Patients treated for non-squamous (non-Sq) non-small cell lung cancer (NSCLC) often require repeat biopsies to determine the optimal subsequent treatment. However, the differences between rebiopsy and initial biopsy in terms of their diagnostic yields and their ability to test the molecular profiles using bronchoscopy with radial endobronchial ultrasound guidance in patients with advanced NSCLC remain unclear. Hence, we aimed to compare the diagnostic yields and ability for molecular analyses of rebiopsies with those of initial biopsies.
Methods
We investigated 301 patients with advanced non-Sq NSCLC who underwent radial endobronchial ultrasound-guided transbronchial biopsy (TBB) for peripheral pulmonary lesions (PPLs) between August 2014 and July 2017. Patients were divided into the rebiopsy and initial biopsy groups: the latter referred to the biopsy that determined the definitive diagnosis. The diagnostic yields and ability for molecular analyses were compared between the two groups, and the factors affecting the TBB diagnostic yield were identified using univariate and multivariate analyses.
Results
The diagnostic yields of the rebiopsy and initial biopsy groups were comparable (86.8 and 90.8%, respectively; p = 0.287). Furthermore, 93.0 and 94.0% of the patients in the rebiopsy and initial biopsy groups, respectively, had adequate specimens for gene profiling and mutational analysis (p = 0.765). The factors that increased the diagnostic yield were a positive bronchus sign (p < 0.001) and tumour location within the internal two-thirds of the lungs (p = 0.026).
Conclusions
The PPL diagnostic yield of the rebiopsy group was as high as that of the initial biopsy group. Hence, TBB for PPLs is feasible for patients requiring rebiopsy as well as for those with initial diagnoses. Adequate, high-quality biopsy specimens can be obtained by transbronchial rebiopsy for molecular testing.
Hinweise
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Abkürzungen
Non-Sq NSCLC
Non-squamous non-small cell lung cancer
TPS
Tumour proportion score
PD-L1
Programmed cell death ligand 1
EGFR
Epidermal growth factor receptor
ALK
Anaplastic lymphoma kinase
ROS1
ROS proto-oncogene 1
BRAF
B-Raf proto-oncogene
TKIs
Tyrosine kinase inhibitors
NGS
Next-generation sequencing
TBB
Transbronchial biopsy
R-EBUS
Radial endobronchial ultrasound
PPLs
Peripheral pulmonary lesions
GS
Guide-sheath
Background
Lung cancer is the leading cause of mortality worldwide [1, 2]. Cytotoxic chemotherapies such as platinum-based regimens have been the primary therapeutic option for advanced non-small cell lung cancer (NSCLC) [3]. However, recently developed molecular targeted therapies and immune checkpoint inhibitors have improved the survival of patients with corresponding gene mutations or a sufficiently high tumour proportion score (TPS) for programmed cell death ligand 1 (PD-L1) [4, 5]. Targeted therapies directed at tumour cells harbouring epidermal growth factor receptor (EGFR) gene mutations, anaplastic lymphoma kinase (ALK) gene rearrangements, ROS proto-oncogene 1 (ROS1) gene fusions, and B-Raf proto-oncogene (BRAF) gene mutations have produced impressive results [6‐9]. One of the mechanisms underlying the resistance to EGFR tyrosine kinase inhibitors (EGFR-TKIs) is the threonine-to-methionine amino acid change at position 790 (i.e. T790M mutation) [10, 11]. The efficacy of osimertinib in T790M-positive patients with advanced NSCLC who experienced disease progression after receiving the first-line EGFR-TKI therapy was demonstrated in the AURA3 clinical trial [12]. However, a rebiopsy is required for detecting the T790M mutation in such patients [11, 13].
With the development of more advanced examination techniques, clinicians are employing novel diagnostic tests based on the individual’s genetics profile, other molecular mechanisms, and the TPS to establish a more personalised targeted therapy [14]. Next-generation sequencing (NGS) has been introduced to detect almost all the relevant gene mutations in patients with cancer in clinical practice [15, 16]; however, this procedure also requires obtaining adequate, high-quality biopsy specimens.
Anzeige
Rebiopsy in patients with non-squamous (non-Sq) NSCLC is important when selecting the subsequent lines of chemotherapeutic agents, EGFR-TKIs, or immune checkpoint inhibitors if their initial treatments are no longer effective. Previous studies have been performed to investigate rebiopsies for T790M analysis [17‐20]; however, the differences between rebiopsy and initial biopsy in terms of diagnostic yields and their ability to test the molecular profiles using bronchoscopy with radial endobronchial ultrasound (R-EBUS) guidance have not yet been explored. Thus, this study aimed to compare the diagnostic yields obtained from rebiopsy to those obtained from initial biopsy (first diagnosis) and their ability to test the molecular profiles by means of bronchoscopy with R-EBUS guidance.
Methods
Patient selection
Data of consecutive patients who underwent R-EBUS-guided transbronchial biopsy (TBB) for peripheral pulmonary lesions (PPLs) at the National Cancer Center Hospital between August 2014 and July 2017 were reviewed. All patients with advanced non-Sq NSCLC were included in this study and were divided into a) the rebiopsy group (i.e. those who underwent repeat biopsies after receiving drug treatments) and b) the initial biopsy group (i.e. those who only had one biopsy for definitive diagnosis before receiving any treatments).
The clinical characteristics of the patients including age at the time of biopsy, sex, tumour size, location, and morphology (solid or part-solid), presence of bronchus sign, and visibility on chest radiography were recorded. The diagnostic yields and ability to test the molecular profiles were compared between the two groups; moreover, the factors affecting the diagnostic yield of TBB were identified using univariate and multivariate analyses. This study was approved by the National Cancer Center Institutional Review Board (no. 2018–090), and written informed consent was obtained from all patients.
Bronchoscopy procedures
All bronchoscopy procedures were performed via the oral route under local anaesthesia. TBB procedures were carried out using any one of the following conventional flexible bronchoscopes (Olympus Ltd.): BF-1 T260, BF-260, BFP260, BF-F260, BF-1TQ290, BF-Q290, BF-P290, LF-TP, or BF-Y0053 [21]. A radial ultrasound probe (UM-S20-20R or UM-S20-17S; Olympus, Tokyo, Japan) was used in all cases; a guide-sheath (GS) kit (K-201 or K-203; Olympus Ltd., Tokyo, Japan) was used when warranted. A virtual bronchoscope was constructed using a workstation (Ziostation2; Ziosoft Ltd., Tokyo, Japan) to simulate the bronchial route that leads to the target PPLs [22]. A PPL was defined as an abnormal growth surrounded by the normal lung parenchyma that was not accessible with a conventional bronchoscope. Upon reaching the target bronchus, which leads to the PPL, the R-EBUS probe with or without a GS was inserted through the working channel of the bronchoscope and advanced towards the PPL under fluoroscopic guidance (VersiFlex VISTAVR; Hitachi Ltd., Tokyo, Japan). Ultrasonographic scanning was performed while manipulating the R-EBUS probe until the lesion was localised within the corresponding R-EBUS image. X-ray fluoroscopy (VersiFlex VISTA, Hitachi, Japan) was used in all cases to guide the insertion of the R-EBUS probe regardless of PPL visibility on chest radiography. The bronchus sign on computed tomography was defined as the presence of a bronchus leading directly to the PPL. Five or more specimens were collected from the patients as possible. The number of TBB specimens obtained from all cases was counted.
Anzeige
Pathologic evaluation and mutational analysis
A positive diagnostic result obtained by TBB was defined as the identification of non-Sq NSCLC based on the histological and cytological features. The overall detection rate was determined on the basis of a positive diagnosis via histology and/or cytology.
EGFR mutation analyses of genomic DNA extracted from the tumour samples were performed using the Scorpion amplification-refractory mutation system. Additionally, the ALK rearrangements were analysed using immunohistochemistry (ALK iAEP® Nichirei Biosciences Inc., Tokyo, Japan) and fluorescence in situ hybridization (Vysis®, Abbott Laboratories, Abbott Park, IL, USA).
Statistical analysis
The correlations between patient characteristics and biopsy success rate were analysed using the Fisher’s exact test for categorical variables. The comparison of R-EBUS detection rate between the two groups were analysed using a chi-squared test. A multivariate analysis using logistic regression was performed to determine the factors affecting the yield, although age and sex were excluded from the factors affecting the diagnostic yield. All tests were two sided, and a p value of < 0.05 was considered significant. All of the statistical analyses were conducted using the JMP 10 software (SAS Institute, Inc., Cary, NC, USA).
Results
A total of 1763 patients underwent R-EBUS-guided bronchoscopy procedures for PPLs during the study period: among them, 301 were diagnosed with advanced non-Sq NSCLC. At least three specimens were taken from all patients. Five or more specimens were collected from 89.9% of the patients in the rebiopsy group and from 88.3% of those in the initial biopsy group.
The rebiopsy and initial biopsy groups comprised 106 and 195 patients, respectively; their characteristics are listed in Table 1, and a flowchart of the study process is shown in Fig. 1. There were significant differences in the median ages of patients in the rebiopsy and initial biopsy groups (64 [range, 57–69] years vs. 68 [range, 59–75] years, p = 0.001) as well as sex (males, 38.7% vs. 53.8%, p = 0.012) and distance from the costal pleura (mm) (≥ 10.0, 44.3% vs. 31.8%, p = 0.031). No other significant differences were observed between the two groups, including tumour sizes, locations, and features, presence of bronchus sign, and visibility on chest radiography.
Table 1
Summary of patients’ clinical characteristics (n = 301).
Variables
Rebiopsy
n = 106
Initial biopsy n = 195
p-value
Age, median (IQR)
64 (57–69)
68 (59–75)
0.001
Sex, no (%)
0.012
Male
41 (38.7)
105 (53.8)
Female
65 (61.3)
90 (46.2)
Lobe, no (%)
0.077
Upper
42 (39.6)
101 (51.8)
Middle/Lingular
21 (19.8)
24 (12.3)
Lower
43 (40.6)
70 (35.9)
Location, no (%)
0.077
Internal 2/3
73 (68.9)
102 (52.3)
External 1/3
33 (31.1)
93 (47.7)
Distance from costal pleura (mm), no (%)
0.031
≥ 10.0
47 (44.3)
62 (31.8)
< 10.0
39 (55.7)
133 (68.2)
Size (mm), no (%)
0.845
≥ 30.0
74 (69.8)
134 (68.7)
< 30.0
32 (30.2)
61 (31.3)
Morphology, no (%)
0.053
Solid
79 (74.5)
124 (63.6)
Part-solid
27 (25.5)
71 (36.4)
Bronchus sign, no (%)
0.166
Positive
94 (88.7)
182 (93.3)
Negative
12 (11.3)
13 (6.7)
Visibility on chest radiography, no (%)
0.229
Visible
100 (95.2)
171 (91.4)
Invisible
6 (4.8)
24 (8.6)
IQR, interquartile range.
Fig. 1
Flowchart of the study. The rebiopsy and initial biopsy groups were extracted and analysed according to the flowchart. *Failure, failed to pathological diagnosis; †Success, succeeded in pathological diagnosis; ‡Due to clinical trial, the purpose of biopsy was to collect specimens for the registration of clinical trials; NSCLC, non-small cell lung cancer; SCLC, small cell lung cancer; Sq, squamous; TBB, transbronchial biopsy
×
There was no significant difference between the rebiopsy and initial biopsy groups in terms of diagnostic yield (86.8% [92/106] vs. 90.8% [177/195]; p = 0.287). Moreover, no significant differences were found between the two groups in terms of lesion detection via R-EBUS: the rates of detection “within” the image for the rebiopsy and initial biopsy groups were 75.5% (80/106) vs. 73.9% (144/195), those of “adjacent to” were 22.6% (24/106) vs. 22.0% (43/195), and those of “invisible” were 1.9% (2/106) vs. 4.1% (8/195); p = 0.592 (Table 2). The factors affecting the diagnostic yield of TBB are shown in Table 3. In the multivariate analysis, the diagnostic yield was significantly higher for those with a positive bronchus sign (p < 0.001) and for those located in the internal two-thirds of the lungs (p = 0.026). By contrast, no significant difference was observed between the two groups depending on the purpose of rebiopsy (p = 0.400).
Table 2
Summary of diagnostic yield and R-EBUS detection (n = 301)
Variables
Rebiopsy
n = 106
Initial biopsy
n = 195
p-value
Diagnostic yield, no (%)
92 (86.8)
177 (90.8)
0.287
R-EBUS detection, no (%)
0.592
Within
80 (75.5)
144 (73.9)
Adjacent to
24 (22.6)
43 (22.0)
Invisible
2 (1.9)
8 (4.1)
Table 3
Univariate and Multivariate regression analyses of factors affecting diagnostic yield.
Variables
n (%)
total 301
Univariate analysis
Multivariate analysis
p-value
p-value
Adjusted OR (95% CI)
Rebiopsy
106 (35.2)
0.287
0.400
–
Lobe
0.041
0.176
–
Upper
143 (47.5)
Middle/lingular
90 (29.9)
Lower
68 (22.6)
Size ≥30.0 mm
208 (69.1)
0.016
0.311
–
Bronchus sign positive
276 (91.7)
< 0.001
< 0.001
132.6 (30.5–990.6)
Location in the internal 2/3 segments
175 (58.1)
0.015
0.026
4.6 (1.2–24.1)
Distance from costal pleura ≥10.0 mm
109 (36.2)
0.317
0.113
–
Visible on chest radiography
271 (90.0)
0.051
0.796
–
OR, odds ratio; CI, confidence interval.
Molecular profiles were evaluated in a proportion of cases (71 in the rebiopsy group and 134 in the initial biopsy group for EGFR mutation analysis, 8 in the rebiopsy group and 123 in the initial biopsy group for ALK rearrangements analysis). Adequate tumour samples were obtained from 93.0% (66/71) rebiopsy and 94.0% (126/134) initial biopsy patients for EGFR mutation analysis (p = 0.765), and from 100% (8/8) rebiopsy and 99.1% (122/123) initial biopsy patients for ALK rearrangements analysis (p = 1.000).
Although moderate bleeding (defined as 25–100 ml of blood) rates were relatively higher in the rebiopsy group than in the initial biopsy group (3.7% vs. 2.5%), none of the patients from both groups developed severe complications.
Anzeige
Discussion
We conducted this study to compare the diagnostic yield of R-EBUS-guided TBB for PPLs between initial biopsy and rebiopsy after treatment. The diagnostic yield of R-EBUS-guided TBB in patients undergoing rebiopsy was as high as that in those undergoing initial biopsy (86.8% vs. 90.8%). In the multivariate analysis, the factors affecting the diagnostic yield of TBB were positive bronchus sign and tumour location within the internal two-thirds of the lungs. There was no significant difference between the two groups depending on the purpose of rebiopsy.
Previous investigations have found that the diagnostic yield of TBB using various modalities is approximately 70% [23‐25]. Although no study has investigated the outcomes of patients with advanced non-Sq NSCLC, our diagnostic yield of 89.4% was considered sufficient. We believe that the high within-rate of R-EBUS detection contributed to our satisfactory diagnostic yield. The particularly large sizes of the tumours observed in advanced lung cancer, the high rate of positive bronchus sign (which are associated with tumour size), and the accurate guidance provided by some typess of navigation systems (achieved using a workstation), possibly contributed to the good results of R-EBUS detection [26].
Previous studies of patients undergoing rebiopsies produced TBB diagnostic yields of 73.2–80.7% [18, 20, 27]; however, these studies had a relatively small sample size and provided information only on patients undergoing rebiopsy. To our knowledge, no previous studies have compared the diagnostic data from rebiopsies and initial biopsies. In this study, we found that the diagnostic yield in the rebiopsy group was as high as that in the initial biopsy group with no significant difference (p = 0.287).
Previous studies revealed that tumour size, a positive bronchus sign, tumour location, and R-EBUS use are all factors that influenced the diagnostic yields [23, 24, 28]. Similar results were obtained in our study, with a positive bronchus sign and a tumour location in the internal two-thirds of the lungs producing higher diagnostic yields; moreover, a rebiopsy did not produce a significantly different diagnostic yield compared with an initial biopsy. Although rebiopsies are considered more difficult to perform than initial biopsies because of the increased tumour stiffness and haemorrhaging due to the administration of anticancer treatments, our results were not surprising because we used R-EBUS in all patients together with GS in those prone to bleeding. Wedging the GS in the target bronchus might help stop the bleeding after TBB [21]. Moreover, we used 30 mm as the cut-off tumour size as majority of the tumours were larger than the upper limit of T1 factor; the median length was 38 mm.
Anzeige
Two previous studies that investigated the feasibility of mutation analyses in rebiopsy specimens found that adequate tissue samples for mutational analyses were obtained from 74.4 and 89.7% of patients who underwent rebiopsies, respectively; the proportions of patients undergoing TBB for rebiopsy were 52 and 28%, respectively [29, 30]. In our study, 93.0% of successfully diagnosed patients in the rebiopsy group yielded adequate specimens for mutational analysis, while 94.0% in the initial biopsy group; the difference was not significant (p = 0.765). The high rate of successful mutational analyses in our study is likely related to the relatively large number of specimens obtained; at least five specimens were collected from 89.8% of the patients in the rebiopsy group and from 88.3% of those in the initial biopsy group.
Based on the results of the FLAURA trial, which demonstrated the efficacy of osimertinib as a first-line treatment for patients with EGFR mutation-positive NSCLC, this agent can be administered as a first-line therapy to eligible patients without requiring T790M mutation analysis beforehand [31]. However, many patients receiving first- and second-generation EGFR-TKIs will require rebiopsies when their cancers acquire resistance. Additionally, a rebiopsy is necessary not only for patients with EGFR mutation-positive NSCLC to detect T790M, but also for analysing ALK rearrangement, PD-L1 TPS, and aberrations in BRAF and ROS1, and to detect other genes including using NGS.
The collection of pathological specimens upon tumour progression following treatment with previous regimens can assist in understanding resistance mechanisms [32, 33]. Furthermore, new genomic mutations are continuously revealed along with the novel treatments that target them. Thus, rebiopsy still plays an important role in decision-making concerning subsequent-line treatments for patients with NSCLC. TBB is well-established as a minimally invasive method for lung biopsy, including rebiopsy.
This study has some limitations. First, the study was of a retrospective in nature. Second, the data were obtained from patients at a single institution that is specialises in cancer treatment. Third, the reasons for performing biopsies were multifactorial, in contrast to those in clinical trials where biopsies have a common purpose such as T790M detection or TPS evaluation. Hence, the assessments of mutations and of TPS were unsystematic. In addition, NGS had not been evaluated in all cases. However, selection bias was minimal, as this study reflects real-life clinical situations.
Anzeige
Conclusions
The data from diagnostic bronchoscopic rebiopsies were comparable to those from initial biopsies. TBB for PPLs is a good an option for patients requiring rebiopsy as well as those requiring initial diagnostic biopsy. Adequate, high-quality biopsy specimens can be obtained by transbronchial rebiopsy for molecular testing.
Acknowledgements
We would like to thank Editage (www.editage.jp) for English language editing.
Ethics approval and consent to participate
This study was approved by the National Cancer Center Institutional Review Board, and the requirement for informed consent was waived due to the retrospective observational nature (No. 2018–090).
Consent for publication
Not applicable.
Competing interests
The authors have no conflicts of interest to declare.
Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
