Material and Method: The observers reviewed all the slides of the malignant pleural mesotheliomas diagnosed during the period ranging from 2004 to 2017. The Cohen Kappa was performed in order to evaluate the agreement between both observers into classifying mesotheliomas, subtyping and grading epithelioid mesotheliomas. Two rounds of examination were planned with a delay period of one month. After the first round, the reviewers discussed the different difficulties and challenges they faced. All the statistic tests were performed using the SPSS software version 12.0.
Results: After the first round, a fair agreement between both observers was reported. After the second round, an improvement of the concordance rate with a good agreement in subtyping epithelioid mesotheliomas was noticed. Concerning the grading of mesotheliomas, the interobserver agreement was poor even after the second round examination. The intraobserver reproducibility of epithelioid mesothelioma subtyping was fair or moderate for both reviewers. The intraobserver agreement was poor concerning the grading of epithelioid mesothelioma.
Conclusion: Integrating subtyping and grading of epithelioid mesotheliomas into a new classification necessitates an important training of the pathologists. The architectural features definitions have to be clarified in order to avoid using own subjective opinions and habits by pathologists.
The authors aimed to assess the inter-observer and intra-observer reproducibility of classifying pleural mesotheliomas and subtyping epithelioid mesotheliomas according to the predominant architecture and the grade.
Inclusion Criteria
All the malignant pleural mesotheliomas diagnosed during
the period of the study were retrieved from the archives of
the Department of Pathology.
Exclusion Criteria
The specimen for which no paraffin blocks were available,
were excluded.
Non-Inclusion Criteria
Other pleural tumours were excluded from this study.
Reviewers Characteristics
All the slides were reviewed by 2 pathologists who were
used to thoracic pathology. The first pathologist had 25
years of experience and the second pathologist had 10 years
of experience in thoracic pathology.
Slides Reviewing
The authors were given a sheet with different items to record
including the number of slides reviewed, the number of
samples, the mesothelioma subtypes including epithelioid,
sarcomatoid, biphasic and the architecture-based
subtyping in case of epithelioid mesothelioma including
trabecular, solid, micropapillary, tubulo-papillary, acinar,
adenomatoid, transitional, deciduoid or special variant
including pleomorphic cells or signet ring cells. The grade
was also recorded in epithelioid mesotheliomas. Two
rounds of evaluation, with an interval of one month, were
performed. After the first round, the two reviewers met for a clarification session to present the different difficulties
and challenges they faced.
Subtyping Criteria
Subtyping of pleural mesothelioma was made according
to the WHO classification [1]. Epithelioid mesothelioma
was defined as a tumour made of polygonal or ovoid cells.
Sarcomatoid mesothelioma was characterized by elongated
and tapered mesothelial cells with various degrees of
atypia and mitoses. Biphasic tumours were defined by the
association of an epithelioid component to a sarcomatoid
one with a minimum proportion of 10 % for each
component. Concerning the epithelioid mesotheliomas,
the trabecular subtype consisted in small cells arranged into
thin cords or single files (Figure 1A). Nests of tumour cells
defined the solid subtype (Figure 1B). Papillary subtype was
characterized by papillary structures with a fibrovascular
core (Figure 1C). Micropapillary structures were digitiform
structures without a fibrovascular core. Acinar structures
were glandular structures (Figure 1D). Adenomatoid
structures were characterized by pseudoglandular
structures (Figure 1E). Deciduoid subtype was composed
by large cells with atypical nuclei, abundant cytoplasm with
pronounced eosinophilia, and glassy cytoplasm mimicking
deciduoid cells. The description of the transitional subtype
was not clear in the WHO classification, and that is why
the authors adopted the definition of Galateau Sallé, et al.
Transitional subtype was defined as sheets of plump cells
starting to lose their epithelioid morphology but not overtly
spindle shaped and lacking frank sarcomatous features [6].
Grading was performed according to the IASLC proposition criteria and was based on the nuclear grading, mitotic index and necrosis [3]. A two-tier system was established with low-grade tumours consisting of grade I or II tumours without necrosis and high-grade tumours consisting of grade III tumours and grade II tumours with necrosis. Nuclear grade was scored 1, 2 or 3 for respectively mild, moderate or severe nuclear atypia. Mitotic count was scored 1, 2 or 3 for tumours with respectively less than 1 mitosis per 2 mm2, 2 to 4 mitoses per 2 mm2 and more than 5 mitoses per 2 mm2. A sum of 2 or 3 was considered as a grade I, a sum of 4 or 5 was considered as a grade II, and a sum of 6 was consistent with grade III tumour. The reviewers had no limit of time to review the cases (Figure 2A,B).
Statistical Analysis
The Cohen Kappa was performed in order to evaluate
the agreement between both pathologists into classifying
mesotheliomas, subtyping epithelioid mesotheliomas and
reporting the grade in epithelioid mesothelioma.
Two rounds of examination were planned with a delay
period of one month. After the first round, the reviewers
discussed the different difficulties and challenges they faced.
Interobserver agreement and intraobserver agreement
were performed. The strength of agreement was considered
excellent for kappa >0.8, good for 0.61
All the blocks included were anonymized and no
information concerning the patients was used in this study.
A reference number was attributed to each case.
Interobserver Reproducibility Concerning the
Subtyping of Mesotheliomas
This study included 50 malignant pleural mesotheliomas.
Both pathologists reviewed all cases with a mean of 7 blocks
(slides)/ case (min 1 block, max 21 blocks). The different
cases consisted of epithelioid mesotheliomas in 44 cases (88%), sarcomatoid mesothelioma in 4 cases (8%), and
biphasic mesothelioma in 2 cases (4%).
The concordance rate accounted for 32% (16/50) when taking into account the subtyping and the grading. It reached 44% (22/50) when taking into account only the subtyping of mesotheliomas without the grading. The pathologists were confused when differentiating solid from deciduoid subtypes (4 cases), papillary from trabecular subtypes (4 cases), acinar from trabecular subtypes (4 cases), signet-ring cell from solid subtypes (2 cases), trabecular from micropapillary subtype (2 cases), solid from trabecular subtype (2 cases), solid from acinar subtype (2 cases), sarcomatoid from pleomorphic (2 cases), sarcomatoid from trabecular subtypes (2 cases), and biphasic from epithelioid subtypes (4 cases) (Figures 3A,B). The highest concordance rates were observed in the tubulopapillary, trabecular, solid, biphasic, and sarcomatoid subtypes with ratios reaching respectively 8/12, 14/18, 6/6, 2/2 and 4/6. The deciduoid and the acinar subtypes presented the lowest concordance rates, reaching 0/2 and 2/4 respectively. The first reviewer recognized 8 trabecular mesotheliomas, 6 acinar, 6 solid, 14 tubulo-papillary, 2 micropapillary, and 8 special variants consisting of 2 pleomorphic cases, 2 signet ring cells cases, 2 deciduoid cases, and 6 sarcomatoid mesotheliomas. The second reviewer identified 14 trabecular mesotheliomas that were judged by the first reviewer as trabecular in 4 cases, acinar in 4 cases, tubulo-papillary in 2 cases, micropapillary in 2 cases, and sarcomatoid in 2 cases. The second reviewer recognized 16 solid mesotheliomas classified by the first reviewer as trabecular in 2 cases, acinar in 2 cases, and solid in 6 cases. The second reviewer identified also 6 biphasic mesotheliomas classified as trabecular in 2 cases, papillary in 2 cases, and a special variant in 6 cases by the first reviewer. The Cohen Kappa reached the value of 0.34 corresponding to a fair agreement.
After the second session, the inter-observer agreement was good with a weighted Kappa value of 0.62. The highest concordance rates were observed for solid, acinar, and sarcomatoid subtypes reaching 100%. The concordance rate accounted for 50% for papillary subtype.
Interobserver Reproducibility Concerning Nuclear
Grading
Concerning the nuclear grading of the epithelioid
mesotheliomas, the first reviewer considered 16 high-grade
and 28 low-grade tumours. The second reviewer considered
22 low-grade and 22 high-grade tumours. Among the 32
high-grade tumours recorded by the second reviewer,
16 cases were also considered as high-grade by the first
reviewer. Among the 12 low-grade tumours recorded by
the second reviewer, 10 cases were also recorded as lowgrade
by the first one. The concordance between the judges
accounted for 59% (26/44). The agreement between the
reviewers was fair (Cohen Kappa=0.28). After the second
round, the agreement of nuclear grade was poor with a
weighted Kappa accounting for 0.
Intraobserver Reproducibility Concerning the
Subtyping of Mesotheliomas and the Grading of
Epithelioid Mesothelioma
Between both sessions of examination, the intraobserver
agreement of mesothelioma subtyping was fair (Kappa=
0.27) and moderate (Kappa=0.44) for the first and the
second reviewer respectively. For the first reviewer, the
worse concordance rates were recorded for solid, trabecular,
acinar, the special variants, and micro-papillary subtypes.
For the second reviewer, the worse concordance rates were
recorded for the trabecular and biphasic subtypes.
Concerning the grading, the intraobserver agreement was very poor (Kappa=0) and poor (Kappa=0.2) for reviewer 1 and 2 respectively.
The different values of the weighted kappa are represented in Table I.
Table I: The distribution of kappa scores for subtyping mesotheliomas and assessing nuclear grade.
In a study including 108 pleural mesotheliomas, Brcic L, et al. reported a good agreement with a Kappa coefficient reaching 0.72 [9]. In 2018, the same authors assessed the interobserver and intraobserver agreement between the main types of mesotheliomas and the subtypes of epithelioid mesothelioma in a study about 200 patients. In opposition to their first manuscript, they reported a fair interobserver agreement, which was substantially improved after a clarification session between the observers. In this study, the clarification between both reviewers induced an improved agreement between pathologists. The clarification had no effect on the reproducibility of the grading of epithelioid mesotheliomas. In this study, the clarification between both observers made the first observer realize the accurate definition of the special variants including deciduoid or signet ring cell mesothelioma. Brcic L, et al. noticed the highest agreement for sarcomatoid and epithelioid mesotheliomas and the lowest agreement for biphasic ones [9]. In this study, the most reproducible subtypes consisted in solid, tubulo-papillary, and sarcomatoid subtypes. Difficulties in classifying biphasic tumours may be explained by the cut-off of 10%, which may be difficult to be assessed unanimously or the difficulty of highlighting the sarcomatoid component, which can be confused with active fibroblasts. The ASCO guideline for the treatment and diagnosis of malignant mesothelioma made a recommendation to quantify epithelioid versus sarcomatoid components in surgical, thoracoscopic or open pleural biopsies [4]. In opposition to these guidelines, the reproducibility of classifying biphasic mesotheliomas between MESOPATH pathologists and the International Mesothelioma Panel pathologists was reported to be moderate with a weighted Kappa value of 0.45 [10]. Brcic L attributed the better reproducibility of tubulo-papillary, pleomorphic and trabecular patterns to the striking character of these patterns that can be easily identified and may be over-estimated by the pathologists [9]. The most challenging pattern reported by the authors and which was not reported a few years before was the acinar pattern. This fact was also noticed in this study and can be explained by the difficulties to differentiate trabecular pattern from acinar one when dealing with slit-like spaces. Acinar and adenomatoid patterns may be also difficult to distinguish because of the definition of glands and of differentiating them from microcysts. After the second round, Brcic et al. reported the highest improvements in micropapillary, deciduoid and solid patterns with the same concern for the acinar pattern [11]. The transitional subtype was not reported in this study. It has been clearly defined by Galateau Salle, et al. [6]. This subtype was reported to be hardly distinguished from sarcomatoid subtype. Dacic S, et al. reported a fair interobserver agreement for diagnosing transitional subtype and an interobserver agreement dependant on the percentage of specific foci when dealing with sarcomatoid features. This agreement was excellent when the proportion of sarcomatoid features accounted for more than 75% [12]. Some authors reported that the sample size may be a limiting factor because they noticed a low agreement between observers when dealing with needle biopsies [11]. These results were in contradiction with those of Chirieac LR et al. who reported a high concordance of the diagnosis made on needle biopsies and surgical biopsies in a study on 759 cases [13]. They put emphasis on the high accuracy of biopsies in sarcomatoid subtypes in comparison to epithelioid subtypes. Besides, they reported that the accuracy of histologic classification increases with the number of tissue blocks examined with a 100% concordance when more than 9 biopsies were included. Another limitation reported by Crzs et al. was the pathologists expertise. In fact, they reported moderate intraobserver agreement with the lowest value attributed to the least experienced pathologist. This fact was not reflected by this studys results because the highest intraobserver variability was attributed to the most experienced pathologist. This study puts emphasis on the difficulties of subtyping the epithelioid mesotheliomas. These difficulties are added to the challenges described when differentiating the mesotheliomas from the multiple mimickers including lung or breast carcinomas [14]. In spite of all these difficulties, pathologists have to adopt the subtyping of epithelioid mesotheliomas because morphologic features reflect molecular pathways. Blum Y, et al. reported that mesotheliomas may be decomposed as a combination of epithelioid-like and sarcomatoid-like components that reflect different oncogenic pathways and whose proportions are highly related to the prognosis [15].
In conclusion, this study puts emphasis on the difficulty of subtyping epithelioid mesotheliomas according to their architecture features and grade. Training and more accurate details in the definition of the different features are needed in order to integrate these characteristics in the classification of malignant mesotheliomas and to make them relevant in predicting the prognosis of mesotheliomas.
CONFLICT of INTEREST
The authors declare no conflict of interest.
FUNDING
The authors declared that this study has received no
financial support.
1) (IARC WHO Classification of Tumours) International Agency
for Research on Cancer - WHO Classification of Tumours of the
Lung, Pleura, Thymus and Heart-World Health Organization
(2015).
2) Alcala N, Mangiante L, Le-Stang N, Gustafson CE, Boyault
S, Damiola F. Redefining malignant pleural mesothelioma
types as a continuum uncovers immune-vascular interactions.
EBioMedicine. 2019;48:191-202.
3) Nicholson AG, Sauter JL, Nowak AK, Kindler HL, Gill RR,
Remy-Jardin M. EURACAN/IASLC proposals for updating
the histologic classification of pleural mesothelioma: Towards a
more multidisciplinary approach. J Thorac Oncol. 2019;1:12-20.
4) Kindler HL, Ismaila N, Hassan R. Treatment of malignant pleural
mesothelioma: American Society of Clinical Oncology Clinical
Practice Guideline Summary. J Oncol Pract. 2018;14:256-64.
5) Husain AN, Colby TV, Ordóñez NG, Allen TC, Attanoos RL,
Beasley MB. Guidelines for pathologic diagnosis of malignant
Mesothelioma: 2017 Update of the consensus statement from
the International Mesothelioma Interest Group. Arch Pathol Lab
Med. 2018;142:89-108.
6) Galateau Salle F, Le Stang N, Nicholson AG, Pissaloux D,
Churg A, Klebe S. New insights on diagnostic reproducibility
of biphasic mesotheliomas: A multi-institutional evaluation by
the International Mesothelioma Panel From the MESOPATH
Reference Center. J Thorac Oncol. 2018;13(8):1189-203.
7) Rosen LE, Karrison T, Ananthanarayanan V, Gallan AJ,
Adusumilli PS, Alchami FS. Nuclear grade and necrosis predict
prognosis in malignant epithelioid pleural mesothelioma: A
multi-institutional study. Mod Pathol. 2018;31:598-606.
8) Churg A, Galateau-Salle F, Roden AC, Attanoos R, von der Thusen
JH, Tsao MS. Malignant mesothelioma in situ: Morphologic
features and clinical outcome. Mod Pathol. 2019;2:10-25.
9) Brcic L, Vlacic G, Quehenberger F, Kern I. Reproducibility of
malignant pleural mesothelioma histopathologic subtyping.
Arch Pathol Lab Med. 2018;142:747-52.
10) Churg A, Galateau-Salle F. The separation of benign and
malignant mesothelial proliferations. Arch Pathol Lab Med.
2012;136:1217-26.
11) Brčić L, Jakopović M, Brčić I, Klarić V, Miloević M, epac A.
Reproducibility of histological subtyping of malignant pleural
mesothelioma. Virchows Arch. 2014;465:679-85.
12) Dacic S, Le Stang N, Husain A, Weynand B, Beasley MB, Butnor
K. Interobserver variation in the assessment of the sarcomatoid
and transitional components in biphasic mesotheliomas. Mod
Pathol. 2019;3:12-24.
13) Chirieac LR, Hung YP, Foo WC, Hofer MD, VanderLaan
PA, Richards WG. Diagnostic value of biopsy sampling in
predicting histology in patients with diffuse malignant pleural
mesothelioma. Cancer. 2019;125:4164-71.