Background Tumor mutational burden (TMB) is a recently proposed predictive biomarker for immunotherapy in solid tumors, including non-small cell lung cancer (NSCLC). Available assays for TMB determination differ in horizontal coverage, gene content and algorithms, leading to discrepancies in results, impacting patient selection. A harmonization study of TMB assessment with available assays in a cohort of patients with NSCLC is urgently needed.
Methods We evaluated the TMB assessment obtained with two marketed next generation sequencing panels: TruSight Oncology 500 (TSO500) and Oncomine Tumor Mutation Load (OTML) versus a reference assay (Foundation One, FO) in 96 NSCLC samples. Additionally, we studied the level of agreement among the three methods with respect to PD-L1 expression in tumors, checked the level of different immune infiltrates versus TMB, and performed an inter-laboratory reproducibility study. Finally, adjusted cut-off values were determined.
Results Both panels showed strong agreement with FO, with concordance correlation coefficients (CCC) of 0.933 (95% CI 0.908 to 0.959) for TSO500 and 0.881 (95% CI 0.840 to 0.922) for OTML. The corresponding CCCs were 0.951 (TSO500-FO) and 0.919 (OTML-FO) in tumors with <1% of cells expressing PD-L1 (PD-L1<1%; N=55), and 0.861 (TSO500-FO) and 0.722 (OTML-FO) in tumors with PD-L1≥1% (N=41). Inter-laboratory reproducibility analyses showed higher reproducibility with TSO500. No significant differences were found in terms of immune infiltration versus TMB. Adjusted cut-off values corresponding to 10 muts/Mb with FO needed to be lowered to 7.847 muts/Mb (TSO500) and 8.380 muts/Mb (OTML) to ensure a sensitivity >88%. With these cut-offs, the positive predictive value was 78.57% (95% CI 67.82 to 89.32) and the negative predictive value was 87.50% (95% CI 77.25 to 97.75) for TSO500, while for OTML they were 73.33% (95% CI 62.14 to 84.52) and 86.11% (95% CI 74.81 to 97.41), respectively.
Conclusions Both panels exhibited robust analytical performances for TMB assessment, with stronger concordances in patients with negative PD-L1 expression. TSO500 showed a higher inter-laboratory reproducibility. The cut-offs for each assay were lowered to optimal overlap with FO.
- lung neoplasms
- tumor biomarkers
- translational medical research
- B7-H1 antigen
Data availability statement
All data relevant to the study are included in the article or uploaded as supplemental information.
This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See https://creativecommons.org/licenses/by/4.0/.
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Lung cancer has the leading incidence (11.6% of the cases) and mortality (18.4%) rates of malignant diseases worldwide.1 Non-small cell lung cancer (NSCLC) is the most prevalent subtype of lung cancer (85% of cases), and most frequently presents at an advanced stage. Systemic treatments in this setting have evolved, with targeted therapies against specific actionable oncogenic alterations in an increasing list of genes, including EGFR, ALK and ROS1, among others, now being added to chemotherapy.2 However, the emergence of resistances in most patients highlights the urgency for alternative treatment strategies to be developed.
In recent years, the availability of checkpoint inhibitors has had a remarkable impact on outcomes in patients with advanced NSCLC. Treatment with PD-1/PD-L1 inhibitors as single agents or in combination with chemotherapy and/or cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) inhibitors has been particularly successful in pretreated and treatment-naïve patients.3–8 However, most of the benefit from these strategies is restricted to a subset of patients displaying long-term survival. At present, patient selection in the clinical practice is based on the immunohistochemical determination of PD-L1 expression by tumor cells, which presents relevant limitations, particularly when checkpoint inhibitors are given in combination.
These limitations on PD-L1 detection are in part due to its expression pattern, influenced by intra-tumoral heterogeneity, temporal and topographical inter-tumoral heterogeneity, impact of previous treatment lines on its expression, the membranous (functional) versus cytoplasmic expression and the type of cell expressing it. In addition, the preanalytical methods and technology used impact on the observed expression due to the instability of the epitopes during fixation and tissue handling and the different affinities and specificities of the available antibodies.3 9–11
In this context, there is an urgent need to find optimized and complementary predictive biomarkers for checkpoint blockers.12 In recent years, tumor mutational burden (TMB), defined as the total number of mutations per megabase of the tumor genome encoding area, has been identified as a promising predictive tool in many solid tumors,13–15 including melanoma16 and NSCLC,17 18 which present the highest prevalence of somatic mutations.19
While whole-exome sequencing (WES) may serve as a more exact method to determine TMB, this technique is nevertheless demanding in terms of coverage, turnaround-time and the required quality and amount of DNA extracted from formalin-fixed, paraffin-embedded (FFPE) tissue. Foundation One (FO) and MSK-Impact20 are centralized assays based on next generation sequencing (NGS) panels approved by the US Food and Drug Administration (FDA) for this purpose.21–24 Consequently, a range of comprehensive genomic profiling assays (CGPs) has been developed and made commercially available by several companies to facilitate the performing of in-house TMB assessments in the clinical practice.20
The different CGPs have numerous differences. The most important is the enrichment technology used in each case, but also different preanalytical procedures, methodology workflows, sequencing technologies, recommended depth, horizontal coverage, panel size, gene selection, types of mutations detected, sequencing platforms and bioinformatic algorithms for TMB determination. Several studies have evaluated the major influence that these factors can exert on precise TMB calculations,20 25–28 thereby emphasizing the need for standardization studies with the different available approaches. In the present study, we present the results of the “TMB2 Harmonization Project: Tumor Mutational Burden by Two Methods Balanced.” We have evaluated the analytical performance of two distributable commercially available panels: TruSight Oncology 500 (TSO500, Illumina) and Oncomine Tumor Mutation Load (OTML, Thermo Fisher) compared with one of the above-mentioned reference methods (FO, Roche). The most important difference is the enrichment method used in each case: TSO500 uses hybrid capture and OTML uses an amplicon-based method. Differences in the methodologies of these two panels include: (i) that TSO500 requires the DNA to be fragmented by sonication previous to library preparation, in order to start with an homogeneous and accurate sample size for the hybrid capture, whereas OTML requires to treat the DNA samples with an uracyl DNA glycosylase enzyme in order to reduce possible deamination events during the amplicon generation; and (ii) that TSO500 uses unique molecular identifiers (UMIs) in the library preparation whereas OTML does not. Ultimately, the main objective of this study is to determine specific TMB cut-off values for each panel to guarantee a correct patient stratification, thus improving the clinical utility of this biomarker.
This section can be found in Online supplemental material.
Analytical performance of the novel NGS panels in TMB determination
A set of 96 resected early-stage NSCLC tumors in FFPE format was used to assess the analytical performance of the TSO500 and the OTML panels. The median total TMB (TMBtotal, synonymous and non-synonymous mutations) calculated by the TSO500 panel was 8.8 mutations/Mb, spanning a range from 0.8 to 84 muts/Mb. In contrast, the median TMBtotal calculated by the OTML panel was 9.7 muts/Mb, ranging from 0 to 59.8 muts/Mb. A linear regression analysis of TMBtotal calculated with OTML versus TSO500 is shown in figure 1A, where R2=0.8545. A Bland-Altman plot describing agreement between the two analytical methods is shown in figure 1B. The systematic difference in absolute terms was close to zero (0.253 (−12.200; 12.707)), with seven measurements (7.29%) outside of the 95% limits of confidence for agreement between OTML and TSO500, showing higher values for TSO500. In general, the mean values (horizontal axis) between each pair of measurements showed higher differences (vertical axis). These differences were corrected when data were plotted according to relative values (figure 1C). The concordance correlation coefficients (CCC) for TSO500 versus OTML was 0.886 (figure 1D) (95% CI 0.851 to 0.920).
Analytical performance of the NGS panels compared with the reference standard method
Total TMB values obtained with FO in the 96 sample set had a median value of 10 muts/Mb, spanning a range of TMB values from 0 muts/Mb to 74 muts/Mb. Linear regression analyses of TMB values calculated with TSO500 versus those obtained by FO resulted in a R2=0.8775 (figure 1E), while that for OTML versus FO was R2=0.8119 (figure 1I). The level of agreement between each pair of methods is shown in figure 1F,G,J,K. The systematic differences were close to zero (0.215 (−10.139; 10.569)), with six measurements (6.25%) outside of the 95% limits of confidence for agreement between FO and TSO500, and 0.469 (−11.548; 12.485) with five measurements (5.21%) outside of the 95% limits of confidence for agreement between FO and OTML. CCCs were 0.933 (95% CI 0.908 to 0.959) for FO versus TSO500, and 0.881 (95% CI 0.840 to 0.922) for FO versus OTML (figure 1H,L). A summary of all TMB results with the three panels is provided in online supplemental table S1.
TMB concordance within tests in patients grouped according to PD-L1 expression
We analyzed the extent of agreement among the tests in subgroups of NSCLC samples separated by PD-L1 expression. Percentages of cells expressing PD-L1 were analyzed in patient samples and classified as PD-L1<1% (N=55) or PD-L1≥1% (N=41). Correlation analyses of tumors with PD-L1 expression<1% (N=55) provided R2 values of 0.9120 for TSO500 versus FO and 0.8768 for OTML versus FO (figure 2A–D). In the group expressing PD-L1≥1% (N=41), R2 values of 0.7466 for TSO500 versus FO and 0.5735 for OTML versus FO (figure 2E–H) were obtained. CCC values of 0.951 (95% CI 0.926 to 0.975) for TSO500 versus FO and 0.919 (95% CI 0.882 to 0.956) for OTML versus FO (figure 2I and online supplemental figure S3) were consistent with the correlation analyses in PD-L1<1% tumors. In contrast, in samples expressing PD-L1≥1%, a CCC value of 0.861 (95% CI 0.781 to 0.942) for TSO500 versus FO was determined compared with 0.722 (95% CI 0.586 to 0.858) for OTML versus FO (figure 2J and online supplemental figure S4). Data for the graphs shown and statistical analyses of the differences in the demographic data between the two groups of patients are presented in online supplemental table S2.
Reproducibility analysis: inter-laboratory cross-validation studies
To evaluate the inter-laboratory reproducibility of each NGS panel, a subset of samples was analyzed using the same test in two different laboratories. Results are shown in figure 3 and online supplemental table S3. The concordance was very good for both panels. More robust data were obtained for TSO500, with a CCC of 0.987 (95% CI 0.976 to 0.999) and R2=0.9789, whereas for OTML the CCC was 0.851 (95% CI 0.736 to 0.965) and R2=0.7275. Of note, the limits of agreement at 95% were much narrower for TSO500 (−3.322 to 2.149) than for OTML (−12.231 to 11.014).
Performance of the NGS panels selecting TMBhigh tumors
We analyzed four different cut-off values to define TMB status (high vs low) with FO: 10, 13, 16 and 20 muts/Mb. We focused in those four cut-off values as they were previously used as predictive in different clinical trials (10 muts/Mb in Checkmate 2277; 13 muts/Mb in Checkmate 02629; 16 and 20 muts/Mb in the Mystic Trial30). When using a cut-off value of 10 muts/Mb, FO categorized 51% of patients from the cohort as TMBhigh (≥10 muts/Mb), whereas TSO500 and OTML assigned the same status to 45.83% and 50% of patients, respectively (figure 4A). Among patients identified as TMBhigh by FO, 20.40% and 18.40% scored as TMBlow (<10 muts/Mb) with the TSO500 and OTML assays, respectively (figure 4B). In addition, out of the 47 tumors with TMBlow, 10.60% and 17% scored as TMBhigh in the TSO500 and OTML assays, respectively (online supplemental figure S5). If a higher cut-off point is desired, such as 13, 16 or 20 muts/Mb, the percentage of patients classified as TMBhigh with panel TSO500 or panel OTML would be lower than the percentage of patients that would be categorized as TMBhigh by FO (using those same cut-off values; figure 4C–E). Consistently, the percentage of patients categorized as TMBlow would be higher with TSO500 or OTML than with FO (online supplemental figure S5).
Selection of adjusted cut-off points for each NGS panel
To determine the adjusted cut-offs for TSO500 and OTML corresponding to TMBs ≥10, 13, 16 and 20 with FO, characteristics of the area under the receiver operating characteristic (ROC) curve were calculated (figure 5). The discriminatory capacities of TSO500 and OTML tests with respect to a FO value of TMB ≥10 were 0.90 (95% CI 0.83 to 0.97; figure 5A) and 0.89 (95% CI 0.83 to 0.96; figure 5B), respectively (p value=0.8398). Similarly, no significant differences between the discriminatory capacities of TSO500 and OTML with respect to FO were found for TMB≥13 (p value=0.8625), TMB≥16 (p value=0.2284) or TMB≥20 (p value=0.2308) (figure 5C–H and online supplemental table S4).
Table 1 shows the adjusted cut-off values calculated for both TSO500 and OTML, corresponding to cut-off points of 10, 13, 16 and 20 muts/Mb for the FO assay. These values represent a compromise between maximum sensitivity (>88%) and specificity obtained from the ROC curves. A comprehensive list of continuous values for both tests, analyzed in relation to each of the desired cut-off points by FO (10, 13, 16 and 20 muts/Mb), including sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) for each point are shown in online supplemental table S4. Cut-off points that guarantee a sensitivity >88% corresponding to 10 muts/Mb by FO would be 7.847 (for TSO500) and 8.380 (for OTML), corresponding to 13 muts/Mb by FO would be 9.434 (for TSO500) and 9.240 (for OTML), respectively, corresponding to 16 muts/Mb by FO would be 10.995 and 10.90 and for 20 muts/Mb by FO would be 13.842 and 11.73, respectively.
Degree of immune infiltration in tumors with different TMBs
At last, we wanted to analyze the presence of different immune infiltrates in the tumors with respect to their mutation burden. For that, we stained four additional slides of each of the 96 tumors with markers for four different populations of immune infiltrates: CD4+ T cells, CD8+ T cells, CD20+ B cells and CD68+ macrophage/monocytic populations. We did not find significant differences that indicated a correlation between higher TMB and higher or lower immune infiltration of these four cell categories. However, we found a trend indicating that CD4+ T cells tend to be more infiltrated in the tumors with lower TMB, and CD68+ macrophage/monocytic populations tend to concentrate in tumors with higher TMB. The results are shown in online supplemental figure S6 and table S5.
The calculation of TMB as a guiding biomarker for treatment with checkpoint inhibitors in clinical practice largely lies in the implementation of NGS gene panels. In this work, we used a cohort of 96 NSCLC samples to determine the technical performance of TSO500 and OTML assays in comparison to a reference standard method (FO). We verified an adequate degree of agreement among the methods, with concordance values tending to be higher for tumors expressing lower levels of PD-L1. We provided a range of cut-off values for both TSO500 and OTML corresponding to different levels of TMB that have been of interest in previous immuno-oncology trials in NSCLC, and estimated their sensitivities, specificities, PPVs and NPVs.
Immunotherapy with checkpoint inhibitors has impacted treatment outcomes in many solid tumors, including lung cancer.4 31 32 However, up to 60%–80% of patients with advanced NSCLC will not benefit to any significant extent from PD-1/PD-L1 inhibitors.5 31 33 34 The only clinically validated biomarker in this context is the tumor expression of PD-L1, as measured by immunohistochemistry, and its predictive capacity is far from optimal, particularly when PD-1/PD-L1 inhibitors are combined with chemotherapy, radiotherapy or CTLA-4 inhibitors.6 7 33 35–37 The role of TMB in this context is unclear, as the survival benefit with ipilimumab plus nivolumab over chemotherapy in the Checkmate 227 trial—the only trial performed in this setting that had patients selected for a primary end-point on the basis of tumor TMB (≥10/Mb)—was independent of the TMB scores, even though TMB was predictive of objective response rate and progression free survival.37 Relevantly, TMB may also be predictive of overall survival benefit for high PD-L1 expression patients when treated with pembrolizumab as single agent.38 However, TMB may not be predictive of survival when pembrolizumab is administered in combination with chemotherapy.39 Other studies demonstrated that using higher TMB values, the selection of patients was more accurate in predicting the greatest benefit from therapy.30 Of note, recently the US FDA approved pembrolizumab for the treatment of adult and pediatric patients with unresectable or metastatic solid tumors with tissue TMB-high (TMB-H; ≥10 mutations/megabase), as determined by an FDA-approved test, who have progressed following prior treatment and have no satisfactory alternative treatment options.40
Calculation of the TMB by WES is highly time-consuming, making it less feasible to guarantee an appropriate turnaround time in the clinical practice. Several NGS panels with predictive capacity in the clinic are currently approved by the FDA for the determination of TMB: FO, F1CDx, MSK Impact, Omics Core and PGDx elio tissue complete.22–24 41 42 Recently, several biotech companies specializing in NGS have released their own panels for TMB determination from tumor tissue samples.20 Their agreement with the gold standard method (WES) or with approved large panels able to estimate the TMB -such as FO- are currently being independently analyzed in large cohorts of clinical samples.43 This is one of the first harmonization studies of TMB determination, in which we evaluated 96 clinical NSCLC samples. There was a high correlation among the overall TMB values obtained with the three different NGS panels analyzed (FO-TSO500 R2=0.8775; FO-OTML R2=0.8119; TSO500-OTML R2=0.8545). More importantly, the actual values obtained with each method were highly concordant as reflected by their CCCs (ie, there was a high correlation among the overall TMB values obtained with the three different NGS panels analyzed (FO-TSO500 CCC=0.933; FO-OTML CCC=0.881; TSO500-OTML CCC=0.886)). We have noticed a few deviations such as a small percentage of samples that show higher values of TMB with TSO500 than with OTML (figure 1B, 5% of samples outside of the limits of confidence). Those six samples have specific genes frequently mutated that, in a high percentage (52%), are not included in the design of the OTML panel, but they are included in the design of the TSO500. That can slightly change the total TMB number calculated with one panel versus another. These results are providing numeric proof that gene content is as important as horizontal coverage in the design of NGS panels for TMB determination, a concept in continuous open discussion in the field. This is the main reason why cut-offs need to be optimized and adjusted for each different panel.
The need for standardization and harmonization of TMB assessments across the available methodologies is obvious owing to their inherent differences in megabases of exonic coverage, selection of genes under study (some genes have hotspots that are more prone to mutate than others, and each panel has a different gene content), amplification and library generation technologies, presence or absence of UMIs, sequencing technology, and TMB calculation algorithm (including the method of correction for deaminations caused by formalin fixation, as well as the reading depth), among others. Countless efforts have been made to address this common goal.27 44 Some studies approached the TMB harmonization from an in silico perspective45 or with relatively reduced cohorts,46 while other studies have overcome the cohort size difficulties but still lack certain critical evaluations such as the definition of specific TMB cut-offs equivalent to those established with the reference method47 or inter-laboratory reproducibility assays.43 Apart from the present study, two other broad studies of TMB standardization have been carried out: one by Friends of Cancer Research and other by Quality in Pathology (QuIP) study investigators. In the first case, a first phase of the study analyzed data from The Cancer Genome Atlas with WES and 11 simulated NGS panels in order to create a calibration and validation set for TMB calculation. The performance of this validation set was evaluated in a second phase of the study with 25 FFPE samples.48 49 In the QuIP initiative, 20 FFPE samples were evaluated in 15 participating institutions, each of which assessed six panels. Specific TMB cut-offs were defined corresponding to 199 mutations determined by WES, and equivalent to 10 mutations per megabase as determined by FO.50 For most of the panels evaluated, including TSO500, the calculated TMB cut-offs were in the range of 9.4 to 11.5 muts/Mb. Among the exceptions, OTML cut-offs were 7.8–7.9, depending on the regression methodology used.
It was relevant to us to evaluate that the performance of the tests was still robust in the population of PD-L1 positives, compared to the general population. That is the specific population of patients with NSCLC for which the FDA has approved the use of pembrolizumab (anti-PD-1). Indeed, exploratory analysis of the Keynote 042 trial suggests that among patients with tumors expressing PD-L1 in ≥50% of cells, only those whose TMB was higher than the median exhibited any therapeutic benefit with PD-1/PD-L1 inhibitors as compared to chemotherapy.38 We consider particularly relevant to analyze the agreement of the three methods in the two separated subgroups, because the PD-L1 positive patients are the ones in which the TMB evaluation will have putative clinical utility. The results in our cohort of 96 patients seem to indicate that the higher the PD-L1 the lower the TMB. Moreover, linear regression values were stronger in the PD-L1-negative tumors, with a N of 55 samples, than in PD-L1-positive tumors, with a N of 41 samples.
One of the best attributes of TMB as a biomarker is its ease of quantification on a continuous scale. However, biomarkers in the clinic are frequently used in a binary fashion (eg, high or low). When this was done with TMB, regardless of the cut-off point used to define high and low, we found that a significant number of patients (around one third) are misclassified as compared to the reference test using the same threshold. In fact, when we analyzed the ROC curves, it could be appreciated that for any cut-off with the FO panel, the corresponding cut-off point with the TSO500 panel needed to be lowered, and even more so with the OTML panel. We have thus obtained here a set of empirical, adjusted cut-off values—representing reasonable compromises between acceptable sensitivity and specificity—for a variety of different cut-off points from the FO panel that have been pursued in different clinical scenarios. Indeed, the cut-point of TMB for patient selection might depend on the treatment context including line of therapy (first line or salvage treatment), specific therapy (single agent immunotherapy or in combination with chemotherapy or radiotherapy), stage of disease (adjuvant setting, stage III or metastatic disease) and further research in this area is warranted. We have selected in this study four relevant cut-off values in lung cancer that were previously used as predictive in different clinical trials: 10 muts/Mb (Checkmate 2277); 13 muts/Mb (Checkmate 02629); 16 and 20 muts/Mb (Mystic Trial30). We have also provided cut-off values for the novel tests that would increase sensitivity (reducing the false negative rate) in relation to the FO test, always taking into account the concurrent effect on increasing the false positive rate. However, it must be mentioned that other small studies obtained different cut-off values for TSO500 when compared with FO.43 Efforts to standardize the cut-off for a TMB high population across platforms may be influenced by several factors, including cohort specific effects, preanalytical differences in tissue processing, and the statistical approaches utilized to select the appropriate threshold, which may lead to differences across studies.
We were also interested here in determining the reproducibility of each test when used in different hospital laboratories by different operators. When around one quarter of the sample cohort was studied with TSO500 and OTML in two paired institutions, the outcomes for both assays were highly reproducible. To this end, TSO500 was found to be more robust, with a R2 of 0.9789 and a CCC of 0.987 (N=21) compared with a R2 of 0.7275 and a CCC of 0.851 for OTML (N=23). The TSO500 panel is a hybrid capture panel, not amplicon-based, thereby resulting in a lower number of artifacts which may account for its better reproducibility. TSO500 uses UMIs, which avoids artifacts caused by errors in the polymerase and also by incorrect interpretation of deamination, because each of the original DNA strands are specifically labeled with a barcode that distinguishes original mutations from mutations that appear during the library preparation. Furthermore, the pipeline analysis included an automatic algorithm that corrects for deaminations occurring as a consequence of the formalin fixation of the tissue in the case of the TSO500 assay. In contrast, when using the OTML assay, the operator must manually correct cases of high deamination as per the manufacturer’s guidelines. Therefore, an obvious conclusion is that, in order to use the OTML panel for TMB determination across laboratories, it is essential to standardize the processing criteria when testing samples with high deaminations.
At last, we evaluated the degree of infiltration of different immune populations (CD8+ T cells, CD4+ T cells, B cells and macrophages) with respect to the TMB of each tumor. We observed that none of the four populations seem to correlate with the TMB with statistical significance, although the infiltration with CD4+ T cells shows a trend of higher accumulation in tumors with lower TMB and less presence in tumors with higher TMB, and CD68+ macrophages seem to present the opposite trend where more macrophages are infiltrated in tumors with higher TMB. It is feasible to hypothesize that, in the case of macrophages, they would be called to the tumors that harbor more mutations and resultant antigens. In the case of the CD4+ T cells, it would depend on the specific cell subtypes of cells that are being recruited to the tumor. Therefore, further investigation regarding the determination of specific cell subtypes (regulatory vs active CD4+ T cells, M1 vs M2 macrophages) will be needed.
In conclusion, our work presents a comprehensive harmonization study for TMB determination using the TSO500 and OTML panels versus the FO reference standard method. Our results obtained on FFPE tumor tissues from a cohort of 96 patients are empirical and not in silico. The results are satisfactory, and both tests on the FFPE samples performed very well both analytically and clinically. Bland-Altman analyses demonstrated good concordance between both tests and the FO reference standard. For the specific characteristics of our study, we described in detail that in order to appropriately select TMBhigh patients and not overlook any putative candidates for therapy, the cut-offs needed to be lowered compared to those selected for FO. The fact that cut-offs in FO resulted higher than for TSO500 and OTML could indicate that the selection of genes that are included in FO are more prone to be mutated than the selection of genes included in the other two panels. Or that the algorithm that FO introduces to discriminate deamination artifacts due to formalin fixation of the samples is better optimized. Moreover, we determined the adjusted cut-offs for different sensitivities and specificities, equivalent to four different FO cut-off points: 10, 13, 16 and 20 muts/Mb. The results should thus serve as a highly valuable tool for laboratories and hospitals to select appropriate cut-offs when using these two panels, providing information about different empirical values of specificity and sensitivity, and thus facilitating patient selection. Moreover, we have studied the reproducibility of both tests from an inter-laboratory perspective, and the behavior of the tests in two different groups of tumors based on their different PD-L1 expression levels. These findings should have an immediate impact on clinical practice and in the personalized management of patients with lung cancer.
Data availability statement
All data relevant to the study are included in the article or uploaded as supplemental information.
We gathered a cohort of 110 resected early stage NSCLC tumors. After resection, tumor samples were formalin-fixed and paraffin-embedded (FFPE) and stored in the Pathology Department of 12 de Octubre University Hospital, under signed agreed consent. Protocol was approved by the Ethics Committee of the Hospital 12 de Octubre with identification number #18/385.
We would like to acknowledge the patients and their families for the donation of tumor tissue, and the technical support provided by Estrella López-Sabroso. FL-R is most grateful to Ilaria Alborelli (University Hospital Basel), Phillip Jermann (University Hospital Basel) and Luca Quagliata (Thermo Fisher Scientific) for their help with the TML panel implementation and to T Crean for his constant support.
This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.
Twitter @TamaraCaniego, @urbicioperez
EMG-M and LP-A contributed equally.
Contributors LP-A, EMG-M and FL-R conceived the study. JR-P, EMG-M, DL, AR, SH-P, ES, NC, ABE, MTM-J, DG-S, TC-C, BR, IF and ANB performed experiments and/or data analysis. Clinical information and specimens were provided by UP-G and SPA. Manuscript preparation was performed by EMG-M and JR-P. Manuscript revisions were performed by EMG-M, JR-P, LP-A, FL-R, PG, JP. All authors read and approved the final manuscript.
Funding This project was funded by Bristol Myers Squibb under the reference BMS#OT123-367, by Fondos FEDER and the Plan Estatal de I+D+I 2008–2011 (PI11/02866), 2013–2016 (PI17/00778, PI17-01001 and PI14-01176), the iLUNG Program (B2017/BMD-3884) from Comunidad de Madrid, the Spanish Network of Biomedical Research in Cancer (CIBERONC, group CB16/12/00442), and the Fundación CRIS contra el cáncer (Unidad Integral CRIS de Inmuno-oncología). TruSight Oncology 500 kits were made available free of charge by Illumina as part of an early access agreement. EMG-M was supported by a Marie Skłodowska-Curie Post-doctoral Research Fellowship awarded by the European Respiratory Society under the RESPIRE3 (REspiratory Science Promoted by International Research Exchanges 3) program, that receives funds from the European Union’s Horizon 2020 research and innovation program under the Marie Skłodowska-Curie Actions Grant agreement No#713 406 (MSCA COFUND scheme). JR-P is funded by an FPU predoctoral fellowship from the Spanish Ministry of Education #FPU16/00382.
Competing interests LP-A has received honoraria for scientific advice and speaker fees from Lilly, Merck Sharp & Dohme, Bristol-Myers Squibb, Roche, PharmaMar, Merck, Astra-Zeneca, Novartis, Boehringer Ingelheim, Celgene, Servier, Sysmex, Amgen, Incyte, Pfizer, Ipsen, Adacap, Sanofi, Bayer and Blueprint, and participates as external member of the board of Genómica. He is founder and board member of Altum sequencing and has received institutional support for contracted research from Merck Sharp & Dohme, Bristol-Myers Squibb, Astra-Zeneca and Pfizer. EMG-M has received honoraria for scientific advice from Bristol-Myers Squibb and speaker fees from Illumina Inc and Pfizer and she is currently employee of PharmaMar. PG has received consultant and advisory fees from Roche, Merck Sharp & Dohme, Bristol-Myers Squibb, Boehringer Ingelheim, Pfizer, Abbvie, Guardant Health, Novartis, Lilly, Astra-Zeneca, Janssen, Sysmex, Blueprint Medicines and Takeda. She has been the recipient of speaker fees from Takeda, Astra Zeneca, Roche, Merck Sharp & Dohme, Bristol-Myers Squibb, Pfizer, Novartis, Boehringer Ingelheim, Gilead and Rovi, and institutional support for clinical trials from Roche, Merck Sharp & Dohme, Bristol-Myers Squibb, Takeda, Lilly, Pfizer, Novartis, PharmaMar, Celgene, Sanofi, GlaxoSmithKline, Theradex Oncology and BluePrint Medicines. She has also received funding for contracted research from Guardant Health and Sysmex. FL-R. has received honoraria from Astra Zeneca, Abbvie, Bayer, Lilly, Merck Sharp & Dohme, Pfizer, Bristol-Myers Squibb, Roche, Thermo Fisher, and has received research funding from Bristol-Myers Squibb, Lilly, Roche and Thermo Fisher. SPA has received honoraria from Roche, Bristol-Myers Squibb, Merck Sharp and Dohme, Astra-Zeneca and Targovax, is a board member of Oncosur, and has received direct research funding as project lead from Roche, Merck Sharp & Dohme, Bristol-Myers Squibb and Lilly. The remaining authors declare no competing financial interests. SHP has received honoraria from Roche and Bristol-Myers Squibb. ES has received grants from Thermo Fisher Scientific and Bristol-Myers Squibb.
Provenance and peer review Not commissioned; externally peer reviewed.
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