Pharmacotherapeutic group: Endocrine therapy. Hormone antagonists and related agents: aromatase inhibitor.
ATC code: L02BG04.
PHARMACOLOGY: Pharmacodynamics: Pharmacodynamic effects: The elimination of estrogen-mediated growth stimulation is a prerequisite for tumor response in cases where the growth of tumor tissue depends on the presence of estrogen and endocrine therapy is used. In postmenopausal women, estrogen are mainly derived from the action of the aromatase enzyme, which converts adrenal androgens - primarily androstenedione and testosterone - to estrone and estradiol. The suppression of estrogen biosynthesis in peripheral tissues and the cancer tissue itself can therefore be achieved by specifically inhibiting the aromatase enzyme.
Letrozole is a non-steroidal aromatase inhibitor. It inhibits the aromatase enzyme by competitively binding to haem of the aromatase cytochrome P450, resulting in a reduction of estrogen biosynthesis in all tissues where present.
In healthy postmenopausal women, single doses of 0.1 mg, 0.5 mg and 2.5 mg letrozole suppress serum estrone and estradiol by 75%, 78% and 78% from baseline, respectively. Maximum suppression is achieved in 48 - 78 hours.
In postmenopausal patients with advanced breast cancer, daily doses of 0.1 mg to 5 mg suppressed plasma concentration of estradiol, estrone, and estrone sulfate by 75 - 95% from baseline in all patients treated. With doses of 0.5 mg and higher, many values of estrone and estrone sulfate were below the limit of detection in the assays, indicating that higher estrogen suppression is achieved with these doses. Estrogen suppression was maintained throughout treatment in all these patients.
Letrozole is highly specific in inhibiting aromatase activity. Impairment of adrenal steroidogenesis has not been observed. No clinically relevant changes were found in the plasma concentrations of cortisol, aldosterone, 11-deoxycortisol, 17-hydroxyprogesterone, and ACTH or in plasma renin activity among postmenopausal patients treated with a daily dose of letrozole 0.1 to 5 mg. The ACTH stimulation test performed after 6 and 12 weeks of treatment with daily doses of 0.1 mg, 0.25 mg, 0.5 mg, 1 mg, 2.5 mg, and 5 mg did not indicate any attenuation of aldosterone or cortisol production. Thus, glucocorticoids and mineralocorticoids supplementation is not necessary.
No changes were noted in plasma concentrations of androgens (androstenedione and testosterone) among healthy postmenopausal women after 0.1 mg, 0.5 mg, and 2.5 mg single doses of letrozole or in plasma concentrations of androstenedione among postmenopausal patients treated with daily doses of 0.1 to 5 mg, indicating that the blockade of estrogen biosynthesis does not lead to accumulation of androgenic precursors. Plasma levels of LH and FSH are not affected by letrozole in patients, nor is thyroid function as evaluated by TSH, T4, and T3 uptake test.
Adjuvant treatment: Study BIG 1-98: BIG 1-98 was a multicenter, double-blind study in which over 8,000 postmenopausal women with hormone receptor positive early breast cancer were randomized to one of the following treatments: A. tamoxifen for 5 years; B. letrozole for 5 years; C. tamoxifen for 2 years followed by letrozole for 3 years; D. letrozole for 2 years followed by tamoxifen for 3 years.
The primary endpoint was disease-free survival (DFS); secondary efficacy endpoints were time to distant metastasis (TDM), distant disease-free survival (DDFS), overall survival (OS), systemic disease-free survival (SDFS), invasive contralateral breast cancer and time to breast cancer recurrence.
Efficacy results at a median follow-up of 26 and 60 months: Data in Table 1 reflect the results of the Primary Core Analysis (PCA) based on data from the monotherapy arms (A and B) and from the two switching arms (C and D) at a median treatment duration of 24 months and a median follow-up of 26 months and at a median of treatment duration of 32 months and a median follow-up of 60 months.
The 5-year DFS rates were 84% for letrozole and 81.4% for tamoxifen. (See Table 1.)
Click on icon to see table/diagram/image
Results at a median follow-up of 96 months (monotherapy arms only): The Monotherapy Arms Analysis (MAA) long-term update of the efficacy of letrozole monotherapy compared to tamoxifen monotherapy (median duration of adjuvant treatment: 5 years): is presented in Table 2. (See Table 2.)
Click on icon to see table/diagram/image
Sequential Treatment Analysis (STA): The Sequential Treatment Analysis (STA) addresses the second primary question of BIG 1-98, namely whether sequencing of tamoxifen and letrozole would be superior to monotherapy. There were significant differences in DFS, OS, SDFS, or DDFS from switch with respect to monotherapy (Table 3). (See Table 3.)
Click on icon to see table/diagram/image
There were no significant differences in DFS, OS, SDFS, DDFS in any of the STA from randomization in pairwise comparisons (Table 4). (See Table 4.)
Click on icon to see table/diagram/image
Study D2407: Study D2407 is an open-label, randomized, multicentre post approval safety study designed to compare the effects of adjuvant treatment with letrozole and tamoxifen on bone mineral density (BMD) and serum lipid profiles. A total of 262 patients were assigned either letrozole for 5 years or to tamoxifen for 2 years followed by letrozole for 3 years.
At 24 months there was a statistically significant difference in the primary end-point; the lumbar spine BMD (L2-L4) showed a median decrease of 4.1% for letrozole compared to a median increase of 0.3% for tamoxifen.
No patient with a normal BMD at baseline became osteoporotic during 2 years of treatment and only 1 patient with osteopenia at baseline (T score of 1.9) developed osteoporosis during the treatment period (assessment by central review).
The results for total hip BMD were similar to those of lumbar spine but less pronounced.
There was no significant difference between treatments in the rate of fracture - 15% in the letrozole arm, 17% in the tamoxifen arm.
Median total cholesterol levels in the tamoxifen arm were decreased by 16% after 6 months compare to baseline and this decrease was maintained at subsequent visits up to 24 months. In the letrozole arm, total cholesterol levels were relatively stable over time, giving a statistically significant difference in favour of tamoxifen at each time point.
Extended adjuvant treatment (MA-17): In a multicentre, double-blind, randomized, placebo-controlled study (MA-17), over 5,100 postmenopausal women with receptor-positive or unknown primary breast cancer who had completed adjuvant treatment with tamoxifen (4.5 a 6 years) were randomized to either letrozole or placebo for 5 years.
The primary endpoint was disease-free survival, defined as the interval between randomization and the earliest occurrence of loco-regional recurrence, distant metastasis, or contralateral breast cancer.
The first planned interim analysis at a median follow-up of around 28 months (25% of patients being followed up for at least 38 months), showed that letrozole significantly reduced the risk of breast cancer recurrence by 42% compared with placebo (HR 0.58; 95% CI 0.45, 0.76; P = 0.00003). The benefit in favor of letrozole was observed regardless of node status. There was no significant difference in overall survival: (letrozole 51 deaths; placebo 62; HR 0.82; 95% CI 0.56, 1.19).
Consequently, after the first interim analysis the study was unblinded and continued in an open-label fashion and patients in the placebo arm were allowed to switch to letrozole for up to 5 years. Over 60% of eligible patients (disease-free at unblinding) opted to switch to letrozole. The final analysis included 1,551 women who switched from placebo to letrozole at a median of 31 months (range 12 to 106 months) after completion of tamoxifen adjuvant therapy. Median duration for letrozole after switch was 40 months.
The final analysis conducted at a median follow-up of 62 months confirmed the significant reduction in the risk of breast cancer recurrence with letrozole. (See Table 5.)
Click on icon to see table/diagram/image
In the MA-17 bone substudy in which concomitant calcium and vitamin D were given, greater decreases in BMD compared to baseline occurred with letrozole compared with placebo. The only statistically significant difference occurred at 2 years and was in total hip BMD (letrozole median decrease of 3.8% vs placebo median decrease of 2.0%).
In the MA-17 lipid substudy, there were no significant differences between letrozole and placebo in total cholesterol or in any lipid fraction.
In the updated quality of life substudy there were no significant differences between treatments in physical component summary score or mental component summary score, or in any domain score in the SF-36 scale. In the MENQOL scale, significantly more women in the letrozole arm than in the placebo arm were most bothered (generally in the first year of treatment) by those symptoms deriving from estrogen deprivation - hot flushes and vaginal dryness. The symptom that bothered most patients in both treatment arms was aching muscles, with a statistically significant difference in favor of placebo.
Neoadjuvant treatment: A double blind trial (P024) was conducted in 337 postmenopausal breast cancer patients randomly allocated either letrozole 2.5 mg for 4 months or tamoxifen for 4 months. At baseline all the patients had tumors stage T2-T4c, N0-2, M0, ER and/or PgR positive and none of the patients would have qualified for breast-conserving surgery. Based on clinical assessment there were 55% objective responses in the letrozole arm versus 36% for the tamoxifen arm (
P<0.001). This finding was consistently confirmed by ultrasound (letrozole 35% vs tamoxifen 25%,
P=0.04) and mammography (letrozole 34% vs tamoxifen 16%,
P<0.001). In total 45% of patients in the letrozole group versus 35% of patients in the tamoxifen group (
P=0.02) underwent breast-conserving therapy. During the 4-month pre-operative treatment period, 12% of the patients treated with letrozole and 17% of the patients treated with tamoxifen had disease progression on clinical assessment.
First-line treatment: A controlled double-blind trial was conducted comparing letrozole 2.5 mg to tamoxifen 20 mg as first-line therapy in postmenopausal women with advanced breast cancer. In 907 women, letrozole was superior to tamoxifen in time to progression (primary endpoint) and in overall objective response, time to treatment failure and clinical benefit.
The results are summarized in Table 6: See Table 6.
Click on icon to see table/diagram/image
Time to progression was significantly longer, and response rate significantly higher for letrozole irrespective of whether adjuvant antiestrogens has been given or not. Time to progression was significantly longer for letrozole irrespective of dominant site of disease. Median time to progression was 12.1 months for letrozole and 6.4 months for tamoxifen in patients with soft tissue disease only and a median of 8.3 months for letrozole and 4.6 months for tamoxifen in patients with visceral metastases.
Study design allowed patients to cross over upon progression to the other therapy or discontinue from the study. Approximately 50% of patients crossed over to the opposite treatment arm and crossover was virtually completed by 36 months. The median time to crossover was 17 months (letrozole to tamoxifen) and 13 months (tamoxifen to letrozole).
Letrozole treatment in the first-line therapy of advanced breast cancer resulted in a median overall survival of 34 months compared with 30 months of tamoxifen (logrank test
P=0.53, not significant).
The absence an advantage for letrozole on overall survival could be explained by the crossover design of the study.
Second-line treatment: Two well-controlled clinical trials were conducted comparing two letrozole doses (0.5 mg and 2.5 mg) to megestrol acetate and to aminoglutethimide, respectively, in postmenopausal women with advanced breast cancer and previously treated with antiestrogens.
Time to progression was not significantly different between letrozole 2.5 mg and megestrol acetate (
P=0.07). Statistically significant differences were observed in favor of letrozole 2.5 mg compared to megestrol acetate in overall objective tumor response rate (24% vs 16%,
P=0.04), and in time to treatment failure (
P=0.04). Overall survival was not significantly different between the 2 arms (
P=0.2).
In the second study, the response rate was not significantly different between letrozole 2.5 mg and aminoglutethimide (
P=0.06). Letrozole 2.5 mg was statistically superior to aminoglutethimide for time to progression (
P=0.008), time to treatment failure (
P=0.003) and overall survival (
P=0.002).
Male breast cancer: Use of letrozole in men with breast cancer has not been studied.
Pharmacokinetics: Absorption: Letrozole is rapidly and completely absorbed from the gastrointestinal tract (mean absolute bioavailability: 99.9%). Food slightly decreases the rate of absorption (median t
max 1 hour fasted versus 2 hours fed; and C
max 129 ± 20.3 nmol/l fasted versus 98.7 ± 18.6 nmol/l fed) but the extent of absorption (AUC) is not changed. This minor effect on the absorption rate is not considered to be of clinical relevance, and therefore letrozole may be taken without regard to mealtimes.
Distribution: Plasma proteins binding of letrozole is approximately 60%, mainly to albumin (55%). The concentration of letrozole in erythrocytes is about 80% of that in plasma. After administration of 2.5 mg of
14C-labeled letrozole, approximately 82% of the radioactivity in plasma was unchanged compound. Systemic exposure to metabolites is therefore low. Letrozole is rapidly and extensively distributed to tissues. Its apparent volume of distribution at steady state is about 1.87 ± 0.47 l/kg.
Biotransformation: Metabolic clearance to a pharmacologically inactive carbinol metabolite is the major elimination pathway of letrozole (CL
m = 2.1 l/h) but is relatively slow when compared to hepatic blood flow (about 90 l/h). The cytochrome P450 isoenzymes 3A4 and 2A6 were found to be capable of converting letrozole to this metabolite. Formation of minor unidentified metabolites and direct renal and fecal excretion play only a minor role in the overall elimination of letrozole. Within 2 weeks after administration of 2.5 mg of
14C-labeled letrozole to healthy postmenopausal volunteers, 88.2 ± 7.6% of the radioactivity was recovered in urine and 3.8 ± 0.9% in faeces. At least 75% of the radioactivity recovered in the urine up to 216 hours (84.7 ± 7.8% of the dose) was attributed to the glucuronide of the carbinol metabolite, about 9% to two unidentified metabolites; and 6% to unchanged letrozole.
Elimination: The apparent terminal elimination half-life in plasma is about 2 to 4 days. After daily administration of 2.5 mg steady-state levels are reached within 2 to 6 weeks. Plasma concentrations at steady-state are approximately 7 times higher than concentrations measured after a single dose of 2.5 mg, while they are 1.5 to 2 times higher than the steady-state values predicted from the concentrations measured after a single dose, indicating a slight non-linearity in the pharmacokinetics of letrozole upon daily administration of 2.5 mg. Since steady-state levels are maintained over time, it can be concluded that no continuous accumulation of letrozole occurs.
Linearity/non-linearity: The pharmacokinetics of letrozole were dose proportional after single oral doses up to 10 mg (dose range: 0.01 to 30 mg) and after daily doses up to 1.0 mg (dose range: 0.1 to 5 mg). After a 30 mg single oral dose there was a slightly dose over-proportional increase in AUC value. The dose over-proportionality is likely to be the result of a saturation of metabolic elimination processes. Steady levels were reached after 1 to 2 months at all dosage regimens tested (0.1-5.0 mg daily).
Special populations: Elderly: Age had no effect on the pharmacokinetics of letrozole.
Renal impairment: In a study involving 19 volunteers with varying degrees of renal function (24-hour creatinine clearance 9-116 ml/min) no effect on the pharmacokinetics of letrozole was found after a single dose of 2.5 mg. In addition to the previously mentioned study assessing the influence of renal impairment on letrozole, a covariate analysis was performed on the data of two pivotal studies (Study AR/BC2 and Study AR/BC3). Calculated creatinine clearance (CLcr) [Study AR/BC2 range: 19 to 187 mL/min; Study AR/BC3 range: 10 to 180 mL/min] showed no statistically significant association between letrozole plasma trough levels at steady-state (Cmin). Futhermore, data of Study AR/BC2 and Study AR/BC3 in second-line metastatic breast cancer showed no evidence of an adverse effect of letrozole on CLcr or an impairment of renal function.
Therefore, no dose adjustment is required for patient with renal impairment (CLcr ≥10 mL/min). Little information is available in patients with severe impairment of renal function (CLcr <10 mL/min).
Hepatic impairment: In a similar study involving subjects with varying degrees of hepatic function, the mean AUC values of the volunteers with moderate hepatic impairment (Child-Pugh B) was 37% higher than in normal subjects, but still within the range seen in subjects without impaired function. In a study comparing the pharmacokinetics of letrozole after a single oral dose in eight male subjects with liver cirrhosis and severe hepatic impairment (Child-Pugh C) to those in healthy volunteers (N=8), AUC and the t
1/2 increased by 95 and 187%, respectively. Thus, letrozole should be administered with caution to patients with severe hepatic impairment and after consideration of the risk/benefit in the individual patients.
Toxicology: Preclinical safety data: In a variety of preclinical safety studies conducted in standard animal species, there was no evidence of systemic or target organ toxicity.
Letrozole showed a low degree of acute toxicity in rodents exposed up to 2,000 mg/kg. In dogs letrozole caused signs of moderate toxicity at 100 mg/kg.
In repeated-dose toxicity studies in rats and dogs up to 12 months, the main findings observed can be attributed to the pharmacological action of the compound. The no-adverse-effect level was 0.3 mg/kg in both species.
Oral administration of letrozole to female rats resulted in decreases in mating and pregnancy ratios and increases in pre-implantation loss.
Both
in vivo and
in vitro investigation of letrozole's mutagenic potential revealed no indications of any genotoxicity.
In a 104-week rat carcinogenicity study, no treatment-related tumors were noted in male rats. In female rats, a reduced incidence of benign and malignant mammary tumors at all the doses of letrozole was found.
In a 104-week mouse carcinogenicity study, no treatment-related tumors were noted in male mice. In female mice, a generally dose-related increase in the incidence of benign ovarian granulosa theca cell tumors was observed at all doses of letrozole tested. These tumors were considered to be related to the pharmacological inhibition of estrogen synthesis and may be due to increased LH resulting from the decrease in circulating estrogen.
Letrozole was embryotoxic and fetotoxic in pregnant rats and rabbits following oral administration at clinically relevant doses. In rats that had live fetuses, there was an increase in the incidence of fetal malformations including domed head and fusion of cervical/centrum vertebral fusion. An increased incidence of fetal malformations was not seen in the rabbits. It is not known whether this was an indirect consequence of the pharmacological properties (inhibition of estrogen biosynthesis) or a direct drug effect (see Contraindications and Use in Pregnancy & Lactation).
Preclinical observations were confined to those associated with the recognized pharmacological action, which is the only safety concern for human use derived from animal studies.
Sign Out
Click on icon to see table/diagram/image
Click on icon to see table/diagram/image
Click on icon to see table/diagram/image
Click on icon to see table/diagram/image
Click on icon to see table/diagram/image
Click on icon to see table/diagram/image
Click on icon to see table/diagram/image
Click on icon to see table/diagram/image
Click on icon to see table/diagram/image
