Skip to main content

Fertility drugs, reproductive strategies and ovarian cancer risk


Several adverse effects have been related to infertility treatments, such as cancer development. In particular, the relationship between infertility, reproductive strategies, and risk of gynecological cancers has aroused much interest in recent years. The evaluation of cancer risk among women treated for infertility is very complex, mainly because of many factors that can contribute to occurrence of cancer in these patients (including parity status). This article addresses the possible association between the use of fertility treatments and the risk of ovarian cancer, through a scrupulous search of the literature published thus far in this field. Our principal objective was to give more conclusive answers on the question whether the use of fertility drug significantly increases ovarian cancer risk. Our analysis focused on the different types of drugs and different treatment schedules used. This study provides additional insights regarding the long-term relationships between fertility drugs and risk of ovarian cancer.


In the world the number of people with problems of infertility has increased since 1990, resulting in a consistent increase in the use of strategies to improve fertility and reproductive rates. The highest incidence of infertility was found in western countries and in these countries a consistent proportion of the infertile women receive fertility treatments [1, 2]. Moreover, the clinical use of fertility drugs and other reproductive strategies is expected to increase for the large number of women who postpone pregnancy for economic and social reasons [1, 2].

In recent years, a great interest has been addressed to a supposed correlation between infertility treatments and cancers development, mainly breast, uterus and ovarian cancer [36].

Infertility appears to increase itself the incidence of ovarian carcinoma, while the potential additional risk associated with the use of fertility drugs is still debated. From many years nulliparity constitutes an established risk factor for ovarian cancer [7, 8]. Conversely, several case-control studies failed to detect a significant correlation between fertility drugs use and ovarian cancer risk [914]. The work conducted by Ness et al. [9], analyzed 8 case-control studies. Among nulliparous women the risk of ovarian cancer increased by 2.67-fold (95% confidence interval (CI): 1.91 - 3.74). Among nulligravid women, neither any fertility drug use (odds ratio (OR) 1.60; 95% CI: 0.90-2.87) nor more than 12 months of use (OR 1.54; 95% CI: 0.45-5.27) was associated with increased risk of ovarian cancer. Fertility drug use in nulliparous women was associated with borderline serous tumors (OR 2.43; 95% CI: 1.01-5.88) but not with invasive epithelial cancers. These data suggest a role for the infertile status, but not for fertility drugs in the risk of epithelial ovarian cancer.

On the other hand, as reported in other studies, ovulation-stimulating therapies seem to be related to an increased risk of epithelial or borberline ovarian cancer [1517].

However the literature data regarding an hypothetic correlation between ovarian cancer and infertility treatments, are conflicting and hard to interpret. This can be due to several factors. For example many studies evaluate fertility schedules of treatment containing drugs used in the past. Furthermore many reports did not show an optimal control on potential confounding factors such as the small number of patients, the frequent retrospective nature of the studies, the difficulty to evaluate the role of other reproductive factors influencing ovarian cancer risk.

The aim of this review is to analyze in detail the most important papers published on this topic in recent years.

Materials and methods

We performed a review of the scientific literature concerning the association between the use of fertility treatments and the risk of ovarian cancer. We searched digital databases including Pubmed, EMBASE and the Cochrane Library. The survey was carried out using keywords such as “infertility”, “ovarian stimulation”, “ ovarian cancer risk”, “gynecological cancer”, “gynecological cancer risk”, “gonadotropins” , “human chorionic gonadotropin”, “clomiphene citrate”, “cancer risk”, “in vitro fertilization”, “progesterone”, “fertility drugs”, “infertility treatment” “gonadotropin-releasing hormone analogs”, variously associated together.

No period, language or study design restrictions have been applied in this stage of research. Reference lists of the most important papers were also examined and several authors were contacted by e-mail for more information about their work. The majority of the studies was excluded according to the title and to the content of the abstract.

In this review we did not include case reports and case series. Moreover were excluded studies exclusively assessing the fertility preservation after cancer treatment; also in vitro reports or animal studies were excluded. We analyzed the full versions of all relevant studies. We evaluated the selected information with a particular attention to the relationship between the occurrence of ovarian cancer and the treatments with fertility drugs. In particular we have focused our attention on the sample size, the type of infertility treatment regimens used, the time of follow-up and on the number of ovarian cancer reported.


Using the search criteria described in the previous section, we examined 970 papers and excluded 843 as irrelevant, on the basis of the title and abstract. The remaining 127 studies were considered in their full versions. Of these works, 97 were literature reviews or meta-analysis reports, 11 were case-control studies and 19 were cohort studies. The case-control studies often have been limited by the small number of subjects reporting prior drug use; therefore only some of these studies and the related meta-analysis have been discussed in this review. The 19 cohort studies selected are described in the Table 1, Table 2 and in the text. Just some meta-analyses, considered as the most significant, are extensively discussed in the text.

Table 1 Fertility drugs and ovarian cancer (Cohort studies)
Table 2 IVF and ovarian cancer (Cohort studies)

Clomiphene citrate and risk of ovarian cancer

Clomiphene citrate (CC) was used since the 1960s and is still considered one of the most important agents for women with anovulatory infertility; the drug have extensively showed to be able to reverse oligoovulation or anovulation in different reproductive pathologies; furthermore this agent was used, alone or in association with other agents, to induce ovarian hyperstimulation for in vitro fertilization (IVF) procedures [18, 19].

This agent is a selective estrogen receptor modulator (SERM) that increases both estradiol and progesterone levels [20] and it is also able to increase cell proliferation; thus, an association between the use of CC and the risk of cancer has been hypothesized for gynecologic tumors, such as breast, ovarian cancer and endometrial cancer [36]. In the last years many authors investigated the relationship between ovarian cancer occurrence and the medical treatment with fertility drugs. Unfortunately all studies failed to give a definitive answer to the question. The causes of this conflicting result are several. We will discuss more in detail some of these studies with specific attention to the use of CC in the treatment of infertility and its association with ovarian cancer (Table 1).

Rossing et al. [21] evaluated the development of ovarian cancer (and in particular ovarian epithelial tumors) in a cohort study of 3837 women. There were 11 invasive or borderline malignant ovarian tumors, as compared with an expected number of 4.4 (standardized incidence ratio (SIR) 2.5; 95% CI: 1.3 - 4.5). Nine of the women in whom ovarian cancer developed were treated with CC; the adjusted relative risk (RR) among these women, as compared with infertile women who had not treated with this drug, was 2.3 (95% CI: 0.5-11.4). Five of the nine women had taken CC during 12 or more monthly cycles. This period of treatment was associated with an increased risk of ovarian tumors (RR 11.1; 95% CI: 1.5-82.3), whereas treatment with the drug for less than one year was not associated with an increased risk.

Similar results were reached by Sanner et al. [22]. They evaluated the incidence of ovarian cancer in a cohort of 2780 patients who received CC or gonadotropins. Also in women with gonadotropin treatment for non-ovulatory disorders, the risk was elevated (SIR 5.89; 95% CI: 1.91-13.75) but 4 of the 5 cases reported human Chorionic Gonadotropin (hCG) treatment only. A multivariate analysis indicated that treatment with gonadotropins only was associated with an increased risk of invasive cancer (RR 5.28; 95% CI: 1.70-16.47). For borderline tumors, a more than threefold overall increase of tumors (SIR 3.61; 95% CI: 1.45-7.44) was observed; women exposed to CC, because of ovulatory disorders, showed the highest risk (SIR 7.47; 95% CI: 1.54-21.83).

Most of other investigations did not confirm a link between fertility drugs use and ovarian cancer risk [2325].

In a retrospective study Brinton et al. [26] evaluated 12193 infertile women followed for a median of 18.8 years and reported 45 ovarian cancers. This study used a detailed collection of informations about drug exposures, causes of infertility, and other potential cancer risk factors. The results were largely reassuring, showing no risk increase associated with the use of either CC or gonadotropins. The recent published study by Trabert et al. [27] is actually a 30 year follow-up to the original study by Brinton et al. [26] and examined the association between the use of ovulation-inducing drugs and the risk of ovarian cancer in a retrospective cohort study of 9825 women. In this study an increase in ovarian cancer risk was not observed after an extensive use of CC (adjusted RR 1.34; 95% CI: 0.86-2.07) or gonadotropins (RR 1.00; 95% CI: 0.48-2.08), with the only exception of those patients who used CC and failed to become pregnant. In fact they had a higher risk than those who successfully conceived compared with nonusers (respectively, RR 3.63; 95% CI: 1.36-9.72 vs RR 0.88; 95% CI: 0.47-1.63). Despite these results, the reason for an association between CC use and ovarian cancer risk among persistently nulligravid women was not clearly determined.

Jensen et al. [28] identified 156 ovarian cancer cases, through a linkage with the Danish Cancer Registry. The authors did not suggest an increased ovarian cancer risk associated with the use of gonadotropins (RR 0.83; 95% CI: 0.50-1.37), CC (RR 1.14; 95% CI: 0.79-1.64), hCG (RR 0.89; 95% CI: 0.62-1.29), or gonadotropin releasing hormone (GnRH) (RR 0.80; 95% CI: 0.42-1.51). Furthermore, no positive or negative associations were found considering all four groups of fertility drugs used, the number of cycles, the length of follow-up, or the rates of parity.

Dos Santos Silva et al. [29] identified 21 ovarian cancers among 7355 women followed for infertility for over 20 years, in order to assess long-term health effects of ovarian-stimulation drugs. They observed no significant differences in the risk of ovarian and other tumors in women treated or not treated with ovarian stimulating drugs.

Other fertility drugs and risk of ovarian cancer

In the treatment of female infertility several drugs are now more spread than CC. GnRH analogues/agonists, human menopausal gonadotropin (hMG), progesterone, follicle stimulating hormone (FSH), luteinizing hormone (LH) and hCG are commonly used as single agents or in combination with CC. Moreover, several other associations among these different drugs have been tested or are under investigation [3033].

We know that gonadotropins, hCG, progesterone, FSH and LH, have been recognized as growth factors in ovarian cancer. In a recent study Hilliard et al. [34] evaluated the pathways activated by FSH and LH in normal ovarian surface epithelium (OSE) growth. The purpose of this study was to identify the pathways downstream of the gonadotropins in normal OSE and their contribution towards proliferation and oncogenesis. The data obtained suggest that the gonadotropins stimulate some of the same proliferative pathways activated in normal OSE and in ovarian cancers too.

Due to the evidence that in the treatment of infertile women these different agents are commonly used together and in combination with CC, it is very difficult to evaluate separately the role of every single agent in development of ovarian cancer. For this reason we have analyzed in the previous section and in the Table 1 the majority of studies on this topic. Only two studies are discussed in detail on this chapter [35, 36].

Lerner-Geva et al. [35] presented a study to evaluate the possible risk for cancer development in a cohort of 2431 women who were treated for infertility with gonadotropins and other fertility drugs in Israel, with over 30 years of follow-up. They calculated the SIR between the observed cancer cases and the expected cancer rates in the general population. The investigators observed 18 cases of ovarian tumors compared to 18.1 expected (SIR 1.0; 95% CI: 0.59-1.57). Ovarian cancer risk was not found to be elevated and the authors were not able to demonstrate a significant high risk associated with ovulation stimulating treatments.

In a recent work Rizzuto et al. [36] included 11 case-control studies and 14 cohort studies, for a total of 182972 women. They did not show an increased ovarian cancer risk in women exposed to CC alone or CC plus gonadotropin, compared with unexposed women. For borderline ovarian tumors, exposure to any fertility drug was associated with a two to three-fold increased risk in two case-control studies. One case-control study reported an OR of 2,8 (95% CI: 1.5-5.16), which was based on only 4 cases. In another cohort study, there was more than a two-fold increase in the incidence of borderline tumors compared with the general population (SIR 2.6; 95% CI: 1.4-4.6), while in another report a Hazard Ratio (HR) of 4.23 (95% CI: 1.25-14.33) for the risk of a borderline ovarian tumor was reported (subfertile treated women compared with non-treated group with more than one year of follow-up).

IVF and risk of ovarian cancer

IVF is used for the treatment of all types of infertility. This is a medical technique by which an egg is fertilised by sperm outside the body. The fertilised egg (zygote) is then transferred into the patient's uterus with the intent to establish a successful pregnancy. IVF requires a pharmacological ovarian hyperstimolation. Generally the intensive ovulation induction treatments are represented by injectable gonadotropins (FSH analogues), GnRH agonist and GnRH antagonist [3740].

Some studies suggested an association among the use of ovulation-inducing drugs, IVF, and ovarian cancer risk, but only few cases of ovarian cancer have been described in women followed in IVF programs [41, 42]. Therefore the relationship between IVF and development of ovarian cancer is still under investigation (Table 2).

Lerner-Geva et al. [43] evaluated the association between ovarian hyperstimolation with IVF and an increased risk of cancer development, using a cohort of 1082 women, who were followed with a mean follow-up of 6.5 ± 2.2 years. They observed 21 cases of cancer as compared to the 11 expected (SIR 1.91; 95% CI: 1.18-2.91). These included 11 cases of gynecological tumors and in particular 3 cases of ovarian cancer as compared to 0.60 expected (SIR 5.0; 95% CI: 1.02-14.6). However SIR decreased to 1. 67 (95% CI: 0.02-9.27) while cases developing within 1 year were excluded; the authors concluded that the higher than expected cancer rate could not be attributed to IVF treatments.

Venn et al. in the first of two studies [44] observed 6 ovarian cancers, among 29666 women. For ovarian cancer SIRs were 1.70 (95% CI: 0.55-5.27) and 1.62 (95% CI: 0.52-5.02), respectively in exposed and unexposed women. In the second study Venn et al. [45] not confirmed these results. The cohort consisted of 29700 women: 20656 were exposed to fertility drugs and 9044 were not. Thirteen ovarian cancers occurred among these women. The incidence was no greater than expected in the exposed group (SIR 0.88; 95% CI: 0.74-1.13) and in unexposed group (SIR 1.16; 95% CI: 0.52-2.59). Women with unexplained infertility had significantly more ovarian cancers than expected (SIR 2.64; CI: 1.10-6.35).

Other contrasting results regarding IVF and ovarian cancer risk derive from a study conducted in Sweden and focused on cancer developing among women who gave birth following IVF treatment. In this experience Kallen et al. [46] found a significantly elevated risk of ovarian cancer following IVF treatments (RR 2.09; 95% CI: 1.39-3.12). Nevertheless many other investigators stressed the hypothesis that risk of ovarian cancer was not associated with effect of IVF [47, 48]. In a cohort of 25152 women Klip et al. [48] reported 17 ovarian cancer and showed no difference in the risk of ovarian cancer between treated and untreated women.

On the other hand, in a recent study van Leeuwen et al. [49], identified a cohort of 19146 women who received IVF and a comparison group of 6006 sub-fertile women who were not treated with IVF. The incidence of ovarian malignancies was assessed through linkage with disease registries. The risk of ovarian malignancies in the IVF group was compared with the risk observed in the general population and in the sub-fertile comparison group. After a median follow-up of 14.7 years, the risk of borderline ovarian tumors was increased in the IVF group compared with the general population (SIR 1.76; 95% CI: 1.16-2.56). The overall SIR for invasive ovarian cancer was not significantly elevated, but increased when the follow-up was extended after first IVF (P = 0.02); the SIR reached 3.54 (95% CI: 1.62-6.72) after 15 years. The risk of borderline ovarian tumors and of all ovarian malignancies in the IVF group were significantly increased compared with the risk in the sub-fertile control group (HR 4.23; 95% CI: 1.25-14.33 and 2.14; 95% CI: 1.07-4.25, respectively, adjusted for age, parity and subfertility cause).

Yli-kuha et al. [50] compared cancer risk among patients receiving IVF with that found in the general population. During the follow-up period after IVF, the investigators observed 9 (OR 2.57; 95% CI: 0.69-9.23) invasive ovarian cancers and 4 (OR 1.68; 95% CI: 0.31-9.27) borderline ovarian tumors. These results confirmed that IVF women had three times more invasive ovarian cancers than controls (only three case about 9175 women), but this difference was not statistically significant. The limitations of this study were: the small number of cases, the absence of subgroups and the very limited information about the different drugs used and their dosages.

Brinton et al. [51] also evaluated long-term cancer risk associated with IVF, calculating HRs for different gynecological cancers. The investigators included in their study a total of 87403 women treated for infertility on or after September 1994, who were followed for cancer development through June 2011. Only 45 ovarian cancers were identified. So they did not find a significant relationship between IVF technique and gynecological cancer risk. However, compared with women with no fertility treatment, the HR for ovarian cancer associated with IVF was 1.58 (95% CI: 0.75-3.29), with higher risk among those receiving ≥ 4 IVF cycles (HR 1.78; 95% CI: 0.76-4.13). The authors concluded that women receiving this treatment should continue to be monitored during the years.

Two recent meta-analyses have recently been published on this topic [41, 42]. In the study of Siristatidis et al. [41], nine cohort studies were analyzed (109969 women exposed to IVF with 76 cases of ovarian cancer). The comparison of studies, considering the general population as the reference group, found a statistically significant association between the use of IVF and an increased risk for ovarian cancer (RR 1.50; 95% CI:1.17-1.92). On the contrary, when infertile women were used as the reference group, no significant associations with ovarian cancer were noted (RR 1.26; 95% CI: 0.62-2.55). So IVF does not seem to be associated with elevated ovarian cancer risk when the confounding effect of infertility was neutralized. Of note, only one study provided follow-up longer than 10 years for the group exposed to IVF. In this meta-analysis borderline tumours were not included.

In the meta-analysis published by Li et al. in 2013 [42], eight cohort studies involving 746455 patients were included. In this work authors evaluated the association between IVF and all-site cancers and in particular observed a RR of 1.59 (95% CI:1.24-2.03) for ovarian cancer. A high risk of ovarian cancer was observed in the analysis of subgroups and especially in women who were diagnosed with cancer during or shortly after IVF (<1 year after treatment).


Several investigators explored the safety profile of fertility drugs and the risks associated with their use [5257], (Tables 1 and 2). The results emerging from the studies included in our review are contrasting. Some works suggest the hypothesis that fertility drugs do not significantly contribute to ovarian cancer risk [914, 2329, 35, 41, 43, 45, 47, 48]. Other studies have reported an increased risk of ovarian cancer in women treated with fertility drugs [1517, 21, 22, 42, 44, 46, 4951]. Finally some studies have reported an increased risk especially for borderline ovarian tumors [16, 21, 22, 36, 42, 49, 50].

Establishing the correlation between fertility drugs use and ovarian cancer risk is complex because it is know that infertility itself determines an increased risk of cancer [7, 8]. Three major theories have been proposed to explain the ovarian cancer pathogenesis [5865]. The “Fallopian tube theory”, hypothesized by Kurman et al., suggested that serous ovarian carcinomas developed from normal residual fimbrial epithelium localized on the ovarian surface after ovulation. The author supposed that, following implantation of tubal epithelium in the ovary, the adjacent stromal cells are activated and secrete steroid hormones that can stimulate malignant transformation [58, 59].

The “Incessant ovulation theory” hypothesizes that the frequent and repetitive trauma to the ovarian epithelium, caused during ovulation, contributes to DNA damage, increasing ovarian cancer risk. In nulliparous women this damage is incessant, so that DNA injuries are facilitated. This can lead to malignant cells transformation [6063]. The last hypothesis is the “Gonadotropin theory”. It suggests that an increase in FSH and LH lead to an overstimulation of the ovarian epithelium by increasing local levels of estrogen. This plays an important role in ovarian cancer development. A support to this theory arises from the observation that ovarian cancer incidence increases considerably during menopause, when gonadotropin levels grow [64, 65].

According to these three theories, fertility drugs should be related to an increase in ovarian cancer risk, because they can cause a gain in LH and FSH levels, and stimulate ovulation. But women who assume fertility drugs have per se a high risk because of their infertility [7, 8]. It is clear that one of the main difficulties in this field is to separate these risk factors, presenting together in infertile women treated with fertility drugs.

Three large meta-analyses have been conducted about our issue [41, 42, 66]. Two of them [44, 66] concluded that there was no difference in ovarian cancer risk between infertile women treated for their infertility and infertile not treated women. The third meta-analysis [44] show an increased risk of ovarian cancer in patients who have used fertility drugs.

We can conclude that past and recent scientific reports reached different results because these studies are characterized by some methodological limitations: low sample size; low follow-up period; low number of ovarian cancers reported; self-reported drugs assumption; lack of information on the type of drugs used, the dosage and the number of cycles administered; lack of attention to the other reproductive risk factors for ovarian cancer; lack of a clear distinction between epithelial tumors and borderline tumors.

Considering all the studies included in our review, the most recent works appear reassuring regarding the potential risk of ovarian cancer, and more accurate compared to the past, because they are conceived in order to avoid the interrelationships and potential bias derived from the different risk factors.


In the next years, the incidence of female infertility is expected to increase. A lot of new drugs are under investigation while other recent drugs are already in current use, such as aromatase inhibitors [6770]. Moreover preservation of fertility and reproduction in cancer patients, constitutes today an emerging problem in clinical oncology, and the new reproductive technologies begin to be used also in this group of patients [70, 71]. These new drugs and technologies will need to be tested for their safety in the perspective of an hypothetic correlation with ovarian and gynaecological cancers development. New studies are expected to be designed differently from the past, in particular to reduce confounding factors. Furthermore, the new studies would look even at borderline ovarian tumors, because they are often not included in cancer registries or are improperly associated with other ovarian tumors.

Another crucial point is the improvement in knowledge about ovarian cancer and its pathogenesis. In fact the three main theories about ovarian cancer development seem to be equally plausible and not necessarily contradict each other.

This issue is fascinating and has a notable social impact.

Authors’ information

FT: MD phd, GLR: MD, GPS: MD, phd, VS: MD, AAP: MD, NP: MD, MS: MD, PV: MD, AP: MD, MSC: MD, PBP: MD, ST: MD.



Confidence interval


Odds ratio


Clomiphene citrate


in vitro fertilization


Selective estrogen receptor modulator


Standardized incidence ratio


Relative risk


Human chorionic gonadotropin


Gonadotropin releasing hormone


Human menopausal gonadotropin


Follicle stimulating hormone


Luteinizing hormone


Ovarian surface epithelium


Hazard ratio.


  1. Mascarenhas MN, Flaxman SR, Boerma T, Vanderpoel S, Stevens GA: National, Regional, and Global Trends in Infertility Prevalence Since 1990: A Systematic Analysis of 277 Health Surveys. PLoS Med 2012,9(12):e1001356. 10.1371/journal.pmed.1001356

    Article  PubMed Central  PubMed  Google Scholar 

  2. CDC: Outline for a national plan for the prevention, detection and management of infertility. Outline Version 050710. 2010, 1: 1–44.

    Google Scholar 

  3. Lo Russo G, Spinelli GP, Tomao S, Rossi B, Frati L, Panici PB, Vici P, Codacci Pisanelli G, Tomao F: Breast cancer risk after exposure to fertility drugs. Expert Rev Anticancer Ther 2013,13(2):149–157. 10.1586/era.12.181

    Article  CAS  PubMed  Google Scholar 

  4. Schüler S, Ponnath M, Engel J, Ortmann O: Ovarian epithelial tumors and reproductive factors: a systematic review. Arch Gynecol Obstet 2013,287(6):1187–1204. 10.1007/s00404-013-2784-1

    Article  PubMed  Google Scholar 

  5. Sergentanis TN, Diamantaras AA, Perlepe C, Kanavidis P, Skalkidou A, Petridou ET: IVF and breast cancer: a systematic review and meta-analysis. Hum Reprod Update 2014,20(1):106–123. 10.1093/humupd/dmt034

    Article  PubMed  Google Scholar 

  6. Althuis MD, Scoccia B, Lamb EJ, Moghissi KS, Westhoff CL, Mabie JE, Brinton LA: Melanoma, thyroid, cervical, and colon cancer risk after use of fertility drugs. Am J Obstet Gynecol 2005,193(3 Pt 1):668–674.

    Article  PubMed  Google Scholar 

  7. Adami HO, Hsieh CC, Lanbe M, Trichopoulos D, Leon D, Persson I, Ekbon A, Janson PO: Parity, age at first childbirth, and risk of ovarian cancer. Lancet 1994, 344: 1250–1254. 10.1016/S0140-6736(94)90749-8

    Article  CAS  PubMed  Google Scholar 

  8. Risch HA, Marrett LD, Howe GR: Parity, contraception, infertility, and the risk of epithelial ovarian cancer. Am J Epidemiol 1994,140(7):585–597.

    CAS  PubMed  Google Scholar 

  9. Ness RB, Cramer DW, Goodman MT, Kjaer SK, Mallin K, Mosgaard BJ, Purdie DM, Risch HA, Vergona R, Wu AH: Infertility, fertility drugs, and ovarian cancer: a pooled analysis of case-control studies. Am J Epidemiol 2002,155(3):217–224. 10.1093/aje/155.3.217

    Article  PubMed  Google Scholar 

  10. Franceschi S, La Vecchia C, Negri E, Guarneri S, Montella M, Conti E, Parazzini F: Fertility drugs and risk of epithelial ovarian cancer in Italy. Hum Reprod 1994,9(9):1673–1675.

    CAS  PubMed  Google Scholar 

  11. Rossing MA, Tang MT, Flagg EW, Weiss LK, Wicklund KG: A case-control study of ovarian cancer in relation to infertility and the use of ovulation-inducing drugs. Am J Epidemiol 2004,160(11):1070–1078. 10.1093/aje/kwh315

    Article  PubMed  Google Scholar 

  12. Parazzini F, Pelucchi C, Negri E, Franceschi S, Talamini R, Montella M, La Vecchia C: Use of fertility drugs and risk of ovarian cancer. Hum Reprod 200 2001,16(7):1372–1375. 10.1093/humrep/16.7.1372

    Article  CAS  Google Scholar 

  13. Parazzini F, Negri E, La Vecchia C, Moroni S, Franceschi S, Crosignani PG: Treatment for infertility and risk of invasive epithelial ovarian cancer. Hum Reprod 1997,12(10):2159–2161. 10.1093/humrep/12.10.2159

    Article  CAS  PubMed  Google Scholar 

  14. Mosgaard BJ, Lidegaard O, Kjaer SK, Schou G, Andersen AN: Infertility, fertility drugs, and invasive ovarian cancer: a case-control study. Fertil Steril 1997,67(6):1005–1012. 10.1016/S0015-0282(97)81431-8

    Article  CAS  PubMed  Google Scholar 

  15. Whittemore AS, Harris R, Itnyre J: Characteristics relating to ovarian cancer risk: collaborative analysis of 12 U.S. case-control studies. IV. Invasive epithelial ovarian cancer in with woman. Am J Epidemiol 1992,136(10):1184–1203.

    CAS  PubMed  Google Scholar 

  16. Cusidó M, Fábregas R, Pere BS, Escayola C, Barri PN: Ovulation induction treatment and risk of borderline ovarian tumors. Gynecol Endocrinol 2007,23(7):373–376. 10.1080/09513590701350341

    Article  PubMed  Google Scholar 

  17. Modan B, Ron E, Lerner-Geva L, Blumstein T, Menczer J, Rabinovici J, Oelsner G, Freedman L, Mashiach S, Lunenfeld B: Cancer incidence in a cohort of infertile women. Am J Epidemiol 1998,147(11):1038–1042. 10.1093/oxfordjournals.aje.a009397

    Article  CAS  PubMed  Google Scholar 

  18. Practice Committee of the American Society for Reproductive Medicine: Use of clomiphene citrate in women. Fertil Steril 2004,82(1S):90–96.

    Google Scholar 

  19. Practice Committee of the American Society for Reproductive Medicine: Use of clomiphene citrate in infertile women: a committee opinion. Fertil Steril 2013,100(2):341–348.

    Article  Google Scholar 

  20. Goldstein SR, Siddhanti S, Ciaccia AV, Plouffe L Jr: A pharmacological review of selective oestrogen receptor modulators. Hum Reprod Update 2000,6(3):212–224. 10.1093/humupd/6.3.212

    Article  CAS  PubMed  Google Scholar 

  21. Rossing MA, Daling JR, Weiss NS, Moore DE, Self SG: Ovarian tumors in a cohort of infertile women. N Engl J Med 1994,147(12):1038–1042.

    Google Scholar 

  22. Sanner K, Conner P, Bergfeldt K, Dickman P, Sundfeldt K, Bergh T, Hagenfeldt K, Janson PO, Nilsson S, Persson I: Ovarian epithelial neoplasia after hormonal infertility treatment: long-trm follow-up of historical cohort in Sweden. Fertil Steril 2009,91(4):1152–1158. 10.1016/j.fertnstert.2008.01.073

    Article  PubMed  Google Scholar 

  23. Doyle P, Maconochie N, Beral V, Swerdlow AJ, Tan SL: Cancer incidence following treatment for infertility at a clinic in the UK. Hum Reprod 2002,17(8):2209–2213. 10.1093/humrep/17.8.2209

    Article  PubMed  Google Scholar 

  24. Calderon-Margalit R, Friedlander Y, Yanetz R, Kleinhaus K, Perrin MC, Manor O, Harlap S, Paltiel O: Cancer risk after exposure to treatments for ovulation induction. Am J Epidemiol 2009,169(3):365–375.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  25. Potashnik G, Lerner-Geva L, Genkin L, Chetrit A, Lunenfeld E, Porath A: Fertility drugs and the risk of breast and ovarian cancers: results of a longterm follow-up study. Fertil Steril 1999,71(5):853–859. 10.1016/S0015-0282(99)00085-0

    Article  CAS  PubMed  Google Scholar 

  26. Brinton LA, Lamb EJ, Moghissi KS, Scoccia B, Althuis MD, Mabie JE, Westhoff CL: Ovarian cancer risk associated with varying causes of infertility. Fertil Steril 2004,82(2):405–414. 10.1016/j.fertnstert.2004.02.109

    Article  PubMed  Google Scholar 

  27. Trabert B, Lamb EJ, Scoccia B, Moghissi KS, Westhoff CL, Niwa S, Brinton LA: Ovulation-inducing drugs and ovarian cancer risk: results from an extended follow-up of a large US infertility cohort. Fertil Steril 2013,100(6):1660–1666. 10.1016/j.fertnstert.2013.08.008

    Article  CAS  PubMed  Google Scholar 

  28. Jensen A, Sharif H, Frederiksen K, Kjaer SK: Use of fertility drugs and risk of ovarian cancer: Danish Population Based Cohort Study. BMJ 2009, 338: b249. 10.1136/bmj.b249

    Article  PubMed Central  PubMed  Google Scholar 

  29. Silva Idos S, Wark PA, McCormack VA, Mayer D, Overton C, Little V, Nieto J, Hardiman P, Davies M, MacLean AB: Ovulation-stimulation drugs and cancer risks: a long-term follow-up of a British cohort. Br J Cancer 2009,100(11):1824–1831. 10.1038/sj.bjc.6605086

    Article  PubMed  Google Scholar 

  30. Diedrich K, Felberbaum R: New approaches to ovarian stimulation. Hum Reprod 1998,13(3):1–13.

    Article  CAS  PubMed  Google Scholar 

  31. Leibowitz D, Hoffman J: Fertility drug therapies: past, present, and future. J Obstet Gynecol Neonatal Nurs 2000,29(2):201–210. 10.1111/j.1552-6909.2000.tb02040.x

    Article  CAS  PubMed  Google Scholar 

  32. Holzer H, Casper R, Tulandi T: A new era in ovulation induction. Fertil Steril 2006,85(2):277–284. 10.1016/j.fertnstert.2005.05.078

    Article  CAS  PubMed  Google Scholar 

  33. Gips H, Hormel P, Hinz V: Ovarian stimulation in assisted reproduction. Andrologia 1996,28(1):3–7.

    PubMed  Google Scholar 

  34. Hilliard TS, Modi DA, Burdette JE: Gonadotropins activate oncogenic pathways to enhance proliferation in normal mouse ovariansurface epithelium. Int J Mol Sci 2013,14(3):4762–4782. 10.3390/ijms14034762

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  35. Lerner-Geva L, Rabinovici J, Olmer L, Blumstein T, Mashiach S, Lunenfeld B: Are infertility treatments a potential risk factor for cancer development? Perspective of 30 years of follow-up. Gynecol Endocrinol 2012,28(10):809–814. 10.3109/09513590.2012.671391

    Article  PubMed  Google Scholar 

  36. Rizzuto I, Behrens RF, Smith LA: Risk of ovarian cancer in women treated with ovarian stimulating drugs for infertility. Cochrane Database Syst Rev 2013, 8: CD008215.

    PubMed  Google Scholar 

  37. Kolibianakis EM, Tarlatzis B, Devroey P: GnRH antagonists in IVF. Reprod Biomed Online 2005,10(6):705–712. 10.1016/S1472-6483(10)61113-3

    Article  CAS  PubMed  Google Scholar 

  38. Check JH, Slovis B: Choosing the right stimulation protocol for in vitro fertilization- embryo transfer in poor, normal, and hyper-responders. Clin Exp Obstet Gynecol 2011,38(4):313–317.

    CAS  PubMed  Google Scholar 

  39. Oehninger S: Ovulation induction in IVF. Minerva Ginecol 2011,63(2):137–156.

    CAS  PubMed  Google Scholar 

  40. Zarek SM, Muasher SJ: Mild/minimal stimulation for in vitro fertilization: an old idea that needs to be revisited. Fertil Steril 2011,95(8):2449–2455. 10.1016/j.fertnstert.2011.04.041

    Article  PubMed  Google Scholar 

  41. Siristatidis C, Sergentanis TN, Kanavidis P, Trivella M, Sotiraki M, Mavromatis I, Psaltopoulou T, Skalkidou A, Petridou ET: Controlled ovarian hyperstimulation for IVF: impact on ovarian, endometrial and cervical cancer–a systematic review and meta-analysis. Hum Reprod Update 2013,19(2):105–112. 10.1093/humupd/dms051

    Article  CAS  PubMed  Google Scholar 

  42. Li LL, Zhou J, Qian XJ, Chen YD: Meta-analysis on the possible association between in vitro fertilization and cancer risk. Int J Gynecol Cancer 2013,23(1):16–24. 10.1097/IGC.0b013e318277608b

    Article  PubMed  Google Scholar 

  43. Lerner-Geva L, Geva E, Lessing JB, Chetrit A, Modan B, Amit A: The possible association between in vitro fertilization treatments and cancer development. Int J Gynecol Cancer 2003,13(1):23–27. 10.1046/j.1525-1438.2003.13041.x

    Article  CAS  PubMed  Google Scholar 

  44. Venn A, Wartson L, Lumley J, Giles G, King C, Healy D: Breast and ovarian cancer incidence after infertility and in vitro fertilization. Lancet 1995,346(8981):995–1000. 10.1016/S0140-6736(95)91687-3

    Article  CAS  PubMed  Google Scholar 

  45. Venn A, Watson L, Bruinsma F, Giles G, Healy D: Risk of cancer after use of fertility drugs with in-vitro fertilisation. Lancet 1999,354(9190):1586–1590. 10.1016/S0140-6736(99)05203-4

    Article  CAS  PubMed  Google Scholar 

  46. Källén B, Finnström O, Lindam A, Nilsson E, Nygren KG, Olausson PO: Malignancies among women who gave birth after in vitro fertilization. Hum Reprod 2011,26(1):253–258. 10.1093/humrep/deq307

    Article  PubMed  Google Scholar 

  47. Dor J, Lerner-Geva L, Rabinovici J, Chetrit A, Levran D, Lunenfeld B, Mashiach S, Modan B: Cancer incidence in a cohort of infertile women who underwent in vitro fertilization. Fertil Steril 2002,77(2):324–327. 10.1016/S0015-0282(01)02986-7

    Article  PubMed  Google Scholar 

  48. Klip H, Burger CW, Van Leeuwen FE: The Omega Project Group. Risk of hormone-related cancers after ovarian stimulation for in-vitro fertilization in a cohort of 25,152 women. Enschede Netherlands PrintPartners Ipskamp BV 2002, 1: 55–82.

    Google Scholar 

  49. van Leeuwen FE, Klip H, Mooij TM, van de Swaluw AM: Risk of borderline and invasive ovarian tumours after ovarian stimulation for in vitro fertilization in a large Dutch cohort. Hum Reprod 2011,26(12):3456–3465. 10.1093/humrep/der322

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  50. Yli-Kuha AN, Gissler M, Klemetti R, Luoto R, Hemminki E: Cancer morbidity in a cohort of 9175 Finnish women treated for infertility. Hum Reprod 2012,27(4):1149–1155. 10.1093/humrep/des031

    Article  PubMed  Google Scholar 

  51. Brinton LA, Trabert B, Shalev V, Lunenfeld E, Sella T, Chodick G: In vitro fertilization and risk of breast and gynecologic cancers: a retrospective cohort study within the Israeli Maccabi Healthcare Services. Fertil Steril 2013,99(5):1189–1196. 10.1016/j.fertnstert.2012.12.029

    Article  PubMed Central  PubMed  Google Scholar 

  52. Asch RH, Greenblatt RB: Update on the safety and efficacy of clomiphene citrate as a therapeutic agent. J Reprod Med 1976,17(3):175–180.

    CAS  PubMed  Google Scholar 

  53. Kulkarni R, McGarry JM: Follicular stimulation and ovarian cancer. BMJ 1989,299(6701):740.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  54. Chatterjee SK: Infertility and ovarian cancer. J Indian Med Assoc 1999,97(2):69.

    CAS  PubMed  Google Scholar 

  55. Ayhan A, Salman MC, Celik H, Dursun P, Ozyuncu O, Gultekin M: Association between fertility drugs and gynecologic cancers, breast cancer, and childhood cancers. Acta Obstet Gynecol Scand 2004,83(12):1104–1111. 10.1080/j.0001-6349.2004.00669.x

    Article  PubMed  Google Scholar 

  56. Sills ES, McLoughlin LJ, Genton MG, Walsh DJ, Coull GD, Walsh AP: Ovarian hyperstimulation syndrome and prophylactic human embryo cryopreservation: analysis of reproductive outcome following thawed embryo transfer. J Ovarian Res 2008,1(1):7. 10.1186/1757-2215-1-7

    Article  PubMed Central  PubMed  Google Scholar 

  57. Shushan A, Paltiel O, Iscovich J, Elchalal U, Peretz T, Schenker JG: Human menopausal gonadotropin and the risk of epithelial ovarian cancer. Fertil Steril 1996,65(1):13–18.

    CAS  PubMed  Google Scholar 

  58. Kurman RJ, Shih IM: The origin and pathogenesis of epithelial ovarian cancer: a proposed unifying theory. Am J Surg Pathol 2010,34(3):433–443. 10.1097/PAS.0b013e3181cf3d79

    Article  PubMed Central  PubMed  Google Scholar 

  59. Kurman RJ: Origin and molecular pathogenesis of ovarian high-grade serous carcinoma. Ann Oncol 2013,24(10):16–21.

    Article  Google Scholar 

  60. Cramer DW, Welch WR: Determinants of ovarian cancer risk. Inferences regarding pathogenesis. J Natl Cancer Inst 1983,71(4):717–721.

    CAS  PubMed  Google Scholar 

  61. Fathalla MF: Incessant ovulation: a factor in ovarian neoplasia? Lancet 1971,2(7716):163.

    Article  CAS  PubMed  Google Scholar 

  62. Whittemore AS, Harris R, Itnyre J: Characteristics relating to ovarian cancer risk: collaborative analysis of 12 U.S. case-control studies. IV. The pathogenesis of epithelial ovarian cancer. Am J Epidemiol 1992,136(10):1212–1220.

    CAS  PubMed  Google Scholar 

  63. Preston-Martin S, Pike MC, Ross RK, Jones PA, Henderson BE: Increased cell division as a cause of human cancer. Cancer Res 1990,50(23):7415–7421.

    CAS  PubMed  Google Scholar 

  64. Tung KH, Wilkens LR, Wu AH, McDuffie K, Nomura AM, Kolonel LN, Terada KY, Goodman MT: Effect of anovulation factors on pre- and postmenopausal ovarian cancer risk: revisiting the incessant ovulation hypothesis. Am J Epidemiol 2005,161(4):321–329. 10.1093/aje/kwi046

    Article  PubMed  Google Scholar 

  65. Godwin AK, Testa JR, Handel LM, Liu Z, Vanderveer LA, Tracey PA, Hamilton TC: Spontaneous transformation of rat ovarian surface epithelial cells: association with cytogenetic changes and implications of repeated ovulation in the etiology of ovarian cancer. J Natl Cancer Inst 1992,84(8):592–601. 10.1093/jnci/84.8.592

    Article  CAS  PubMed  Google Scholar 

  66. Kashyap S, Moher D: Fung Kee Fung M, Rosenwaks Z: Assisted reproductive technology and the incidence of ovarian cancer: a meta-analysis. Obstet and Gynecol 2004,103(4):785–794. 10.1097/01.AOG.0000119226.39514.1d

    Article  Google Scholar 

  67. Tomao F, Spinelli G, Vici P, Pisanelli GC, Cascialli G, Frati L, Panici PB, Tomao S: Current role and safety profile of aromatase inhibitors in early breast cancer. Expert Rev Anticancer Ther 2011,11(8):1253–1263. 10.1586/era.11.96

    Article  CAS  PubMed  Google Scholar 

  68. Polyzos NP, Tzioras S, Badawy AM, Valachis A, Dritsas C, Mauri D: Aromatase inhibitors for female infertility: a systematic review of the literature. Reprod Biomed Online 2009,19(4):456–471. 10.1016/j.rbmo.2009.06.008

    Article  CAS  PubMed  Google Scholar 

  69. Polyzos NP, Tzioras S, Mauri D, Tsappi M, Cortinovis I, Tsali L, Casazza G: Treatment of unexplained infertility with aromatase inhibitors or clomiphene citrate: a systematic review and meta-analysis. Obstet Gynecol Surv 2008,63(7):472–479. 10.1097/OGX.0b013e31817d4e8d

    Article  PubMed  Google Scholar 

  70. Tomao F, Benedetti Panici P, Tomao S: Gonadotropin-releasing hormone agonists for the preservation of ovarian function during chemotherapy. J Clin Oncol 2012,30(26):3310–3311.

    Article  CAS  PubMed  Google Scholar 

  71. Tomao F, Spinelli GP, Panici PB, Frati L, Tomao S: Ovarian function, reproduction and strategies for fertility preservation after breast cancer. Crit Rev Oncol Hematol 2010,76(1):1–12. 10.1016/j.critrevonc.2009.12.005

    Article  PubMed  Google Scholar 

Download references


The authors wish to thanks the Director of Distretto ASL 1, Dr. Belardino Rossi for his contribution in the study development and the nurses Mara Arduin and Cinzia Sciarretta for their support.

Author information

Authors and Affiliations


Corresponding author

Correspondence to Federica Tomao.

Additional information

Competing interests

The authors have no relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript. This includes employment, consultancies, honoraria, stock ownership or options, expert testimony, grants or patents received or pending, or royalties. No writing assistance was utilized in the production of this manuscript.

Authors’ contributions

FT, GLR, GPS, PBP, PV and ST have contributed to conception and design of review, acquisition, analysis and interpretation of data and to the drafting of manuscript; VS, AAP, NP, MS, AP, MSC have contributed to acquisition, analysis and interpretation of data and to the drafting of manuscript. All authors read and approved the final manuscript.

Federica Tomao, Giuseppe Lo Russo contributed equally to this work.

Rights and permissions

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Tomao, F., Lo Russo, G., Spinelli, G.P. et al. Fertility drugs, reproductive strategies and ovarian cancer risk. J Ovarian Res 7, 51 (2014).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: