Kurman, Robert J. MD; Shih, Ie-Ming MD, PhD
“Nothing will come from nothing”
King Lear, Act I
The origin and pathogenesis of epithelial ovarian cancer has perplexed investigators for decades. Despite numerous studies that have carefully scrutinized the ovaries for precursor lesions, none have been found. This has led to the proposal that ovarian cancer develops de novo.2 “Nothing will come from nothing,” but each year in the United States, approximately 21,550 women develop ovarian cancer “de novo,” and 14,600 women die from this disease.18 Ovarian cancer is, in fact, the most lethal gynecologic malignancy. It is clear that de novo reflects our ignorance about the early events of ovarian carcinogenesis rather than our insight into its perplexing origin. The time-honored concepts that have forged our views of ovarian carcinogenesis can be summarized as follows: (1) although it is recognized that there are profound differences among the various histologic types, the vast majority of ovarian carcinomas are high-grade serous carcinomas and therefore ovarian cancer is regarded as a single disease; (2) ovarian cancer originates from the ovarian surface epithelium (mesothelium) that invaginates into the underlying stroma resulting in inclusion cysts that eventually undergo malignant transformation; (3) ovarian cancer spreads from the ovary to the pelvis, abdomen, and distant sites. On the basis of these views of ovarian carcinogenesis, efforts at improving the survival have focused on early detection of ovarian cancer, when it is still confined to the ovary, and on the development of new chemotherapeutic drugs and routes of delivery irrespective of the histologic type. Unfortunately, these efforts have not been successful as evidenced by the fact that the overall survival for women with ovarian cancer has not changed over the last 50 years. The reasons for this are that the concepts of histogenesis, on which these approaches are based, are flawed.
Recent morphologic and molecular genetic studies have illuminated our understanding of ovarian carcinogenesis in ways that have been quite unexpected and have challenged the conventional wisdom regarding their origin and development. Indeed, they have resulted in a paradigm shift that has important implications for research and for radically changing our approaches to early detection, prevention, and treatment.
THE MORPHOLOGIC AND MOLECULAR HETEROGENEITY OF EPITHELIAL OVARIAN CANCER
One of the major problems in elucidating the pathogenesis of ovarian cancer is that it is a heterogeneous disease composed of different types of tumors with widely differing clinicopathologic features and behavior. On the basis of a series of morphologic and molecular genetic studies, we have proposed a dualistic model that categorizes various types of ovarian cancer into two groups designated type I and type II.43 Type I tumors are clinically indolent and usually present at a low stage. They exhibit a shared lineage between benign cystic neoplasms and the corresponding carcinomas, often through an intermediate (borderline tumor) step, supporting the morphologic continuum of tumor progression in these neoplasms. This stepwise sequence of events parallels the adenoma-carcinoma sequence that occurs in colorectal carcinoma. Type I tumors include low-grade serous, low-grade endometrioid, clear cell and mucinous carcinomas. In contrast to the clear-cut and distinctive morphologic differences among type I tumors, the morphologic differences among the type II tumors are more subtle and, as a result, there is considerable overlap in the diagnosis of these tumors by different pathologists. Type II tumors exhibit papillary, glandular, and solid patterns and are diagnosed as high-grade serous, high-grade endometrioid. and undifferentiated carcinomas depending on the dominant pattern. Generally, most pathologists classify them as high-grade serous carcinomas even though they bear little resemblance to tubal-type epithelium (the basis for typing a tumor as serous); arguably many of those lacking distinctive serous or endometrioid features could be classified as “high-grade adenocarcinoma”. In addition to these neoplasms, malignant mixed mesodermal tumors (carcinosarcomas) are included in the type II category, because they have epithelial components identical to the pure type II carcinomas. Type II tumors are highly aggressive and almost always present in advanced stage. As they account for approximately 75% of all epithelial ovarian carcinomas and have relatively similar morphologic features and a uniformly poor outcome, ovarian cancer has been erroneously regarded as a single disease. The morphologic differences between type I and type II tumors are mirrored by marked differences in their molecular genetic features.7 As a group, type I tumors are genetically more stable than type II tumors and display specific mutations in the different histologic cell types.21 Thus, KRAS, BRAF, and ERBB2 mutations occur in approximately two thirds of low-grade serous carcinomas, whereas TP53 mutations are rare in these tumors. Low-grade endometrioid carcinomas have aberrations in the Wnt signaling pathway involving somatic mutations of CTNNB1 (encoding β-catenin), PTEN and PIK3CA.7 Mucinous carcinomas have KRAS mutations in more than 50% of specimens.1,28 Clear cell carcinoma is unique in that it has a high percentage of PIK3CA activating mutations when purified tumor samples and cell lines are analyzed.22 There is little available molecular genetic data on transitional cell (Brenner) tumors. High-grade serous carcinoma, the prototypic type II tumor is characterized by very frequent TP53 mutations (>80% of cases) and CCNE1 (endcoding cyclin E1) amplification but rarely mutations that characterize most type I tumors, such as KRAS, BRAF, ERBB2, PTEN, CTNNB1, and PIK3CA.7 Although only a small number of malignant mixed mesodermal tumors have been analyzed molecularly, the few that have been analyzed, display a similar molecular genetic profile. In summary, type I tumors as a group, are genetically more stable than type II tumors and display a distinctive pattern of mutations that occur in specific cell types (low-grade serous, low-grade endometrioid, clear cell and mucinous). In contrast, the type II tumors (high-grade serous, high-grade endometrioid, malignant mixed mesodermal tumors, and undifferentiated carcinomas) show greater morphologic and molecular homogeneity, are genetically unstable, and have a very high frequency of TP53 mutations. These findings suggest that different types of ovarian carcinomas develop along different molecular pathways.
THE CELL OF ORIGIN OF MOST EPITHELIAL OVARIAN CANCER IS NOT OVARIAN
The cell of origin of ovarian cancer and the mechanisms by which cancer develops have been long debated. The traditional view of ovarian carcinogenesis has been that the various tumors are all derived from the ovarian surface epithelium (mesothelium), and that subsequent metaplastic changes lead to the development of the different cell types [serous, endometrioid, clear cell, mucinous, and transitional cell (Brenner)], which morphologically resemble the epithelia of the fallopian tube, endometrium, gastrointestinal tract, or endocervix and urinary bladder, respectively. The normal ovary, however, has no constituents that resemble these tumors. Moreover, the cervix, endometrium, and fallopian tubes are derived from the müllerian ducts, whereas the ovaries develop from mesodermal epithelium on the urogenital ridge separate from the müllerian ducts. Therefore, an alternate theory proposes that tumors with a müllerian phenotype (serous, endometrioid, and clear cell) are derived from müllerian-type tissue and not from mesothelium.11 This müllerian-type tissue (columnar epithelium, often ciliated) lines cysts located in paratubal and paraovarian locations that have been referred to collectively as the “secondary müllerian system”.23 According to this theory, ovarian tumors develop from these cysts. As the tumor enlarges, it compresses and eventually obliterates ovarian tissue resulting in an adenxal tumor that seems to have arisen in the ovary. More recently, another theory has been advanced, which argues that the majority of ovarian carcinomas that are high-grade serous carcinomas, arise from high-grade intraepithelial serous carcinomas in the fallopian tube, which then spread to the ovary. These conflicting views led us to undertake a review of the literature in an effort to determine which of the theories is best able to explain the various aspects of ovarian carcinogenesis.
Evaluating these theories is problematic, because it is difficult to construct experimental systems to test their validity. Accordingly, our evaluation is based on critical analysis of these studies in the light of observations we have made in the course of pathologic examination of ovarian tumors. The discussion that follows is an attempt to distill the most plausible components from the various theories of cellular origin and integrate them with the clinicopathologic and molecular genetic data from the dualistic model to construct a unifying theory of ovarian carcinogenesis.
The theory of origin from ovarian surface epithelium (mesothelium) has a number of limitations. Histologically, the single layer of generally attenuated mesothelium overlying the ovaries bears no resemblance to serous, endometrioid, mucinous, clear cell, or transitional (Brenner) carcinomas. As noted above to account for this apparent contradiction, it was proposed that the mesothelium overlying the ovary invaginates into the underlying stroma to form so-called “cortical inclusion cysts”. These cysts under the influence of local factors, possibly steroid hormones, undergo a metaplastic change, which results in the mesothelium being converted to müllerian-type epithelium. These inclusion cysts, with their newly acquired müllerian phenotype, can then undergo malignant transformation resulting in carcinomas corresponding to the different cell types (serous, endometrioid and clear cell carcinomas).6 Although cortical inclusion cysts lined by ciliated (müllerian-type epithelium) are frequently observed in the ovarian cortex, well-documented examples of what can be interpreted as a transition from these cysts to carcinoma have not been reported. Moreover, cortical inclusion cysts lined by intestinal-type epithelium to account for the development of mucinous carcinomas are distinctly rare. The same can be said for the absence of transitional-type epithelium lining cortical inclusion cysts to account for the development of Brenner tumors.
The limitations of the secondary müllerian system theory are that precursor lesions resembling serous, endometrioid, and clear cell carcinomas have rarely, if ever, been reported in paratubal and paraovarian cysts. Moreover, the vast majority of mucinous tumors display intestinal rather than endocervical-type mucinous differentiation and therefore do not qualify as müllerian-type tumors. A similar problem exists for transitional cell (Brenner) tumors resembling urothelium that is not müllerian in origin.
The most compelling evidence suggests that the vast majority of what seems to be primary ovarian cancers, namely serous, endometrioid, and clear cell carcinomas, are derived from the fallopian tube and endometrium and not directly from the ovary. Sporadic reports of tubal carcinoma and “dysplasia” had been reported in the past,15 but in 2001, a group of Dutch investigators described these lesions that closely resemble high-grade ovarian serous carcinoma in women with a genetic predisposition to ovarian cancer.33 This was a surprising finding, as numerous studies over the past two decades that carefully examined the ovaries of women with a genetic predisposition to ovarian cancer never reported similar lesions. In addition, other studies of normal appearing ovaries contralateral to sporadic (nonhereditary) unilateral ovarian carcinomas had never identified a convincing precursor lesion. These latter studies reported a number of morphologic changes in grossly normal appearing ovaries, such as an increased number of surface papillae and cortical inclusion cysts, including some displaying minor degrees of atypia. The data, however, have been conflicting, some studies reporting a significant difference of these changes in cases versus controls, and other studies reporting no difference. In any event, none of these changes even remotely resemble high-grade serous carcinoma. It was precisely because of a lack of convincing precursor lesions that the de novo hypothesis was invoked.
In hindsight, because it was assumed that precursors of ovarian carcinoma would logically be in the ovaries, the fallopian tubes were not carefully examined.10,42 Subsequent studies, in which fallopian tubes were more carefully examined, confirmed that in situ and small, early invasive tubal carcinomas occurred in women with a genetic predisposition for the development of ovarian cancer.4,5,8,12,27,29,41 This led to fallopian tube carcinoma being included as part of the cancer spectrum associated with inherited BRCA mutations. It was subsequently proposed that a proportion of ovarian carcinomas might develop as a result of implantation of malignant cells from the tubal carcinoma to the ovary.34,35 The next important step linking what had been termed “tubal intraepithelial carcinoma” and, subsequently, “serous tubal intraepithelial carcinoma” (STIC) with ovarian carcinoma was the observation that over 70% of sporadic (nonhereditary) ovarian and peritoneal high-grade serous carcinomas showed mucosal tubal involvement including STICs.19 This observation gave substantial support to the proposal that STICs, which almost always are detected in the fimbria, may be the source of ovarian high-grade serous carcinoma in both women with hereditary mutations in BRCA and women who did not have a known genetic predisposition for ovarian cancer. Although it can be argued that mucosal tubal involvement could represent secondary spread from an ovarian carcinoma present in the same specimen, the presence of focal noncontiguous intraepithelial lesions (STICs) would be an unusual manifestation of metastasis. Furthermore, the identification of STICs in prophylactic specimens from women with a hereditary predisposition to ovarian cancer, in which complete microscopic evaluation of the fallopian tubes and ovaries failed to identify invasive carcinoma in these organs, lends additional support to the concept that the serous neoplastic process may well begin in the fallopian tube rather than in the ovary. Further support for this argument is the finding that nearly all STICs overexpress p53, similar to high-grade serous carcinoma (Fig. 1). Laser capture microdissection studies of these lesions have shown that they harbor mutated TP53.19 In addition, STICs associated with a concomitant ovarian carcinoma share not only morphologic features but also identical TP53 mutations indicating a clonal relationship between them. Adnexal malignant mixed mesodermal tumors (another type II tumor) have also been associated with STICs supporting the existence of a common precursor lesion for type II tumors.14 Further evidence implicating the fallopian tube rather than ovarian surface epithelium as the site of origin of serous neoplasms comes from a gene profiling study showing that the gene expression profile of high-grade serous carcinoma is more closely related to the fallopian tube than to the ovarian surface epithelium.25 In addition, high-grade serous carcinomas express PAX8, a müllerian marker, but not calretinin, a mesothelial marker (Shih, Unpublished data).
A recent finding has been the identification of benign tubal epithelium, specifically secretory as opposed to ciliated cells, that express p53 and in which laser capture microdissection studies have reported TP53 mutations in 57% of cases.24 These lesions termed “p53 signatures” are found in association with STICs and in normal appearing fallopian tubes of women without STICs or carcinoma; they have been observed in approximately one third of women with and without BRCA mutations.13,17,41 Like STICs, p53 signatures express γ-H2AX that localizes to areas of DNA damage in nuclei.24 When associated with STICs and ovarian carcinoma, the p53 signature has had the identical TP53 mutation as the STIC and the carcinoma in some cases but not in others. Based on these findings, a sequence of pathogenetic events has been proposed beginning with genotoxic DNA damage, followed by TP53 mutation and progressive loss of cell cycle control, which then eventuate in the development of carcinoma.24 There are a number of questions that must be resolved, however, before this hypothesis can be completely accepted. First, as noted in some instances, TP53 mutations, when present in the p53 signature, are not always identical with the mutations in the STICs and carcinomas in the same specimen. Second, women at high risk have the same frequency of p53 signatures as women who are not at high risk. Third, the high prevalence of p53 signatures (a third of all women) compared with the low prevalence of high-grade serous ovarian carcinoma suggests that either a small minority of p53 signatures progress or that they are not related to carcinoma. It is conceivable that p53 signatures reflect an appropriate and physiologic upregulation of p53 in response to DNA damage based on the observation that TP53 mutations are absent in nearly half of p53 signatures. Although the proposal that the p53 signature is a precursor lesion is intriguing, its role in the genesis of ovarian high-grade serous carcinoma is far from clear at this time. As fallopian tubes are more carefully examined and these lesions studied, the nature of p53 signatures and their relationship to STICs will become better defined.
Generally, before a carcinoma acquires the ability to metastasize, it must first invade and gain access to blood vessels or lymphatics. We have observed that the fimbria contain a rich angiolymphatic vasculature. Moreover, they are in almost direct contact with the basement membrane of the tubal epithelium, and therefore a tubal carcinoma may not need to attain a very large size to invade this highly accessible angiolymphatic network. In addition, invasion in the case of a STIC may not be a necessary prerequisite for dissemination. Tubal intraepithelial carcinomas are morphologically and immunohistochemically similar to endometrial intraepithelial carcinomas that are regarded as precursors or early forms of uterine serous carcinoma. These lesions have also been termed “uterine surface serous carcinomas”. They have been shown to disseminate throughout the peritoneal cavity presumably by the passage of malignant cells through the fallopian tube without requisite myometrial invasion.45 The cells that comprise both endometrial and tubal intraepithelial carcinomas are highly anaplastic and identical morphologically to high-grade serous carcinoma. The lesions form papillary tufts and the constituent cells are loosely cohesive. Presumably, these cells can shed and implant on the surface of the ovary and the peritoneum in the absence of invasive growth in the fallopian tube. Evidence supporting this possibility are the reports of positive pelvic washings in women whose only lesion was a STIC.4
As earlier noted, in studies of ovarian and primary peritoneal high-grade serous carcinomas in which the entire fallopian tubes were carefully sectioned, mucosal involvement of the tube, including STICs, was identified in approximately 70% of cases.19 The question arises as to the source of the remaining ovarian carcinomas that lack evidence of tubal involvement. There are a number of possible explanations. First, despite thorough sectioning, a small STIC could have been missed (unpublished data). Second, occasionally high-grade serous carcinomas are intimately associated with serous borderline tumors and low-grade serous carcinomas. In these cases, the high-grade tumors have had KRAS mutations identical to those in the serous borderline tumors and lacked TP53 mutations.9 This finding suggests that some high-grade serous carcinomas arise from low-grade serous tumors and not by the usual (type II) pathway that begins with a TP53 mutation. Third, clear-cut mucosal tubal involvement could have been obscured by overgrowth of the pelvic carcinoma. Fourth, the fimbria of the fallopian tube normally is in intimate contact with the ovarian surface at the time of ovulation. It is conceivable that when the ovarian surface epithelium is disrupted at the time of ovulation, normal tubal epithelial cells from the fimbria may be dislodged and implant in the ovary to form an inclusion cyst (Fig. 2) from which a high-grade serous carcinoma could develop (see below). Evidence to support this notion is the observation that fallopian tube epithelial cells are easily obtained for culture by flushing the fallopian tube (Shih, Unpublished data).34 This mechanism could also explain the development of endosalpingiosis, a lesion composed of glands and papillary structures lined by tubal-type epithelium that is found on peritoneal surfaces in the pelvis, omentum, and beneath the capsule of pelvic and para-aortic lymph nodes. Endosalpingiosis is frequently found in association with low-grade serous tumors and has been viewed as a possible precursor of these tumors. Finally, the possibility that some high-grade serous carcinomas arise in cortical inclusion cysts as a metaplastic process from the ovarian surface epithelium rather than from implantation of normal fallopian tube epithelium cannot be entirely dismissed.
Direct implantation of tubal epithelium into the ovary to form an inclusion cyst, which in turn is the site of origin of ovarian serous carcinoma, although not yet shown, is an attractive alternative theory to that of metaplasia from the surface epithelium (mesothelium). Implantation of fallopian tube epithelium from the fimbria at the time of ovulation when the surface epithelium is disrupted can explain the derivation of low-grade and high-grade serous carcinomas. In the case of a low-grade serous carcinoma, the process develops slowly from a serous cystadenoma and then a serous borderline tumor after a KRAS or BRAF mutation, whereas in the case of a high-grade serous carcinoma, the process evolves rapidly, presumably from a cortical inclusion cyst after a TP53 mutation with the development of an intraepithelial carcinoma as an intermediate step. According to this view, both low-grade and high-grade serous carcinomas are ultimately of tubal (müllerian) origin, and, in a sense, the ovary is involved secondarily (Fig. 3).
It has been well established both by morphologic and, more recently, by molecular genetic studies that low-grade endometrioid and clear cell carcinomas develop from endometriotic cysts (endometriomas)that are frequently associated with implants of endometriosis elsewhere in the pelvis.44 Although the precise origin of endometriosis has not been completely established, specifically, whether it develops in situ in the peritoneum through a process of metaplasia or from retrograde menstrual flow, the preponderance of data favor the latter mechanism.3 Admittedly, the former theory is more difficult to prove experimentally. Thus, if retrograde menstruation accounts for most cases of endometriosis, it is logical to assume that endometrioid and clear cell tumors develop from endometrial tissue (müllerian derived) that implanted on the ovary and therefore the ovary is involved secondarily26 (Fig. 4). Of further interest has been the observation that the eutopic endometrium in women with endometriosis exhibits intrinsic molecular abnormalities, including activation of oncogenic pathways. Presumably, these changes permit the endometrial tissue to implant, survive, and invade on ovarian and peritoneal surfaces.3 This hypothesis, by which endometrioid and clear cell carcinoma develop from endometrial tissue implanted on the ovary, is supported by epidemiologic evidence showing that a protective effect for tubal ligation was seen only for endometrioid and clear cell carcinoma of the ovary.37
Finally, the derivation of mucinous tumors of gastrointestinal type and transitional cell (Brenner) tumors may also not involve the ovaries directly. The origin of these tumors is puzzling, as unlike serous, endometrioid, and clear cell tumors, they do not display a müllerian phenotype. Although it has been argued that these mucinous tumors bear some relationship with the endocervix, the mucinous epithelium that characterizes these neoplasms more closely resembles gastrointestinal mucosa. It seems most unlikely that they develop from cortical inclusion cysts. as mucinous metaplasia involving cortical inclusion cysts is a very rare finding. On the other hand, the association of Brenner tumors and mucinous tumors has been recognized for many years. In a provocative study of mucinous cystadenomas and Brenner tumors, it was reported that after extensive sectioning, mucinous cystadenomas contained foci of Brenner tumor in 18% of cases.40 Interestingly, mucinous tumors were frequently associated with Walthard cell nests that are composed of benign transitional-type epithelium, frequently found in paraovarian and paratubal locations. This raises the possibility that mucinous tumors and Brenner tumors have the same histogenesis arising from these microscopic transitional cell nests at the tubal-mesothelial junction in keeping with their nonmüllerian appearance. The study reported that Brenner tumors are small (median size 0.5 cm, range 0.02 to 20 cm), whereas mucinous cystadenomas are large (median size 9 cm, range 1 to 30 cm). The investigators speculated that as a small Brenner tumor grows, the mucinous component becomes dominant resulting in the development of a mucinous cystadenoma that, as it enlarges, compresses and eventually obliterates the adjacent ovary giving the appearance that it arose in the ovary. The findings in this study are intriguing but must be regarded as preliminary. Additional morphologic and molecular genetic studies are necessary to determine whether this concept is valid.
In summary, none of the existing theories adequately reconciles all aspects of ovarian carcinogenesis. All of them have something to offer in explaining the development of ovarian carcinomas, but none are all inclusive. It does seem that the vast majority of what have been thought to be primary epithelial ovarian and primary peritoneal carcinomas are, in fact, secondary. Thus, the most persuasive data support the view that serous tumors develop from the fimbriated portion of the fallopian tube, endometrioid, and clear cell tumors from endometrial tissue passing through the fallopian tube resulting in endometriosis and mucinous, and Brenner tumors from transitional-type epithelium located at the tubal-mesothelial junction where the fimbria makes contact with the peritoneum. The concept that the majority of epithelial ovarian carcinomas originates outside the ovary and involves it secondarily has emerged only recently, because in the past, the default diagnosis of carcinomas involving the pelvis and abdomen was that they were ovarian. A carcinoma was classified as tubal in origin only when the bulk of the tumor involved the fallopian tube rather than the ovary, and there was evidence of an intraepithelial (in situ) tubal carcinoma.39 A diagnosis of primary peritoneal carcinoma is even more restrictive. Even with extensive tumor involving the peritoneum, omentum, and other abdominal organs, a carcinoma is classified as primary ovarian, if there is as little as 5 mm of tumor involving the ovaries. Thus, there has been an inherent bias in classifying pelvic tumors as being ovarian in origin.
Although the data suggesting that epithelial ovarian carcinoma arises in extraovarian sites and involves the ovaries secondarily are compelling, serous neoplasms (low- and high-grade) involve the ovaries and other pelvic and abdominal organs, such as the omentum and mesentery, much more extensively than the fallopian tubes. Similarly, although endometrioid carcinomas develop from endometriosis that frequently involves multiple sites in the pelvis, these neoplasms are almost always confined to the ovaries. It is likely that the propensity for growth in the ovary is mulifactorial, but the precise reasons for this are unknown.
IMPLICATIONS FOR RESEARCH, SCREENING, PREVENTION, AND TREATMENT
The implications of this new paradigm of ovarian carcinogenesis for investigators, clinicians, and women are significant. For researchers, the implication of tubal origin of ovarian serous carcinoma challenges many of the earlier reports showing “overexpressed” ovarian cancer- associated genes in which their expression levels in carcinoma are almost always compared with their “normal” counterpart, ovarian surface epithelium. As the gene expression profiles in ovarian surface epithelium that is of mesothelial origin, are distinct from fallopian tube epithelium which is of müllerian origin, experiments in which ovarian surface epithelium (mesothelium) has been used as a control may not be valid. Whether the overexpressed genes that have been reported are indeed upregulated, when they are compared with the more likely source of ovarian serous carcinoma, that is, fallopian tube epithelium, needs to be revisited. In fact, a recent molecular genetic study showed that the different histologic types of ovarian cancer do indeed display distinct expression profiles that are concordant with the normal tissues they resemble and show little similarity to ovarian surface epithelium (mesothelium). Thus, the genes expressed in serous carcinoma were similar to those expressed in normal fallopian tube, whereas the expression profiles of endometrioid and clear cell carcinomas resembled endometrial epithelium. Interestingly, the expression profile of mucinous tumors resembled normal colonic epithelium.25 We have also observed (unpublished data) that PAX8, a marker of müllerian-type epithelium, is expressed in ovarian serous carcinoma but not in ovarian surface epithelium (mesothelium), whereas calretinin, a mesothelial marker, reacts with ovarian surface epithelium and mesothelioma but not with tubal epithelium or ovarian serous carcinoma (Fig. 5). In the future, the analysis of overexpressed genes in ovarian cancer should take into account the histologic type of the tumors being studied and the data compared with the appropriate normal tissue.
From a clinical perspective, the implications of this new paradigm are even more far reaching. For the last two decades, numerous studies, including large clinical trials, have been conducted in an effort to develop screening tests for ovarian cancer. The goal of these studies is to detect tumors, when they are still confined to the ovaries, thereby increasing the likelihood of cure and reducing the mortality of the disease. The modalities that are currently being used to screen women are pelvic examination, transvaginal ultrasound, and measurement of serum CA 125. An awareness of the dualistic model, which highlights the heterogeneity of ovarian carcinoma, clearly indicates that one screening test will not be effective in detecting all the different types of ovarian carcinomas. Type I tumors (low-grade serous, low-grade endometrioid, clear cell, and mucinous) are slow growing and attain a large size while still confined to the ovary. They are easily detected by pelvic examination and/or transvaginal ultrasound. They constitute, however, only 25% of ovarian cancers and account for approximately 10% of ovarian cancer deaths.16 Therefore, it can be argued that the development of a biomarker screening test is not urgently needed for type I tumors. More importantly, the recognition that the majority of type II tumors [high-grade serous and undifferentiated carcinomas, and malignant mixed mesodermal tumors (carcinosarcomas)] originate outside the ovary illustrates the underlying flaws in screening approaches designed to detect these tumors while confined to the ovary. Moreover, type II tumors represent approximately 75% of all ovarian carcinomas and are responsible for 90% of ovarian cancer deaths.16 It is the type II tumors that should be targeted for screening, but unfortunately these tumors are rarely confined to the ovary, even at their inception. In a study of nearly 400 patients who were carefully staged from the Washington Center Hospital in Washington DC, which is largely a primary care hospital, less than 1.25% of high-grade serous carcinomas were confined to the ovary (Seidman et al, unpublished data). Similarly, the British Columbia Tumor Registry reported that only 0.5% of high-grade serous carcinomas were limited to the ovary at diagnosis.38 The futility of detecting early-stage ovarian cancer was recently underscored in a large multiinstitutional prospective study [Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial] in which, despite intensive annual screening of nearly 35,000 women with CA 125 and transvaginal ultrasound, 70% of the women presented with advanced stage disease. This was no different from unscreened populations.31 For the type II tumors, the goal in screening should be the detection of low volume, not low stage disease. This can only be accomplished by developing a panel of sensitive and specific biomarkers that are expressed early in ovarian carcinogenesis.
As with early detection, the treatment of type I and type II tumors must be individualized. Type I tumors are generally low-grade, slow growing and localized to the ovary at diagnosis spreading late in their evolution. Accordingly, when confined to the ovary, salpingo-oophorectomy may suffice. On the other hand, when they have spread beyond the ovary, chemotherapeutic agents that are effective against the more rapidly proliferating type II tumors are not as effective for type I tumors, because the latter are slow growing. Therefore, new approaches for advanced- stage type I tumors are needed. Deregulation of protein kinase activity as a result of somatic mutation in these genes occurs in many type I tumors. Mutations in these genes constitutively activate the signaling pathways they control, and tumor cells with mutations become dependent on those mutations for progression. Therefore, these genes could provide potential targets for therapeutic intervention. For example, in many type I carcinomas, there is constitutive activation of the MAPK signaling pathway because of mutations in ERBB2, KRAS or BRAF, the upstream regulators of MAPK. It is therefore conceivable that BRAF inhibitors and other MAPK kinase inhibitors could prolong disease-free interval and improve overall survival in patients with these types of advanced stage type I tumors, when combined with conventional therapeutic modalities.
The approach to the treatment of type II tumors should be completely different from that of the type I tumors. Treatment for type II tumors should be initiated on the basis of detection of sensitive and specific biomarkers before the appearance of morphologically recognizable disease, when therapy will likely be more effective. A precedent exists for this approach, as women with hereditary BRCA mutations are treated on the basis of that information only. Another important treatment issue that needs to be considered is whether patients found to have a STIC require adjuvant chemotherapy. The finding of positive pelvic washings in patients with only a STIC indicates that these microscopic lesions can shed malignant cells.4 At present there is no consensus as to whether or not these women should be treated. This will have to be determined by a randomized clinical trial.
Finally, the mounting evidence that ovarian cancer does not develop in the ovary, and the lack of success of ovarian cancer screening provides a strong rationale for directing efforts at primary prevention. It has been well established in epidemiologic studies that the use of oral contraceptives reduces the risk of ovarian cancer substantially. The risk is reduced by about 50% for women using oral contraceptives for 5 or more years.36 Parity hasalso been shown to be protective conferring approximately a 50% decrease in risk compared with nulliparity.32 Accordingly, the entire approach to prophylaxis, not only for women at high risk of developing ovarian cancer but also for the general female population, needs to be reevaluated in the light of the evolving new paradigm of ovarian carcinogenesis as discussed here. The traditional approach for reducing risk for women with a family history of ovarian carcinoma or who are found to have BRCA1/2 mutations has been hysterectomy and bilateral salpingo-oophorectomy. The ovarian tumors that develop are almost always high-grade serous carcinomas and there has been no convincing evidence that these women are at a higher risk of developing uterine serous carcinomas. If it can be unequivocally shown that the serous carcinomas in these women develop almost exclusively in the fimbria, then salpingectomy alone would be sufficient to reduce the risk of ovarian cancer. This approach would have to be evaluated in a randomized clinical trial comparing it to the standard treatment of bilateral salpingo-oophorectomy. For women who are not considered to be at high risk but who undergo a hysterectomy for benign uterine disease, many gynecologists have argued that bilateral oophorectomy should be carried out to reduce the risk of developing ovarian cancer. In a recent prospective study of nearly 30,000 women in the Nurses' Health Study, it was shown that compared with ovarian conservation, bilateral oophorectomy at the time of hysterectomy was associated with an increased risk of all-cause mortality, fatal and nonfatal coronary heart disease, and lung cancer.30 Accordingly, for women undergoing a hysterectomy for benign uterine disease, removal of only the fallopian tubes with sparing of the ovaries would improve quality of life and overall survival while still reducing the risk of ovarian carcinoma. Such an approach has important public health implications, as approximately 300,000 women in the United States undergo elective oophorectomy each year.
A new paradigm for the pathogenesis of ovarian cancer based on a dualistic model and the recognition that the majority of “ovarian” carcinomas originate outside the ovary assist in organizing this complex group of neoplasms and facilitates the development of new and novel approaches to prevention, screening, and treatment. One group of tumors (type I) is generally indolent, presents in stage I (tumor confined to the ovary) and develops from well-established precursors, so-called borderline tumors. These tumors are characterized by specific mutations, including KRAS, BRAF, ERBB2, CTNNB1, PTEN and PIK3CA, but rarely TP53. They are relatively genetically stable. The other group (type II) is composed of tumors that are aggressive, present in advanced stage, and develop from intraepithelial carcinomas in the fallopian tube. They have a very high frequency of TP53 mutations but rarely harbor the mutations detected in type I tumors. They are genetically highly unstable.
This proposed model is intended to serve as a framework for studying ovarian cancer. It is not complete and does not resolve all issues. For example, clear cell carcinoma is classified as a type I tumor based on having a characteristic PIK3CA mutation, relative genetic stability, frequent presentation in stage I, and association with endometriosis, a well-established precursor lesion. But unlike other type I tumors, clear cell carcinoma is high-grade at presentation. The inability to reconcile all of the many issues relating to ovarian pathogenesis does not invalidate or negate the utility of the paradigm. Thomas Kuhn, who introduced the concept of paradigms as a way of explaining how science progresses, pointed out: “To be accepted as a paradigm, a theory must seem better than its competitors, but it need not, and in fact never does, explain all the facts with which it can be confronted.”20
Recent studies on the origin of ovarian cancer have directed attention to a putative precursor lesion in the fallopian tube that morphologically and molecularly resembles high-grade ovarian serous carcinoma, and that has been designated “serous intraepithelial tubal carcinoma (STIC)”. Thus, rather than developing de novo from the ovary, as earlier proposed, the majority of type II tumors seem to arise from a STIC in the fimbriated end of the fallopian tube that spreads to the ovary. Another possible mechanism for the development of “ovarian” carcinoma is dislodgement of normal tubal epithelium from the fimbria, which implants on the site of rupture where ovulation occurred resulting in the formation of an inclusion cyst that may then undergo malignant transformation. Thus, serous tumors may develop from inclusion cysts, as has been thought, but by a process of implantation of tubal (müllerian-type) tissue rather than by a process of metaplasia from ovarian surface epithelium (mesothelial). Endometrioid and clear cell carcinomas may also originate from nonovarian, müllerian-type tissue, as it is widely accepted that these tumors develop from endometriosis that is thought to develop as a result of retrograde menstruation. The origin of mucinous and transitional cell (Brenner) tumors is still not well established, although recent data suggest a possible origin from transitional epithelial nests located in paraovarian locations. Thus, there is mounting evidence that type I and type II ovarian tumors develop independently along different molecular pathways, and that both types develop outside the ovary and involve it secondarily. This explains why current screening strategies designed to detect ovarian cancer, when it is confined to the ovary, are ineffective in accomplishing this goal.
Given the obstacles in early detection (screening) and the significant but relatively limited success in treatment, attention should be directed to primary prevention. This takes on particular relevance with the recognition that the majority of ovarian carcinomas are derived from cells in the fallopian tube or from passage of the endometrial tissue through the fallopian tubes and the important role of ovulation in ovarian carcinogenesis. Salpingectomy alone may be sufficient to accomplish this, as removal of the fallopian tubes would reduce the risk of ovarian cancer while preserving ovarian function. Ovarian conservation seems to be particularly important for a woman's health, as it has been shown that oophorectomy is associated with increased overall mortality and a higher frequency of nonfatal coronary heart disease. Other approaches should also be explored, for example the use of oral contraceptives that presumably by preventing ovulation reduces the risk of ovarian cancer by as much as 50%. In any case, new diagnostic, prevention and therapeutic approaches must be developed on the basis of our evolving understanding of ovarian carcinogenesis.
The authors thank Drs Kathleen Cho, Lora Hedrick Ellenson, Brigitte M. Ronnett, Jeffrey, D. Seidman, and Russell Vang for their critical review of the manuscript and helpful suggestions.
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