Progress in the pathological arena of gynecological cancers.

It was previously thought that HGSC could arise at multiple independent sites through some form of “field effect.” However, it has been convincingly shown that HGSC at different sites are clonal, with one site representing the primary and the others being metastatic. Almost all extrauterine HGSC exhibit TP53  mutation as an early founder event, and mutational analysis of ovarian and peritoneal HGSC with concurrent STIC has shown these to harbor identical TP53  mutations in the vast majority of cases. 7 , 8 The demonstration of an identical TP53  mutation in tumors at different sites is strong evidence for clonality, as the probability of an identical mutation occurring simultaneously at multiple sites is extremely low. It can be summarized that there is irrefutable evidence that almost all HGSC arises from a single tumor clone and that multiple foci of disease do not result from a multifocal origin or a field effect. 7 , 8 Similarly, it has been shown that cases of uterine serous carcinoma with involvement of the fallopian tube (even when confined to the tubal mucosa) mostly represent tubal metastases and not independent primary tubal lesions. 9

In WHO 2020, the classification of ovarian sex cord–stromal tumors is largely unchanged from the prior classification. 1 The category of gynandroblastoma (mixed sex cord–stromal tumor) has been reintroduced having been removed from the prior classification. This is one area of ovarian pathology where significant advances have been made in recent years. Sex cord–stromal tumors represent a heterogenous group of uncommon neoplasms that, when they exhibit classical morphology, are relatively easy to diagnose. However, there may be considerable morphological overlap between the different tumor types, and immunohistochemistry, while useful in confirming a sex cord–stromal tumor, is of minimal value in distinguishing between the different tumor types. Recent significant advances (see Table  4 ) include the demonstration that adult granulosa cell tumors contain somatic FOXL2  mutations in well over 90% of cases, 52 while a significant proportion of moderately and poorly differentiated Sertoli–Leydig cell tumors contain DICER1  mutations; these may be somatic or germline, the latter signifying DICER1 syndrome. 53 , 54 Ongoing studies are elucidating the molecular events in several other tumor types within the sex cord–stromal category. For example, microcystic stromal tumor contains CTNNB1 or less frequently APC mutations and is occasionally an extracolonic manifestation of familial adenomatous polyposis. 55 , 56 In problematic cases, demonstration of the appropriate molecular abnormality assists in tumor classification. Recently described molecular events in ovarian sex cord–stromal and miscellaneous neoplasms Small cell carcinoma of the ovary of hypercalcemic type (SCCOHT), which is included in the category of miscellaneous ovarian neoplasms in WHO 2020, has been shown to be characterized by deleterious germline or somatic mutations in a single gene SMARCA4 57 , 58 , 59 in well over 90% of cases. SMARCA4 is part of the SWI/SNF complex, which is implicated in the pathogenesis of a growing number of other malignancies. Demonstration of this mutation and/or loss of immunohistochemical staining with SMARCA4 (BRG1) may, in the correct morphological context, be crucial in the diagnosis of this highly aggressive neoplasm. 60 , 61 It is recommended that all patients diagnosed with SCCOHT should be referred for germline SMARCA4  mutation testing. 62 , 63

In 1983, in a seminal and widely cited paper, Bokhman proposed that there were two broad types of endometrial carcinoma, type I and type II. 10 Broadly speaking, type I carcinomas (prototypically endometrioid‐type) arise in perimenopausal or early postmenopausal women, are low‐grade, typically early‐stage neoplasms arising on a background of atypical hyperplasia and are positive with hormone receptors. Type II carcinomas (prototypically serous‐type) arise in elderly postmenopausal women, are high‐grade, typically advanced‐stage neoplasms arising in atrophic endometria and are negative with hormone receptors. However, although useful as a broad concept, it was always clear that there is too much overlap in the clinical and pathological features in many individual tumors and the Bokhman classification never gained widespread acceptance among pathologists. The current 2020 WHO Classification of endometrial carcinomas, 1 like prior classifications, is based on morphology and in practice pathologists often use a variety of immunohistochemical markers to assist in classifying problematic neoplasms. However, especially with “high‐grade” endometrial carcinomas (serous, clear cell, grade 3 endometrioid, mixed, undifferentiated, and dedifferentiated carcinoma and carcinosarcoma), there is significant interobserver variation even among expert gynecological pathologists. 11 For example, in one study, three observers examined 56 high‐grade endometrial carcinomas and in 20 of 56 (35.8%) cases there was a major disagreement, including no consensus regarding the major subtype diagnosis or even whether a component of high‐grade carcinoma was present. 11 In 2013, TCGA published a seminal comprehensive molecular study of 373 endometrial carcinomas; the study was restricted to endometrioid, serous, and mixed endometrioid – serous carcinomas with no inclusion of other high‐grade carcinomas. 12 Tumors were analyzed using a variety of modalities, including exome sequencing, somatic copy number alteration, whole genome sequencing, mRNA expression, protein expression, microRNA expression, and DNA methylation. The study revealed that endometrial carcinoma is a complex disease consisting of four intrinsic molecular types: POLE (ultramutated), microsatellite instability (MSI, hypermutated), copy‐number low (also referred to as microsatellite stable or no specific molecular profile), and copy‐number high (serous‐like). It was demonstrated that the four molecular types are of prognostic significance, with POLE tumors having the best prognosis (even though they often look high grade morphologically) and copy‐number high the worst. 12 Regarding the percentages of the four molecular types, copy‐number low is the most prevalent accounting for approximately 39%, followed by MSI hypermutated (28%), copy‐number high (26%), and POLE ultramutated (7%). Since the delineation of the four molecular types and the demonstration of prognostic significance, there has been an explosion of studies investigating how to incorporate molecular typing into routine reporting of endometrial carcinomas, and a simplified combined morphological–molecular classification (such as the ProMisE classifier 13 ) is likely to be incorporated into routine practice in the near future. The recommendation in WHO 2020 is to integrate microscopic features with molecular characteristics in regions where the resources are available. 1 Molecular classification is likely to be of particular value in high‐grade endometrioid carcinomas by picking out the POLE ‐mutated (good actors) and the copy‐number high (poor actor) neoplasms. 14 POLE mutation analysis may not be necessary in typical low‐grade endometrioid carcinomas since POLE mutations are not common in this group and these neoplasms would not qualify for adjuvant therapy unless they are advanced stage at diagnosis. Typical serous carcinomas may also not require POLE mutation analysis. CTNNB1  mutation analysis (or perhaps beta‐catenin immunohistochemistry as a surrogate), L1 cell adhesion molecule (L1CAM), and p53 may be of value in low‐grade endometrioid carcinomas in identifying those cases likely to have a worse outcome. 15 An obvious drawback is that currently POLE mutation analysis is not available in most pathology laboratories and, as such, development of an appropriate infrastructure will be required; this will likely entail centralization of testing in a limited number of reference laboratories. It is also clear that the molecular classification will be complementary to morphology since parameters such as depth of myometrial invasion, lymphovascular space invasion and cervical and nodal involvement, which are prognostically significant, can only be identified on morphological examination. Recent studies have shown that TCGA classification also has prognostic significance in other endometrial carcinoma types such as carcinosarcoma, clear cell carcinoma, undifferentiated/dedifferentiated carcinoma and neuroendocrine carcinoma. 16 , 17 , 18

The author is responsible for the design and writing of the paper.

Similar to the cervix, vaginal and vulval SCC are now divided into HPV‐associated and HPV‐independent types in WHO 2020. 1 This replaces those types included in the prior classification, namely keratinizing, nonkeratinizing, papillary, basaloid, warty, and verrucous; the reasons underlying these changes are exactly analogous to those discussed in the section on cervical SCC. Although primary vaginal SCC are considerably more uncommon than in the cervix and the vulva, there is convincing evidence that, similar to other sites, HPV‐independent neoplasms have a worse prognosis. 42 , 43 It is recommended that the type of vaginal SCC (HPV‐associated or HPV‐independent) be documented on the pathology report. However, as at other sites, a morphological diagnosis of SCC NOS is acceptable when resources required to differentiate between the two, such as p16 immunohistochemistry and HPV testing, are not available. Similarly in the vulva, traditional histologic typing of vulval SCC has been superseded by HPV status as the major determinant of classification. HPV‐independent SCC have a worse prognosis with significantly worse recurrence‐free and overall survival compared with HPV‐associated SCC. 44 , 45 , 46 , 47 , 48 There is also growing evidence that HPV‐independent SCC are less responsive to radiotherapy. 47 The majority of HPV‐associated SCC exhibit basaloid or warty morphology, while HPV‐independent SCC tend to be keratinizing; however, a significant percentage of cases (15%–20%) show overlapping morphologic features. While the nature of any adjacent precursor lesion may be useful in helping to determine the HPV status, in practice, ancillary testing (p16 or HPV testing) is necessary given the overlap in morphology. As in the cervix and vagina when HPV status cannot be confidently determined or resources are not available to undertake ancillary testing, a diagnosis of SCC NOS is acceptable, although this is not recommended. Most, but not all, HPV‐independent vulval SCC are associated with TP53  mutations. 49 However, a proportion are TP53 wild type and there is growing evidence that these may have an intermediate prognosis between HPV‐associated SCC (best prognosis) and HPV‐independent TP53  mutated neoplasms (worst prognosis). 49 There have also been changes to the classification of primary vaginal adenocarcinomas with the description of new entities such as HPV‐associated and gastric‐type adenocarcinomas, 50 , 51 both of which may arise in adenosis; the latter are aggressive primary vaginal adenocarcinomas morphologically and immunophenotypically identical to their cervical counterparts. Broadly, with some minor differences, the classification of primary vaginal adenocarcinomas mirrors that in the cervix. 50 , 51

Traditionally (including in WHO 2014), cervical adenocarcinomas were classified based on morphology and were divided into clinically meaningless and poorly reproducible categories with no biological basis, including villoglandular, endometrioid, and serous. Analogous to cervical SCC, cervical adenocarcinomas are now categorized in WHO 2020 into HPV‐associated and HPV‐independent types (Table  3 ). Most cervical adenocarcinomas are HPV‐associated but a higher percentage than SCC (about 15%–20%) are HPV‐independent. 34 , 35 , 36 , 37 , 38 , 39 HPV‐independent cervical adenocarcinomas typically present at higher stage and have a worse prognosis. 34 , 35 , 36 , 37 , 38 , 39 The 2020 WHO Classification also divides adenocarcinoma precursor lesions into HPV‐associated and HPV‐independent types, the latter including gastric‐type adenocarcinoma in situ and atypical lobular endocervical glandular hyperplasia. 1 , 40 Comparison of the 2014 and 2020 WHO classifications of cervical adenocarcinoma Endocervical adenocarcinoma, usual type Mucinous carcinoma NOS Mucinous carcinoma, gastric type Mucinous carcinoma, intestinal type Mucinous carcinoma, signet ring cell type Villoglandular carcinoma Mesonephric carcinoma Serous carcinoma Clear cell carcinoma Serous carcinoma Adenocarcinoma NOS HPV‐associated cervical adenocarcinoma (includes several subtypes; see text) HPV‐independent cervical adenocarcinoma Gastric type Mesonephric type Clear cell type Other adenocarcinomas Abbreviations: NOS, not otherwise specified. HPV‐associated adenocarcinomas are typified by easily identifiable mitotic figures and apoptotic bodies and almost always exhibit diffuse block‐type immunoreactivity with p16. Subtypes of HPV‐associated adenocarcinoma include usual type and mucinous type; the former encompasses villoglandular and micropapillary variants and mucinous type encompasses stratified mucin producing carcinoma, intestinal, signet ring, and NOS variants. 1 , 41 HPV‐independent types of cervical adenocarcinoma are gastric type (the most common), mesonephric, and clear cell. 36 , 37 , 38 , 39 As discussed, these typically have a worse prognosis than HPV‐associated adenocarcinomas and are almost always p16 negative or focally positive (nonblock‐type immunoreactivity). Serous carcinoma of the cervix is not included in the 2020 WHO Classification. Most tumors previously diagnosed as such represent usual‐type HPV‐associated cervical adenocarcinomas with papillary architecture and high‐grade nuclear features or direct involvement by or a drop metastasis of a tubo‐ovarian or endometrial serous carcinoma.

It is not uncommon for a patient to have an endometrioid carcinoma in the endometrium and one, or occasionally both, ovaries and a variety of clinicopathological parameters are used by pathologists to distinguish between synchronous independent primaries and metastasis usually from the endometrium to the ovary. Especially when both neoplasms are low grade, it has long been assumed that most of these represent dual primaries and the prognosis has been assumed to be good, although there are few studies with long‐term follow‐up. It has recently been demonstrated that such neoplasms involving the uterine corpus and ovary are clonal and probably represent metastasis from one site to the other, usually from the endometrium to the ovary. 19 , 20 , 21 Thus, there is a dilemma in that, although molecularly these are clonal neoplasms, and most represent Stage IIIA endometrial carcinomas, the prognosis is thought to be good and there is potential for overtreatment with the unnecessary administration of adjuvant therapy. In WHO 2020 it is recommended that conservative management is undertaken and management should be as for synchronous neoplasms when the following four criteria are met: (1) both tumors are low grade; (2) <50% myometrial invasion; (3) no involvement of any other site; (4) absence of extensive lymphovascular invasion at any location. 1

The updated 2020 World Health Organization (WHO 2020) Classification of Female Genital Tract Tumours (5th edition) was published online and in the traditional “Blue Book” in Autumn 2020. 1 The present review covers the significant developments and major changes in the classification of gynecological cancers, some of which emanate from the new WHO Classification. In a review such as this, most of the topics cannot be covered in detail and the reader is referred to the key references provided herein.

The author has no conflicts of interest to declare.

It is now well established that a significant majority of extrauterine (primary ovarian, tubal, or peritoneal) high‐grade serous carcinomas (HGSC) arise from the distal fimbrial end of the fallopian tube from a precursor lesion known as STIC (serous tubal intraepithelial carcinoma). The evidence is compelling, both in sporadic cases and cases associated with germline BRCA mutations. 2 , 3 , 4 , 5 Unfortunately, this has not translated uniformly into clinical and pathological practice; in other words, the same extrauterine HGSC in a resection specimen could be categorized as of tubal, ovarian, or peritoneal origin by different pathologists. Although typically not important for management, this has obvious implications for epidemiological reasons and cancer registration and the tubal origin raises the possibility of prophylactic salpingectomy with ovarian preservation in premenopausal women at increased risk of the development of HGSC. Criteria for site assignment in extrauterine HGSC have been proposed 3 , 4 , 5 (Table  1 ) and the use of these criteria results in a high proportion (approximately 80%) being classified as tubal in origin, while primary peritoneal HGSC are exceedingly rare; this diagnosis should only be made when there is no ovarian parenchymal involvement and no mucosal STIC or HGSC within either tube, both of which should be grossly visible in their entirety and examined in total histologically using a SEE‐FIM (sectioning and extensively examining the fimbriated end of the fallopian tube) protocol. 2 , 3 , 4 , 5 , 6 These recommendations have been endorsed by the International Collaboration on Cancer Reporting (ICCR) and in the cancer datasets of the Royal College of Pathologists in the UK and the College of American Pathologists. 6 Criteria for primary site assignment in extrauterine high‐grade serous carcinomas Both tubes should be clearly visible and fully examined by a standardized SEE‐FIM protocol Regardless of presence and size of peritoneal disease Abbreviations: HGSC, high‐grade serous carcinoma; SEE‐FIM, sectioning and extensively examining the fimbriated end; STIC, serous tubal intraepithelial carcinoma.