Induz in Ovulation Induction
Dr Sujoy Dasgupta
MBBS (Gold Medalist, Hons) MS (Obst & Gynae- Gold Medalist)
DNB, FIAOG, Fellow- Reproductive Endocrinology and Infertility (ACOG, USA)
Assistant Professor: SRIMSH, Durgapur
Consultant:
RSV Hospital, Kolkata
Iris Hospital, Kolkata
Behala Balananda Brahmachary Hospital, Kolkata
Secretary, Perinatology Committee: Bengal Obstetric and Gynaecological Society (BOGS)- 2016-17
Managing Committee Member: BOGS- 2016-17
15 Publications: National and International Journals
NOTICE
Medicine is an ever-changing science. As new research and clinical
experience broaden our knowledge, changes in treatment and drug
therapy are required. The authors and the publisher of this work have
checked with sources believed to be reliable in their efforts to provide
information that is complete and generally in accord with the standards
accepted at the time of publication. However, in view of the possibility of
human error or changes in medical sciences, neither the authors nor the
publisher nor any other party who has been involved in the preparation or
publication of this work warrants that the information contained herein is in
every respect accurate or complete, and they disclaim all responsibility for
any errors or omissions or for the results obtained from use of the information
contained in this work. Readers are encouraged to confirm the information
contained herein with other sources.
Incidence of all malformations was not different between
the two groups (p= 0.25, 95%CI 0.78-4.71).
However, the incidence of locomotor malformations (p= 0.0005, 95% CI
2.64-27.0) and cardiac anomalies (p= 0.0006 95% CI 3.30-58.1) were
higher than in the control groups
Fertil Steril. 2006 Jun;85(6):1761-5
 No difference in overall rates of major & minor congenital
malformations among newborns from mothers who conceived after
LTZ or CC treatments
 It appears that congenital cardiac anomalies are less frequent in LTZ
group
 The concern that LTZ use for ovulation induction could be
teratogenic is unfounded based on this data
Number of newborns with major malformations
Percent of newborns with malformations
Hum Reprod. 2017 Jan;32(1):125-132
N= 3928
LTZ stimulation reduces risk of miscarriage, with no increase in risk of major
congenital anomalies or adverse pregnancy
Sharma S, et al. PLoS ONE. 2014; 9(10): e108219
Structural
malformations &
chromosomal
abnormalities
N= 623
Natural conception
group
5 / 171 babies
(2.9%)
LTZ group
5 / 201 babies
(2.5%)
CC group
10 / 251 babies
(3.9%)
Other Studies
Reference No of patients
Forman R, et al. J Obstet Gynaecol Can 2007;29:668-71. 430
Dehbashi S, et al. Iran J Med Sci 2009;34:23-8. 100
Legro RS, et al. N Engl J Med. 2014 Jul 10;371(2):119-29. 750
Banerjee Ray P, et al. Arch Gynecol Obstet. 2012 Mar;285(3):873-7. 147
Roy KK, et al. J Hum Reprod Sci. 2012 Jan-Apr; 5(1): 20–25 204
Wu XK, et al. Fertil Steril 2016;106:757-765 644
Requena A, et al. Hum Reprod Update. 2008 Nov-Dec;14(6):571-82.
(Meta-analysis)
2573
Diamond MP, et al. N Engl J Med 2015;373:1230-40. 900
Wang R, et al. BMJ. 2017; 356: j138.
15th Jan 2017
Ban On Letrozole Lifted After 5 Long Years By DCGI
13
Letrozole Revoked
MINISTRY OF HEALTH AND FAMILY WELFARE [(Department of Health and
Family Welfare) NOTIFICATION: New Delhi, the 17th February, 2017 G.S.R. 145(E)]
Current Clinical Guidelines
For women with PCOS and BMI >30, letrozole should be
considered as first-line therapy for ovulation induction
because of the increased live birth rate compared with
clomiphene citrate
Endocrine Society Clinical Guideline (2013) recommends:
 Clomiphene citrate (or comparable estrogen modulators such as
Letrozole) as the first-line treatment of anovulatory infertility in women
with PCOS.
American Association of Clinical Endocrinologists, American College of
Endocrinology, And Androgen Excess & PCOS Society (2015)
 Treatment for women with PCOS and anovulatory infertility should
begin with an oral agent such as clomiphene citrate or Letrozole, an
aromatase inhibitor.
 CC should be first-line pharmacotherapy for ovulation induction and letrozole can also be
used as first-line therapy.
Letrozole as
Ovulation
Inducer
Clomiphene Citrate
 Ovulation: 70-80% cases
 Pregnancy rate: 10-20%/cycle*
not more then 6 cycle continuously and not more then 12 cycles in life time
..to avoid possible Risk of (?) Ovarian Malignancy (NICE, 2013)
In doses of 50 mg/d /cycle and can be increased to 150 mg until ovulation is
achieved
*Pavone ME, et al. J Clin Endocrinol Metab. 2013 May; 98(5): 1838–1844.
CC Resistance/ Failure
 CC RESISTANT:
If patient fails to ovulate despite 3 CC cycles
 About 20-25% of Anovulatory women are CC- resistant*
 CC FAILURE:
 CC-resistant
 women who ovulate, but do not get pregnant
 Women who get pregnant but end in miscarriage
*Mitwally MF, et al. Fertil Steril. 2001 Feb;75(2):305-9, Azargoon A, et al. Iran J Reprod Med. 2012 Jan; 10(1): 33–40.
Management of PCOS-Anovulation
Life Style Modification
CC
1st Line Treatment
No Ovulation (CC Resistance)
Metformin + CC FSH Lap Ovarian Drilling Letrozole
Ovulates
Management of PCOS-Anovulation
Life Style Modification
CC
1st Line Treatment
No Ovulation (CC Resistance)
Metformin + CC FSH Lap Ovarian Drilling Letrozole
Ovulates
Letrozole
3rd generation aromatase inhibitor (AI)
Non-steroidal, potent & selective
1st study (Mitwally & Casper, 2001): OI
Mitwally MF, et al. Fertil Steril. 2001 Feb;75(2):305-9.
granulosa cells
FSH
aromatase
LH
theca cells
androstenedione
estrogen
Follicular Physiology
Aromatase
1. Ovary
2. Adipose tissue
3. Brain
Exogenous FSH
CC binds to ER & depletes
receptor concentrations
aromatase inhibitors
Follicular Development
Pituitary gland
FSH
Stimulates follicular growth Estrogen
Large follicles (more FSH receptors) Smaller follicles (less FSH receptors)
Continues to grow (mono follicular) Atresia
Ovulation
Journal of Human Reproductive Sciences / Volume 6 / Issue 2 / Apr - Jun 2013
Follicular Development
Pituitary gland
FSH
Stimulates follicular growth Estrogen
Large follicles (more FSH receptors) Smaller follicles (less FSH receptors)
Continues to grow (mono follicular) Atresia
Ovulation
CC → No feedback inhibition
Journal of Human Reproductive Sciences / Volume 6 / Issue 2 / Apr - Jun 2013
Follicular Development
Pituitary gland
FSH
Stimulates follicular growth Estrogen
Large follicles (more FSH receptors) Smaller follicles (less FSH receptors)
Continues to grow (mono follicular) Atresia
Ovulation
CC → No feedback inhibition
Journal of Human Reproductive Sciences / Volume 6 / Issue 2 / Apr - Jun 2013
Follicular Development
Pituitary gland
FSH
Stimulates follicular growth Estrogen
Follicles with FSH receptors Smaller follicles (less FSH receptors)
Continues to grow (multi follicular) Atresia
Ovulation
CC → No feedback inhibition
Journal of Human Reproductive Sciences / Volume 6 / Issue 2 / Apr - Jun 2013
Follicular Development
Pituitary gland
FSH
Stimulates follicular growth Estrogen
Large follicles (more FSH receptors) Smaller follicles (less FSH receptors)
Continues to grow (mono follicular) Atresia
Ovulation
Letrozole → maintains feedback
inhibition
Journal of Human Reproductive Sciences / Volume 6 / Issue 2 / Apr - Jun 2013
Follicular Development
Pituitary gland
FSH
Stimulates follicular growth Estrogen
Large follicles (more FSH receptors) Smaller follicles (less FSH receptors)
Continues to grow (mono follicular) Atresia
Ovulation
Letrozole → maintains feedback
inhibition
Journal of Human Reproductive Sciences / Volume 6 / Issue 2 / Apr - Jun 2013
Letrozole vs CC
Letrozole vs CC
Letrozole (Aromatase Inhibitor)
Blocks Aromatase Does not block ER
Increased intraovarian androgen 1. No adverse effect on
endometrium/
cervix
Augment FSH receptors Stimulates IGF-I 2. No hot flush
Synergistically promotes follicular growth
Clomiphene (Anti-estrogen)
Blocks ER
1. ↓ endometrial thickness
↓glandular density
↓ uterine blood flow in luteal
phase
2. ↓quantity/ quality of Cx mucus
3. Hot flushes (prolonged
accumulation in tissues→
prolonged depletion of ER)
J Clin Endocrinol Metab, March 2006, 91(3):760 –771 J Hum Reprod Sci 2011 May-Aug; 4(2): 76–79. J Hum Reprod Sci 2013 Apr-Jun; 6(2): 93–98
Letrozole vs CC
Letrozole (Aromatase Inhibitor)
Blocks Aromatase Does not block ER
Increased intraovarian androgen 1. No adverse effect on
endometrium/
cervix
Augment FSH receptors Stimulates IGF-I 2. No hot flush
Synergistically promotes follicular growth
Clomiphene (Anti-estrogen)
Blocks ER
1. ↓ endometrial thickness
↓glandular density
↓ uterine blood flow in luteal
phase
2. ↓quantity/ quality of Cx mucus
3. Hot flushes (prolonged
accumulation in tissues→
prolonged depletion of ER)
J Clin Endocrinol Metab, March 2006, 91(3):760 –771 J Hum Reprod Sci 2011 May-Aug; 4(2): 76–79. J Hum Reprod Sci 2013 Apr-Jun; 6(2): 93–98
Letrozole vs CC
Letrozole (Aromatase Inhibitor)
Blocks Aromatase Does not block ER
Increased intraovarian androgen 1. No adverse effect on
endometrium/
cervix
Augment FSH receptors Stimulates IGF-I 2. No hot flush
Synergistically promotes follicular growth
Clomiphene (Anti-estrogen)
Blocks ER
1. ↓ endometrial thickness
↓glandular density
↓ uterine blood flow in luteal
phase
2. ↓quantity/ quality of Cx mucus
3. Hot flushes (prolonged
accumulation in tissues→
prolonged depletion of ER)
J Clin Endocrinol Metab, March 2006, 91(3):760 –771 J Hum Reprod Sci 2011 May-Aug; 4(2): 76–79. J Hum Reprod Sci 2013 Apr-Jun; 6(2): 93–98
Clomiphene citrate vs Letrozole
Letrozole Uses
 Letrozole has been used in the following three
situations:
 OI in polycystic ovary syndrome (PCOS)
 OI in intrauterine insemination (IUI)
 Ovarian stimulation for IVF/ICSI
Letrozole for OI in polycystic ovary
syndrome (PCOS)
Clinical Evidence
CONCLUSION: letrozole showed a better endometrial response and pregnancy rate
compared to CC
Endometrial thickness on the day of hCG
administration (mm) 9.1±0.3 6.3±1.1 0.014 (S)
Roy KK, et al. J Hum Reprod Sci. 2012 Jan-Apr; 5(1): 20–25.
Population Studied
7 studies out of 232 selected
• N= 1833 patients
– LTZ: 906
– CC: 927
• N= 4999 ovulation cycles
– LTZ: 2455
– CC: 2544
OUTCOME MEASURES
 Primary outcome measure:
Live birth rate (LBR)
 Secondary outcomes measures:
Ovulation rate per cycle
Clinical pregnancy rate
Miscarriage rate
Multiple pregnancy rates
 Result
 statistically significant increase in the live birth and pregnancy rates in the letrozole group when
compared to the CC group
 Conclusion
 LTZ is superior to CC considering live birth & pregnancy rates in patients with PCOS
CC 100 mg for at least 6 cycles → failure to form the DF, then put on letrozole ; 5 mg for 5 days for 4 cycles →
unable to form the DF, combination therapy (letrozole 5 mg + CC100 mg) for 5 days
PCOS patients resistant to clomiphene and letrozole used alone as single agents, Letrozole with CC
combination may be used as a first-line therapy to induce ovulation in severe cases of PCOS in order
to save time and expense
 Statistically significantly increased the ovulation rate by 33.3% in the treatment group
 letrozole can be used as an effective and simple alternate ovulation-inducing agent in these
women
Fertility and Sterility Vol. 94, No. 7, December 2010
 N=94 : letrozole ( 2.5 mg/day) + HMG,
 N= 90: CC (50 mg/day) + HMG,
 N=71: HMG only.
 All women received one treatment regimen in one treatment cycle.
 All patients were given HMG 75 IU on alternate days daily starting on day 3 or day 7 until the day of
administration of hCG.
 hCG 10,000 IU : when at least 1 follicle with mean diameter ≥18 mm
 Pts advised natural intercourse after 24-36 hours after hCG
Results
Ovulation rate and Clinical Pregnancy Rates
Other parameters
Conclusion
Letrozole in combination
with hMG
reduced duration of
stimulation and total HMG
dose needed for stimulation
significantly higher
monofollicular
development
The regimen of letrozole + HMG is more effective and safer than CC + HMG or HMG
alone for ovulation induction in cases of CC resistance
Letrozole vs. LOD in CC Failure
LTZ had superior reproductive outcomes compared with LOD in women with
CC-resistant PCOS
LTZ could be used as 1st line treatment for women with CC-resistant PCOS
Liu W, et al. Experimental and Therapeutic Medicine. 2015; 10: 1297-1302.
Comparison of Letrozole vs. Tamoxifen
LTZ
superior to
TMX
Higher
pregnancy
rate
Higher
ovulation
rate
El-Gharib et al. J Reprod Infertil. 2015; 16(1): 30-35.
 60 moderately obese patients with PCOS
 N=31 clomiphene citrate-metformin
 N=29 letrozole-metformin therapy.
 Stimulation was carried out for the procedures of intrauterine insemination (IUI).
 60 moderately obese patients with PCOS
 N=31 clomiphene citrate-metformin
 N=29 letrozole-metformin therapy.
 Stimulation was carried out for the procedures of intrauterine insemination (IUI).
 RESULTS:
0
2
4
6
8
10
letrozole+metformin CC+metformin
8.9
6.3
EndometrialThickness(mm)
0
5
10
15
20
25
Letrozole+metformin CC+Metformin
20.6
9.6
PregnancyRateafterthirdIUI
cycle(%)
Fig : Showing Endometrial Thickness Fig : Preg Rate after third IUI cycle
Conclusion: Study demonstrated the advantages of the use of letrozole over clomiphene citrate in
combination with metformin in moderately obese patients with PCOS who are resistant to
stimulation with clomiphene citrate alone.
Letrozole for OI in intrauterine
insemination (IUI)
Clinical Evidence
 Methods
 group A :Letrozole (5 mg) for five days and gonadotrophins (HMG) 75 IU once daily for 3−5 days
 group B : Clomiphene Citrate (50 mg) for 5 days and gonadotrophins (HMG) in a dose of 75 IU for 3–
5days
 Results
 Patients co-treated with Letrozole required fewer gonadotrophins administrations and had a thicker
endometrium
 The pregnancy rate was not significantly different between two groups (11% vs. 12.6%)
J Reprod Infertil 2013 Jul-Sep; 14(3): 138–142.
Conclusion:
The addition of Letrozole to gonadotrophins decreases gonadotrophins requirements and improves
endometrial thickness, without a significant effect on pregnancy rates
180 infertile women:
 Group A: 5 mg/day letrozole on day 3-7 of menstrual cycle.
 Group B: 100 mg/day clomiphene in the same way as letrozole.
 hMG administered in both groups every day starting on day between 6-8 of
cycle.
 hCG(5000 IU) trigger when have two follicles of ≥16 mm.
 IUI was performed 36 hr later.
Int J Reprod Biomed (Yazd).2017 Jan;15(1):49-54.
Results
0
5
10
Letrozole+ HMG
CC+HMG
3.8
3.7
8.99
8.46
EndometrialThickness(mm)
Fig 2: Showing Endometrial Thickness
Before treatment
After Treatment
0
2
4
6
Letrozole+ HMG CC+HMG
5.7
anHyperstimulation(%)
Fig 3: Showing Ovarian
Hyperstimulation
0
10
20
30
Letrozole+ HMG
CC+HMG
26.51
12.64
ClinicalPregnancyRate(%)
Fig 1: Showing Clinical Pregnancy Rate
 Letrozole for OI in In Vitro
Fertilization (IVF)
Clinical Evidence
RCTs regarding use of letrozole for ovulation induction in
IVF/ICSI cycles
Journal of Human Reproductive Sciences / Volume 6 / Issue 2 / Apr - Jun 2013
Letrozole in IVF
 Normal ovarian response
 Addition of letrozole showed higher implantation and ongoing pregnancy rates
and significantly improved endometrial thickness
 Poor responders
 Lower dose of gonadotropin required in the letrozole cotreatment group in all
trials
Summary
 Better pregnancy outcomes & higher live births compared to
CC in PCOS patients
 Effective even in patients with CC-resistant PCOS
 Reduces Gonadotrophin dose & superior alternative to CC in
combined Gonadotrophin cycles
 Monofollicular development & lower multiple pregnancies
 No anti-estrogenic effects on endometrium & cervical mucus
 Lower cycle cancellation & risk of hyperstimulation is
negligible
 Safety established in clinical studies
Letrozole in Ovulation Induction

Letrozole in Ovulation Induction

  • 1.
    Induz in OvulationInduction Dr Sujoy Dasgupta MBBS (Gold Medalist, Hons) MS (Obst & Gynae- Gold Medalist) DNB, FIAOG, Fellow- Reproductive Endocrinology and Infertility (ACOG, USA) Assistant Professor: SRIMSH, Durgapur Consultant: RSV Hospital, Kolkata Iris Hospital, Kolkata Behala Balananda Brahmachary Hospital, Kolkata Secretary, Perinatology Committee: Bengal Obstetric and Gynaecological Society (BOGS)- 2016-17 Managing Committee Member: BOGS- 2016-17 15 Publications: National and International Journals
  • 2.
    NOTICE Medicine is anever-changing science. As new research and clinical experience broaden our knowledge, changes in treatment and drug therapy are required. The authors and the publisher of this work have checked with sources believed to be reliable in their efforts to provide information that is complete and generally in accord with the standards accepted at the time of publication. However, in view of the possibility of human error or changes in medical sciences, neither the authors nor the publisher nor any other party who has been involved in the preparation or publication of this work warrants that the information contained herein is in every respect accurate or complete, and they disclaim all responsibility for any errors or omissions or for the results obtained from use of the information contained in this work. Readers are encouraged to confirm the information contained herein with other sources.
  • 5.
    Incidence of allmalformations was not different between the two groups (p= 0.25, 95%CI 0.78-4.71). However, the incidence of locomotor malformations (p= 0.0005, 95% CI 2.64-27.0) and cardiac anomalies (p= 0.0006 95% CI 3.30-58.1) were higher than in the control groups
  • 6.
    Fertil Steril. 2006Jun;85(6):1761-5  No difference in overall rates of major & minor congenital malformations among newborns from mothers who conceived after LTZ or CC treatments  It appears that congenital cardiac anomalies are less frequent in LTZ group  The concern that LTZ use for ovulation induction could be teratogenic is unfounded based on this data
  • 7.
    Number of newbornswith major malformations Percent of newborns with malformations
  • 8.
    Hum Reprod. 2017Jan;32(1):125-132 N= 3928 LTZ stimulation reduces risk of miscarriage, with no increase in risk of major congenital anomalies or adverse pregnancy
  • 9.
    Sharma S, etal. PLoS ONE. 2014; 9(10): e108219 Structural malformations & chromosomal abnormalities N= 623 Natural conception group 5 / 171 babies (2.9%) LTZ group 5 / 201 babies (2.5%) CC group 10 / 251 babies (3.9%)
  • 10.
    Other Studies Reference Noof patients Forman R, et al. J Obstet Gynaecol Can 2007;29:668-71. 430 Dehbashi S, et al. Iran J Med Sci 2009;34:23-8. 100 Legro RS, et al. N Engl J Med. 2014 Jul 10;371(2):119-29. 750 Banerjee Ray P, et al. Arch Gynecol Obstet. 2012 Mar;285(3):873-7. 147 Roy KK, et al. J Hum Reprod Sci. 2012 Jan-Apr; 5(1): 20–25 204 Wu XK, et al. Fertil Steril 2016;106:757-765 644 Requena A, et al. Hum Reprod Update. 2008 Nov-Dec;14(6):571-82. (Meta-analysis) 2573 Diamond MP, et al. N Engl J Med 2015;373:1230-40. 900
  • 11.
    Wang R, etal. BMJ. 2017; 356: j138.
  • 12.
    15th Jan 2017 BanOn Letrozole Lifted After 5 Long Years By DCGI
  • 13.
  • 14.
    Letrozole Revoked MINISTRY OFHEALTH AND FAMILY WELFARE [(Department of Health and Family Welfare) NOTIFICATION: New Delhi, the 17th February, 2017 G.S.R. 145(E)]
  • 15.
  • 16.
    For women withPCOS and BMI >30, letrozole should be considered as first-line therapy for ovulation induction because of the increased live birth rate compared with clomiphene citrate
  • 17.
    Endocrine Society ClinicalGuideline (2013) recommends:  Clomiphene citrate (or comparable estrogen modulators such as Letrozole) as the first-line treatment of anovulatory infertility in women with PCOS. American Association of Clinical Endocrinologists, American College of Endocrinology, And Androgen Excess & PCOS Society (2015)  Treatment for women with PCOS and anovulatory infertility should begin with an oral agent such as clomiphene citrate or Letrozole, an aromatase inhibitor.
  • 19.
     CC shouldbe first-line pharmacotherapy for ovulation induction and letrozole can also be used as first-line therapy.
  • 20.
  • 21.
    Clomiphene Citrate  Ovulation:70-80% cases  Pregnancy rate: 10-20%/cycle* not more then 6 cycle continuously and not more then 12 cycles in life time ..to avoid possible Risk of (?) Ovarian Malignancy (NICE, 2013) In doses of 50 mg/d /cycle and can be increased to 150 mg until ovulation is achieved *Pavone ME, et al. J Clin Endocrinol Metab. 2013 May; 98(5): 1838–1844.
  • 22.
    CC Resistance/ Failure CC RESISTANT: If patient fails to ovulate despite 3 CC cycles  About 20-25% of Anovulatory women are CC- resistant*  CC FAILURE:  CC-resistant  women who ovulate, but do not get pregnant  Women who get pregnant but end in miscarriage *Mitwally MF, et al. Fertil Steril. 2001 Feb;75(2):305-9, Azargoon A, et al. Iran J Reprod Med. 2012 Jan; 10(1): 33–40.
  • 23.
    Management of PCOS-Anovulation LifeStyle Modification CC 1st Line Treatment No Ovulation (CC Resistance) Metformin + CC FSH Lap Ovarian Drilling Letrozole Ovulates
  • 24.
    Management of PCOS-Anovulation LifeStyle Modification CC 1st Line Treatment No Ovulation (CC Resistance) Metformin + CC FSH Lap Ovarian Drilling Letrozole Ovulates
  • 25.
    Letrozole 3rd generation aromataseinhibitor (AI) Non-steroidal, potent & selective 1st study (Mitwally & Casper, 2001): OI Mitwally MF, et al. Fertil Steril. 2001 Feb;75(2):305-9.
  • 27.
    granulosa cells FSH aromatase LH theca cells androstenedione estrogen FollicularPhysiology Aromatase 1. Ovary 2. Adipose tissue 3. Brain Exogenous FSH CC binds to ER & depletes receptor concentrations aromatase inhibitors
  • 28.
    Follicular Development Pituitary gland FSH Stimulatesfollicular growth Estrogen Large follicles (more FSH receptors) Smaller follicles (less FSH receptors) Continues to grow (mono follicular) Atresia Ovulation Journal of Human Reproductive Sciences / Volume 6 / Issue 2 / Apr - Jun 2013
  • 29.
    Follicular Development Pituitary gland FSH Stimulatesfollicular growth Estrogen Large follicles (more FSH receptors) Smaller follicles (less FSH receptors) Continues to grow (mono follicular) Atresia Ovulation CC → No feedback inhibition Journal of Human Reproductive Sciences / Volume 6 / Issue 2 / Apr - Jun 2013
  • 30.
    Follicular Development Pituitary gland FSH Stimulatesfollicular growth Estrogen Large follicles (more FSH receptors) Smaller follicles (less FSH receptors) Continues to grow (mono follicular) Atresia Ovulation CC → No feedback inhibition Journal of Human Reproductive Sciences / Volume 6 / Issue 2 / Apr - Jun 2013
  • 31.
    Follicular Development Pituitary gland FSH Stimulatesfollicular growth Estrogen Follicles with FSH receptors Smaller follicles (less FSH receptors) Continues to grow (multi follicular) Atresia Ovulation CC → No feedback inhibition Journal of Human Reproductive Sciences / Volume 6 / Issue 2 / Apr - Jun 2013
  • 32.
    Follicular Development Pituitary gland FSH Stimulatesfollicular growth Estrogen Large follicles (more FSH receptors) Smaller follicles (less FSH receptors) Continues to grow (mono follicular) Atresia Ovulation Letrozole → maintains feedback inhibition Journal of Human Reproductive Sciences / Volume 6 / Issue 2 / Apr - Jun 2013
  • 33.
    Follicular Development Pituitary gland FSH Stimulatesfollicular growth Estrogen Large follicles (more FSH receptors) Smaller follicles (less FSH receptors) Continues to grow (mono follicular) Atresia Ovulation Letrozole → maintains feedback inhibition Journal of Human Reproductive Sciences / Volume 6 / Issue 2 / Apr - Jun 2013
  • 34.
  • 35.
    Letrozole vs CC Letrozole(Aromatase Inhibitor) Blocks Aromatase Does not block ER Increased intraovarian androgen 1. No adverse effect on endometrium/ cervix Augment FSH receptors Stimulates IGF-I 2. No hot flush Synergistically promotes follicular growth Clomiphene (Anti-estrogen) Blocks ER 1. ↓ endometrial thickness ↓glandular density ↓ uterine blood flow in luteal phase 2. ↓quantity/ quality of Cx mucus 3. Hot flushes (prolonged accumulation in tissues→ prolonged depletion of ER) J Clin Endocrinol Metab, March 2006, 91(3):760 –771 J Hum Reprod Sci 2011 May-Aug; 4(2): 76–79. J Hum Reprod Sci 2013 Apr-Jun; 6(2): 93–98
  • 36.
    Letrozole vs CC Letrozole(Aromatase Inhibitor) Blocks Aromatase Does not block ER Increased intraovarian androgen 1. No adverse effect on endometrium/ cervix Augment FSH receptors Stimulates IGF-I 2. No hot flush Synergistically promotes follicular growth Clomiphene (Anti-estrogen) Blocks ER 1. ↓ endometrial thickness ↓glandular density ↓ uterine blood flow in luteal phase 2. ↓quantity/ quality of Cx mucus 3. Hot flushes (prolonged accumulation in tissues→ prolonged depletion of ER) J Clin Endocrinol Metab, March 2006, 91(3):760 –771 J Hum Reprod Sci 2011 May-Aug; 4(2): 76–79. J Hum Reprod Sci 2013 Apr-Jun; 6(2): 93–98
  • 37.
    Letrozole vs CC Letrozole(Aromatase Inhibitor) Blocks Aromatase Does not block ER Increased intraovarian androgen 1. No adverse effect on endometrium/ cervix Augment FSH receptors Stimulates IGF-I 2. No hot flush Synergistically promotes follicular growth Clomiphene (Anti-estrogen) Blocks ER 1. ↓ endometrial thickness ↓glandular density ↓ uterine blood flow in luteal phase 2. ↓quantity/ quality of Cx mucus 3. Hot flushes (prolonged accumulation in tissues→ prolonged depletion of ER) J Clin Endocrinol Metab, March 2006, 91(3):760 –771 J Hum Reprod Sci 2011 May-Aug; 4(2): 76–79. J Hum Reprod Sci 2013 Apr-Jun; 6(2): 93–98
  • 38.
  • 39.
    Letrozole Uses  Letrozolehas been used in the following three situations:  OI in polycystic ovary syndrome (PCOS)  OI in intrauterine insemination (IUI)  Ovarian stimulation for IVF/ICSI
  • 40.
    Letrozole for OIin polycystic ovary syndrome (PCOS) Clinical Evidence
  • 41.
    CONCLUSION: letrozole showeda better endometrial response and pregnancy rate compared to CC Endometrial thickness on the day of hCG administration (mm) 9.1±0.3 6.3±1.1 0.014 (S) Roy KK, et al. J Hum Reprod Sci. 2012 Jan-Apr; 5(1): 20–25.
  • 42.
    Population Studied 7 studiesout of 232 selected • N= 1833 patients – LTZ: 906 – CC: 927 • N= 4999 ovulation cycles – LTZ: 2455 – CC: 2544 OUTCOME MEASURES  Primary outcome measure: Live birth rate (LBR)  Secondary outcomes measures: Ovulation rate per cycle Clinical pregnancy rate Miscarriage rate Multiple pregnancy rates
  • 43.
     Result  statisticallysignificant increase in the live birth and pregnancy rates in the letrozole group when compared to the CC group  Conclusion  LTZ is superior to CC considering live birth & pregnancy rates in patients with PCOS
  • 44.
    CC 100 mgfor at least 6 cycles → failure to form the DF, then put on letrozole ; 5 mg for 5 days for 4 cycles → unable to form the DF, combination therapy (letrozole 5 mg + CC100 mg) for 5 days PCOS patients resistant to clomiphene and letrozole used alone as single agents, Letrozole with CC combination may be used as a first-line therapy to induce ovulation in severe cases of PCOS in order to save time and expense
  • 45.
     Statistically significantlyincreased the ovulation rate by 33.3% in the treatment group  letrozole can be used as an effective and simple alternate ovulation-inducing agent in these women Fertility and Sterility Vol. 94, No. 7, December 2010
  • 46.
     N=94 :letrozole ( 2.5 mg/day) + HMG,  N= 90: CC (50 mg/day) + HMG,  N=71: HMG only.  All women received one treatment regimen in one treatment cycle.  All patients were given HMG 75 IU on alternate days daily starting on day 3 or day 7 until the day of administration of hCG.  hCG 10,000 IU : when at least 1 follicle with mean diameter ≥18 mm  Pts advised natural intercourse after 24-36 hours after hCG
  • 47.
    Results Ovulation rate andClinical Pregnancy Rates
  • 48.
  • 49.
    Conclusion Letrozole in combination withhMG reduced duration of stimulation and total HMG dose needed for stimulation significantly higher monofollicular development The regimen of letrozole + HMG is more effective and safer than CC + HMG or HMG alone for ovulation induction in cases of CC resistance
  • 50.
    Letrozole vs. LODin CC Failure LTZ had superior reproductive outcomes compared with LOD in women with CC-resistant PCOS LTZ could be used as 1st line treatment for women with CC-resistant PCOS Liu W, et al. Experimental and Therapeutic Medicine. 2015; 10: 1297-1302.
  • 51.
    Comparison of Letrozolevs. Tamoxifen LTZ superior to TMX Higher pregnancy rate Higher ovulation rate El-Gharib et al. J Reprod Infertil. 2015; 16(1): 30-35.
  • 52.
     60 moderatelyobese patients with PCOS  N=31 clomiphene citrate-metformin  N=29 letrozole-metformin therapy.  Stimulation was carried out for the procedures of intrauterine insemination (IUI).
  • 53.
     60 moderatelyobese patients with PCOS  N=31 clomiphene citrate-metformin  N=29 letrozole-metformin therapy.  Stimulation was carried out for the procedures of intrauterine insemination (IUI).  RESULTS: 0 2 4 6 8 10 letrozole+metformin CC+metformin 8.9 6.3 EndometrialThickness(mm) 0 5 10 15 20 25 Letrozole+metformin CC+Metformin 20.6 9.6 PregnancyRateafterthirdIUI cycle(%) Fig : Showing Endometrial Thickness Fig : Preg Rate after third IUI cycle Conclusion: Study demonstrated the advantages of the use of letrozole over clomiphene citrate in combination with metformin in moderately obese patients with PCOS who are resistant to stimulation with clomiphene citrate alone.
  • 54.
    Letrozole for OIin intrauterine insemination (IUI) Clinical Evidence
  • 55.
     Methods  groupA :Letrozole (5 mg) for five days and gonadotrophins (HMG) 75 IU once daily for 3−5 days  group B : Clomiphene Citrate (50 mg) for 5 days and gonadotrophins (HMG) in a dose of 75 IU for 3– 5days  Results  Patients co-treated with Letrozole required fewer gonadotrophins administrations and had a thicker endometrium  The pregnancy rate was not significantly different between two groups (11% vs. 12.6%) J Reprod Infertil 2013 Jul-Sep; 14(3): 138–142. Conclusion: The addition of Letrozole to gonadotrophins decreases gonadotrophins requirements and improves endometrial thickness, without a significant effect on pregnancy rates
  • 56.
    180 infertile women: Group A: 5 mg/day letrozole on day 3-7 of menstrual cycle.  Group B: 100 mg/day clomiphene in the same way as letrozole.  hMG administered in both groups every day starting on day between 6-8 of cycle.  hCG(5000 IU) trigger when have two follicles of ≥16 mm.  IUI was performed 36 hr later. Int J Reprod Biomed (Yazd).2017 Jan;15(1):49-54.
  • 57.
    Results 0 5 10 Letrozole+ HMG CC+HMG 3.8 3.7 8.99 8.46 EndometrialThickness(mm) Fig 2:Showing Endometrial Thickness Before treatment After Treatment 0 2 4 6 Letrozole+ HMG CC+HMG 5.7 anHyperstimulation(%) Fig 3: Showing Ovarian Hyperstimulation 0 10 20 30 Letrozole+ HMG CC+HMG 26.51 12.64 ClinicalPregnancyRate(%) Fig 1: Showing Clinical Pregnancy Rate
  • 58.
     Letrozole forOI in In Vitro Fertilization (IVF) Clinical Evidence
  • 59.
    RCTs regarding useof letrozole for ovulation induction in IVF/ICSI cycles Journal of Human Reproductive Sciences / Volume 6 / Issue 2 / Apr - Jun 2013
  • 60.
    Letrozole in IVF Normal ovarian response  Addition of letrozole showed higher implantation and ongoing pregnancy rates and significantly improved endometrial thickness  Poor responders  Lower dose of gonadotropin required in the letrozole cotreatment group in all trials
  • 61.
    Summary  Better pregnancyoutcomes & higher live births compared to CC in PCOS patients  Effective even in patients with CC-resistant PCOS  Reduces Gonadotrophin dose & superior alternative to CC in combined Gonadotrophin cycles  Monofollicular development & lower multiple pregnancies  No anti-estrogenic effects on endometrium & cervical mucus  Lower cycle cancellation & risk of hyperstimulation is negligible  Safety established in clinical studies

Editor's Notes

  • #18 Endocr Pract. 2015 Dec;21(12):1415-26.
  • #39 Half life of CC is 5 d to 3 wk depending on isomer
  • #45 A dose of 5 mg Letrozole every night and 100 mg clomiphene every day after lunch was prescribed for 5 days. In Patients with oligomenorrhea the medication (letrozole and clomiphene) started after induction of bleeding with progesterone, and for those patients with regular cycles the medications (letrozole and clomiphene) were started from