILAG, CLASI-Activity, TJC/SJC, and PGA at week 52	Pelvic infection and lower abdominal pain	Pelvic abscessa, pyelonephritisa, noncardiac chest pain, SLE flare with hospitalization, and ulcerative keratitis

AEs adverse events, BILAG British Isles Lupus Assessment Group index, CLASI-Activity Cutaneous Lupus Erythematosus Disease Area and Severity Index-Activity, ESR erythrocyte sedimentation rate, FACIT-Fatigue Functional Assessment of Chronic Illness Therapy-Fatigue scale, hSLEDAI hybrid Systemic Lupus Erythematosus Disease Activity Index, Lupus QoL Lupus Quality of Life scale, PGA Physician Global Assessment, PtGA Patient Global Assessment, RCI repository corticotropin injection, SAE serious adverse event, SLE systemic lupus erythematosus, SLEDAI-2K Systemic Lupus Erythematosus Disease Activity Index 2000, SJC swollen joint count, SRI-4 Systemic Lupus Erythematosus Responder Index-4, TJC tender joint count

aSAE determined to be related to RCI treatment

The efficacy and safety of RCI in reducing disease activity, when used as an adjunctive treatment in patients with moderate–severe SLE, was evaluated in a 28-day open-label study in 10 female patients [32], followed by a 6-month extension in 5 female patients [33]. Outcomes included physician (PGA) and patient global assessments (PtGA); SLE Disease Activity Index-2000 (SLEDAI-2K); British Isles Lupus Assessment Group 2004 (BILAG-2004) index; swollen, tender, and total joint counts; Lupus Quality of Life (Lupus QoL) questionnaire; Functional Assessment of Chronic Illness Therapy-Fatigue (FACIT-F) questionnaire; erythrocyte sedimentation rate (ESR); and C-reactive protein (CRP) [32, 33]. Outcomes were assessed weekly for 28 days, then every 3 months for 6 months. The study results showed that SLEDAI-2K scores (primary endpoint) significantly improved from baseline at day 28, month 3, and month 6 [32, 33]. Significant improvements in all clinical outcome measures, except CRP, were observed at day 28, whereas tender joint count, swollen joint count, and the combined total joint count also significantly improved from baseline at month 3 and month 6 [32, 33]. No serious adverse events (SAEs) after RCI initiation were reported in these studies [32, 33]. These results suggested that RCI may significantly and safely reduce SLE disease activity among patients who were not responsive to conventional treatments.

A pilot study [34] and post hoc analyses [35] assessed the efficacy and safety of RCI in patients with glucocorticoid-treated SLE over an 8-week double-blind, placebo-controlled period, and an optional 44-week open-label extension period. Although the proportion of patients showing a response to treatment based on a hybrid SLEDAI (hSLEDAI) measured at week 4 (primary endpoint) did not reach statistical significance, several secondary endpoints were attained (BILAG-2004; Cutaneous Lupus Erythematosus Disease Area and Severity Index [CLASI]-Activity; tender and swollen joint count; PGA). Several post hoc analyses have demonstrated that RCI treatment was associated with improvements in disease activity measures in patients with persistent disease activity despite glucocorticoid treatment [34, 35]. No new safety signals were identified, although the incidence of infections was higher in the RCI group than in the placebo group; the most common treatment-emergent AE after administration of RCI was weight gain [34, 35].

A multicenter, double-blind, randomized, placebo-controlled study [29] evaluated the efficacy and safety of RCI in patients with persistently active SLE despite the use of moderate-dose glucocorticoids. Although the proportion of SLE Responder Index-4 (SRI-4) responders at week 16 (primary endpoint) did not reach statistical significance, there were improvements for subjects treated with RCI versus placebo in the secondary endpoints of 28 swollen joint count/tender joint count and CLASI-Activity scores [29]. Post hoc analyses of data from subjects with high levels of disease activity revealed significantly more SRI-4 responders among those who received RCI versus placebo [29]. RCI treatment resulted in a greater number of BILAG-based Combined Lupus Assessment (BICLA) responders than placebo in a post hoc analysis of the modified intention-to-treat population [29]. Further, cytokine analysis showed that BAFF levels significantly decreased from baseline values in subjects receiving RCI compared to the placebo group [29]. BAFF increases B cell activity and function and is central to the pathophysiology of SLE [38]. Therefore, the reduction of BAFF after treatment of SLE with RCI may contribute to the observed clinical outcomes of reduced disease activity.

Safety results were consistent with the established safety profile of RCI, and no new safety signals were observed [29]. The most common AEs reported by patients treated with RCI were upper respiratory tract infection, insomnia, headache, hypertension, and urinary tract infection; SAEs included SLE flare, herpes zoster, hyperglycemia, and nephrotic syndrome (Table 2) [29]. Notably, more subjects treated with RCI reported hypertension and hyperglycemia, whereas twice as many subjects in the placebo group reported SAEs (Table 2) [29]. No changes in the bone turnover markers N-terminal propeptide of type I collagen (PINP) and C-terminal crosslinking telopeptide of type I collagen (CTX-I) were observed, suggesting that RCI treatment had no adverse effect on bone [29].

Table 2

TEAEs and SAEs reported by Askanase et al. [31] during 16 weeks of treatment with RCI or placebo

	No. (%) of patients
	RCI (n = 86)	Placebo (n = 86)
Any AE	61 (70.9)	55 (64.0)
Most common TEAEs (≥ 3% in either treatment group)
Upper respiratory tract infection	9 (10.5)	1 (1.2)
Insomnia	7 (8.1)	4 (4.7)
Headache	6 (7.0)	5 (5.8)
Hypertension	6 (7.0)	0
Urinary tract infection	6 (7.0)	10 (11.6)
Herpes zoster	4 (4.7)	0
Influenza	4 (4.7)	2 (2.3)
Nasopharyngitis	3 (3.5)	6 (7.0)
Urticaria at the injection site	3 (3.5)	1 (1.2)
Bronchitis	3 (3.5)	0
Hyperglycemia	3 (3.5)	0
Nausea	2 (2.3)	3 (3.5)
Gastroenteritis	1 (1.2)	3 (3.5)
SAEs	4 (4.7)	8 (9.3)
SLE flare	2 (2.3)	1 (1.2)
Herpes zoster	1 (1.2)	0
Nephrotic syndrome	1 (1.2)	0
Appendicitis	0	1 (1.2)
Drug abuse	0	1 (1.2)
Gastroenteritis	0	1 (1.2)
Peritonitis	0	1 (1.2)
Pneumonia	0	1 (1.2)
Pyelonephritis	0	1 (1.2)
Soft tissue infection	0	1 (1.2)

AE adverse event, RCI repository corticotropin injection, SAE serious adverse event, SLE systemic lupus erythematosus, TEAE treatment-emergent adverse event

Post hoc analyses of these clinical trial data [29] further investigated the molecular and cellular biomarkers underlying the effects of RCI on B cell immunomodulation [39]. Data were analyzed in subgroups stratified by disease activity at baseline, comparing results from subjects with SLEDAI-2K ≥ 10 versus SLEDAI-2K < 10 or anti-dsDNA ≥ 15 IU/mL versus anti-dsDNA < 15 IU/mL or from BICLA responders versus BICLA nonresponders [39]. BAFF levels were reduced from baseline with RCI treatment compared with placebo in nearly every subgroup, and time point analyzed [39]. Lower levels of IL-6 were observed in patients treated with RCI versus placebo at most time points across all disease-activity subgroups [39]. RCI treatment decreased numbers of CD19+ B cells in all subgroups at weeks 16 and 24 compared with placebo in patients with high disease activity [39]. RCI-treated subjects with high baseline disease activity showed lower levels of CD19+IgD−CD27−CD95+ atypical activated memory B cells than placebo-treated subjects; similar results were noted in BICLA nonresponders [39]. Elevated levels of CD19+ B cells or CD19+IgD−CD27−CD95+ memory B cells correlate with increased SLE disease activity [40, 41]; therefore, this reduction in B cells with RCI therapy may provide insights into the clinical outcomes observed in the clinical trial and the mechanisms of action of RCI [29]. Analysis of complement levels revealed that, after RCI treatment, C3 and C4 levels increased in subjects with high baseline disease activity. Since complement C3 and C4 are often low in patients with immune-mediated diseases, these results suggest that RCI may restore normality of the complement system in patients with SLE [39].

Patient-reported outcomes from subjects in the aforementioned clinical trial [29] were analyzed using the Lupus QoL questionnaire and the Work Productivity and Activity Impairment (WPAI)-Lupus questionnaire [42]. Post hoc analysis uncovered significant improvements with RCI treatment in quality of life and work productivity, particularly in patients with high disease activity. Compared with placebo, subjects treated with RCI reported significant improvements in the Lupus QoL pain, planning, and fatigue domains and in the domains of WPAI-Lupus percentage impairment while working and percentage work time missed [42].

To further define the effects of RCI in a larger population of patients with SLE, data from week 4 and week 8 of the clinical trial [29] were pooled with those from the pilot study [34]. Analysis of the pooled data revealed a significantly larger reduction from baseline in 28-joint count (tender and swollen) total scores (Fig. 3) and BILAG-2004 total scores (Fig. 4) in subjects receiving RCI than in those receiving placebo.

Fig. 3

Pooled data analysis of 28-joint count (tender and swollen) total scores by visit. RCI repository corticotropin injection. Data were pooled from a recent clinical trial (Askanase et al. [29]) and a pilot study (Furie et al. [34]). Symbols represent mean change ± SEM. Data were analyzed using analysis of covariance models with the change from baseline as the dependent variable, treatment as the factor, and baseline value of the corresponding endpoint as the covariate. Data were adjusted for the stratification variables used for randomization, location (US and outside the US), and prednisone equivalent dose (≤ 20 and > 20 mg/day)

Fig. 4

Pooled data analysis of BILAG-2004 total scores by visit. BILAG-2004 British Isles Lupus Assessment Group-2004 index, RCI repository corticotropin injection. Data were pooled from a recent clinical trial (Askanase et al. [29]) and a pilot study (Furie et al. [34]). Symbols represent mean change ± SEM. Data were analyzed using analysis of covariance models with the change from baseline as the dependent variable, treatment as the factor, and baseline value of the corresponding endpoint as the covariate. Data were adjusted for the stratification variables used for randomization, location (US and outside the US), and prednisone equivalent dose (≤ 20 and > 20 mg/day)

Pooled data analyses also demonstrated greater reductions from baseline in SLEDAI (SLEDAI-2K and hSLEDAI), CLASI-Activity, and PGA scores in the RCI group compared with the placebo group (Table 3). A greater proportion of SRI-4 and BICLA responders were observed with RCI treatment compared with placebo (Table 4).

Table 3

Additional clinical assessments from pooled data analysis

	RCIweek 4 (n = 109)	Placeboweek 4 (n = 96)	LS mean difference (95% CI)	p valuea	RCIweek 8 (n = 109)	Placeboweek 8 (n = 96)	LS mean difference (95% CI)	p valuea
SLEDAIb (range 0–105) change from baseline, mean (SD)	− 2.0 (3.0) n = 108	− 1.0 (2.0) n = 93	− 0.3 (− 1.1 to 0.4)	0.37	− 3.0 (4.0) n = 105	− 2.0 (3.0) n = 94	− 0.74 (− 1.7 to 0.2)	0.12
CLASI-Activity (range 0–70) change from baseline, mean (SD)	− 2.0 (4.0) n = 105	− 1.0 (3.0) n = 93	− 0.7 (− 1.4 to 0.1)	0.09	− 3.0 (4.0) n = 102	− 2.0 (3.0) n = 94	− 0.7 (− 1.6 to 0.1)	0.08
PGA (range 0–100) change from baseline, mean (SD)	− 15.8 (17.14) n = 106	− 11.7 (15.6) n = 90	− 3.7 (− 8.1 to 0.7)	0.10	− 23.3 (19.3) n = 105	− 18.9 (16.0) n = 92	− 3.7 (− 8.3 to 0.9)	0.12

Data were pooled from a recent clinical trial (Askanase et al. [31]) and a pilot study (Furie et al. [29])

CLASI Cutaneous Lupus Erythematosus Disease Area and Severity Index, hSLEDAI hybrid Systemic Lupus Erythematosus Disease Activity Index, LS least squares, PGA Physician Global Assessment, RCI repository corticotropin injection, SLEDAI Systemic Lupus Erythematosus Disease Activity Index

aEndpoints were analyzed using analysis of covariance models with the change from baseline as the dependent variable, treatment as the factor, and baseline value of the corresponding endpoint as the covariate. Data were adjusted for the stratification variables used for randomization, location (US and outside the US), and prednisone equivalent dose (≤ 20 and > 20 mg/day)

bPooled results included hSLEDAI [29] and SLEDAI-2K data [31]

Table 4

Results of pooled data analysis for clinical responders

	RCIweek 4 (n = 109)	Placeboweek 4 (n = 96)	Odds ratioa (95% CI)	p valuec	RCIweek 8 (n = 109)	Placeboweek 8 (n = 96)	Odds ratio (95% CI)	p valueb
SRI-4 responders,c No. (%)	27 (24.8)	17 (17.7)	1.53 (0.77–3.02)	0.23	44 (40.4)	33 (34.4)	1.28 (0.73–2.26)	0.38
BICLA responders,d No. (%)	37 (33.9)	21 (21.9)	1.84 (0.98–3.43)	0.11	44 (40.4)	28 (29.2)	1.64 (0.92–2.94)	0.14

Data were pooled from a recent clinical trial (Askanase et al. [31]) and a pilot study (Furie et al. [29])

BICLA British Isles Lupus Assessment Group-Based Combined Lupus Assessment, BILAG British Isles Lupus Assessment Group, PGA Physician Global Assessment, RCI repository corticotropin injection, SLEDAI-2K Systemic Lupus Erythematosus Disease Activity Index 2000, SRI-4 Systemic Lupus Erythematosus Responder Index-4

aOdds ratios were calculated by the formula: [(number of responders in RCI group) × (number of nonresponders in placebo group)]/[(number of nonresponders in RCI group) × (number of responders in placebo group)]

bp value is from the Cochran–Mantel–Haenszel test, adjusted for the stratification variables used for randomization, location (US and outside the US), and prednisone equivalent dose (≤ 20 and > 20 mg/day)

cSRI-4 responders were defined as subjects with a 4-point reduction from baseline in SLEDAI-2K, no new BILAG A and no more than 1 new BILAG B organ domain scores compared with baseline, and no worsening in PGA (≥ 10% increase from baseline). Subjects who did not provide data were classified as nonresponders

dBICLA responders were subjects with ≥ 1 improvement gradation in baseline BILAG scores in all body systems with moderate or severe disease activity at entry; no new BILAG A scores or no more than one new BILAG B score; no worsening of total SLEDAI-2K score from baseline; no significant deterioration (≥ 10% increase from baseline) in PGA; and no treatment failure. Subjects who did not provide data were classified as nonresponders

Discussion

This article provides a review of the recently published data on RCI in SLE. The results of pooled data from a pilot study and a clinical trial revealed early improvement in the 28-joint counts (total and swollen) and BILAG-2004 scores in patients with SLE receiving RCI, as well as greater proportions of SRI-4 and BICLA responders in the RCI group compared with placebo, supporting a role for RCI in the treatment of SLE.

No new safety signals were observed in these clinical trials, comparable to composing the long-established safety profile of RCI, and few SAEs were observed [29, 32–37]. Treatment-related SAEs included chest discomfort/gastroesophageal disease, pelvic abscess, and pyelonephritis [34, 35]. A 26-week study of RCI for the treatment of rheumatoid arthritis in 259 subjects reported a similar low frequency of SAEs: 1 case each of chest pain, craniocerebral injury, and pneumonia [31, 43]. The acceptable safety profile of RCI is advantageous when considering patients with refractory SLE who require additional therapies or increased doses of corticosteroids.

RCI likely derives its efficacy via activation of all five MCRs [20, 32, 37]. In vitro studies have found that treatment with RCI directly reduced cytokine release from macrophages [26] and inhibited B cell proliferation [23]. In the clinical trial, patients with SLE treated with RCI had reduced levels of IL-6 and BAFF [39]. Elevated levels of IL-6 in patients with SLE result in systemic and local inflammatory effects, including induction of leukocyte differentiation (B and T cells) and proliferation (T cells and macrophages), autoantibody production, and increased SLE disease activity [44]. Dysfunctional BAFF signaling underlies mouse models of SLE, in which increased BAFF levels cause an SLE-like autoimmune disease, and reduced BAFF levels cause immunodeficiency [38]. BAFF is primarily secreted by macrophages, dendritic cells, and neutrophils and activates multiple BAFF-receptor subtypes expressed on B cells, increasing their maturation and survival [38]. Notably, treatment of patients with SLE with RCI reduced total B cells (CD19+) and atypical activated memory B cells (CD19+IgD−CD27−CD95+) [39], which correlate with SLE disease activity [39-41]. Together, these data suggest that RCI effects on IL-6 and BAFF signaling may reduce activated B cells [29, 39].

While glucocorticoids are central to the treatment of SLE, the long-term side effects, such as hypertension, osteoporosis, diabetes, and their contribution to organ damage accrual, limit their use [16-18]. Despite standard treatment, many patients experience continued disease activity and SLE flares and require additional therapies. Patients with SLE showed improvement in disease activity scores and clinical outcomes after treatment with RCI in addition to stable doses of glucocorticoids (7.5–30 mg prednisone equivalent) [29, 32–37], suggesting that the effectiveness of RCI is due to a mechanism that is additive to or separate from its classical steroidogenic mechanism of action via MC2R activation in the adrenal cortex. Additionally, RCI may have a steroid-sparing effect, as reported by Fietchner et al. [33] and Li et al. [37]. While data are limited, the current review supports the positive effects of RCI in the treatment of SLE and substantiates the need for a larger clinical trial to further define the role of RCI in SLE and to assess its potential to be a safer alternative to the current glucocorticoid regimens.

Conclusions

There are unmet needs in the treatment of SLE, especially for patients who continue to experience flares despite receiving standard-of-care therapies. Currently, there is no defined role for RCI in SLE clinical guidelines. The data presented here suggest that RCI may be a safe and effective adjunctive treatment for patients with refractory SLE. The unique mechanism of action of RCI provides an alternative treatment option for patients with insufficient disease control using current standard-of-care treatments. Given its few treatment-related SAEs, positive efficacy results, and distinct mechanisms of action, clinicians may consider using RCI as an early-line therapy, particularly for patients with refractory SLE.

Many patients with systemic lupus erythematosus (SLE) have refractory disease that is not responsive to standard-of-care therapies, such that alternative treatments are needed.

Repository corticotropin injection (RCI; Acthar® Gel) is a naturally sourced complex mixture of adrenocorticotropic hormone analogs and other pituitary peptides indicated for the treatment of SLE that has anti-inflammatory and immunomodulatory effects beyond its steroidogenic effect.

The clinical trial results and the pooled data analysis presented here demonstrate that RCI treatment provided early reduction in the SLE Disease Activity Index (SLEDAI), the British Isles Lupus Assessment Group 2004 (BILAG-2004) index, and swollen and tender joint counts.

Treatment with RCI showed an acceptable safety profile with generally mild–moderate adverse events and few serious adverse events.

The data reported in these clinical trials suggest that RCI may be safe and effective for the treatment of moderate–severe refractory SLE.