Methods. This prospective US multicenter trial of leuprolide acetate 1-month depot (7.5–15 mg) for central precocious puberty utilized an open-label treatment period, long-term follow-up, and adult callback. Forty-nine females <9 years old with Tanner breast stage ≥2 before 8 years and 6 males <10 years old with Tanner genital stage ≥2 before 9 years with stimulated LH ≥10 IU/L and bone age advance ≥1 year were enrolled. Results. Subjects were treated for years. Mean peak GnRH-stimulated LH and FSH were prepubertal after the first dose and remained suppressed throughout treatment. During treatment, mean estradiol decreased to the limit of detection and mean testosterone decreased but remained above prepubertal norms. During posttreatment follow-up ( years), all patients achieved a pubertal hormonal response within 1 year and menses were reported in all females ≥12 years old. No impairment of reproductive function was observed at adulthood (mean age: 24.8 years).
1. Introduction
Children with central precocious puberty (CPP) prematurely develop pubertal pulsatile release of gonadotropin-releasing hormone (GnRH), leading to an increase in gonadotropin and sex steroid levels, development of secondary sexual characteristics, advancement of bone age (BA), and consequent reduction in adult height (AH) [1]. Treatment goals include hormonal suppression, cessation of development of secondary sex characteristics, halting or preventing menarche, and preservation of AH. If left untreated, children with CPP can also face psychological challenges resulting from premature physical maturation that contrasts with their immature emotional development [2].
GnRH analogs (GnRHa) have been the standard of care for CPP for over 15 years [1]. Continuous exposure to GnRHa desensitizes pituitary gonadotroph receptors and suppresses luteinizing hormone (LH) and follicle stimulating hormone (FSH) secretion. Efficacy of various GnRHa in CPP has been established [3‐14], but truly long-term studies are limited, particularly for leuprolide. Furthermore, most GnRHa studies have not utilized sensitive gonadotropin assays that can accurately assess the extent of hormonal suppression. The objectives of this open-label treatment study of leuprolide acetate 1-month depot and long-term observational extension study were to evaluate the suppression of the pituitary-gonadal axis and the clinical sexual characteristics during treatment and to examine the long-term impact on the growth pattern, AH, and reproductive function of children treated for CPP. Initial results from the treatment period led to FDA approval of leuprolide acetate 1-month depot for the treatment of CPP. Here we report hormonal suppression during the treatment period, safety, recovery of hormone secretion, and long-term reproductive outcomes. A separate paper reports the auxological outcomes [15].
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2. Patients and Methods
2.1. Patients
All patients were naïve to GnRHa therapy. Females with Tanner breast stage ≥2 before 8.0 years old and chronological age (CA) <9.0 years at initiation of therapy and males with Tanner genital stage ≥2 before 9.0 years and CA <10.0 years were eligible. Inclusion criteria included GnRH-stimulated peak LH ≥10 IU/L, BA advance ≥1 year beyond CA by Fels Method [16], no prior treatment with GnRHa, no history of central nervous system irradiation, and anticipated treatment for ≥1 year. Patients had an MRI of the brain, hypothalamus, and pituitary prior to the initiation of therapy. Institutional review board approval was obtained at each site, and written informed consent was provided by the subject and the subject's parent or legal guardian prior to any study-related procedures.
2.2. Methods
This study at 9 US centers consisted of an open-label treatment period with leuprolide acetate 1-month depot and a long-term follow-up period. Clinical sexual characteristics, LH, FSH, and sex steroids during and after treatment were assessed. After a screening visit, treatment period study visits occurred at week 0, 4, 8, 12, 24, 36, and 48, and then every 24 weeks. Study visits included a physical examination with Tanner staging, weight, and triplicate heights by stadiometer. Laboratory assessments included GnRH stimulation testing to determine basal and peak stimulated LH and FSH using Factrel 100 μ g IV with blood samples at 0, 20, 40, 60, and 90 minutes. LH and FSH were measured by dissociation-enhanced lanthanide fluorescence immunoassay (DELFIA), with a sensitivity of 0.15 IU/L for LH and 0.5 IU/L for FSH (University of Pittsburgh Children's Hospital; Pittsburgh, PA). Estradiol (or testosterone) levels were obtained at 0 and 90 minutes and were measured by radioimmunoassay (University of Pittsburgh Children's Hospital, Pittsburgh, PA) with a lower limit of 18.36 pmol/L (5 pg/mL) for estradiol and 0.347 nmol/L (10 ng/dL) for testosterone. Hematology and chemistry analyses were performed by Covance (formerly Scicor, Indianapolis, IN). Adverse events were assessed at each study visit. Treatment-emergent adverse events were coded using the Coding Symbols for Thesaurus of Adverse Reaction Terms (COSTART) dictionary.
Leuprolide acetate 1-month depot was started at a dose of at least 300 μ g/kg (7.5, 11.25, or 15.0 mg) administered intramuscularly (IM) every 28 days. Incremental dose adjustments of 3.75 mg were made at each clinic visit for specific criteria or for weight increase. Doses were increased at the week 8 study visit if the peak LH value from the week 4 GnRH stimulation test exceeded 1.75 IU/L. At week 12 and beyond, doses were to be increased for peak LH value >1.75 IU/L, testosterone >0.347 nmol/L (10 ng/dL), estradiol >18.36 pmol/L (5 pg/mL), or menstrual bleeding or spotting. Therapy was discontinued at an age appropriate for reinitiation of puberty at the discretion of the investigator.
After discontinuation of treatment, patients could enter a long-term observational follow-up study with visits occurring every 6 months (1 month equal to 28 days) until laboratory measurements reached pubertal levels, then annually until the age of 21 years. Follow-up study visits included Tanner staging, height and weight, and a questionnaire on menstrual history. Basal and stimulated gonadotropins and estradiol/testosterone were measured at each visit until a pubertal response was observed; thereafter only basal levels were measured. Pubertal response was defined by all of the following: females, peak LH >6 IU/L, peak FSH ≥5 IU/L, estradiol ≥55.1 pmol/L (15 pg/mL); males, peak LH >10 IU/L, peak FSH ≥2.5 IU/L, testosterone ≥2.60 nmol/L (75 ng/dL). Menses was defined as ≥3 consecutive days of uterine bleeding. A final visit at adulthood was conducted to assess adult height and reproductive function by questionnaire and pelvic ultrasound.
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2.3. Statistics
Clinical suppression was defined as an improvement or no change in Tanner staging. The development of clinical sexual characteristics posttreatment was defined as an increase in Tanner stage from the end of treatment. Patients who entered the study at Tanner stage 5 were not included in these analyses. Summary statistics were calculated for age, menses, adverse events, and gonadotropin and sex steroid levels. For levels below the detection thresholds, calculations substituted the relevant threshold value. Standard deviations or ranges (parentheses) are reported in text. Significance tests for change versus no change were performed using paired t-tests.
3. Results
Subjects were treated for an average of 3.9 ± 2.0 years and followed for an average posttreatment period of 3.5 ± 2.2 years.
3.1. Baseline Characteristics
Fifty-five patients, naïve to GnRHa treatment, met the inclusion criteria of peak LH ≥10 IU/L and BA advance ≥1 year and entered the study. Subject demographics and baseline characteristics for the female () and male () patients are summarized in Table 1. Twenty patients (18/49 females and 2/6 males) had a history of neurological disorder, including head trauma (), seizure disorder (), suprasellar cyst (), meningitis (), hypothalamic tumor, hamartoma, spina bifida, hydrocephalus, developmental delay, and hypotonia (all ). The remaining patients (35/55) were diagnosed with idiopathic CPP.
Table 1
Subject demographics and baseline characteristics.
Characteristic
Female subjects
Male subjects
Race, n
Caucasian
30
4
African American
11
0
Asian
0
1
Hispanic
8
1
Age, years
Mean (SD)
7.3 (1.9)
7.9 (2.0)
Range
1.2–9.4a
4.1–9.5
Weight, kg
Mean (SD)
33.6 (9.72)
32.4 (8.96)
Range
13.0–52.2
19.9–41.8
Height, cm
Mean (SD)
131.6 (15.0)
134.4 (18.1)
Range
84.6–154.7
106.7–156.8
Height standardized score
Mean (SD)
1.5 (1.29)
1.4 (1.75)
Range
−1.4–3.4
−0.4–4.3
Tanner stage, n
Breast/genitalia I
1b
0
II
9
2
III
25
3
IV
13
1
V
1
0
Basal LH, IU/L
Mean (SD)
2.0 (2.06)
1.6 (0.77)
Range
<0.15–11.1
0.73–2.6
Peak LH, IU/L
Mean (SD)
36.7 (21.8)
21.2 (9.1)
Range
12.0–119.2
13.5–38.8
History of menstrual bleeding, n
No
36
—
Yes
12
—
aStart of study drug was delayed beyond 9 years old in one girl.
bA one-year-old patient was enrolled in the trial with breast Tanner stage I based on qualifying peak stimulated LH (84.7 IU/L) and E2 (90 pg/mL).
Mean peak GnRH-stimulated LH was 35.1 ± 21.32 IU/L at baseline. The peak LH occurred at the 20- or 40-minute blood draw in 51/55 subjects, and in all patients the diagnostic threshold of 10 IU/L was surpassed at both timepoints. Mean basal LH was 1.98 IU/L (range: <0.15–11.1); 6/55 pretreatment basal LH levels were <0.5 IU/L. Peak LH and basal LH were moderately correlated (), but peak LH was more strongly correlated with peak FSH (). Serum estradiol levels at 0 and 90 minutes were undetectable (<18.36 pmol/L (5 pg/mL)) in 16/49 and 21/49 females, respectively. The 0- and 90-minute mean estradiol concentrations were 56.9 pmol/L (15.5 pg/mL) and 56.2 pmol/L (15.3 pg/mL), respectively. In males, 0- and 90-minute mean testosterone concentrations were 6.9 nmol/L (199.8 ng/dL) and 12.1 nmol/L (347.7 ng/dL), respectively ().
3.2. Treatment Period: Females
Mean age entering the study was 7.3 ± 1.9 years, mean age at discontinuation of treatment was 11.1 ± 1.1 years (7.3–13.3), and mean treatment duration was 3.8 years (0.23–9.8). Mean peak GnRH-stimulated LH and FSH in females declined into the prepubertal range after the first dose and remained suppressed throughout treatment (Figure 1). Mean peak LH decreased to 0.75 IU/L (<0.15–3.9) by week 4 and numerically decreased after week 12 (Figure 1(a)). During treatment, 8/49 females had a peak stimulated LH value ≥1.75 IU/L. Mean peak FSH decreased from 14.0 IU/L at baseline to 0.9 IU/L (<0.5–3.19) by week 4 then numerically increased but remained <1.7 IU/L (Figure 1(b)).
Figure 1
Mean peak stimulated LH (a, log scale) and FSH (b) for females during the treatment and follow-up periods. Mean concentrations for peak LH and FSH at each study visit are displayed adjacent to the respective points. Maximum individual concentrations for peak LH at each study visit are indicated on panel (a). The number of subjects at each study visit is indicated beneath panel (b).
×
Mean basal LH in females decreased from 2.0 IU/L at baseline to 0.48 IU/L (<0.15–1.82) at week 4 and numerically declined during the treatment period (Figure 2(a)). Mean basal FSH decreased from 4.1 IU/L at baseline to 0.8 IU/L (0.15–1.97) by week 4 and was <1.5 IU/L for the duration of treatment (Figure 2(b)). Mean basal estradiol decreased from 57.28 pmol/L (15.6 pg/mL) at baseline to the lower limit of detection (18.36 pmol/L (5.0 pg/mL)) by study week 4. Almost all postbaseline estradiol levels (99.2%) were below the threshold of detection.
Figure 2
Mean basal LH (a, log scale) and FSH (b) for females during the treatment and follow-up periods. Mean values for basal LH and FSH are displayed adjacent to the respective points. Maximum individual concentrations for basal LH at each study visit are indicated on panel (a). The number of subjects at each study visit is indicated beneath panel (b).
×
The mean peak LH : peak FSH ratio in females was 2.6 (1.0–6.2) at baseline, decreased to 0.9 (0.2–3.0) at week 4, and trended downward during the course of treatment (Figure 3(a)). The mean ratio was ≤0.5 from the second year onward. The mean basal LH : basal FSH ratio numerically decreased as treatment progressed (Figure 3(b)), coordinate with the opposite trends in basal LH and FSH.
Figure 3
Mean peak LH : peak FSH ratio (a) and mean basal LH : basal FSH ratio (b) for females during the treatment period and at the 6 month follow-up visit. The mean ratios at each study visit are displayed adjacent to the respective points. The number of subjects at each study visit is indicated beneath panel (b).
×
Regression or no progression of breast Tanner stage was observed at week 4 in 81.8% of females. Over 4 years, the percentage of patients with regression or no progression of breast stage from baseline at each visit ranged from 66.7% to 90.6%. Uterine bleeding or spotting occurred in 15 females (31%) during the first 4 weeks of treatment (8/15 with prior history of bleeding). Those 15 girls exhibited a higher mean serum basal estradiol at baseline compared with the 33 girls who did not have subsequent bleeding (83.2 ± 53.2 pmol/L (22.7 ± 14.5 pg/mL) versus 44.1 ± 58.6 pmol/L (12.0 ± 16.0 pg/mL), ). They also had higher baseline basal LH levels (3.46 ± 2.95 IU/L versus 1.41 ± 1.08 IU/L, ). Uterine bleeding or spotting after week 4 was reported in 7 females, all in the absence of detectable estradiol.
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3.3. Treatment Period: Males
In males, mean start age was 7.9 ± 2.0 years, mean age at discontinuation was 12.4 ± 1.2 years (11.1–14.1), and mean duration was 4.6 years (1.9–7.9). Mean peak LH decreased from 21.2 IU/L at baseline to 0.7 IU/L at week 4. During the treatment period, one male had a peak stimulated LH value ≥1.75 IU/L. Mean peak FSH decreased from 5.6 IU/L at baseline to 0.5 IU/L at week 4. Comparable to the females, mean basal LH was suppressed to 0.5 IU/L at week 4 and was ≤0.4 IU/L for the duration of treatment. Mean basal FSH in males decreased from 2.4 IU/L at baseline to 0.5 IU/L by week 4 and was ≤0.8 IU/L during the treatment period. Mean basal testosterone decreased from 6.93 nmol/L (199.8 ng/dL) at baseline to 0.62 nmol/L (17.8 ng/dL) at week 4 and never exceeded 0.84 nmol/L (24 ng/dL) during treatment, but 5/6 males had treatment levels above the prepubertal threshold/limit of detection of 0.35 nmol/L (10 ng/dL). Testosterone in 3 males was intermittently above 1.04 nmol/L (30 ng/dL), with a maximum testosterone of 1.94 nmol/L (56 ng/dL). Regression or nonprogression of genital Tanner stage was observed in 5/6 males. Progression from 2 to 3 occurred in the male with the highest testosterone level and a transient peak LH ≥1.75 IU/L.
3.4. Dose Modifications and Adverse Events during Treatment
The dose was increased in eight patients. Five were females with stimulated LH >1.75 IU/L, including the 2 youngest subjects (1 year olds, one with a hamartoma). The dose was also increased in the male patient with elevated testosterone, peak LH >1.75 IU/L, and Tanner stage progression. All 6 patients suppressed to peak stimulated LH ≤1.75 IU/L after the first year. In 2 additional females, a dose adjustment was made due to weight increase.
Long-term treatment with leuprolide acetate 1-month depot was well tolerated. There were no clinically relevant changes in hematology or chemistry values. Adverse events reported in ≥5% of patients possibly or probably related to study drug are shown in Table 2. Eleven patients had >1 adverse event related to injections, including reported pain (), reaction (), inflammation (), and/or edema (). None of the injection-site adverse events were serious or led to premature discontinuation. Two serious events possibly related to study drug occurred, a severe asthma exacerbation and an increase in size of a preexisting optic glioma with deteriorating vision. There was a death during the study considered unrelated by the investigator, a cardiopulmonary arrest following respiratory infection. Nine patients discontinued study drug prematurely for reasons including patient request to leave the study, noncompliance with visit schedule, lost to follow-up, and the death described above. No patients withdrew due to injection reaction or failure to achieve adequate suppression.
Table 2
Adverse events possibly or probably related to study drug in ≥5% of subjects.
Number of subjects (%)
COSTART term
Any adverse event
34 (62)
Emotional lability
10 (18)
Injection site pain
8 (15)
Headache
6 (11)
Acne
5 (9)
Pain
4 (7)
Vasodilatationa
4 (7)
Growth retardedb
4 (7)
Vaginitis
4 (7)
Injection site reactionc
3 (5)
Menstrual disorderd
3 (5)
Weight gain
3 (5)
aVasodilation = flushing and/or hot flashes.
bGrowth retarded = slowing of growth.
cInjection site reaction = injection site reaction, injection site hypersensitivity, edema, mass, pain, cyst, atrophy, fibrosis, rash, necrosis, inflammation, abscess, hematoma, granuloma, induration.
dMenstrual disorder = menstrual spotting, vaginal bleeding, and cramping.
3.5. Posttreatment Follow-Up Period
Thirty-five females entered the posttreatment follow-up period. Most (66.7%) had breast stage advance by the first posttreatment visit. Tanner breast stage 5 was achieved by 78% of females within the first 3 years of follow-up and in 100% of female patients within the 5 year follow-up. Mean peak LH and FSH concentrations in females increased to 21.3 IU/L (0.28–52.9) and 10.4 IU/L (1.2–18.4), respectively, at the 6 month visit (Figure 1). Mean peak LH : peak FSH ratio rose to 1.9 ± 0.9 IU/L at the 6 month visit (Figure 3(a)). All females achieved a pubertal GnRH-stimulated response within 1 year of treatment discontinuation. Mean basal LH increased to 3.4 IU/L (<0.15–9.3) by 6 months posttreatment and to 11.7 IU/L in the females who still remained in the study at the 5 year follow-up (Figure 2(a)). Mean basal FSH increased to 5.4 IU/L (0.95–9.3) in females at 6 months and was 5.8 IU/L at the 5 year follow-up (Figure 2(b)). Mean basal LH : basal FSH ratio rose to 0.6 ± 0.3 by the 6 month visit (Figure 3(b)) and further increased during reestablishment of puberty, reaching 1.8 ± 1.3 at the 5 year visit. Mean estradiol increased to 60.4 pmol/L (16.4 pg/mL) by 6 months and to 281.7 pmol/L (76.7 pg/mL) by 5 years.
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Menses were reported for 27/32 female patients during the follow-up period. The remaining 5 patients were less than 12 years of age when they discontinued from long-term follow-up. Mean time from discontinuation to first menses was 1.5 ± 0.5 years (0.5–2.5 years), and the mean age was 12.9 ± 0.9 years (11.6–14.9 years). In those patients who had menses prior to treatment (), the average time to resumption of menses was 1.4 ± 0.5 years (0.5–2.1 years), and for those patients without menses prior to treatment (), elapsed time was 1.6 ± 0.5 years (0.5–2.5 years).
Five males entered the follow-up study, 4 of whom showed Tanner genital stage advance by 6 months. Mean peak LH and FSH rose to 16.0 IU/L and 8.7 IU/L, respectively, mean basal LH and FSH were 2.8 IU/L and 4.4 IU/L, respectively, and basal testosterone was 6.7 nmol/L (194 ng/dL) at 6 months. All 5 males achieved the defined pubertal response by 1 year posttreatment.
3.6. Adult Follow-Up
Data to assess reproductive function, including menstrual cycles, pregnancy, and reported history of ovarian cysts, were collected in a post-study survey of 20 girls who reached adulthood (ages 18–26). Menstrual cycles were reported to be normal in 80% of women and use of birth control medication was reported in 7/20 patients. Ovarian volumes were assessed by ultrasound in 11 patients and revealed normal ranges; only small follicular cysts were reported, including in the 2 females with reported polycystic ovarian syndrome. Twelve pregnancies were reported in 7/20 patients, including multiple pregnancies for 4. There were 6 live births, 5 spontaneous or elective terminations, and 1 ongoing pregnancy; no stillbirths were reported. Four out of 4 women who attempted to become pregnant became pregnant. Two women who reported difficulty conceiving had achieved live births.
4. Discussion
Treatment with leuprolide acetate 1-month depot has been routine therapy for CPP for over 15 years. This report from the initial US multicenter trial provides details regarding suppression of gonadotropins and sex steroids during treatment, hormonal and clinical progression during long-term posttreatment follow-up, and review of reproductive health at adulthood.
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During the treatment period, on average 4 years, leuprolide acetate depot rapidly controlled clinical signs of puberty and suppressed hormones to prepubertal levels. In females, mean peak LH dropped by over 97% after the first injection. However, the protocol called for an increase in dose for any peak LH >1.75 IU/L, a rigorous outcome measure equivalent to prepubertal means (17, 18, 21, 22). This resulted in dose increases in the first year of treatment in 6 subjects, but no stimulated LH levels surpassed this cutoff after the 48 week visit. It is unknown whether that outcome was solely attributable to duration of treatment or partially to increases in dose in some patients. Overall, mean peak LH in females trended downward during therapy, whereas mean peak FSH trended slightly upward. As a consequence, the peak LH : peak FSH ratio gradually declined during therapy, returning subjects to the gonadotropin pattern seen in normal prepubertal girls.
At baseline, the age, sex ratio, and Tanner stage were typical of patients with CPP. However, the conservative entry threshold of peak LH ≥10 IU/L, plus the BA advance criterion, likely excluded some patients who in current clinical practice might be treated. Thus the cohort might have been more advanced in puberty than in other CPP studies, as the mean peak LH of 36 IU/L in females and BA advance of approximately 3 years demonstrate. The relatively advanced puberty may explain the high percentage of girls with menses prior to treatment (25%), which in turn could be linked to the proportion of girls with bleeding following estrogen withdrawal in the first month (31%). Girls with bleeding during therapy had higher baseline estradiol and LH levels; however, a surprising number of girls showed continued spotting after hormonal suppression was established.
This study was initiated when GnRH for stimulation testing was still available in the US. The peak LH levels at diagnosis of CPP were observed in almost all subjects within 40 minutes after GnRH injection, and with highly consistent levels among timed samples, supporting the concept that stimulation testing using multiple samples or for extended duration is unnecessary [17‐19]. Basal LH has been recommended as a surrogate for peak LH in diagnosis of CPP [20, 21]; in this study basal LH correlated modestly with peak LH at diagnosis, although in some subjects the diagnostic peak LH was not associated with a clearly pubertal basal LH. Thus, basal LH has reasonable sensitivity as a screen and perhaps in most instances is adequate to diagnose CPP [22], while stimulation testing (now using aqueous leuprolide acetate) may sometimes be required and may help differentiate FSH-predominant nonprogressive premature thelarche from LH-predominant CPP.
The DELFIA LH and FSH assays utilized in the study are highly sensitive and widely used double-antibody assays [23]. The rigorous lower LH detection limit of 0.15 IU/L was not relevant at the relatively high concentrations of basal and peak LH at diagnosis. However, as treatment progressed, increasing percentages of basal and peak LH levels were at or below the threshold of detectability. Accordingly, the mean values for basal and peak LH during therapeutic monitoring are possibly overstated, as many of the true levels were likely less than the threshold 0.15 IU/L used to calculate the means.
The standard for monitoring the early phase of GnRHa therapy has been the observation of clinical parameters, especially pubertal staging and growth rate, and assessment of peak LH. In the US, the latter now requires blood obtained after aqueous leuprolide injection or following leuprolide acetate depot itself [17]. For convenience, some practitioners monitor therapy using unstimulated basal LH levels. Our data demonstrate that this practice should be used cautiously, particularly in the first year of therapy, when basal LH levels are routinely elevated above prepubertal norms [20, 21, 24]. Like peak LH, basal LH showed a downward trend during treatment, with the mean falling to approximately 0.3 IU/L by 24 weeks. However, many subjects with suppressed peak LH exhibited basal LH concentrations in the 0.5–1 IU/L pubertal range.
Despite the high peak LH threshold required for study entry, 33% of girls did not have detectable estradiol at baseline, demonstrating its limited utility for diagnosis of CPP. This is plausibly attributable to assay threshold or to physiologic variability. The study RIA measured to 18.36 pmol/L (5 pg/mL), whereas estradiol can now be measured by MS/MS to approximately 7.34 pmol/L (2 pg/mL). Even that threshold is well above normal prepubertal levels [25], and as a consequence estradiol was not detectable during the treatment phase of our study. Estradiol measurement during therapy can at best confirm complete treatment failure.
The testosterone RIA in our study measured to 0.347 nmol/L (10 ng/dL), close to the prepubertal threshold reported for MS/MS. For reasons of assay sensitivity, testosterone can generally be considered a better screen of CPP (in combination with confirmatory LH) in males compared with estradiol in females. Testosterone levels fell steeply after the first injection, but 5/6 males intermittently exceeded the prepubertal norm, despite suppressed LH levels. This presents a clinical management dilemma whether to accept marginally detectable testosterone levels, which may not respond to more aggressive dosing. Alternative explanations for incompletely suppressed testosterone include assay inaccuracy in the lower range, testosterone of adrenal origin, or persistent gonadal testosterone secretion despite apparent gonadotropin suppression.
After discontinuation of treatment, subjects were followed for an average of 3.5 years. All subjects had resumption of the pubertal hypothalamic-pituitary-gonadal axis within 12 months, and most by 6 months, with LH, FSH, and estradiol or testosterone all returning to pubertal levels. The resumption of puberty was also evidenced by progression of Tanner stages in both females and males. In females, the mean time to onset of menses was approximately 1.5 years, consistent with previous studies in females treated with GnRHa, in which the interval ranged from 2 to 61 months, with an average of approximately 16 months [6, 13, 26‐28]. Furthermore, the mean age at the onset of menarche or re-menarche in our study was 12.9 years, which is consistent with the average age of menarche of 12.53 years in the US [29]. Reassuringly, all females over 12 years old reported menses by the end of the follow-up phase.
At callback of adult subjects we did not find impairment in reproductive function, consistent with previous studies [6, 8, 13, 30]. A study by Heger et al. reported 12 pregnancies in 34 women who wished to have children [6]. In the current study, 7 women reported a total of 12 pregnancies. Although definitive conclusion regarding long-term reproductive function is weakened by the limited number of patients that could be located at callback more than a decade after the end of treatment, the universal normalcy of hormone levels and menses during the follow-up period and lack of reported problems in adulthood are all reassuring.
In summary, treatment with leuprolide acetate 1-month depot effectively suppressed the GnRH axis for the duration of therapy in all subjects. It was well tolerated, with no clinically relevant injection-site reactions in any of the 55 subjects. Most subjects exhibited recovery to pubertal hormone levels 6 months after discontinuation of treatment, and mean onset of menses was 1.5 years after discontinuation. Long-term follow-up and adult callback revealed that the interruption of the GnRH axis in children with CPP did not impair reproductive function in adulthood.
Disclosure
E. Kirk Neely has received grant/research support from and has been a consultant and scientific advisory board member for Abbott. Peter A. Lee has been a consultant for Abbott and Novo Nordisk with grants from Abbott, Eli Lilly, Novo Nordisk, Pfizer, and Ipsen. Clifford A. Bloch has been a consultant to Abbott. Lois Larsen, Di Yang, Cynthia Mattia-Goldberg, and Kristof Chwalisz are all employees of Abbott and Lois Larsen, Cynthia Mattia-Goldberg, and Kristof Chwalisz all own Abbott stock.
Acknowledgments
Financial support for this study was provided by Abbott Laboratories, formerly TAP. Medical writing support was provided by A. J. Fein, PhD on behalf of Abbott. The authors would like to thank the following investigators for their participation in the study: B. B. Bercu, MD; S. A Chalew, MD; F. A. Conte, MD; R. Hintz, MD; J. S. Fuqua, MD; M. S. Kappy, MD; G. J. Klingensmith, MD; E. O. Reiter, MD.
Open AccessThis article is published under license to BioMed Central Ltd. This is an Open Access article is distributed under the terms of the Creative Commons Attribution 2.0 International License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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) and male (
) patients are summarized in Table 1. Twenty patients (18/49 females and 2/6 males) had a history of neurological disorder, including head trauma (
), seizure disorder (
), suprasellar cyst (
), meningitis (
), hypothalamic tumor, hamartoma, spina bifida, hydrocephalus, developmental delay, and hypotonia (all
). The remaining patients (35/55) were diagnosed with idiopathic CPP.
), but peak LH was more strongly correlated with peak FSH (
). Serum estradiol levels at 0 and 90 minutes were undetectable (<18.36 pmol/L (5 pg/mL)) in 16/49 and 21/49 females, respectively. The 0- and 90-minute mean estradiol concentrations were 56.9 pmol/L (15.5 pg/mL) and 56.2 pmol/L (15.3 pg/mL), respectively. In males, 0- and 90-minute mean testosterone concentrations were 6.9 nmol/L (199.8 ng/dL) and 12.1 nmol/L (347.7 ng/dL), respectively (
).
). They also had higher baseline basal LH levels (3.46 ± 2.95 IU/L versus 1.41 ± 1.08 IU/L,
). Uterine bleeding or spotting after week 4 was reported in 7 females, all in the absence of detectable estradiol.
), reaction (
), inflammation (
), and/or edema (
). None of the injection-site adverse events were serious or led to premature discontinuation. Two serious events possibly related to study drug occurred, a severe asthma exacerbation and an increase in size of a preexisting optic glioma with deteriorating vision. There was a death during the study considered unrelated by the investigator, a cardiopulmonary arrest following respiratory infection. Nine patients discontinued study drug prematurely for reasons including patient request to leave the study, noncompliance with visit schedule, lost to follow-up, and the death described above. No patients withdrew due to injection reaction or failure to achieve adequate suppression.
), the average time to resumption of menses was 1.4 ± 0.5 years (0.5–2.1 years), and for those patients without menses prior to treatment (
), elapsed time was 1.6 ± 0.5 years (0.5–2.5 years).