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Risk of Fetal Harm with Letrozole Use in Fertility Treatment: A Systematic Review and Meta-Analysis

29 Pages Posted: 13 Jul 2020

See all articles by Jyotsna Pundir

Jyotsna Pundir

St. Bartholomew’s Hospital (Barts) - Centre for Reproductive Medicine

Chiara Achilli

Liverpool Women's Hospital - Hewitt Fertility Centre

Priya Bhide

Queen Mary University of London - Centre for Women's Health

Luca Sabatini

St. Bartholomew’s Hospital (Barts) - Centre for Reproductive Medicine

Richard S. Legro

Pennsylvania State University - Department of Obstetrics and Gynecology

Luk Rombauts

Monash University

Helena J. Teede

Monash University, School of Public Health and Preventive Medicine, Monash Centre for Health Research and Implementation ; Monash Health - Diabetes and Vascular Medicine Unit; Monash Partners Academic Health Sciences Centre

Arri Coomarasamy

University of Birmingham - Tommy’s National Centre for Miscarriage Research

Javier Zamora

Queen Mary University of London - Women's Health Research Unit

Shakila Thangaratinam

University of Birmingham - Institute of Metabolism and Systems Research

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Abstract

Background: The aromatase inhibitor letrozole is increasingly recommended for ovulation induction, as it is more effective with fewer side-effects than other agents. But many clinicians are reluctant to use the drug for fertility treatment due to a strong-label warning against its use, which warns about congenital malformation risk to the fetus in women seeking pregnancy.   

Objective: To determine the risks of congenital malformations and pregnancy loss with letrozole compared with clomiphene primarily, and against other fertility drugs and natural conception.

Methods: A systematic review and meta-analysis.

Findings: We included 45 studies (18 randomised trials; 20 comparative cohorts; 7 non-comparative cohorts). We did not observe a significant increase in congenital malformations with letrozole vs clomiphene in the randomised trials (Risk Difference RD 0.01, 95% CI -0.02, 0.03; I2 = 0%; 14 studies), and found a significant reduction in the cohort studies (RD -0.02, 95% CI -0.03, -0.004; I2 = 0%, 10 studies). The risks of pregnancy loss were not increased with letrozole vs clomiphene in the 14 randomised trials (RD -0.01, 95% CI -0.06, 0.04; I2 = 0%), and the risks were reduced in the six cohort studies (RD -0.09, 95% CI -0.17, -0.00; I2 = 68%). The GRADE quality of evidence was low to moderate for congenital malformations and pregnancy loss. We did not find any increased congenital malformation risk with letrozole vs gonadotrophins, natural conception or natural cycle assisted reproductive technology, but the number of studies was small.  

Interpretation: There is no evidence that letrozole increases the risk of congenital fetal malformation or pregnancy loss than clomiphene, natural conception or other fertility agents to warrant warning against its use. Given its therapeutic benefits and lack of evidence of harm to the fetus, clinicians should consider letrozole as first-line agent for ovulation induction.

Funding Statement: None.

Declaration of Interests: None.

Keywords: Letrozole, Harm, Congenital malformations

Suggested Citation

Pundir, Jyotsna and Achilli, Chiara and Bhide, Priya and Sabatini, Luca and Legro, Richard S. and Rombauts, Luk and Teede, Helena J. and Coomarasamy, Arri and Zamora, Javier and Thangaratinam, Shakila, Risk of Fetal Harm with Letrozole Use in Fertility Treatment: A Systematic Review and Meta-Analysis (4/14/2020). Available at SSRN: https://ssrn.com/abstract=3576837 or http://dx.doi.org/10.2139/ssrn.3576837

Jyotsna Pundir (Contact Author)

St. Bartholomew’s Hospital (Barts) - Centre for Reproductive Medicine ( email )

London
United Kingdom

Chiara Achilli

Liverpool Women's Hospital - Hewitt Fertility Centre

Crown Street
Liverpool
United Kingdom

Priya Bhide

Queen Mary University of London - Centre for Women's Health

London
United Kingdom

Luca Sabatini

St. Bartholomew’s Hospital (Barts) - Centre for Reproductive Medicine

London
United Kingdom

Richard S. Legro

Pennsylvania State University - Department of Obstetrics and Gynecology

PA
United States

Luk Rombauts

Monash University

23 Innovation Walk
Wellington Road
Clayton, Victoria 3800
Australia

Helena J. Teede

Monash University, School of Public Health and Preventive Medicine, Monash Centre for Health Research and Implementation

Australia

Monash Health - Diabetes and Vascular Medicine Unit

Australia

Monash Partners Academic Health Sciences Centre

Australia

Arri Coomarasamy

University of Birmingham - Tommy’s National Centre for Miscarriage Research

Birmingham
United Kingdom

Javier Zamora

Queen Mary University of London - Women's Health Research Unit

London
United Kingdom

Shakila Thangaratinam

University of Birmingham - Institute of Metabolism and Systems Research

Birmingham
United Kingdom

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