Figures
Abstract
Background and Purpose
Molecular profiling should be performed on all advanced non-small cell lung cancer with non-squamous histology to allow treatment selection. Currently, this should include EGFR mutation testing and testing for ALK rearrangements. ROS1 is another emerging target. ALK rearrangement status is a critical biomarker to predict response to tyrosine kinase inhibitors such as crizotinib. To promote high quality testing in non-small cell lung cancer, the European Society of Pathology has introduced an external quality assessment scheme. This article summarizes the results of the first two pilot rounds organized in 2012–2013.
Materials and Methods
Tissue microarray slides consisting of cell-lines and resection specimens were distributed with the request for routine ALK testing using IHC or FISH. Participation in ALK FISH testing included the interpretation of four digital FISH images.
Results
Data from 173 different laboratories was obtained. Results demonstrate decreased error rates in the second round for both ALK FISH and ALK IHC, although the error rates were still high and the need for external quality assessment in laboratories performing ALK testing is evident. Error rates obtained by FISH were lower than by IHC. The lowest error rates were observed for the interpretation of digital FISH images.
Citation: Tembuyser L, Tack V, Zwaenepoel K, Pauwels P, Miller K, Bubendorf L, et al. (2014) The Relevance of External Quality Assessment for Molecular Testing for ALK Positive Non-Small Cell Lung Cancer: Results from Two Pilot Rounds Show Room for Optimization. PLoS ONE 9(11): e112159. https://doi.org/10.1371/journal.pone.0112159
Editor: Ramon A. de Mello, University of Algarve, Portugal
Received: May 30, 2014; Accepted: October 13, 2014; Published: November 11, 2014
Copyright: © 2014 Tembuyser et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: The authors confirm that all data underlying the findings are fully available without restriction. All relevant data are within the paper.
Funding: This work was supported by an unrestricted grant from Pfizer: grant number ZL520506, www.pfizer.com/. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: Patrick Pauwels received a scientific grant from Pfizer and receives occasional speaker fees from Pfizer, Ventana (Roche) and Abbott. Lukas Bubendorf receives consultation and lecture fees from Roche and Pfizer. Keith Kerr receives consultation and lecture fees from Pfizer, Novartis and Abbott. Ed Schuuring has board membership (Roche, Pfizer and Novartis) and receives lecture fees (Roche and Abbott). Erik Thunnissen received an unrestricted grant from Pfizer and travel and speaker’s fee for presentation (Pfizer). Elisabeth M. C. Dequeker received an unrestricted grant from Pfizer and remuneration from AstraZeneca. The other authors have no competing interests to declare. The competing interests of the authors of this manuscript do not alter the authors' adherence to PLOS ONE policies on sharing data and materials.
Introduction
Lung cancer is amongst the leading causes of cancer related mortality worldwide [1]. Approximately 85% of lung cancers are non-small cell lung cancers (NSCLC), traditionally divided into three major cell types: adenocarcinoma, squamous cell carcinoma and large cell carcinoma [2]. Over the past decade, the availability of molecular targeted therapies has increased the progression-free survival for patients with NSCLC, adenocarcinoma in particular [3]–[6].
The approach of using biomarkers to select treatments that are tailored to individual patient profiles is referred to as precision medicine. In advanced NSCLC, EGFR gene mutations and ALK rearrangements are currently critical biomarkers to predict treatment response. The fusion protein from ROS1 rearrangement is an emerging target.
In 2007, it was first reported that an inversion on chromosome 2p resulted in the creation of an EML4-ALK fusion gene in lung cancer [7]. Multiple EML4-ALK variants, represented by different EML4 breakpoints, have been identified, as well as other fusion partners for ALK, such as KIF5B and TFG [8]–[10]. ALK rearrangements result in oncogenic fusions which lead to constitutive activity of the ALK tyrosine kinase with subsequent effects on proliferation, migration and survival [11]. Lung cancers harboring ALK rearrangements represent a unique subpopulation of lung cancer patients. The frequency of the EML4-ALK rearrangement ranges from 2% to 7% in unselected NSCLC patients [3], [12]. The frequency is higher in NSCLC patients with adenocarcinoma histology, non or light cigarette smoking history, and younger age, regardless of ethnicity [3], [12], [13]. However, these clinical characteristics are not shared by all carriers and molecular characterization is necessary to determine treatment eligibility [3], [14], [15].
ALK rearrangements are pharmacologically targetable with the small molecule tyrosine kinase inhibitor (TKI) crizotinib. In 2011, the FDA granted accelerated approval of crizotinib in response to the manifested clinical benefit.
Routine molecular diagnostics need to include evaluations for both EGFR mutations and ALK rearrangements [13], [15], [16]. It is expected that testing for ROS1 rearrangements will be included soon. ROS1 is another receptor tyrosine kinase that forms fusions in NSCLC and has shown responsiveness to crizotinib [17]. Diagnostic testing laboratories have been expected to rapidly introduce and perform molecular testing for NSCLC. For successful patient treatment, it is of great importance that molecular test results are accurate, highly reliable, and presented in a timely fashion. In 2012, the European Society of Pathology (ESP) proposed an external quality assessment (EQA) scheme to promote high quality biomarker testing in NSCLC for EGFR mutation analysis and ALK rearrangement detection. From 2014 on, ROS1 testing is also included. The scheme aims to assess and improve the current status of molecular testing in NSCLC, to provide education and remedial measures, to permit inter-laboratory comparison and to allow validation of test methods by distributing validated material harboring well-defined aberrations. For EGFR, EQA results have been reported [18]. This article summarizes the results of the two ALK testing pilot rounds of the ESP Lung EQA scheme, organized in 2012–2013 with the purpose to reflect the current status of ALK rearrangement testing practices and to issue recommendations for the improvement of testing quality.
Materials and Methods
A pilot EQA scheme consisting of two rounds was set up. Tissue microarray (TMA) slides that consisted of NSCLC cell-lines and resection specimens were distributed. Three expert laboratories (University of Groningen, the Netherlands, UK NEQAS ICC & ISH, United Kingdom and VU University Medical Center, Amsterdam) provided material for this EQA program. All patient samples were leftover tissues that were obtained as part of routine care and testing from the three laboratories mentioned above and then handed over to the researchers anonymously. These laboratories signed a statement that the patient material was obtained according to the national legal requirements for the use of patient samples. Informed consent is not a mandatory prerequisite for the use of patient derived material, since samples for test validation are exempt from research regulations requiring informed consent. The treating physician was responsible to obtain informed consent from the patients to use their tissues and data for research purposes and this consent is kept in the patient’s medical file. The authors had no contact with the patients or received any patient identifying information. The samples were to be analyzed for the presence of ALK rearrangements using IHC or FISH. In addition to the TMA slides, participation in ALK FISH included the interpretation of four digital FISH images which were accessible online. The ALK FISH digital cases were provided in close collaboration with UK NEQAS ICC & ISH.
In both rounds, mock clinical information was provided for several cases, for which the delivery of a full written report was requested. Report content was assessed in agreement with established standards/guidelines on reporting [19]–[21].
A central database was used for the submission of the results, accessible through the ESP Lung EQA Scheme website. Through their personal account, participants could access their results, scheme documentation and assessor feedback. Upon registration, each laboratory was assigned a unique EQA identity number to guarantee anonymity. A team of medical and technical experts supported the validation of the samples and the evaluation of the scheme results. Results were discussed during an assessment meeting to obtain final consensus scores. Participants received individual feedback and a general report with aggregated scheme results.
The set-up of both rounds slightly differed and the scheme was a pilot for the development and standardization of homogeneous testing material. Eight samples (four resection specimens and four cell lines) and twelve samples (six resection specimens and six cell lines) were prepared and send to the participants for respectively the first and second round. Different cell lines either with or without ALK break were routinely fixed with neutral-buffered formalin, mixed with agar and embedded in paraffin (reflecting routine pathology tissue block) were included. Results from samples for which less than 75% of the participants were able to obtain a result were not taken into account to assess performance [22]. Consequently, for ALK FISH, 3/8 and 7/12 samples were regarded as educational samples for respectively the first and second round. For the assessment, the accepted cases were two resection specimens and three cell lines for the first round of ALK FISH, and for the second round, five resection specimens were included. For ALK IHC, all samples were approved in both rounds.
For ALK FISH, it was requested for each case to report the number of neoplastic cell nuclei without hybridization signals, the number of neoplastic nuclei with fused signal, with split signal and with a single red signal. An algorithm automatically generated the number of neoplastic nuclei with FISH signal, the number of neoplastic nuclei with split or single red, and the fraction of FISH positive and negative nuclei. Participants were asked to then determine the outcome of the ALK FISH test (positive/negative). Samples for which a laboratory did not obtain results due to sample quality or technical failures were not assessed. For ALK FISH TMA and ALK FISH Digital, error rates were calculated based on the samples for which a minimum of 50 nuclei were enumerated, in order to exclude uninformative cases. This paper does not emphasize the marking criteria and assigned scores, as the scoring criteria slightly differed for the pilot rounds, but the study aims to reflect the current status of ALK rearrangement testing practices in molecular pathology laboratories.
For ALK IHC, it was requested to use the H-score procedure as described by Ruschoff et al. [23]. This modified H-score procedure is educational as it gives a better understanding of the ALK IHC sensitivity and reliability [14]. In the first round, a cut-off IHC score of 32 was determined by the mean score plus standard deviation from the laboratories on the IHC negative specimens (except outliers with H-score >100). The same threshold for positivity/negativity was applied in the second round.
For the statistical analysis, scheme error rates from both rounds for FISH digital and FISH TMA were compared using the Mann-Whitney U test. Scheme error rates for IHC were compared using an unpaired t-test. The level of significance was set at α = 0,05.
Results
In total, 173 different laboratories (primarily from European Union countries) participated in the pilot rounds. In the first round, 29 laboratories submitted results for ALK IHC, 55 for ALK FISH TMA, and 67 laboratories performed the interpretation of the digital ALK FISH images. In the second round, 58 laboratories submitted results for ALK IHC, 104 for ALK FISH TMA, and 106 for the ALK FISH digital cases. For the data-analysis, missing values were ignored and only valid answers to questions were included, which explains why sample sizes slightly differ. Laboratory characteristics are listed in Table 1. The total number of laboratories that provided information was used as the denominator to calculate percentages. Because it was sometimes possible to indicate more than one answer, percentages may not add up to 100%.
The majority of the participants were set in a community hospital or university hospital environment. The analysis was mostly performed under the authority of the department of pathology. Regarding the interpretation of ALK FISH, a pathologist was most frequently involved (23% and 27% of laboratories in the first and second round, respectively), in some cases assisted by a scientist (18% and 27%) or a technician (20% and 13%). A scientist alone performed the FISH reading in 15% of the laboratories in both the first and second round. The final reading conclusion was the responsibility of a pathologist alone in more than half of the laboratories (52% and 59% in the first and second round). A pathologist in cooperation with a scientist was responsible in 13% and 14% of the laboratories. A scientist alone was responsible for the final reading conclusion in 16% and 12% of the laboratories in the first and second round.
ALK FISH digital results
Results for both rounds of the ALK FISH digital subscheme are summarized in Table 2. There were no clear differences in the error rates depending on the number of nuclei enumerated. Enumeration practices were evaluated on sample level and on laboratory level. In both rounds, the bulk of the participants enumerated 50–100 nuclei for each case. At laboratory level, in the first round, 34/67 laboratories (51%) counted ≥50 cells for each sample. In the second round, an increase was observed to 77/106 (73%). Table 3 illustrates the performance of the labs that participated in both rounds for each subscheme. Improvement in enumeration practices was defined as enumeration of ≥50 cells in a larger number of samples in the second round compared to the first round.
A decrease was observed in the error rates between both rounds (error rates were calculated taking only the samples for which ≥50 nuclei were enumerated into account). In the first round, 7 out of 195 scored samples were incorrectly assigned (3,6%), while in the second round, 4 errors out of 366 scored samples (1,1%) occurred. The comparison of the number of errors made for laboratories that participated in both rounds and that counted ≥50 nuclei for each case can be found in Table 3.
ALK FISH TMA results
Table 4 summarizes the ALK FISH TMA results for both rounds. In both rounds, the majority of the participants enumerated 50–100 nuclei for each case. Again, there were only small differences in the error rates depending on the number of nuclei enumerated. In the first round, 30/55 laboratories (55%) counted ≥50 cells for each sample; in the second round there was an increase to 81/104 (78%).
For the TMA cases there was also a decrease in the error rates between the two rounds. In the first round, 14 out of 193 scored samples were incorrectly assigned (7,3%), while in the second round, 22 errors out of 423 scored samples (5,2%) occurred. Comparison of the enumeration performance and number of errors made for laboratories participating in both rounds can be found in Table 3.
ALK IHC results
Results for both ALK IHC rounds are provided in Table 5. In the first round, 30/230 scored cases (13,0%) were incorrectly called (false positive or false negative). In the second round, a decrease to 44/540 (8,2%) was observed. Table 3 illustrates the performance for the labs that participated in both IHC rounds.
Summary scheme error rates
The Mann-Whitney U test revealed no significant differences between both rounds for Digital FISH (U = 7, z = –0.308, p = 0.758) or FISH TMA (U = 9, z = –0.731, p = 0.465). For IHC, an unpaired t-test showed no significant difference between the first (M = 0.13, SD = 0.06) and second round (M = 0.08, SD = 0.05); t(18) = 1.845, p = 0.082. Although not statistically significant, comparing the error rates in both rounds suggests a learning effect (Table 6). The smallest error rates were observed for the digital cases, assessing only the post-analytical interpretation phase. In both rounds, the error rate for ALK FISH TMA was lower than the error rate for ALK IHC TMA.
Methods used
The most frequently used method for FISH analysis was the Vysis ALK break apart FISH probe kit (Abbott Molecular, Illinois, USA), used by over 70% of the participants. For IHC, the most frequently used antibodies were clone 5A4 and clone D5F3 for the first and second round, respectively. An overview of the used methods and the error rate per method is provided in Tables 7 and 8. For the percentage of laboratories that used a certain method, the total number of laboratories that provided information was used as the denominator. Because it was possible to indicate more than one used method, percentages may not add up to 100%.
For ALK FISH, the Repeat-Free Poseidon ALK/EML4 t(2;2) inv(2) Fusion Probe (Kreatech Diagnostics, Amsterdam, the Netherlands) revealed a high error rate of 50% in the second round (Table 7). For IHC, the smallest error rates were observed for clones 5A4 and D5F3 (Table 8).
Clinical result reporting
Evaluation of the written reports for the second round (n = 102) showed that a case-specific clinical interpretation was missing in 74% and 79% of the reports for an ALK positive and ALK negative case, respectively. Patient name and date of birth were correctly present in the majority of the reports, as well as a specification of the methods used (FISH kit information or IHC antibody). However, a specification of the aberrations tested and the threshold of the method were not mentioned in 46% and 47% of the FISH reports. The total number of neoplastic cells analyzed and the number of cells with split and/or single signal were missing in 23% of the FISH reports. For IHC, the threshold for positivity/negativity was not defined in 81% of the reports, and the staining intensity was missing in 39% of the reports.
Discussion
Major advances have been made in the management of patients with NSCLC, with improved treatment response and survival following the introduction of molecular targeted TKI therapies focusing on EGFR mutations and ALK rearrangements. The increasing importance of morphology-based studies such as IHC or FISH has made the pathologist’s involvement a key element in precision medicine for NSCLC [2], [24].
In reply to the growing demands, laboratories have introduced molecular testing for NSCLC in routine diagnostics. Regular participation in quality assurance programs is crucial to ensure a high quality of testing service and to warrant patient safety [15], [18], [19].
Our results show that in the majority of the participating laboratories, ALK testing is performed under the authority of the pathology department. This is a necessity as FISH and IHC are both histological tests. Pathology review and assessment of section quality is essential considering the diversity and heterogeneity of tumor tissue [19], as false negatives may be due to poor fixation or insufficient neoplastic cell content [14], [18].
Three methods are generally used in routine diagnostics for ALK rearrangement detection: FISH, RT-PCR, and immunohistochemistry for aberrant expression of ALK protein [12], [14], [25]. Importantly, every assay should undergo validation in the laboratory before clinical interpretation and should be subject to regular internal and external quality controls [14], [19], [24]. The FDA approved test to determine ALK status is the Vysis LSI ALK dual color, break apart rearrangement probe (Abbott Molecular, Illinois, USA) [12], [14]. Although other IVD-CE labeled kits are available in Europe, this kit was by far the most frequently used method in both pilot rounds. ALK break apart (or split-signal) probes detect disruption of the ALK 2p23 locus but do not identify the partner fusion gene [3], [25]. Surprisingly, the ALK/EML4 fusion probe is still occasionally used, although these probes miss the translocation of ALK with partners other than EML4. In the second round, the fusion probe revealed a high error rate of 50%. The cut-off values used during the clinical trials to prove the efficacy of crizotinib can be transferred from the Vysis probe to other break apart probes since the design (size + location) is highly similar [26]. The ZytoLight TriCheck (ZytoVision, Bremerhaven, Germany), used by approximately 7% of the participants in both rounds, can identify the presence of an ALK rearrangement and if the rearrangement partner is EML4. Today it is still under discussion whether it is important to know the fusion partner of ALK in relation to expected response to ALK TKIs [27], [28].
According to Abbott Molecular scoring criteria, a nucleus is considered positive if it contains at least one split signal or one isolated red signal. A first enumerator should count 50 nuclei. Cases with >50% and <10% positive nuclei are considered positive and negative respectively. If a sample shows between 10–50% positive nuclei, a second enumerator should also count 50 nuclei. If the average of the two readings contains at least 15% positive cells, the sample is considered positive. The kit specifies uninformative specimens as those in which fewer than 50 nuclei within the scribed area can be enumerated. In our evaluation these cases were therefore not included to calculate and compare the scheme error rates. It has been shown that the sensitivity and specificity of the kit increase as the number of tumor areas and number of nuclei scored increase [29], [30]. Our results showed that ALK rearrangement status was often determined on the evaluation of less than 50 nuclei by many participants. The percentage of false positive and false negative results upon enumeration of <50 nuclei did not reveal a clear difference compared to the percentage upon enumeration of ≥50 tumor nuclei. These findings correlate with the fact that the ALK rearrangement appears to be a homogenous event in the tumor population [26], [29], Enumeration of <50 nuclei is not advisable because this number is based on the minimal number that is statistically needed to be able to reliably define a sample without FISH break signals (<15% of nuclei) as a case without ALK rearrangement. In addition, the predictive value of phase III trial is based on this. Remarkably, some participants enumerated a large number of nuclei (e.g. >600 evaluated nuclei for case 12.215), which is not a requirement for daily practice. FISH interpretation should be performed in areas of the slide with clear signals, which are clearly distinct from the nuclear fluorescent ‘noise’ as well as from the background [15]. Importantly, selection of neoplastic nuclei is essential, and to this end sufficient morphological knowledge in FISH stained slides is obligatory, which stresses involvement of a pathologist.
It is not a surprise that the TMA FISH error rates were substantially higher than those of the digital FISH images. The FISH digital subscheme specifically assesses the interpretation of identical digital images whereas the TMA FISH error rate also incorporates variation in serial TMA sections, technical execution, and reading. Suboptimal ALK FISH procedure may lead to a low signal versus background ratio, increasing the chance for interpretation errors.
Although FISH is used as a standard test, it demonstrates considerable inter-observer variability. Therefore, experienced (>100 cases/year) and well-trained FISH reviewers/enumerators are necessary. If the clinical scientist is well trained and experienced in histo- and cytomorphology with specialized training in solid tumor FISH analysis, he/she can be responsible for the technical performance and molecular interpretation. A pathologist should at least be responsible for the selection of the right cells, the review of the interpretation and the authorization of the pathology report [14], [15]. Our data demonstrate that a pathologist was responsible for the final conclusion in the majority of the laboratories. Participating laboratories indicated that scientists and technicians were often involved in FISH enumeration. In this set-up it is important that the clinical scientist can consult a pathologist at any time in case of doubt concerning the location of the tumor cell area.
ALK IHC, if carefully clinically validated according to ISO 15189, may be considered as a screening method to select specimens for ALK FISH testing [15]. It is a cost-effective screening tool which correlated significantly with ALK FISH, using a number of antibodies including the 5A4 and D5F3 [25], [31]–[33]. However, discrepancies are reported also and need to be elucidated [34]. The 5A4 and D5F3 antibodies were the most frequently used clones in our study and revealed the smallest error rates, which is in accordance with literature [32], [33] and the findings of a recent NordiQC assessment [35]. Not surprisingly however, the error rates for IHC were greater than for FISH. Recently different validation projects for ALK IHC tests were done in collaboration with a lot of laboratories [36]. Moreover, on the website of NORDIQC (http://www.nordiqc.org/), advice on IHC staining protocols is given for several antibody clones.
Our study demonstrates improvement of ALK testing after only two EQA rounds. This suggests that laboratories constructively use the assessors’ feedback from the previous round to enhance their performance. Participation in EQA facilitates rapid exposure of errors and the timely implementation of corrective and preventive actions. However, other factors such as increased expertise and experience may play a part. It is expected that larger datasets, spanning a larger number of EQA participations will demonstrate a statistically significant improvement. On scheme level, the error rates for both ALK FISH and ALK IHC were lower in the second round and the ALK FISH digital scheme demonstrated an error rate of only 1,1%. Error rates for ALK FISH TMA and ALK IHC were still high (>5%), which stresses the need for continued education through EQA. Progress was also seen on individual laboratory level. For FISH analysis, improvements were observed both in the number of errors made and in enumeration practices.
Reporting of test results should take into account sample adequacy relative to the assay performance characteristics and limitations, and clinical reports should be readily interpretable by non-expert clinicians [19], [21]. Previous EQA schemes have exposed existing deficiencies in clinical reporting [18], [37]. Our results show that the content of reports for ALK rearrangement detection should be improved. Especially, a case-specific clinical interpretation, predicting the effect of the rearrangement status on therapy response, should be integrated in each report since a clear and concise assessment of the clinical implications of the result is crucial to fully inform treatment options.
Maintenance of quality assurance measures, including stringent internal quality controls and continued education by repeated EQA participations is essential to ensure high testing quality and rapid exposure of errors in order to warrant appropriate treatment choices. This article has demonstrated improvement in the performance of ALK FISH and ALK IHC in two consecutive EQA rounds. Several recommendations were made to improve the quality of ALK testing.
Acknowledgments
The following laboratories were responsible for the preparation and validation of the samples: Carola Andersson (Sweden), Lukas Bubendorf (Switzerland), Keith Kerr (United Kingdom), Keith Miller (United Kingdom), Patrick Pauwels (Belgium), Ed Schuuring, Lorian Slagter and Rianne Pelgrim (The Netherlands), Erik Thunnissen (The Netherlands). We thank Sofie Delen for her help in the assessment of the scheme results. We also thank the laboratories that participated in the pilot rounds and we thank the administrative office of the European Society of Pathology for their assistance.
Author Contributions
Conceived and designed the experiments: LT KM ES ET ED. Performed the experiments: LT KM ES ET ED. Analyzed the data: LT VT KZ PP KK KM LB ES ET ED. Contributed reagents/materials/analysis tools: LT KM ES ET ED. Contributed to the writing of the manuscript: LT VT PP KZ ED.
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