`
`Annals of Oncology 17: 200-204, 2006
`doi:10.1093/annone/mdj047
`Published online 26 October 2005
`
`Fulvestrant, a new treatment option for advanced
`breast cancer: tolerability versus existing agents
`|. Vergote’* & P. Abram?
`‘University Hospitals, Leuven, Belgium; “Belvoir Park Hospital, Belfast, UK
`
`Received 17 April 2005; revised 10 September 2005; accepted 12 September 2005
`
`
`
`Owingto its favourable tolerability profile versus cytotoxic chemotherapy, endocrine therapy is the treatment of
`choice for postmenopausal women with hormone receptor-positive advanced breast cancer (ABC). However,
`tolerability concerns associated with some endocrine treatments and the potential for cross-resistance has
`helped to drive the need for new, effective and better-tolerated agents. Fulvestrant is a new type of oestrogen
`receptor antagonist with no agonist effects. In phaseIll trials, fulvestrant has been shownto be at least as effective
`as the third-generation aromataseinhibitor (Al) anastrozole in the treatment of postmenopausal women with ABC
`progressing on prior tamoxifen therapy. Fulvestrant is administered as a once-monthly 250 mg intramuscular
`injection into the gluteus muscle. Here wereview thetolerability of fulvestrantin the treatment of postmenopausal
`
`women with hormone-sensitive ABC and compareit with that of the four most frequently prescribed endocrine
`treatments for advanced disease (tamoxifen, anastrozole, letrozole and exemestane). Compared with these
`agents, fulvestrant is well tolerated and is associated with a lowerincidenceof joint disorders compared with the
`non-steroidal Als and none of the potential androgenic side-effects that are sometimes seen with steroidalAls.
`It is also associated with hot flushes compared with tamoxifen. Fulvestrant therefore providesclinicians and
`
`patients with a useful, well-tolerated option for the treatment of hormone-sensitive ABC. Integration of such
`agents into the endocrine treatment sequence may extend the opportunity for using well-tolerated therapies
`
`before chemotherapy needs to be considered and thus may improve quality oflife for patients with ABC. The
`overall safety profiles of newer agents such asfulvestrant will become increasingly clear with their ongoing use.
`Key words:breast, breast cancer, fulvestrant, hormone, neoplasms, therapy
`
`
`
`introduction
`
`For patients with advanced breast cancer (ABC) in whom
`palliation of symptoms and maintenance of quality oflife are
`the primary objectives, it is important that any treatment is
`well tolerated to aid compliance and treatment success. Owing
`to its favourable tolerability profile, endocrine therapy is the
`treatment of choice for postmenopausal women with hormone
`receptor-positive ABC (i.e. about 73% of the total
`postmenopausal ABC population). Currently available
`endocrine treatments for advanced disease include the
`selective oestrogen receptor (ER) modulator tamoxifen, the
`third-generation, non-steroidal aromatase inhibitors (Als)
`anastrozole and letrozole, and the steroidal AI exemestane.
`The most recent addition to the armamentarium of endocrine
`agents is fulvestrant, a novel ER antagonist with no agonist
`effects [1]. It binds, blocks and degrades the ER, thereby
`downregulating cellular ER levels, which in turn leads to
`reduced expression of the progesterone receptor.
`
`“Correspondence to: Dr |. Vergote, University Hospitals Leuven, Department of
`Gynecologic Oncology, Gasthuisberg, Herestraat 49, B-3000 Leuven, Belgium.
`Tel: +32-16-34-46-35; Fax: +32-16-34-46-29;
`E-mail: Ignace.Vergote@uz.kuleuven.ac, be
`
`Here wereview the tolerability profile of fulvestrant [250 mg
`once monthly, intramuscular (i.m.) injection], and compareit
`with tolerability data from the four most frequently prescribed
`endocrine treatments for ABC: tamoxifen (20 mg once daily,
`orally), anastrozole (1 mg oncedaily,orally), letrozole (2.5 mg
`once daily, orally) and exemestane (25 mg oncedaily, orally).
`
`fulvestrant
`
`oestrogen agonistactivity
`In a phaseI trial involving 30 healthy postmenopausal women,
`volunteers received a single dose of 125 or 250 mgfulvestrant or
`placebo im. followed 2 weeks later by 20 mg/day
`ethinyloestradiol for 2 weeks. No evidence of agonist activity in
`the endometrium was observed withfulvestrant [2]. In addition,
`when compared with placebo, after 21 days of treatment the
`mean change in oestrogen-stimulated endometrial thickening
`was prevented using 250 mg fulvestrant (1.5 versus 8.1 mm;
`P < 0.001). Therefore, in contrast to tamoxifen, which has
`well-known agonist effects in the endometrium,fulvestrant
`lacks oestrogen agonist effects and so is unlikely to be associated
`with an increasedrisk of endometrial cancer with long-term use.
`
`© 2005 European Society for Medical Oncology
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`LOZ‘TEA[neuoAptstsatuy)surydoyysuyor/Arerqr]Jamoyuasry“gUOTIe/S1o's[eummol[psoyxoououues/:dyyWoypapropumoc]
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`AstraZeneca Exhibit 2075 p. 1
`InnoPharma Licensing LLC v. AstraZeneca AB IPR2017-00905
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`Annals of Oncology
`
`comparative tolerability: fulvestrant versus
`anastrozole
`
`Two phaseIII studies have shownthat fulvestrantis at least
`as effective as anastrozole in the treatment of postmenopausal
`women (7 = 851) with ABC who have progressed or relapsed
`on prior tamoxifen treatment [3, 4]. This was also borne out in
`the subgroup of patients with visceral metastases [5].
`Study 0020 (7 = 451) was an open-label, randomised,parallel-
`group, multicentre study conducted in Europe, South Africa
`and Australia, in which fulvestrant was delivered in a single 5 ml
`im. injection. The median duration of follow-up in this study
`was 14.4 months[4]. Study 0021 (n = 400) was a double-blind,
`randomised, multicentre, parallel-group study conducted in
`North America in which fulvestrant was delivered in two
`x 2.5 ml im. injections. The median duration of follow-up in
`this study was 16.8 months [3]. Overall, the median duration
`of treatment for both studies was 5.5 months (range 0.9-36.8)
`in the fulvestrant group and 5.5 months (range 0.6-31.4) in the
`anastrozole group.
`Both studies were prospectively designed to allow combined
`analysis of data [6]. Combined analysis of the safety data showed
`that both treatments were well tolerated and there was a low
`incidence of withdrawals due to adverse events (AEs) overall
`(fulvestrant, 2.8%; anastrozole, 1.9%) and those AEs considered
`to be drug related (fulvestrant, 0.9%; anastrozole, 1.2%). The
`most common AEs in these trials were nausea (26% versus
`25.3%), asthenia (22.7% versus 27.0%), pain (18.9% versus
`20.3%), vasodilatation (dizziness, light-headedness,
`symptomatic hypotension) (17.7% versus 17.3%) and headache
`(15.4% versus 16.8%) in the fulvestrant and anastrozole groups,
`respectively [6]. In these studies, seven AEs considered relevant
`to endocrine therapy were pre-defined for statistical analysis. In
`bothtrials, there was no statistically significant difference
`between treatment groups in the incidence of weight gain,
`thromboembolic disease, gastrointestinal disturbance, hot
`flushes or urinary tract infections (Figure 1). However, there
`wasa significantly lower incidence of joint disorders (including
`arthralgia, arthrosis and arthritis) with fulvestrant (5.4%)
`compared with anastrozole (10.6%) (P = 0.0036) (Figure 1).
`The effect of fulvestrant on lipid variables was also monitored
`as part of laboratory investigations in thesetrials; no major
`changes in lipid variables occurred with either treatment
`(AstraZeneca, data on file). In an extended follow-up for
`time to death, conducted when 75% of patients had died,
`no long-term safety concerns were apparent [7].
`Fulvestrant i.m. injection was well tolerated locally; in most
`cases injection-site reactions were non-serious, mild and
`transient: only 4.6% and 1.1% offulvestranti.m. injections in
`trials 0021 and 0020,respectively resulted in injection-site
`events. Across the two studies, only two patients (0.5%) in the
`fulvestrant group withdrew because of injection-site events. In
`a comparison of fulvestrant and placebo injections in trial 0021,
`there was no difference in the incidenceof injection-site
`reactions, demonstrating that the fulvestrant i.m. injection is
`well tolerated in contrast to some other injectable anticancer
`agents such as the steroidal AI formestane. For example, in
`a phase II dose-finding study, formestane treatment (500-1000
`mg monthly) resulted in injection-site events (abscesses, painful
`
`
`
`@ Fulvestrant
`Cl Anastrozole
`
`P=0.91
`87
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`a a i”) oe
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`60 5
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`50 P=0.53
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`£
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`30>
`
`207
`
`0
`
`P=0,0036
`107
`P=0.06
`45
`P=0.68
`
`P=0.51
`P=0.35
`18
`
`
`
`
`Gastrointestinal
`Hot
`Urinarytract
`Joint Thromboembolic Vaginitis
`Weight
`disturbances
`flushes
`infection
`disorders
`disease
`gain
`
`Figure 1. Theincidence of predefined adverse events in a combined analysis
`of two phaseIII trials comparing fulvestrant with anastrozole as second-line
`treatments in patients with advanced breast cancer [6]. Reprinted by
`permission of Wiley-Liss, Inc., a subsidiary of John Wiley & Sons, Inc.
`
`lumpsandallergic-type reactions) in 19% of patients [8].
`To date, there have been no head-to-head clinical studies
`comparing fulvestrant with either letrozole or exemestane.
`
`comparativetolerability: fulvestrant versus
`tamoxifen
`
`A double-blind, double-dummy randomised phase HItrial has
`shown that fulvestrant has similar efficacy to tamoxifen in the
`first-line treatment of postmenopausal women (n = 587) with
`hormonereceptor-positive ABC [9]. The median duration of
`treatment in this study was 8.3 months (range 0.9-26.5) in the
`fulvestrant group and 9.3 months (range 0.9—-25.1) in the
`tamoxifen group.
`At a median follow-up of 14.5 months, the most frequent
`AEs in both groups were nausea (20.3% fulvestrant versus
`22.5% tamoxifen), asthenia (19.4% versus 20.3%),
`vasodilatation (14.8% versus 21.4%), pain (13.9% versus
`19.2%) and bone pain (13.9% versus 17%) [9]. Most AEs
`were mild or moderate in severity. A total of 129 (41.6%)
`patients in the fulvestrant group and 139 (51.3%) patients in
`the tamoxifen group experienced drug-related AEs. The most
`frequent drug-related AEs in both treatment groups were
`vasodilatation, injection-site pain and nausea.
`Of the AEs prospectively defined for statistical comparison,
`there were no significant differences between the two treatment
`groups for vaginitis and thromboembolic disease. There was
`a trend for fewer gastrointestinal disturbances (nausea,
`vomiting, diarrhoea and constipation) with fulvestrant (37.1%
`versus 43.2%; P = 0.16) and the incidence of hot flushes was
`lower in the fulvestrant group than in the tamoxifen group
`(17.7%versus 24.7%; P = 0.05) (Figure 2). The latter
`observation may be related to the fact that fulvestrant does
`not cross the blood—brain barrier (AstraZeneca, data onfile).
`
`tamoxifen
`
`Tamoxifen is generally well tolerated, although with long-term
`use its partial oestrogen agonist properties increase the risk of
`endometrial cancer. In an overview of the randomisedtrials
`of adjuvant tamoxifen including data for 37 000 women,the
`
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`PLO‘TEAnyUoApssoatuy)surydoxysuyor/Aresqry]Jemoyuasry“gUOTIe/S10's[euol[psoyxoououue//:dyyWoypapropumoc]
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`Volume 17 | No. 2 | February 2006
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`doi:10.1093/annone/mdj047 | 201
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`AstraZeneca Exhibit 2075 p. 2
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`PLO‘TEAnyUoApssoatuy)surydoxysuyor/Aresqry]Jemoyuasry“gUOTIe/S10's[euol[psoyxoououue//:dyyWoypapropumoc]
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`Annals of Oncology
`
`P=0.16
`
`117
`
`ne)
`
`P=0.0501
`67
`
`Gastrointestinal
`distubances
`
`Hotflushes
`
`
`@ Fulvestrant
`
`
`Tamoxifen
`
`
`
`P=0.26
`17
`
`Vaginitis
`
`p=0.22
`
`Thromboembolic
`disease
`
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`
`_ 40
`yu
`5 30
`3
`£
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`60
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`50 —
`
`20 +
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`10 —
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`Figure 2. The incidence of predefined adverse events in a phaseIIT trial
`comparing fulvestrant with tamoxifen as first-line treatments in patients
`with advanced breast cancer [9]. Reprinted with permission from the
`American Society of Clinical Oncology.
`
`incidence of endometrial cancer was doubledin trials of 1 or
`2 years’ treatment and approximately quadrupledin trials of
`5 years’ tamoxifen [10]. Tamoxifen treatment may stimulate
`‘tumourflare’ subsequent to an initial response andis also
`associated with hot flushes and an increased risk of stroke
`and thromboembolic disease. In a trial comparing anastrozole
`with tamoxifen in the first-line treatment of ABC, tamoxifen
`was associated with a significantly higher incidence of
`thromboembolic events (6.5% versus 3.6%; P = 0.0434) and
`vaginal bleeding was also reported in fewer anastrozole-treated
`patients (2.2% versus 1%) [11]. The incidence of
`thromboembolic events in a trial comparing tamoxifen with
`letrozole was 2%and 1%,respectively [12]. The agonist activity
`of tamoxifen may, however, have beneficial effects on bone
`mineral density, particularly with long-term treatment,
`e.g. in the adjuvantsetting [13].
`
`aromatase inhibitors
`
`Third-generation Als are effective and generally well tolerated
`in the treatment of postmenopausal women with ABC. The
`selective non-steroidal Als anastrozole and letrozole have been
`shown to beatleast as effective as tamoxifen in this setting and
`anastrozole was associated withsignificantly fewer
`thromboembolic events than tamoxifen [11, 14]. The Als inhibit
`endogenous oestrogen synthesis via aromatase, which in
`postmenopausal womenresults in very low plasmalevels of
`oestrogen, and these agents may therefore be associated with
`somedeleterious effects on bone [15].
`Joint disorders (e.g. arthralgia) have also been reported for
`all of the third-generation Als [6, 16-19]. For example, in a trial
`comparing the efficacy and tolerability of letrozole and
`megestrol acetate in patients with ABC,arthralgia was
`experienced by more letrozole-treated patients (13.2%)
`compared with those receiving the comparator treatment
`(7.9%) [16]. However, in a phase IT] comparative trial of
`letrozole and tamoxifen there was no difference in the incidence
`of arthralgia (16% versus 15%,respectively) [14]. As previously
`stated, significantly more anastrozole-treated patients
`experienced joint disorders compared with fulvestrant (10.6%
`versus 5.4%; P = 0.0036) in comparative phaseIII trials [6]. The
`
`steroidal AI exemestaneis also associated with arthralgia. In
`a recent phase III study comparing the efficacy and tolerability
`of this steroidal AI with tamoxifen, 11% of exemestane-treated
`patients experienced arthralgia compared with 5% of those
`treated with tamoxifen [19].
`The most common AEsassociated with anastrozole are
`transient gastrointestinal disturbances, generally mild-to-
`moderate in intensity, headache, asthenia, bone pain and hot
`flushes [20, 21]. The tolerability profile of letrozole appears to be
`broadly similar to that of anastrozole with the most commonly
`18=”|
`encountered AEs also including nausea/vomiting, headache,
`asthenia, bone pain and hotflushes [16, 22]. In the only study
`to compare directly the efficacy and tolerability of anastrozole
`and letrozole, there were no significant differences in the
`incidence of any AEs [23].
`The most frequently reported drug-related AEs with
`exemestane treatment are hot flushes, nausea and fatigue [24].
`Exemestane has weak androgenic properties and has been
`associated with androgenicside-effects such as weight gain,
`alopecia and acne, particularly when used at higher doses [25].
`In a phase III trial comparing theefficacy and tolerability of
`exemestane (25 mg/day) and megestrol acetate (160 mg/day),
`the incidence of grade 3 or 4 weight gain after a median of
`only 17 weeks’ treatment was 8% in the exemestane group
`and 17% in the megestrol acetate group (P = 0.001) [26].
`Androgenic side-effects such as hair loss, hypertrichosis,
`hoarseness and acne are more commonly reported. with higher
`doses of exemestane, occurring in 10% of patients treated
`with a 200 mg daily dose [27]. In two short-term trials using
`25 mg/day exemestane, hypertrichosis and acne were reported
`in ~2% of patients [28] and grade 2/3 skin disorders were
`reported in 8%of patients (no reports in the tamoxifen group)
`[18]. In a recent phaseIII trial, alopecia was reported in 4% of
`patients receiving exemestane 25 mg/day compared with 1% of
`those receiving tamoxifen [19].
`Compared with tamoxifen, exemestane treatment was also
`associated with a higher incidence of increased. gamma-glutamyl
`transferase (33% versus 26%), increased alkaline phosphatase
`(26%versus 14%), increased bilirubin (11% versus 3%),
`dyspnoea (17% versus 11%) and AEsof the skin (19% versus
`14%), whereas hot flushes (29% versus 24%), bone pain (22%
`versus 17%), nausea (21%versus 14%) and oedema (20%versus
`10%) were all more common in tamoxifen-treated patients [18].
`In a subsequent phaseIII study, exemestane was associated with
`a higher incidence of weight gain (19%versus 14%), arthralgia/
`myalgia (11% versus 5%) and diarrhoea (9% versus 3%)
`compared with tamoxifen. In this study, constipation
`(13% versus 8%) and vaginal discharge (7% versus 2%)
`were more commonly seen in patients receiving tamoxifen [19].
`
`
`
`
`
`summary
`
`More than 1100 postmenopausal women havereceived
`fulvestrant during the clinical study programme. This new
`endocrine agent exhibits a predictable tolerability profile that
`may offer benefits compared with other agents including
`tamoxifen and the three currently available Als: anastrozole,
`letrozole and exemestane.In all the phaseIII trials in
`postmenopausal women with locally advanced or metastatic
`
`202 | Vergote & Abram
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`Volume 17 | No. 2 | February 2006
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`AstraZeneca Exhibit 2075 p. 3
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`. Pippen J, Osborne CK, Howell A, Robertson JFR. Fulvestrant (Faslodex) versus
`anastrozole (Arimidex) for the treatment of advanced breast cancer: a prospective
`combined survival analysis of two multicentertrials. Breast Cancer Res Treat
`2003; 82 (Suppl 1): $101 (Abstr 426}.
`. Goss PE, Powles TJ, Dowsett M et al. Treatment of advanced postmenopausal
`breast cancer with an aromatase inhibitor, 4-hydroxyandrostenedione: phase|
`eport. Cancer Res 1986; 46: 4823-4826.
`. Howell A, Robertson JFR, Abram P et al. Comparison of fulvestrant v tamoxifen
`or the treatment of advanced breast cancer in postmenopausal women
`previously untreated with endocrine therapy: a multinational, double-blind,
`andomized trial. J Clin Oncol 2004; 22: 1605-1613.
`Early Breast Cancer Trialists’ Collaborative Group. Tamoxifen for early breast
`cancer: an overview of
`the randomised trials. Lancet 1998; 351: 1451-1467.
`Bonneterre J, Buzdar A, Nabholtz JM et al. Anastrozole is superior to tamoxifen
`as first-line therapy in hormone receptor positive advanced breast carcinoma.
`Cancer 2001; 92: 2247-2258.
`letrozole versus
`jouridsen H, Gershanovich M, Sun Y et al. Superior efficacy of
`amoxifen asfirst-line therapy for postmenopausal women with advanced breast
`cancer: results of a phaseIll study of the international letrozole breast cancer
`group. J Clin Oncol 2001; 19: 2596-2606.
`Fisher B, Costantino JP, Redmond CK et al. Endometrial cancer in tamoxifen-
`reated breast cancer patients: findings from the National Surgical Adjuvant
`Breast and Bowel Project (NSABP) B-14. J Natl Cancer Inst 1994; 86: 527-537.
`ouridsen H, Gershanovich M, Sun Y et al. PhaseIll study of letrozole versus
`amoxifen as first-line
`therapy of advanced breast cancer in postmenopausal
`women: analysis of survival and update of efficacy from the International
`Letrozole Breast Cancer Group. J Clin Oncol 2003; 21: 2101-2109.
`Buzdar A, Robertson JFR, Eiermann W, Nabholtz JM. An overview of the
`pharmacology and pharmacokinetics of the newer generation aromatase
`inhibitors anastrozole,
`letrozole and exemestane. Cancer 2002; 95: 2006-2016.
`Dombernowsky P, Smith |, Falkson G et al. Letrozole, a new oral aromatase
`b
`inhibitor
`for advanced breast cancer: double-blind randomized trial showing
`a dose effect and improved efficacy and tolerability compared with megestrol
`acetate. J Clin Oncol 1998; 16: 453-461.
`Donnellan PP, Douglas SL, Cameron DA, Leonard RC. Aromatase inhibitors and
`arthralgia. J Clin Oncol 2001; 19: 2767.
`Paridaens R,Dirix L, Lohrisch C et al. Mature results of a randomized phase II
`nulticenter study of exemestane versus tamoxifen asfirst-line hormone therapy
`or postmenopausal women with metastatic breast cancer. Ann Oncol 2003; 14:
`1391-1398.
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`Annals of Oncology
`
`breast cancer fulvestrant was well tolerated; AEs were generally
`mild or moderate in intensity. The higher incidence of joint
`disorders with the Als compared with fulvestrant illustrates
`the value of fulvestrant in a patient population who may be
`predisposed to musculoskeletal conditions.
`Fulvestrant has no proliferative effect on the endometrium
`[2] and is therefore unlikely to lead to an increased risk of
`endometrial cancer following long-term exposure such as that
`produced by tamoxifen [29]. There have been no reports of
`adverse events that may be attributable to androgenicactivity
`and fulvestrant is associated with a lower incidence of hot
`flushes compared with tamoxifen. In contrast to other
`endocrine agents used in the treatment of ABC, fulvestrantis
`administered as a once-monthly im. injection.
`In summary, fulvestrant 250 mg once-monthly i.m. injection
`is a well-tolerated and effective treatment for postmenopausal
`women with hormone-sensitive ABC. Thetolerability profile
`and route of administration of fulvestrant may also lead to
`improved patient compliance and thusbetter patient outcomes,
`although somepatients may prefer to receive their breast cancer
`treatment orally [30]. The previously demonstrated lack of
`cross-resistance of fulvestrant with other endocrine treatments
`along with its favourable tolerability profile means that this
`agent provides clinicians and patients with a useful additional
`option for the treatment of hormone-sensitive ABC. Whilst the
`overall safety profiles of newer endocrine treatments will
`becomeincreasingly clear with their ongoing use, the
`integration of agents such as fulvestrant into the endocrine
`treatment sequence may extend the opportunity for using
`well-tolerated therapies before chemotherapy needs to be
`considered and thus may improve quality of life for patients
`with advanced disease. In addition, the good tolerability profile
`of fulvestrant may suggest possible benefits for this agent in the
`adjuvant setting where longer-term use would be anticipated.
`Although as yet unproven,clinical trials of fulvestrant in the
`adjuvant setting are being planned.
`
`acknowledgements
`
`Editorial assistance was provided by Dawn Batty PhD, with
`financial support from AstraZeneca.
`
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` =
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`PLO‘TEAnyUoApssoatuy)surydoxysuyor/Aresqry]Jemoyuasry“gUOTIe/S10's[euol[psoyxoououue//:dyyWoypapropumoc]
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