|Year : 2019 | Volume
| Issue : 2 | Page : 55-60
Comparative assessment of conventional chromosomal analysis and fluorescence in situ hybridization in the evaluation of suspected myelodysplastic syndromes: A single institution experience
Denyo Adjoa Zakhia1, Olga Voronel1, Feras Zaiem1, Kunil Raval1, Jay Yang2, Deborah Schloff3, Anwar N Mohamed3, Ali M Gabali1
1 Division of Hematopathology, Barbara Ann Karmanos Center and Wayne State University School of Medicine, Detroit, MI, USA
2 Division of Hematology/Oncology, Barbara Ann Karmanos Center and Wayne State University School of Medicine, Detroit, MI, USA
3 Division of Cytogenetics, Wayne State University, Detroit, Michigan, USA
|Date of Web Publication||8-Apr-2019|
Dr. Ali M Gabali
3990, John R Street, Detroit, Michigan 48201
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Background: Myelodysplastic syndromes (MDSs) are a heterogeneous group of clonal hematopoietic neoplasms, roughly half of which harbor cytogenetic abnormalities with diagnostic, prognostic, and therapeutic significance. Fluorescence in situ hybridization (FISH) for the most commonly seen abnormalities (5/5q, –7/7q, +8, and –20/20q–) is routinely performed alongside conventional cytogenetics (CC) in the evaluation of suspected MDS despite conflicting reports of its relative contribution compared to CC alone.Objectives: To assess the additional diagnostic and prognostic value of performing concurrent FISH versus CC alone in cases of suspected MDS.Materials and Methods: A total of 127 bone marrow samples submitted to our cytogenetic laboratory with a presumptive diagnosis of MDS were evaluated by concurrent CC and an MDS FISH panel.Results: CC was used as the gold standard method with 100% sensitivity in detecting suspected MDS-associated cytogenetic abnormalities. FISH alone had a sensitivity of 76%, whereas CC alone achieved a sensitivity of 97%. The addition of FISH did not change the diagnosis nor change the Revised International Prognostic Scoring System score in any patient. Moreover, in 12 cases identified as positive by both CC and FISH, CC identified multiple chromosomal aberrations of clinical significance not interrogated by the FISH probe panel.Conclusion: CC alone is sufficiently sensitive in detecting suspected MDS-associated cytogenetic abnormalities that influence clinical decision-making. Routine FISH testing does not provide a significant increase in test sensitivity when an adequate karyotype is obtained. Therefore, FISH testing is best reserved for suspected MDS cases lacking sufficient metaphases.
Keywords: Chromosomal analysis, fluorescence in situ hybridization, karyotype, myelodysplastic syndrome
|How to cite this article:|
Zakhia DA, Voronel O, Zaiem F, Raval K, Yang J, Schloff D, Mohamed AN, Gabali AM. Comparative assessment of conventional chromosomal analysis and fluorescence in situ hybridization in the evaluation of suspected myelodysplastic syndromes: A single institution experience. Avicenna J Med 2019;9:55-60
|How to cite this URL:|
Zakhia DA, Voronel O, Zaiem F, Raval K, Yang J, Schloff D, Mohamed AN, Gabali AM. Comparative assessment of conventional chromosomal analysis and fluorescence in situ hybridization in the evaluation of suspected myelodysplastic syndromes: A single institution experience. Avicenna J Med [serial online] 2019 [cited 2020 Jan 23];9:55-60. Available from: http://www.avicennajmed.com/text.asp?2019/9/2/55/254474
| Introduction|| |
Myelodysplastic syndromes (MDSs) are a group of clonal hematopoietic neoplasms characterized by ineffective hematopoiesis manifested by morphologic dysplasia, cytopenias, and increased risk of acute myeloid leukemia (AML). Roughly half of the patients with MDS harbor cytogenetic abnormalities, a feature that carries diagnostic, prognostic, and therapeutic significance. Cytogenetic abnormalities are disease defining in some cases and are an integral component of the Revised International Prognostic Scoring System (IPSS-R), which is predictive of overall survival and progression to AML [Table 1]., In the case of an isolated del(5q), the presence of this abnormality defines a specific MDS subtype and predicts favorable response to lenalidomide., At this time, the only curative therapy is allogeneic stem cell transplantation, in which cytogenetic risk subgroup has been found to be the most important variable in predicting event-free survival.,
|Table 1: Revised International Prognostic Scoring System (IPSS-R) cytogenetic categories|
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The importance of accurate cytogenetic data in MDS is well established with conventional cytogenetics (CC) (karyotyping) firmly entrenched as the gold standard methodology. However, CC is a labor-intensive process, which is dependent on the malignant clone’s propensity to divide in culture with analysis limited to a small number of cells (usually no more than 25). In addition, adequate interpretation can be limited by inadequate chromosome spreading and poor quality banding. The addition of interphase fluorescence in situ hybridization (FISH) has permitted more rapid quantitative detection of specific genetic alterations in large numbers of non-mitotic cells. In particular, the most common chromosomal abnormalities in MDS, –5/5q, –7/7q, +8, and del(20q), are now routinely tested by FISH, often in parallel with CC. FISH, however, can only detect the presence or absence of the specific chromosomal abnormalities for which the probe is intended to detect, whereas CC offers an unbiased analysis of chromosomal number and structure. Several studies evaluating the added value of FISH to CC have generated mixed results.,,,,,,,,,, In this study, we evaluated 127 patients with a presumptive diagnosis of MDS using CC and FISH to assess the additional diagnostic and prognostic yield over conventional karyotyping alone.
| Materials and methods|| |
Patient samples and diagnosis
One hundred and thirty-five bone marrow aspirates collected from 63 female and 72 male patients submitted to the cytogenetic laboratory at Detroit Medical Center University Laboratories with a presumptive diagnosis of MDS between 2010 and 2012 were retrospectively identified and selected for this study. The inclusion criteria consisted of patients with at least one persistent cytopenia and clinical suspicion of MDS after exclusion of nutritional and elemental deficiencies, toxins/drugs, autoimmune diseases, congenital disorders, infections, and other neoplastic conditions. Comprehensive evaluation of the electronic medical record, peripheral blood smear, and aspirate/biopsy material was performed by an experienced board-certified hematopathologist. Concurrent, CC analysis and MDS FISH panel were performed on all cases independent of the morphologic assessment.
Bone marrow aspirates were cultured without mitogens for 24h, followed by 48h in 10% conditioned medium. G-banding was performed using the Giemsa–trypsin–Leishman banding technique. Metaphase cells from unstimulated culture were examined and karyotype was defined in accordance with the International System for Human Cytogenetic Nomenclature (ISCN) on 20 metaphase cells per patient.
FISH was performed on all cases using the MDS panel DNA probes that included D5S23:D5S721/5p15.2, EGR1/5q31, D7Z1/CEP-7, D7S486/7q31, D8Z2/CEP-8, and D20S108/20q12. All FISH probes were purchased from Abbott Molecular, Downers Grove IL, USA. 200 interphase cells were examined for each probe to detect –5/5q, –7/7q, +8, and del(20q): 5p15.2 (LSI D5S23), 5q31 (LSI EGR1) (6%), CEP 7, 7q31 (LSI D7S486) (4.4%), CEP 8 (2.3%), and 20q12 (LSI D20S108) (5.7%). Cutoff values, as listed in parentheses, were determined using data from at least 10 normal patients to calculate false-positive cells using a binomial statistical formula to project the upper boundary of the 95th percentile (Standard Cumulative Beta Distribution). An experienced cytotechnologist blinded to the karyotypes analyzed 200 interphase nuclei per case without computer assistance. Results were reported using 2009 ISCN.
| Results|| |
Bone marrow samples from 127 patients with presumptive MDS were analyzed by both metaphase CC and interphase FISH. The patients included 64 males and 63 females with a median age of 64 years (ranging from 4 to 91 years).
FISH and CC results were concordant in 117 patients (117/127; 92%). A tabulation of the concordant/discrepant results is shown in [Table 2]. Eighty-nine patients (89/127; 70%) showed normal karyotypes with no abnormalities detected by FISH. In 28 patients (28/127; 22%), CC revealed clonal abnormalities and abnormal results for at least one FISH probe. The most common FISH abnormality was deletion 5q observed in 13 patients, followed by monosomy 7 in 9 patients, deletion 20q in 8 patients, trisomy 8 in 6 patients, as well as 2 patients each with monosomy 5 and deletion 7q. All of these FISH abnormalities were also detected by CC. Of the 28 patients with abnormalities detected both by FISH and CC, eight were diagnosed with MDS with multilineage dysplasia (MDS-MLD); seven with MDS with excess blasts (MDS-EB); three each with therapy-related MDS (TR-MDS); and AML with myelodysplasia-related changes (AML-MRC); and two cases each with chronic myelomonocytic leukemia (CMML), MDS with isolated deletion (5q), and refractory cytopenia of childhood. One patient showed no morphologic evidence of myelodysplasia or other diagnostic abnormality on bone marrow morphologic evaluation. Details of these clonal defects are summarized in [Table 3]. Among the patients with abnormalities detected by both FISH and CC, additional chromosomal abnormalities including rings, deletions, translocations, inversions, and markers were observed in 15 of the 28 samples (54%), including 12 cases in which the additional/complex abnormalities altered the IPSS-R cytogenetic risk category. Three of these twelve cases with complex karyotypes showed only del(5q) by FISH.
|Table 2: Summary of fluorescence in situ hybridization and conventional chromosomal analysis|
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|Table 3: Summary of 28 patients with abnormal findings on fluorescence in situ hybridization and conventional chromosomal analysis|
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Discordant results between CC and FISH were seen in 10 (10/127; 8%) patients. Nine (9/127; 7%) of those patients were found to have clonal abnormalities by CC with no abnormal findings on FISH. The findings in these patients are summarized in [Table 4]. The discrepancies included four patients with MDS-MLD, one patient with MDS with single lineage dysplasia (MDS-SLD), one patient with MDS-EB, and three patients who showed no evidence of myelodysplasia on bone marrow morphologic evaluation. Loss of chromosome Y was observed in the three morphologically normal patients including one patient with trisomy 14 in addition to –Y. In one (1/127; 0.8%) case of cytogenetically normal MDS-MLD, FISH detected an additional fragment (marker) of chromosome 8 interpreted as a trisomy. On reviewing the CC data, this fragment was identified post hoc and was missed during the initial analysis because of its small size.
|Table 4: Summary of nine patients with normal fluorescence in situ hybridization and abnormal karyotype|
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| Discussion|| |
The identification of cytogenetic abnormalities is of vital importance in the diagnosis, prognosis, and therapeutic decision-making for patients with MDS. The gold standard remains CC, which, under ideal conditions, detects a wide variety of numerical and structural aberrations associated with myeloid malignancy. FISH has emerged as an alternative method of evaluating nondividing (interphase) nuclei for targeted diagnostic and prognostic abnormalities and is particularly useful as a complementary method to detect cryptic genetic abnormalities and small clones that may otherwise fall below the limit of detection of conventional karyotyping. Published studies offer conflicting reports about the added benefit of FISH over CC in patients with MDS. In this study, we compared FISH and CC findings in 127 patients with presumptive MDS, evaluating the concordance/discordance between the two methods and assessing the impact of using both modalities in accurately diagnosing and risk-stratifying patients as opposed to conventional karyotyping alone.
Several studies have suggested a significant role for FISH analysis, especially in chromosomally normal patients with MDS/AML.,, In a study of 57 chromosomally normal patients with MDS, Bernasconi et al. detected occult chromosomal abnormalities by FISH in 15% of patients, resulting in a change in IPSS for five of the nine patients. Furthermore, FISH positivity was associated with an eightfold increase in progression to advanced MDS or AML. These findings were corroborated by Rigolin et al. whose analysis of 101 consecutive patients of MDS with normal karyotypes found occult chromosomal abnormalities by FISH in 18 patients (17.8%) and were associated with higher risk disease and worse outcomes as compared to FISH-negative patients. Of note, a third of the FISH-positive patients showed trisomy 8—a chromosomal abnormality—that is no longer considered disease defining, though remains part of the IPSS-R cytogenetic risk stratification schema. Romeo et al. similarly found that FISH testing conferred a benefit to 4/40 patients (10%) by identifying cytogenetic abnormalities in three patients with normal karyotypes and one patient with no harvestable metaphases for CC.
Other studies, however, have found only a modest benefit to using complementary FISH in patients with MDS. For instance, Beyer et al. investigated 110 patients with AML and high-risk MDS using probes directed at chromosomes 5, 7, and 8 and found discordance between CC and FISH in only 7.3% of patients, concluding that the primary use of FISH in these cases was to increase the resolution of CC by identifying marker chromosomes and breakpoints as well as detecting minor clones with chromosome 8 aneuploidy. Cherry et al. reiterated the superiority of CC over FISH in a study of patients with predominantly low-risk MDS in which CC and FISH results (probes for –5/5q–, –7/7q–, +8, 11q23 abnormalities, 13q–, and 20q–) were concordant in 46 of 48 patients with an occult 11q abnormality detected by FISH in just one of the 30 cytogenetically normal patients (3.3%). Similar results were obtained by Ketterling et al. who tested a wider array of probes by both interphase and metaphase FISH and detected an occult abnormality in just one of the 32 cytogenetically normal patients. More recent studies by Pitchford et al. and Costa et al. have found concordance rates of >99% when adequate high-quality karyotypes can be obtained, asserting that FISH does not confer additional value in those cases. Pitchford et al. further concluded that restricting FISH testing to those patients without adequate karyotypes could generate more savings along with 8.7 weeks of cytotechnologist time in their institution alone. This limited approach is endorsed by He et al. after evaluating 505 patients with possible MDS and finding that FISH results had no diagnostic and only minimal prognostic impact when ≥20 metaphases were analyzed by CC.
Our findings align with the latter group with a very low rate of occult FISH abnormalities in our cohort (1/127; 0.8%), very similar to that of Pitchford et al. Although the concordance rate was high (92%), CC yielded additional and potentially clinically meaningful results. Among the concordant cases, CC detected a complex karyotype in 12% (14/117). Four of these patients were found to only have del(5q) or del(20q) by FISH, which, in the absence of other karyotypic findings, would incorrectly classify these patients into a more favorable prognostic category. Furthermore, CC was able to detect additional chromosomal abnormalities including rings, deletions, translocations, inversion, and markers in the majority (15/28; 54%) of FISH-positive cases. The superiority of CC was also shown among the 10 discordant cases, 9 of which showed clonal abnormalities by CC but were negative by FISH. A single patient was found to have trisomy 8 by FISH with normal CC accounting for 1% of the cytogenetically normal patient cohort, although this additional finding would not have changed the diagnosis or the IPSS-R in this patient.
The discrepancies seen among studies may be at least partially explained by the variability of cutoff values used to assess FISH positivity. The highest discordance rates appear in studies with the lowest cutoff values. In addition, the experience and expertise of the individual cytogenetic laboratories and their personnel may vary between institutions. Our experience suggests that cytotechnologist selection and spreading bias of metaphase nuclei may result in missing undetected aneuploidies, complex metaphases with overlapping chromosomes, and small abnormal clones. Finally, our study largely analyzed cases in which at least 20 metaphases were cultured. FISH may have use in cases in which no metaphases or less than 20 metaphases were available for analysis.
| Conclusion|| |
In conclusion, our data confirm the superiority of CC to FISH in the initial cytogenetic analysis of MDS cases. These findings contribute to the growing body of evidence that FISH should not be used to replace cytogenetic analysis. In addition, FISH does not add significant diagnostic or prognostic value in the setting of an adequate karyotype by CC. FISH can be a valuable complementary tool to identify marker chromosomes and breakpoints in patients with karyotypically abnormal MDS as well as to unmask minor clones with aneuploidy of chromosome 8, once a diagnosis has been established. We recommend that FISH not be routinely performed in the initial diagnostic workup of suspected MDS unless an adequate karyotype cannot be obtained.
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Conflicts of interest
There are no conflicts of interest.
| References|| |
Haase D. Cytogenetic features in myelodysplastic syndromes. Ann Hematol 2008;87:515-26.
Arber DA, Orazi A, Hasserjian R, Thiele J, Borowitz MJ, Le Beau MM, et al
. The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia. Blood 2016;127:2391-405.
Greenberg PL, Tuechler H, Schanz J, Sanz G, Garcia-Manero G, Solé F, et al
. Revised international prognostic scoring system for myelodysplastic syndromes. Blood 2012;120:2454-65.
Bejar R, Steensma DP. Recent developments in myelodysplastic syndromes. Blood 2014;124:2793-803.
Nevill TJ, Fung HC, Shepherd JD, Horsman DE, Nantel SH, Klingemann HG, et al
. Cytogenetic abnormalities in primary myelodysplastic syndrome are highly predictive of outcome after allogeneic bone marrow transplantation. Blood 1998;92:1910-7.
de Witte T, Oosterveld M, Muus P. Autologous and allogeneic stem cell transplantation for myelodysplastic syndrome. Blood Rev 2007;21:49-59.
Arif M, Tanaka K, Damodaran C, Asou H, Kyo T, Dohy H, et al
. Hidden monosomy 7 in acute myeloid leukemia and myelodysplastic syndrome detected by interphase fluorescence in situ
hybridization. Leuk Res 1996;20:709-16.
Brizard F, Brizard A, Guilhot F, Tanzer J, Berger R. Detection of monosomy 7 and trisomies 8 and 11 in myelodysplastic disorders by interphase fluorescent in situ
hybridization. Comparison with acute non-lymphocytic leukemias. Leukemia 1994;8:1005-11.
Bernasconi P, Cavigliano PM, Boni M, Calatroni S, Klersy C, Giardini I, et al
. Is FISH a relevant prognostic tool in myelodysplastic syndromes with a normal chromosome pattern on conventional cytogenetics? A study on 57 patients. Leukemia 2003;17:2107-12.
Rigolin GM, Bigoni R, Milani R, Cavazzini F, Roberti MG, Bardi A, et al
. Clinical importance of interphase cytogenetics detecting occult chromosome lesions in myelodysplastic syndromes with normal karyotype. Leukemia 2001;15:1841-7.
Romeo M, Chauffaille Mde L, Silva MR, Bahia DM, Kerbauy J. Comparison of cytogenetics with FISH in 40 myelodysplastic syndrome patients. Leuk Res 2002;26:993-6.
Beyer V, Castagné C, Mühlematter D, Parlier V, Gmür J, Hess U, et al
. Systematic screening at diagnosis of -5/del(5)(q31), -7, or chromosome 8 aneuploidy by interphase fluorescence in situ
hybridization in 110 acute myelocytic leukemia and high-risk myelodysplastic syndrome patients: Concordances and discrepancies with conventional cytogenetics. Cancer Genet Cytogenet 2004;152:29-41.
Cherry AM, Brockman SR, Paternoster SF, Hicks GA, Neuberg D, Higgins RR, et al
. Comparison of interphase FISH and metaphase cytogenetics to study myelodysplastic syndrome: An Eastern Cooperative Oncology Group (ECOG) study. Leuk Res 2003;27:1085-90.
Ketterling RP, Wyatt WA, VanWier SA, Law M, Hodnefield JM, Hanson CA, et al
. Primary myelodysplastic syndrome with normal cytogenetics: Utility of ‘FISH panel testing’ and M-FISH. Leuk Res 2002;26:235-40.
Pitchford CW, Hettinga AC, Reichard KK. Fluorescence in situ
hybridization testing for -5/5q, -7/7q, +8, and del(20q) in primary myelodysplastic syndrome correlates with conventional cytogenetics in the setting of an adequate study. Am J Clin Pathol 2010;133:260-4.
Costa D, Valera S, Carrió A, Arias A, Muñoz C, Rozman M, et al
. Do we need to do fluorescence in situ
hybridization analysis in myelodysplastic syndromes as often as we do? Leuk Res 2010;34:1437-41.
He R, Wiktor AE, Durnick DK, Kurtin PJ, Van Dyke DL, Tefferi A, et al
. Bone marrow conventional karyotyping and fluorescence in situ
hybridization: Defining an effective utilization strategy for evaluation of myelodysplastic syndromes. Am J Clin Pathol 2016;146:86-94.
[Table 1], [Table 2], [Table 3], [Table 4]