WO1996005833A1

WO1996005833A1 - Methods of inhibiting endometrial cancer

Info

Publication number: WO1996005833A1
Application number: PCT/US1995/010651
Authority: WO
Inventors: Susan Margaret Boss
Original assignee: Eli Lilly And Company
Priority date: 1994-08-22
Filing date: 1995-08-21
Publication date: 1996-02-29
Also published as: AU3370095A; IL115022A0; CZ51897A3; MY113757A; RU2161964C2; FI970717A; NO970783D0; HUT76890A; CA2198119A1; EP0777476A4; MX9701327A; ZA956994B; JPH10504824A; TW404834B; EP0777476A1; NZ292017A; NO970783L; KR970705387A; IL115022A; AU688112B2

Abstract

A method of inhibiting endometrial cancer comprising administering to a human in need thereof an effective amount of a compound having formula (I) wherein R?1 and R3¿ are independently hydrogen, -CH¿3?, (a), or (b), wherein Ar is optionally substituted phenyl; R?2¿ is selected from the group consisting of pyrrolidine, hexamethyleneimino, and piperidino; or a pharmaceutically acceptable salt of solvate thereof.

Description

METHODS OF INHIBITING ENDOMETRIAL CANCER

The uterine lining (endometrium) is composed of tissue, blood vessels, and glands that grow when stimulated by the hormone estrogen. In women with normal menstrual cycles, hormonal fluctuations trigger the growth and shedding of the endometrium each month. If conception occurs, the endometrium nourishes the developing embryo. Most cases of endometrial carcinoma are associated with a precursor lesion termed "endometrial hyperplasia. " The classification of endometrial hyperplasia is based on the presence or absence of cytologic atypia, the presence of dysplasia, and the degree of complexity of the architectural pattern. Cytologic atypia is the most predictive criterion for the likelihood of progression to carcinoma.

In simple or cystic hyperplasia with cytologic atypia present there is about an 8% chance of progression to cancer. With complex or adeno atous hyperplasia with cytologic atypia present, there is 29% chance. When no cytologic atypia is present, the progression rate is 1% for simple and 3% for complex hyperplasia.

With continuously elevated estrogen levels, the endometrium remains in its growth phase at all time, in some cases leading to an overabundance of endometrial tissue or endometrial hyperplasia. Overgrowth of the endometrium is often a benign condition, but it can also be a precursor of endometrial cancer. Because of this risk, doctors urge women to avoid long-term unopposed estrogen therapy, which can cause endometrial overgrowth if the lining is not continually shed, and to seek prompt treatment for conditions that cause excessive estrogen production. (The use of progesterone in hormone replacement therapy causes breakdown bleeding and shedding of endometrial build up) . Doctors base their treatment decisions on several factors. First, they examine the cells obtained in the biopsy or D&C. If the cells are normal but simply over abundant, future development of cancer is less likely than if the cells are atypical, displaying enlarged nuclei and other unusual features. In some cases, a D&C will show that cancer has already developed.

Endometrial cancer is the most common gynecologic pathology and the fourth most common malignancy in women, after breast, colorectal, and lung cancer.

Approximately 30,000-40,000 new cases of endometrial cancer are diagnosed each year. While it is the most common pathology, most patients present in the early stage.

Endometrial cancer affects mainly postmenopausal women, as the average age at diagnosis is 58 years, and fewer than 5% of cases occur prior to age 40. The incidence of endometrial cancer is higher among women with a history of breast, endometrial, or ovarian malignancies, and also in women that belong to a high socioeconomic status.

The most significant risk factors for endometrial cancer are obesity and the presence of estrogen unopposed by progesterone.

The inaccuracy in clinical staging of endometrial carcinoma impedes optimal therapy and analysis of treatment results. Unless metastatic or systemic disease is identified, the initial approach for all medically fit patients is currently a total abdominal hysterectomy/bilateral salpingo-oophorectomy. Adjunctive therapy, if needed, can be planned, depending on whether the surgical-pathologic findings indicate intrauterine only or extrauterine disease. The patient may receive external beam radiation to the pelvis if pelvic nodes are positive and of external beam radiation to the para-aortic fields if those nodes are positive. Patients with other sites of extrauterine disease may require whole abdominal irradiation. Some patients may need systemic therapy in addition to radiation therapy, depending on sites of spread.

Patients with Stage II disease are at higher risk for having extrauterine disease and recurrence. If the cervix is of normal size and grossly normal, one approach is an extrafascial TAH/BSO with complete surgical staging followed by postoperative irradiation. With gross cervical involvement, two options are available. The first is whole pelvic irradiation followed by one intracavitary implant, which is then followed by a TAH/BSO and para- aortic lymph node sampling. The second option is a radical hysterectomy. BSO, and pelvic and para-aortic lymphadenectomy with irradiation tailored to the surgical findings, if necessary.

In surgical Stage III disease, primary surgery with the use of a TAH/BSO with tumor debulking may be attempted. Extrapelvic disease, depending on the site and extent, may necessitate extended field irradiation, systemic chemotherapy, or hormone therapy. Patients with Stage III disease, by virtue of vaginal or parametrial extension, need a thorough metasta ic survey and then irradiation.

Most patients with Stage IV disease are best treated with systemic therapy, which includes hormones or chemotherapy. Pelvic irradiation or hysterectomy is reserved for palliative control purposes.

Patients with recurrent endometrial cancer in the pelvis may be treated with radiotherapy. Unfortunately, the majority of these patients also have distant metastases as well. Isolated central recurrences in the pelvis after irradiation are rare. However, if this situation does occur, selected patients may be candidates for pelvic exenterative surgery. The majority of patients with recurrent disease are treated with hormones or chemotherapy. Progestins have been used for decades to treat recurrent endometrial cancer. The overall response to progestins is approximately 25%, although recent trials demonstrate lower response rates, in the range of 15 to 20%. Patients with endometrial carcinoma with progesterone-positive and estrogen-positive receptors have a better response to endocrine therapy. Most patients with positive receptors respond to progestins, whereas only 15% with negative receptors respond. Medroxyprogesterone acetate (Provera) and megestrol acetate (Megace) are the agents most commonly used. Tamoxifen (Nolvadex) has also been used to treat patients with recurring endometrial cancer, and responses are usually seen in patients who have previously responded to progestins. Several cytotoxic agents have activity for endometrial cancer, but responses are short-lived, and the treatment for advanced and recurrent disease is considered palliative. The two most active single agents are doxorubicin and cisplatin. Many combinations of cytotoxic agents have been used, but the results of multiagent chemotherapy do not appear to be significantly better than those of single-agent chemotherapy.

This invention provides methods of inhibiting endometrial cancer comprising administering to a human in need thereof an effective amount of a compound of formula I

(I) wherein R¹ and R³ are independently hydrogen,

0 0

/I ii

-_CH₃, -C-⁽Cι-C₆ alkyl⁾ _{^ or} C Ar _^ herein Ar is optionally substituted phenyl; R² is selected from the group consisting of pyrrolidino, hexamethyleneimino, and piperidino; and pharmaceutically acceptable salts and solvates thereof.

The current invention concerns the discovery that a select group of 2-phenyl-3-aroylbenzothiophenes

(benzothiophenes) , those of formula I, are useful for inhibiting endometrial cancer.

The therapeutic and prophylactic treatments provided by this invention are practiced by administering to a human in need thereof a dose of a compound of formula

I or a pharmaceutically acceptable salt or solvate thereof, that is effective to inhibit endometrial cancer.

The term "inhibit" includes its generally accepted meaning which includes prohibiting, preventing, restraining, and slowing, stopping or reversing progression, severity or a resultant symptom. As such, the present method includes both medical therapeutic and/or prophylactic administration, as appropriate.

Raloxifene is a preferred compound of this invention and it is the hydrochloride salt of a compound of formula 1 wherein R¹ and R³ are hydrogen and R² is 1- piperidinyl.

Generally, at least one compound of formula I is formulated with common excipients, diluents or carriers, and compressed into tablets, or formulated as elixirs or solutions for convenient oral administration, or administered by the intramuscular or intravenous routes.

The compounds can be administered transdermally, and may be formulated as sustained release dosage forms and the like. The compounds used in the methods of the current invention can be made according to established procedures, such as those detailed in U.S. Patent Nos. 4,133,814, 4,418,068, and 4,380,635 all of which are incorporated by reference herein. In general, the process starts with a benzo[b]thiophene having a 6-hydroxyl group and a 2- (4- hydroxyphenyl) group. The starting compound is protected, acylated, and deprotected to form the formula I compounds. Examples of the preparation of such compounds are provided in the U.S. patents discussed above. The term "optionally substituted phenyl" includes phenyl and phenyl substituted once or twice with C -Cζ alkyl, C₁-C₄ alkoxy, hydroxy, nitro, chloro, fluoro, or tri(chloro or fluoro)methyl. The compounds used in the methods of this invention form pharmaceutically acceptable acid and base addition salts with a wide variety of organic and inorganic acids and bases and include the physiologically acceptable salts which are often used in pharmaceutical chemistry. Such salts are also part of this invention. Typical inorganic acids used to form such salts include hydrochloric, hydrobromic, hydroiodic, nitric, sulfuric, phosphoric, hypophosphoric and the like. Salts derived from organic acids, such as aliphatic mono and dicarboxylic acids, phenyl substituted alkanoic acids, hydroxyalkanoic ^■ and hydroxyalkandioic acids, aromatic acids, aliphatic and aromatic sulfonic acids, may also be used. Such pharmaceutically acceptable salts thus include acetate, phenylacetate, trifluoroacetate, acrylate, ascorbate, benzoate, chlorobenzoate, dinitrobenzoate, hydroxybenzoate, methoxybenzoate, methylbenzoate, o-acetoxybenzoate, naphthalene-2-benzoate, bromide, isobutyrate, phenylbutyrate, β-hydroxybutyrate, butyne-1,4-dioate, hexyne-1,4-dioate, caprate, caprylate, chloride, cinnamate, citrate, formate, fumarate, glycollate, heptanoate, hippurate, lactate, malate, maleate, hydroxymaleate, malonate, mandelate, mesylate, nicotinate, isonicotinate, nitrate, oxalate, phthalate, teraphthalate, phosphate, monohydrogenphosphate, dihydrogenphosphate, metaphosphate, pyrophosphate, propiolate, propionate, phenylpropionate, salicylate, sebacate, succinate, suberate, sulfate, bisulfate, pyrosulfate, sulfite, bisulfite, sulfonate, benzene-sulfonate, p-bromophenylsulfonate, chlorobenzenesulfonate, ethanesulfonate, 2- hydroxyethanesulfonate, ethanesulfonate, naphthalene-1- sulfonate, naphthalene-2-sulfonate, p-toluenesulfonate, xylenesulfonate, tartarate, and the like. A preferred salt is the hydrochloride salt.

The pharmaceutically acceptable acid addition salts are typically formed by reacting a compound of formula I with an equimolar or excess amount of acid. The reactants are generally combined in a mutual solvent such as diethyl ether or benzene. The salt normally precipitates out of solution within about one hour to 10 days and can be isolated by filtration or the solvent can be stripped off by conventional means. Bases commonly used for formation of salts include ammonium hydroxide and alkali and alkaline earth metal hydroxides, carbonates, as well as aliphatic and primary, secondary and tertiary amines, aliphatic diamines. Bases especially useful in the preparation of addition salts include ammonium hydroxide, potassium carbonate, methyla ine, diethylamine, ethylene diamine and cyclohexylamine.

The pharmaceutically acceptable salts generally have enhanced solubility characteristics compared to the compound from which they are derived, and thus are often more amenable to formulation as liquids or emulsions.

Pharmaceutical formulations can be prepared by procedures known in the art. For example, the compounds can be formulated with common excipients, diluents, or carriers, and formed into tablets, capsules, suspensions, powders, and the like. Examples of excipients, diluents, and carriers that are suitable for such formulations include the following: fillers and extenders such as starch, sugars, mannitol, and silicic derivatives; binding agents such as carboxymethyl cellulose and other cellulose derivatives, alginates, gelatin, and polyvinyl pyrrolidone; moisturizing agents such as glycerol; disintegrating agents such as calcium carbonate and sodium bicarbonate; agents for retarding dissolution such as paraffin; resorption accelerators such as quaternary ammonium compounds; surface active agents such as cetyl alcohol, glycerol monostearate; adsorptive carriers such as kaolin and bentonite; and lubricants such as talc, calcium and magnesium stearate, and solid polyethyl glycols.

The compounds can also be formulated as elixirs or solutions for convenient oral administration or as solutions appropriate for parenteral administration, for instance by intramuscular, subcutaneous or intravenous routes. Additionally, the compounds are well suited to formulation as sustained release dosage forms and the like. The formulations can be so constituted that they release the active ingredient only or preferably in a particular part of the intestinal tract, possibly over a period of time. The coatings, envelopes, and protective matrices may be made, for example, from polymeric substances or waxes. - The particular dosage of a compound of formula I required to inhibit endometrial cancer according to this invention will depend upon the severity of the condition, the route of administration, and related factors that will be decided by the attending physician. Generally, accepted and effective daily doses will be from about 0.1 to about 1000 mg/day, and more typically from about 50 to about 200 mg/day. Such dosages will be administered to a subject in need thereof from once to about three times each day, or more often as needed, and for a time to effectively treat or prevent endometrial cancer. It is usually preferred to administer a compound of formula I in the form of an acid addition salt, as is customary in the administration of pharmaceuticals bearing a basic group, such as the piperidino ring. For such purposes the following oral dosage forms are available.

Formulations

In the formulations which follow, "Active ingredient " means a compound of formula I . Formulation 1 : Gelatin Capsules

Hard gelatin capsules are prepared using the following :

Ingredient Quantity (mg/capsule) Active ingredient 0 .1 - 1000

Starch, NF 0 - 650

Starch flowable powder 0 - 650

Silicone fluid 350 centistokes 0 - 15

The ingredients are blended, passed through a No . 45 mesh U. S . sieve, and filled into hard gelatin capsules . Examples of specific capsule formulations of raloxifene that have been made include those shown below:

Formulation 2 : Raloxifene capsule

Ingredient Quantity (mq/capsule ) Raloxifene 1

Starch, NF 112

Starch flowable powder 225 .3

Silicone fluid 350 centistokes 1 .7 Formulation 3 : Raloxifene capsule

Ingredient Quantity (mg/capsule)

Raloxifene 5

Starch, NF 108

Starch flowable powder 225.3

Silicone fluid 350 centistokes 1.7

Formulation 4: Raloxifene capsule

Ingredient Quantity (mg/capsule)

Raloxifene 10

Starch, NF 103

Starch flowable powder 225.3

Silicone f luid 350 centistokes 1.7

Formulation 5 : Raloxifene capsule

Ingredient Quantity (mg/capsule)

Raloxifene 50

Starch, NF 150

Starch flowable powder 397

Silicone fluid 350 centistokes 3.0

The specific formulations above may be changed in compliance with the reasonable variations provided.

A tablet formulation is prepared using the ingredients below: Formulation 6: Tablets

Ingredient Quantity (mg/tablet)

Active ingredient 0.1 - 1000 Cellulose, microcrystalline 0 - 650 Silicon dioxide, fumed 0 - 650 Stearate acid 0 - 15

The components are blended and compressed to form tablets ,

Alternatively, tablets each containing 0.1 - 1000 mg of Active ingredient are made up as follows :

Formulation 7 : Tablets

Ingredient Quantity (mg/tablet )

Active ingredient 0 . 1 - 1000

Starch 45

Cellulose , microcrystalline 35

Polyvinylpyrrolidone 4 (as 10% solution in water)

Sodium carboxymethyl cellulose 4.5

Magnesium stearate 0 .5

Talc 1

The Active ingredient, starch, and cellulose are passed through a No. 45 mesh U.S. sieve and mixed thoroughly. The solution of polyvinylpyrrolidone is mixed with the resultant powders which are then passed through a No. 14 mesh U.S. sieve. The granules so produced are dried at 50°-60° C and passed through a No. 18 mesh U.S. sieve. The sodium carboxymethyl starch, magnesium stearate, and talc, previously passed through a No. 60 U.S. sieve, are then added to the granules which, after mixing, are compressed on a tablet machine to yield tablets. Suspensions each containing 0.1 - 1000 mg of Active ingredient per 5 mL dose are made as follows:

Formulation 8: Suspensions

Ingredient Quantity (mg/5 ml)

Active ingredient 0 . 1 ^■ - 1000 mg

Sodium carboxymethyl cellul Loossee 50 mg

Syrup 1 . 25 mg

Benzoic acid solution 0 . 10 mL

Flavor q . v .

Color q . v .

Purified water to 5 mL

The Active ingredient is passed through a No. 45 mesh U.S. sieve and mixed with the sodium carboxymethyl cellulose and syrup to form a smooth paste. The benzoic acid solution, flavor, and color are diluted with some of the water and added, with stirring. Sufficient water is then added to produce the required volume.

ASSAYS ASSAY 1 Continuous cultures of transformed endometrial cells reflective of endometrial carcinoma are maintained in culture. Estrogen receptor containing cells (such as the Ishikawa line) are assessed for proliferation in response to estrogen and compounds of Formula I. Responsiveness is assessed by monitoring transcription of known estrogen/anti-estrogen regulated genes such as progesterone receptor, PS2 and others.

ASSAY 2 Induced Animal Models - Endometrial carcinoma is induced by injections of estrogenic substances such as 17- β-estradiol or DES during neonatal development. The presence of carcinoma in the adult animal is confirmed by biopsy of affected animals and/or sacrifice and biopsy of syngeneic animals identically treated. After evaluation of the lesions, affected animals are treated with estrogen, compounds of formula I, or progestins for 1-8 weeks. After treatment, lesions of surviving animals are examined for progression, regression or stasis.

ASSAY 3 Five to fifty women are selected for the clinical study. The women suffer from endometrial cancer. The study has a placebo control group, i.e., the women are divided into two groups, one of which receives a compound of formula 1 as the active agent and the other receives a standard treatment for endometrial cancer. Women in the test group receive between 50-200 mg of the drug per day by the oral route. They continue this therapy for 3-12 months. Accurate records are kept as to the symptoms and status of the cancer in both groups and at the end of the study these results are compared. The results are compared both between members of each group and also the results for each patient are compared to the status reported for each patient before the study began.

ASSAY 4

A total of 251 healthy, postmenopausal women are recruited. Each subject has had her last menstrual period more than 6 months but less than 6 years prior to beginning the treatment phase of the study. Postmenopausal status of each subject is confirmed before beginning treatment by serum estradiol <120 pmol/L and by FSH >30 IU/L. Subjects will not have been treated with estrogen over at least the last 3 months before the study and have never been treated with fluoride, calcitonin, or bisphosphonate. Subjects are in good health and range in age from 46 to 60 years. The study is a multi-center, randomized, controlled, double-blind study. Qualified subjects who consent are randomized to one of four treatment groups: placebo, a compound of formula I 200 mg once daily, a compound of formula I 600 mg once daily, or estrogen 0.625 mg once daily. All subjects also receive daily oral calcium carbonate supplements (520 mg/day elemental calcium) . All medications and supplements are taken daily in the morning during the 8-week treatment period. Once treatment is completed (Visit 5), each suject receives Provera® 5 mg/day for 12 days.

Using a Pipelle catheter, a uterine biopsy is performed at baseline and after 8 weeks of treatment. The biopsies are performed in a routine manner and the tissue specimens are placed in 10% buffered formalin. Specimens are retrieved by pouring them into tissue paper filters and then are grossly examined and classified as to appearance (color, texture, and consistency) and volume. Standard histologic processing into paraffin blocks is used and the tissues are serially sectioned onto a minimum of two slides which results in serial strips of 6 to 20 cross sections. Since subjects with clinically significant endometrial abnormalities are to be excluded from the study or are discontinued from the study if they develop abnormalities,' the biopsies are evaluated immediately for a descriptive diagnosis. This is performed by one of two pathologists and immediately reported to the clinical physicians. The primary purpose of the biopsies is to determine the degree of morphologic estrogenic effect of study treatment. Two pathologists are trained to read the biopsies by reviewing a series of Pipelle biopsies obtained outside the study that represent the full spectrum of endometrial morphology. Using standard morphologic criteria associated with estrogen-induced proliferation, a scoring system is devised to quantitate this estrogenic effect and include the more subtle changes that may be encountered. Ten of these outside cases are then scored with this system by each pathologist, and the cases are reviewed together to assure uniform understanding and use of the criteria. After the first twenty cases from the baseline biopsies in the study are blindly scored by each pathologist, the scores are reviewed to verify proper use of the system. The pathologists evaluate the biopsy samples for the following components: 1) specimen adequacy, 2) glandular morphology, 3) stromal morphology, and 4) other changes. Additional findings are entered as textual comments. Point scores are generated from the glandular and stromal morphologic features and are totaled and graded on a -point estrogenicity scale where a grade of 0 indicates typical postmenopausal endometrium and a grade of 2 indicates a marked estrogenic effect. Total scores for both pathologists are averaged and then assigned a final grade of 0 to 3. Scoring occurs well after the initial immediate diagnosis and usually 10 to 20 cases are scored sequentially. It is expected that the rate of scant tissue is relatively high on the initial biopsy since the typical postmenopausal endometrium is inactive and consists of a very shallow (5 mm or less) tissue lining and the Pipelle biopsy is a limited, blind biopsy method. Because endometrial glands are required to score features of glandular and stromal morphology, the final biopsy must have contained glands before any conclusions can be drawn in individual subjects. Specimen adequacy is defined as follows: If no tissue or debatable tissue of endometrial origin is present, the specimen is deemed inadequate and not included in the evaluation. If multiple fragments of endometrial surface epithelium are obtained, the specimen can not be scored. However the biopsy is deemed adequate and is assigned a grade of 0 on the 4-point scale indicating no estrogen effect.

If disrupted endometrium with glands are obtained, the biopsy is adequate and is scored for the glandular and stromal features.

If intact endometrial tissue is obtained, the biopsy is adequate and is scored for the glandular and stromal changes. In addition, the volume of the tissues is taken into account as an indication of estrogen effect.

Glandular morphology is the primary scoring factor for adequate biopsy specimens. Stromal morphology is the secondary scoring factor for adequate biopsy specimens. Tables 1 and 2 display the features to be used to score each specimen that have glands and/or stroma present. Four features are used to classify the glands: shape, cellular nuclear to cytoplasmic cross sectional areas, nuclear pseudostratification, and mitotic activity.-

Table 1. Glandular Features: Scoring of Estrogenicity

Estrogenic Effect/Point Value

No Limited High

Glandular Estrogenicity Estrogeneicity Estrogenicity Feature (0 Points) (1 Point) (2 Points)

Shape Small, Open, straight Open, cystic, tubular tortuous straight

Nucleus-to- Very High Moderate (75% Low (<50%) cytoplasm (> 75%) to 50%) ratio

Nuclear None Limited Diffuse pseudostrati

-fication

Mitoses None Rare Scattered to many

Note: At least 20 gland profiles are used to grade for mitotic activity (four serial sections of scant specimens) .

In more scanty specimens a minimum of 20 gland profiles in serial sections are viewed before concluding no mitoses are evident. In Table 2 the stromal and "other" features are listed. Four features are also used to classify the stroma: density, mitoses, metaplastic changes in epithelia, and tissue volume.

Table 2. Stromal Features: Scoring of Estrogenicity

Estrogenic Effect/Point Value

No Limited High

Stromal Estrogenicity Estrogeneicity Estrogenicity

Feature (0 Points) (1 Point) (2 Points)

Compact, Loosely Edematouε

Density fibrous cellular

Mitoses None Rare Few/Many

Metaplasia³ None Rare Scattered, diffuse

Tissue Volume^b Disrupted or Moderate, much Abundant, few intact being intact intact

Metaplasia includes tubular, eosinophilic, and squamous type. ^bUsed only if glands show some estrogenic effect (1 or 2 points) .

Morphologic features that indicate a lack of estrogenicity generate a score of 0 points and features indicating a limited or significant estrogenic effect generate a score of 1 to 2 points, respectively. Using this approach, a biopsy can receive between 0 to 16 points. In addition to glandular and stromal morphology/ and other important morphologic features including progestational effect, inflammatory processes, breakdown bleeding, polypoid growth, or other pathologic findings are described but are not included in the scoring of proliferative effects since the other changes are primarily nonproliferative.

The sum of the scores obtained from grading the glandular and stromal morphology features result in a 4- point estrogenicity grading scale which is assigned to each sample as follows: Grade 0 = 0 to 3 points Typical postmenopausal endometrium with little or no estrogenic effect Grade 1 = 4 to 6 points Definite but limited estrogenic effect

Grade 2 = 7 to 10 points Moderte estrogenic effect

Grade 3 = >10 points Marked estrogenic effect

As noted earlier, if biopsy specimens contain multiple fragments of endometrial surface epithelium, those specimens are assigned a grade of 0. For each biopsy, there are eight scores: four assessments of the glandular morphology, two assessments of the stromal morphology (density and mitoses scores are combined and metaplasia and tissue volume are combined for statistical analyses) , the sum of these six scores and the grade as defined above.

Intraclass correlation coefficients are calculated to assess agreement between the two readers on the sum of the scores obtained at baseline and at 8 weeks (Fleiss, JL (1981) Statistical Methods for Rates and Proportions. New York: John Wiley and Sons, p. 218.]

The baseline, week 8 and change-from-baseline to week 8 scores for each of the eight scores are analyzed for treatment differences using Cochran-Mantel-Haenazel statistical techniques adjusting for investigator [Landis, RJ Heyman, ER and Koch, GG (1978). "Average Partial

Association in Three-Way Contingency Tables: A Review and Discussion of Alternative Tests". International Statistical Review 46:237-254.].

The occurrence of endometrial glands in the biopsy tissue is evaluated at baseline and 8 weeks for treatment differences using the chi-square test. Pairwise treatment comparisons between each active treatment and placebo are performed if the overall treatment difference is statistically significant. Statistical significance is judged at a two-sided 0.05 level of significance. Al statistical analyses use the SAS system [SAS Institute Inc. (1989) , SAS/STAT User's Guide, Version 6, Fourth Edition, Volumes 1 and 2, Cary, NC: SAS Institute Inc. ]

A positive result in this assay is the reduction of the score for glandular mitoses indicating a decrease in cell replication relative to placebo.

Table 3 illustrates important results of the study. Table 3. Mean (± SEM) Scores for Glandular Fatures At Endpoint

Placebo Raloxifene Raloxifene Estrogen (n = 53) 200 mg 600 mg 0.625 mg

Variable (n = 54) (n = 54) (n = 47)

Shape 0.44 ± 0.08 0.58 ± 0.07 0.51 ± 0.06 1.37 ± 0.06*

Pseudostrat¬ 0.64 ± 0.10 0.57 ± 0.06 0.56 ± 0.06 1.68 ± 0.07* ification

Mitoses 0.19 ± 0.05 0.05 ± 0.02* 0.07 ±0.03/ 0.98 ± 0.08*

Nucleus: 0.48 ± 0.09 0.58 ±0.06 0.58 ±0.05 1.56 ± 0.08* Cytoplasm

* Statistically significantly different from placebo, two- tailed test (p<.050)

/ Marginally significantly different from placebo, two- tailed test (p = .053) Utility of the compounds of formula I is illustrated by the positive impact they have in at least one of the assays described above.

Claims

I claim:

1. A method of inhibiting endometrial cancer comprising administering to a human in need thereof an effective amount of a compound having the formula

(I)

wherein R¹ and R³ are independently hydrogen,

0 0

II II

-_CH₃, -C-(Cι-C₆ alkyl)_{f or} -C-Ar ^ _wnerei_n p^ _s optionally substituted phenyl;

R² is selected from the group consisting of pyrrolidine, hexamethyleneimino, and piperidino; or a pharmaceutically acceptable salt of solvate thereof.

2. The method of Claim 1 wherein said compound is the hydrochloride salt thereof.

3. The method of Claim 1 wherein said administration is prophylactic.

4. The method of Claim 1 wherein said compound is

or its hydrochloride salt.