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World Journal of Oncology

Review

Volume 7, Number 4, August 2016, pages 59-69

Incidence Rates in Low-Grade Primary Brain Tumors: Are There Differences Between Men and Women? A Systematic Review

Incidence rates of adult low-grade primary brain tumors have previously been widely analyzed nationwide across the world, and most of these studies include data on incidence rates in men and women separately [1-3]. However, to our knowledge, no worldwide international comparison has been made on possible differences in incidence rates of low-grade brain tumors between men and women.

Previous studies have shown contradictive data on differences in incidence rate between men and women in low-grade tumors. For example, the low-grade vestibular schwannoma has in some studies shown no significant difference in incidence rate between men and women [4], whilst other has reported differences in incidence rate according to age [5]. Also, differences in incidence rate within genders have been suggested among a study including four Nordic countries; however, interpretation of these results was limited because of differences in reporting and coding the diagnosis between the different countries [6].

Other low-grade tumors such as meningiomas have previously reported higher incidence rate in women compared to that of men [1, 7]. The pathogenicity is under discussion, but studies have shown differences in both gene expression and chromosome abnormalities associated to patients’ gender, which may explain parts of this puzzle [8].

Tumors in the central nervous system are divided based on histopathological assessment as per 2007 WHO classification, using a four-point scale. Per definition, a brain tumor is an abnormal tissue within the cranium including the brain, cranial nerves, meninges, skull, pituitary gland and pineal gland [9]. In the clinical setting, the grading system is an important tool to decide choice of therapy, particularly adjuvant radiation and chemotherapy. The scale ranges from grade I to grade IV, describes the malignancy of the tumors and is used among the different histopathological groupings. Grade I describes tumors with low proliferation rate that may be curable with surgical resection only. Grade II tumors, on the other hand, are generally infiltrative and can transform to higher grades in the classification scale. Grade III tumors have even higher malignancy rates and are mostly treated with adjuvant radiotherapy or chemotherapy. Grade IV tumors are the most malignant in the scale, and include histological groupings of which a high mitotic activity and necrosis are often present. This is also associated with a poorer prognosis [10].

The ICD classification system is a diagnostic tool made by the WHO aimed to classify diseases according to a systematic encoding system [11]. The ICD system has its roots back in the 19th century, and multiple updates of the system have been done since then. In 1975, the nineth revision (ICD-9) and in 1990 the 10th revision (ICD-10) were made [11, 12], and this system is used by most studies included in this review.

The ICD-O is a system developed and revised by the WHO, used to systematically code tumors based on topography (anatomical site) and histology, and the third edition ICD-O-3 was revised in year 2000 [13].

The histologic parts of ICD-O are incorporated into the SNOMED [13], which is a clinical terminology owned by the International Health Terminology Standards Development Organization (IHTSDO) [14].

The Central Brain Tumor Registry of the Unites States (CBTRUS) is an organization aimed to collect and provide epidemiologic data on all benign and malignant primary brain tumors [15]. To gather data information, CBTRUS uses the Surveillance, Epidemiology, and End Results (SEER) program that was established in the United States (US) in 1973, with the aim to collect cancer statistic data from the US population [16]. CBTRUS also uses data from the National Program of Cancer Registries (NPCR) that collect data on cancer occurrence and initial treatments and, together with the SEER program, covers the entire US population [17].

Other countries normally use their respective national cancer registry in order to collect and provide information about cancer statistics in the population [18-22].

The primary aim was to review the incidence rates between men and women in adult low-grade primary brain tumors.

We searched for published articles in internationally peer reviewed journals that were identified through a systematic search of PubMed. The mesh terms used were Brain Cancer Incidence Time Trends. Because of difficulties in interpreting data, we excluded all studies only including patient data before the second edition of WHO histological classification system of brain tumors (1993) [23]. We also excluded studies not written in the English language, studies not including data of primary brain tumors, review articles and articles excluding adult subjects.

For each selected article, the following data were extracted: histology, data source, study period (years), demography, number of subjects included, age interval, and average annual age-adjusted incidence rate by gender.

The STATA 13 program was used for the analysis. Since the data did not have a normal distribution (Shapiro-Wilk W test, P-value < 0.00001), and since the variance of mean age-adjusted incidence rate differed between men and women (1.930 and 9.708, respectively), the Wilcoxon rank-sum (Mann-Whitney) test was used instead of a t-test to estimate differences in incidence rate between men and women.

For trend analysis, we compared the incidence rate within genders between time periods 1995 - 2004 and 2005 - 2010 by using the test for trend across ordered groups (nptrend). The incidence trend was analyzed in men and women separately. Different lengths in time periods were chosen because of very few numbers of studies before year 2005.

A total of 224 articles were found during the search. Exclusions were made because of the following reasons: seven were not written in English, 23 did not include adult patients only, 54 did not include information about incidence rate, 10 did not analyze low-grade brain tumors only, 50 did not study brain cancer, four were laboratory studies, seven were review articles, one did not analyze genders separately, three were excluded due to no online access, 43 only published data before 1993, five studied incidence rates based on non-Western population and three were comments on other articles (Supplementary 1, www.wjon.org). The remaining 14 articles did include incidence data on low-grade brain tumors, and were included in our analysis (Fig. 1). Eleven of these were based on US population, one article was published on four Nordic countries (Sweden, Finland, Denmark and Norway), one included Finnish population only, and one was based on Croatian data (Table 1 [1, 2, 5, 24-34]).

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Figure 1. Article selection process.

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Table 1. Demography and Data Sources

Since the studies analyzing the low-grade tumor pineocytoma made an overall calculation including pinealoma, NOS (ICD-O code 9630) and pineoblastoma (ICD-O code 9362), which is a highly malignant tumor (WHO grade IV), these data were not included in our analysis [1, 2].

Overall mean value in age-adjusted incidence rate in men was 1.07 (SD ± 1.389) per 100,000 compared to 1.70 (SD ± 3.116) per 100,000 in women. However, because of differences in variance between genders, the Wilcoxon rank-sum (Mann-Whitney test) was used to calculate median differences. No significant difference was seen in age-adjusted incidence rate between genders (P = 0.8347). Also, no significant trend of age-adjusted incidence rate was seen in male patients (P = 0.757) nor in women (P = 0.354).

A total of seven studies analyzed age-adjusted incidence rate in tumors of the cranial and paraspinal nerves. Of these, six articles were based on US register data and one study showed results based on Croatian register data.

Three studies reported results on primary nerve sheath tumors, NOS, whereas three articles presented results on vestibular schwannomas and one study differed between the two histopathologic groupings and presented results separately. The incidence rate across all studies ranged from 0.3 to 1.7 per 100,000 population in men and 0.55 to 1.71 per 100,000 population in women between years 1985 and 2010 [1, 2, 5, 24-27].

Nine studies presented results of low-grade astrocytic tumors; however, only five showed data on age-adjusted incidence rate (Table 2 [1, 2, 5, 24-34]). One study analyzed data on astrocytic tumors, NOS among US black population and showed incidence rates of 0.80 per 100,000 in men compared to 0.60 per 100,000 in women during the period 1973 - 2008 (Tables 2 and 3 [1, 2, 5, 24-34]). When analyzing the period of 1998 - 2008, the average male incidence decreased to 0.31 per 100,000 compared to the female incidence of 0.18 per 100,000, which was stated as a “sizable difference”. No incidence rate ratio (IRR) was calculated, nor any statistical power in the differences between the genders [28].

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Table 2. Incidence Rates by Histology

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Table 3. International Classification of Diseases for Oncology (ICD-O) Codes Used

Among the remaining four studies, three were based on US patients using CBTRUS registries, and one showed data based on Croatian population. The incidence rate of pilocytic astrocytoma was reported in the three American studies, ranging from 0.14 to 0.33 per 100,000 in men and 0.13 to 0.33 per 100,000 in women between years 2004 and 2010. Incidence rates of diffuse astrocytoma were presented by two US studies, ranging from 0.66 to 0.68 per 100,000 in men compared to 0.48 to 0.5 per 100,000 in women between years 2005 and 2010.

Six studies analyzed oligodendroglial tumors; however, only three reported incidence rate data. Two of these were based on US population, and one study was made using data on Croatian patients. The incidence rate ranged from 0 to 0.30 per 100,000 in men and 0.24 to 0.4 per 100,000 in women between years 1996 and 2010. The two US studies based on CBTRUS registry data showed male to female IRR of 1.30 and 1.26, respectively, both statistically significant.

In the studied data by Dobec-Meic et al (2006), no male had gotten the diagnosis of oligodendroglioma, thus the incidence rate (not age-adjusted) was 0 per 100,000. The female incidence rate was 0.4 per 100,000, which was a number based on three cases [15].

Two studies reported incidence rate data on oligoastrocytic tumors, both based on US CBTRUS registry data. The age-adjusted incidence rate amongst these tumors was 0.24 per 100,000 in men and 0.17 to 0.18 per 100,000 in women. One study [1] showed a statistically significant male to female IRR of 1.41. However, the other US study [2] presented a non-significant male to female IRR of 1.37.

Three studies showed data on incidence rate of ependymal tumors; two from US CBTRUS registries and one from Croatia. The incidence rate ranged from 0.3 to 0.47 per 100,000 in men and 0.3 to 0.37 in women between years 1996 and 2010. Both US studies had statistically significant male to female IRR of 1.31 and 1.32, respectively.

Only two studies analyzed choroid plexus tumors, both from US, based on CBTRUS data. Age-adjusted incidence rate was 0.05 per 100,000 in men and ranged from 0.05 to 0.06 per 100,000 in women between years 2005 and 2010. No male to female IRR was calculated in neither study.

Two studies presented data of all neuronal and mixed neuronal-glial tumors (ICD-O codes 8680, 8681, 8690, 8693, 9412, 9413, 9442, 9492, 9493, 9505, 9506, 9522 and 9523), thus also including the anaplastic ganglioglioma (WHO grade III) together, yielding incidence rates of 0.29 per 100,000 in men and 0.25 to 0.26 per 100,000 in women between years 2005 and 2010.

Four studies showed results of incidence rates in meningeal tumors, of which three were based on US CBTRUS data and one presented results on Croatian population. Incidence rates ranged from 2.6 to 5.46 per 100,000 in men and 3.5 to 12.42 per 100,000 in women between years 1996 and 2010. Two of these studies included all non-malignant meningiomas (ICD-O codes 9530/0,1; 9531, 9532, 9533, 9534, 9537, 9538 and 9539), whereas two presented average annual age-adjusted incidence rates on meningiomas, NOS (no ICD-O histology codes specified). The Croatian study only included 40 meningioma diagnoses, thus those numbers should be interpreted by caution. The two large US studies both calculated statistically significant male to female IRR of 0.44.

A total of four studies presented incidence rates of tumors of the sellar region, of which two were based on US population, one from Finland and one from Croatia. Three studies showed incidence rates of pituitary tumors (ICD-O codes 8040, 8140, 8146, 8246, 8260, 8270, 8271, 8272, 8280, 8281, 8290, 8300, 8310, 8323, 9492 and 9582) and the Finnish study analyzed the average annual incidence rates of pituitary adenomas (ICD-O codes not specified). The incidence rates ranged from 1.1 to 2.93 per 100,000 in men and 0.6 to 5.86 per 100,000 in women. The US based studies showed male to female IRR of 0.86 and 0.87, respectively, both statistically significant. Raappana et al showed female to male IRR of 2.5 and the Croatian study had a male to female IRR of 1.9 (not statistically significant). However, this study only included 11 cases of pituitary adenomas, thus those numbers should be interpreted carefully.

Three studies showed incidence data on craniopharyngiomas (not the Finnish study). The US studies defined the diagnosis by ICD-O codes 9350, 9351 and 9352, whereas the Croatian study did not specify ICD codes. Incidence rates ranged from 0.18 to 0.2 per 100,000 in men and 0.18 to 0.3 per 100,000 in women between years 1996 and 2010.

The impact of sex differences in human disease is a well-known yet often overlooked aspect. In this regard, cancer is no exception, where there are evident differences between men and women in terms of incidence and prognosis for different tumors.

In this review of reported incidence rates of low-grade primary tumors in adults, we have found no significant difference in overall incidence between men and women. Furthermore, we have found no significant time trend of age-adjusted incidence rate in neither male nor female patients. However, when taking only menigiomas into account, the age-adjusted incidence rates were higher in women and two of three studies with IRR calculations showed a statistically significant male to female IRR of 0.44, meaning menigiomas are diagnosed about twice as often in females as in males. Likewise, the studies reporting incidence rate of pituitary tumors showed higher incidence in women than in men (IRR 0.4 - 0.87).

This is a comprehensive review containing incidence data for men and women from different countries. To our knowledge, it is the first international comparison that has been conducted concerning possible gender differences in incidence rates of low-grade brain tumors. However, the interpretation of these results must be done carefully and no absolute conclusion can be made. One major issue with the present review regards the selection of studies that has been performed. The data search in this study was made in one electronic database only, PubMed, thus relevant articles might have been missed. Also the inclusions were made based on review aim rather than methodological quality. Furthermore, out of the 224 articles that were initially found, 210 were excluded for various reasons leaving only 14 papers available for analysis, which may lead to additional selection bias. One obvious selection regards the dominance of US population patients in the reviewed studies, thus the average annual age-adjusted incidence rate was based on the 2000 US standard population. Furthermore, in some of the studies of US population, there may be overlapping data. The Finnish study by Raappana et al (2010) used the WHO 2000 standard population, Dobec-Meic et al (2006) used 2001 Varazdin County census data in Croatia to make the estimations, and Deltour et al (2009) used national population registers in Sweden, Finland, Denmark and Norway to estimate the incidence rate. This may result in different incidence rates based on the calculation rather than on the absolute incidence rate. Also, similar tumor groupings, for example, primary nerve sheath tumors, NOS, had different ICD-O histology codes between studies, meaning that comparison within the tumor groupings must be made with caution. Some studies even did not state the ICD-O histology codes. Also, the number of inclusions, and thus the statistical power of different incidence rates between men and women varied throughout the studies. For example, the total number of included patients with a diagnosis of tumors of the cranial and paraspinal nerves in Dobec-Meic et al (2006) was 8, compared to the number of inclusions by Ostrom et al (2013) (n = 26,548 cases).

As the general incidence rate of low-grade brain tumors in men and women differs through time, a possible covariate could be that all different tumor groupings are not analyzed in the same time period. This may result in a false change in incidence rate within low-grade tumors over time. For example, meningiomas which have relatively high incidence rates in both men and women only have powerful data between years 2004 and 2010, probably influencing the increase in incidence rate in the later years in our analysis.

When analyzing the incidence of cancers affecting both men and women, the male to female incidence ratios often range from 1.5:1 to 3:1. Males have higher incidence rates for most cancers and usually also poorer overall survival [35-38]. This indicates that sex plays a major role in tumorigenesis. In malignant gliomas, the incidence has previously been reported to be higher in males [39]. Meningiomas, on the other hand, are reported to be much more likely to occur in women. Furthermore, in addition to the difference in incidence, female meningiomas are more commonly low grade, whereas the male menigiomas are more commonly high grade [39]. The reason behind this may be an effect of the different levels of sex steroids in men and women as meningiomas rarely develop in prepubertal children and menigiomas have been shown to express progesterone and estrogen receptors [40]. Also there have been reports of a higher risk of menigioma in women subjected to hormone replacement therapies [41]. Furthermore, there may be a protective effect of testosterone as men with prostate cancer undergoing androgen deprivation therapy have been shown to have an increased risk of meningioma growth [42].

As the results must be interpreted with caution, more large international studies are warranted and should be made in a standardized manner differing low-grade tumors from high-grade tumors according to the WHO 2007 brain tumor classification system. Also future studies should always state the ICD-O histology coding to ease future interpretations.

Conflicts of Interest

None.

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