4th Palermo Conference on INNOVATIVE THERAPIES FOR LYMPHOID MALIGNANCIES
Published online 1 December 2009
Haematologica, Vol 94, Issue 12, 1708-1713 doi:10.3324/haematol.2009.011064
Copyright © 2009 by Ferrata Storti Foundation
This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Google Scholar
Right arrow Articles by Chiecchio, L.
PubMed
Right arrow PubMed Citation
Right arrow Articles by Chiecchio, L.

Monoclonal Gammopathies

Timing of acquisition of deletion 13 in plasma cell dyscrasias is dependent on genetic context

Laura Chiecchio1, Gian Paolo Dagrada1, Ashraf H. Ibrahim1, Elizabet Dachs Cabanas1, Rebecca K.M. Protheroe1, David M. Stockley1, Kim H. Orchard2,3, Nicholas C.P. Cross1, Christine J. Harrison4, Fiona M. Ross1 on behalf of the UK Myeloma Forum

1 Leukaemia Research Fund UK Myeloma Forum Cytogenetics Group, Human Genetics Division, University of Southampton, Wessex Regional Genetics Laboratory, Salisbury District Hospital, Salisbury, Wilts
2 Department of Haematology, Southampton University Hospital NHS Trust, Southampton General Hospital, Southampton
3 Cancer Sciences Division, University of Southampton, Southampton
4 Leukaemia Research Cytogenetics Group, Northern Institute for Cancer Research, Newcastle University, Newcastle-upon-Tyne, UK

Correspondence: Laura Chiecchio, Myeloma Cytogenetics Group, Wessex Regional Genetics Laboratory, Salisbury District Hospital, Salisbury, Wilts SP2 8BJ, UK. E-mail: laura.chiecchio{at}salisbury.nhs.uk


arrow
ABSTRACT
TOP
 ABSTRACT
Introduction
 Design and Methods
 Results
 Discussion
 References
 
Background: Multiple myeloma, monoclonal gammopathy of undetermined significance and smoldering multiple myeloma harbor common chromosomal abnormalities but the prevalence and relative association of aberrations in these diagnostic groups remains controversial. We investigated these aspects in a large series of patients.

Design and Methods: Chromosome 13 deletion ({Delta}13), deletion of TP53, ploidy status and immunoglobulin heavy chain (IgH) translocations were evaluated by fluorescence in situ hybridization in patients with monoclonal gammopathy of undetermined significance (n=189), smoldering multiple myeloma (n=127) and multiple myeloma (n=400).

Results: Overall, {Delta}13 (25%, 34% and 47%), 16q23 deletions (6%, 8% and 21%) and 17p13 deletions (3%, 1% and 10%) were less frequent in patients with monoclonal gammopathy of undetermined significance and smoldering multiple myeloma than in those with multiple myeloma. When distinct genetic groups were considered, no differences in the prevalence of {Delta}13 were found with t(4;14)(p16;q32) and t(14;16)(q32;q23) among the three diagnostic groups; in contrast {Delta}13 was rarer in t(11;14)(q13;q32) in patients with monoclonal gammopathy (1/28) and smoldering myeloma (2/13) than in those with multiple myeloma (40%). Similar results were seen for the few t(6;14)(p21;q32) cases: 0/3 patients with monoclonal gammopathy or smoldering myeloma had the {Delta}13, whereas 4/6 (67%) patients with multiple myeloma and this translocation also had the deletion. In multiple myeloma patients with both an IgH translocation and {Delta}13, the proportions of cells affected by the two abnormalities were similar, as was the case for t(4;14) and t(14;16) monoclonal gammopathy patients positive for {Delta}13. In contrast, in monoclonal gammopathy patients with t(14;20)(q32;q11), the translocation was present in almost all cells, while the {Delta}13 was present in only a sub-population.

Conclusions: These results indicate that the presence and time of occurrence of {Delta}13 depends on the presence of specific concurrent abnormalities. The observation that {Delta}13 was extremely rare in monoclonal gammopathy of undetermined significance and smoldering multiple myeloma with translocations directly involving cyclin D genes (CCND1 and CCND3) suggest a possible role of {Delta}13 in the progression of the disease specifically in these genetic sub-groups. (clinicaltrials.gov identifier: ISRCTN 68454111; UKCRN ID 1176).

Key words: deletion 13, plasma cell dyscrasias, genetic context.


arrow
Introduction
TOP
 ABSTRACT
 Introduction
Design and Methods
 Results
 Discussion
 References
 
Monoclonal gammopathy of undetermined significance (MGUS) and smoldering multiple myeloma (SMM) are characterized by an expansion of monoclonal plasma cells and both can progress to symptomatic multiple myeloma (MM) or other related conditions.1–3 MGUS is the most frequent plasma cell disorder and its incidence increases markedly with age, reaching approximately 3% in subjects over 70 years old.1,3–5 MGUS is defined by a serum M-protein concentration of less than 30 g/L and fewer than 10% of plasma cells in the bone marrow, while patients with SMM meet the diagnostic criteria for MM but are asymptomatic. SMM resembles MGUS in that end-organ damage is absent, but clinically it is far more likely to progress to active MM or amyloidosis.3

The paucity of plasma cells within the bone marrow of patients with MGUS, together with the low proliferative capacity of these cells, has precluded significant karyotypic studies in these patients. Interphase fluorescence in situ hybridization (FISH) provides an alternative approach to investigate chromosomal aberrations in tumor cells from which metaphases are difficult to obtain. Using interphase FISH, chromosomal aberrations were consistently detected in a high proportion of MGUS patients, with roughly 50% of them carrying one of the primary IgH translocations and the remaining patients displaying a hyperdiploid karyotype. These findings suggested that ploidy status and IgH rearrangements were early events delineating different pathogenic pathways.6–9

Conflicting results have been reported on the prevalence of deletion/monosomy 13 ({Delta}13) in MGUS. Avet-Loiseau et al. found a substantially lower frequency of this abnormality in MGUS (~25%) than in MM (~50%),10,11 while others reported a similar incidence in both conditions.7,12 Fonseca et al. also indicated that when {Delta}13 was detected in MGUS it occurred in the majority of clonal plasma cells,7 consistent with that normally observed in MM,13,14 while others reported a greater heterogeneity in MGUS.13 There has also been controversy regarding the prognostic significance of {Delta}13 in MM. This chromosomal aberration, detected by interphase FISH, was one of the first established genetic prognostic factors, independent of the mode of treatment.15 However, it now appears that the dismal prognosis previously thought to be conferred by the deletion is actually due to its association with other poor-risk genetic markers, such as specific primary IgH translocations or TP53 deletions,16,17 and that {Delta}13 on its own probably does not affect prognosis.

In this study, we used interphase FISH to assess the incidence and the association of {Delta}13 with IgH translocations, ploidy status and deletions of 16q23 and TP53 in a large series of MGUS and SMM patients. We compared the results with the frequencies found in a group of newly diagnosed MM patients in order to determine whether the patterns of chromosomal aberrations differ within the different diagnostic groups. We also explored the clonal heterogeneity of MGUS by comparing the frequencies of the different chromosomal aberrations detected in individual patients.10


arrow
Design and Methods
TOP
 ABSTRACT
 Introduction
 Design and Methods
Results
 Discussion
 References
 
Patients
We evaluated a consecutive series of 716 patients with plasma cell disorders reported to the LRF UK Myeloma Forum Cytogenetic Database between November 2000 and January 2007. Samples were received from different centers throughout the UK with informed consent for cytogenetic/FISH analysis. The cohort consisted of 189 patients with MGUS (median age, 69 years; range, 36–92 years) and 127 with SMM (median age, 69 years; range, 31–89 years) not requiring therapy, and 400 newly diagnosed MM patients entered into the MRC Myeloma IX Trial (median age, 64 years; range, 30–89 years). Patients with an IgM heavy chain subtype were not eligible for this study, given the different biology of this disease.15 Patients were classified as having MGUS or SMM according to standard criteria18 and were required to have no evidence of organ damage indicative of MM. All but four SMM and eight MGUS patients were studied at diagnosis.

Cytogenetic testing
Density gradient centrifugation of bone marrow aspirates over Lymphoprep was performed to separate mononuclear cells by standard protocols. CD138+ plasma cells were isolated by magnetic-activated cell sorting using anti-CD138 immunobeads (Miltenyi Biotec Ltd., Bisley, UK). Interphase FISH was performed on plasma cells using a panel of commercial and in-house probes, as previously described.19,20 Results were available for {Delta}13, IgH rearrangements, t(4;14)(p16;q32), CCND3 break-apart (6p21), t(11;14)(q13;q32), t(14;16)(q32;q23), MAFB break-apart (20q11), deletion of TP53 (17p13) together with 17 centromere, and ploidy status. The interphase FISH method used to estimate ploidy and classify patients into groups with and without hyperdiploidy had been previously designed and assessed in MM patients,20 using a modification of the method described by Wuilleme et al.21 Break-apart patterns for the CCND3 or the MAFB probes in cases with a concomitant break-apart of the IgH probe were suggestive of t(6;14) and t(14;20), respectively. Cases with a suspected t(14;20) were tested using a fusion probe approach to confirm the presence of the translocation.

The cut-off levels for interphase FISH scoring recommended by the European Myeloma Network (EMN) FISH workshop (10% for fusion/break-apart probes and 20% for numerical abnormalities) were followed.

Statistical analysis
The frequencies of chromosomal aberrations in the groups of patients were compared by Fisher’s exact test or the Kruskall-Wallis test, as appropriate.


arrow
Results
TOP
 ABSTRACT
 Introduction
 Design and Methods
 Results
Discussion
 References
 
Frequencies of chromosomal abnormalities
FISH analysis was performed according to the availability of patients’ material: a minimum of seven loci were tested (4p16, 5p15, CEP 9, 11q13, 13q14, 14q32 and CEP 15). In more than 80% of patients, 12 different loci were analyzed. We observed copy number changes or structural alterations for at least one of the chromosomal regions tested in 169/189 (89%) MGUS, 124/127 (98%) SMM and 396/400 (99%) MM.

Table 1 summarizes the frequencies of the specific chromosomal aberrations within each diagnostic group. The incidence of {Delta}13 was substantially lower in MGUS (25%) and SMM (34%) than in MM (47%); the difference across the three groups was statistically highly significant (Kruskall-Wallis test: MGUS versus SMM versus MM, p<0.001).


View this table:
[in this window]
[in a new window]
[Download PPT slide]
  		Table 1. Incidence of specific chromosomal abnormalities in the three groups of patients with MGUS, SMM and MM.

Rearrangements involving the IgH heavy chain locus located at 14q32 were detected with similar frequencies in MGUS and MM (41% and 46%, respectively); the incidence in SMM (35%) was lower, but the difference was not statistically significant. When the individual chromosomal partners of the primary translocations were considered, similar frequencies of t(6;14), t(11;14) and t(14;16) were observed among the three groups; t(4;14) was rare in MGUS (4%), but was observed at the same incidence in SMM and MM (13%) (MGUS versus MM, p<0.001). The frequency of t(14;20) was higher in MGUS (5%) than in either SMM (0%) or MM (2%). The difference in the incidence of this translocation was not statistically significant in this analysis, but became so when the incidence in the same MGUS group was compared to that in a larger population of MM patients (unpublished data). Deletion of 16q23 was found to be less common in MGUS (6%) and SMM (8%) than in MM (21%) (MGUS versus MM, p<0.001). Deletion of TP53 was also very rare in MGUS (3%) and SMM (~1%).

Patients with MGUS and SMM were classified as being hyperdiploid or not in the same way as previously described for MM.20 The distribution into the two ploidy classes differed between the diagnostic groups. A hyperdiploid karyotype was indicated in 63% of SMM and 57% of MM patients, while only 42% of MGUS cases were assigned to this category. The non-hyperdiploid MGUS group also included those patients found to be negative for all the interphase FISH tests performed; in MGUS these patients represented 11% of the total group and accounted for most of the difference between the groups.

IgH rearrangements involving the five recurrent loci (4p16, 6p21, 11q13, 16q23 and 20q11) were highly associated with a non-hyperdiploid karyotype in all three diagnostic groups: 94% of MGUS cases, 82% of SMM cases and 73% of MM cases with one of these IgH translocations were found in the context of non-hyperdiploidy (p<0.001 for all diagnostic groups). In contrast 35 of 49 MM cases with an IgH rearrangement not involving one of these loci were found in association with hyperdiploidy (p=0.043). In the SMM group the six unidentified IgH rearrangements were equally distributed between the two ploidy groups. In MGUS, 12 of 16 unidentified IgH rearrangements were found in the context of a non-hyperdiploid karyotype but the association was not statistically significant (p=0.18).

Percentage of plasma cells in patients with chromosome 13 deletion
When present, {Delta}13 involved a variable proportion of plasma cells (Figure 1). The median percentage of plasma cells carrying the abnormality was 65% in MGUS, 88.5% in SMM and 95% in MM. No variation was seen for illegitimate IgH rearrangements: in patients with MGUS the median percentage of cells displaying a 14q32 translocation was 91.5% (range, 24%–100%). The level of plasma cell involvement by different chromosomal aberrations was compared for all MGUS patients who exhibited {Delta}13 with at least one other abnormality (Table 2). Because of the differences in false positive rates between probes, unequivocal evidence of heterogeneity within the neoplastic clone was only accepted when the difference in the proportions of cells affected by distinct chromosomal aberrations was 30% or more. In 16 of 47 patients with {Delta}13, the abnormality was present in 60% or less of plasma cells (cases 1–16 in Table 2); of these 16 cases, 12 had other chromosomal aberrations for comparison. In all but three of these 12, the plasma cell involvement by the non-{Delta}13 abnormality was at least 30% greater than that shown by {Delta}13.


Figure 10941708
View larger version (15K):
[in this window]
[in a new window]
[Download PPT slide]
  		Figure 1. Distribution of the percentages of abnormal plasma cells with {Delta}13 in patients found positive for the abnormality, among the three groups of patients.


View this table:
[in this window]
[in a new window]
[Download PPT slide]
  		Table 2. List of 47 MGUS patients with {Delta}13 ordered on the basis of the percentage of plasma cell involvement by the abnormality. For each case, concomitant numerical or structural abnormalities are specified with the percentage of plasma cell involvement (UIP, unidentified partner).

Interestingly five of six (83%) MGUS cases positive for both t(4;14) and {Delta}13 showed the same proportion (±5%) of plasma cells with the two abnormalities. In contrast, four of five (80%) cases of t(14;20) MGUS with {Delta}13 showed at least 30% fewer {Delta}13-positive plasma cells (median 51%) than t(14;20)-positive ones (median 95%). In MM, seven of nine (78%) cases of t(14;20) were associated with {Delta}13 and the median difference in plasma cell involvement by {Delta}13 and the translocation was 10% (range, 0–27%). In MGUS, 16q23 deletions were often present in a sub-clone of plasma cells (median, 63%; range, 23–100%), while in MM the median percentage of plasma cells with the abnormality was 87% (range, 21–100%). Those MGUS cases in which the proportion of plasma cells carrying the 16q deletion was small displayed at least one of the other chromosomal aberrations in the majority of clonal plasma cells (deletion 16q23 versus other chromosomal aberrations: 23% versus 82% IgH split; 33% versus 93% deletion 14q32; 44% versus 92% IgH split; 47% versus 99% IgH split).

Association of chromosome 13 deletion with other abnormalities
Table 3 shows the association between {Delta}13 and other chromosomal aberrations. The {Delta}13 was less frequently associated with any of the IgH rearrangements in MGUS than in MM (MGUS versus MM, 34% versus 60%; p<0.001). However, when the individual translocations were examined, no differences were found in the frequencies of association of t(4;14), t(14;16), or t(14;20) with {Delta}13 among the three diagnostic groups.


View this table:
[in this window]
[in a new window]
[Download PPT slide]
  		Table 3. Association between {Delta}13 and the different chromosomal abnormalties.

In MM, {Delta}13 was found in 40% of t(11;14) cases and involved a large proportion of plasma cells (>85%) while only one of 28 (3.6%) MGUS cases with t(11;14) had {Delta}13 (p<0.001). Furthermore, in this case, only 45% of the plasma cells had {Delta}13, while the translocation was present in all cells. In SMM only two of t(11;14) cases had {Delta}13 (15%), but this was not significantly different from the percentage found in MM. Both SMM patients had {Delta}13 in 70% of their plasma cells and the translocation in 100%. In this study, the presence of t(6;14) was detected in only 1–2% of patients, in agreement with other reported series. Despite the small number of cases, it was notable that {Delta}13 was present in four of the six (67%) MM cases, while in MGUS the two t(6;14) were both negative for {Delta}13 (in one of these two cases, 12% of the plasma cells carried the deletion).


arrow
Discussion
TOP
 ABSTRACT
 Introduction
 Design and Methods
 Results
 Discussion
References
 
Our analysis of chromosomal aberrations in MGUS and SMM revealed a significantly lower frequency of {Delta}13 in the pre-malignant conditions than in MM. This is in accordance with findings reported by Avet-Loiseau et al.10 The frequency of {Delta}13 progressively increased from MGUS to SMM to MM, suggesting a possible role of this abnormality in disease progression. The incidence of deletion of 16q23 and TP53 also increased progressively from MGUS to MM (p<0.001 and p=0.003, respectively). In contrast, a similar frequency of IgH rearrangements was observed in the three groups. When the individual incidences of the specific translocations were compared, only t(4;14) was significantly less frequent in MGUS, in agreement with other reports.7,10

Interphase FISH was used to classify patients according to their ploidy status into those with hyperdiploidy and those without. {Delta}13 was found more frequently in patients with a non-hyperdiploid karyotype than in those with hyperdiploidy in all three groups of patients (MGUS, 15% versus 32%; SMM, 21% versus 52%; MM, 34% versus 66%), suggesting that the specific association between {Delta}13 and non-hyperdiploidy, extensively reported in MM,15,17 is already established at the stage of MGUS. These findings differ from those reported by Brousseau et al.22 In MGUS, they found {Delta}13 more frequently in patients with hyperdiploidy (11/29, 38%) than in those without (3/27, 11%), although the reverse association was seen in MM. They defined ploidy by measuring the plasma cell DNA content using the Feulgen reaction and image cytometry. We are unable to explain this discrepancy although the fact that ploidy was evaluated by two different methods may be partially responsible. Pseudodiploidy and low chromosome count hyperdiploidy (48–49 chromosomes) are potentially difficult to identify by interphase FISH, compared to true hypodiploidy or high chromosome count hyperdiploidy. However, the comparison of our interphase FISH ploidy results with actual karyotypes for those MGUS (n=8) and SMM (n=24) patients with abnormal cytogenetics showed that all cases but one were accurately classified. Thus interphase FISH misclassification of ploidy is unlikely to account for the significant difference in results between the two series.

Abnormalities of 14q32 were observed in the majority of clonal plasma cells, independently of the stage of the disease, whereas the percentages of plasma cells carrying {Delta}13 or the 16q23 deletion varied significantly between MGUS, SMM and MM, with MGUS patients showing the greatest heterogeneity. In MGUS, {Delta}13 was often present in a sub-clone of the abnormal plasma cells. Although low level clones in MGUS may be due to only a small proportion of the CD138-positive plasma cells being part of the neoplastic clone, our results indicate that, in these cases, the {Delta}13 is a later change following IgH translocations or multiple trisomies. Similar findings were observed for most low level 16q23 deletions in which the cells were found to be 100% positive for other chromosomal aberrations.

Our results clearly show that the time of occurrence of specific abnormalities is crucially dependent on genetic context. The t(4;14), t(14;16) and t(14;20) are highly associated with {Delta}13 in MM.15,17,20 The same association was observed in MGUS and SMM patients. Moreover, in cases with t(4;14) and t(14;16), IgH rearrangement and {Delta}13 were found in a similar proportion of abnormal cells in the three diagnostic groups, suggesting that {Delta}13 occurred early in disease pathogenesis. However, a different time of occurrence of {Delta}13 was observed in relation to t(14;20). In MGUS, {Delta}13 appeared to originate later than t(14;20). A striking difference between MGUS and MM was seen regarding the association of {Delta}13 with t(11;14). While in MM 21/53 of t(11;14) cases also showed {Delta}13, in MGUS only 1/28 of cases with the translocation was associated with {Delta}13 (p<0.001). In MM the median percentage of plasma cells carrying the {Delta}13 in patients with t(11;14) was 98% while in the only case of MGUS with both t(11;14) and {Delta}13, all the plasma cells were positive for t(11;14) but only 48% of the plasma cells had {Delta}13. The translocation t(11;14) has been related to t(6;14) on the basis of a similar biological and clinical behavior.23 Both translocations directly activate a cyclin D family member (CCND1 and CCND3, respectively) and gene expression profiling studies demonstrated that cases carrying either one or the other translocation exhibited dysregulation of similar transcriptional programs showing overlapping gene expression profiles.23,24 As for t(11;14), {Delta}13 was not found in the MGUS cases with t(6;14), while it was present in the majority of MM cases with this translocation.

These findings are consistent with those reported by Bochtler et al.,25 who applied an oncogenic tree model to study patients with amyloid light chain amyloidosis, MGUS and MM, in order to detect clustering of chromosomal abnormalities. Patients with amyloidosis and MGUS showed the t(11;14) branch independent of {Delta}13, while t(4;14), and gain of 1q21 were grouped together with {Delta}13. In our study, {Delta}13 occurred less frequently in SMM cases with t(11;14), but not to a degree that was statistically significantly different from the MM group.

Conclusions
In this study, we examined a range of numerical and structural chromosomal changes in MGUS, SMM and MM patients. None of the chromosomal aberrations tested was exclusive to a single diagnostic group, confirming the extensive overlap between the different conditions from a genetic point of view. However, statistically significant differences were observed in the incidence of specific abnormalities between the three conditions, in particular for {Delta}13, 16q23 deletion and TP53 deletion. In MGUS, the greatest variation in the proportion of abnormal plasma cells carrying the abnormality was seen for {Delta}13 and 16q23 deletion. In particular, the temporal appearance of {Delta}13 was related to the presence of specific concomitant abnormalities: early when t(4;14) or t(14;16) was present, later with t(14;20), and even later with t(11;14) or t(6;14). These data suggest a possible role of {Delta}13 in the transition from MGUS to MM specifically in cases with t(11;14) or t(6;14).


arrow
Acknowledgments
 
the authors would like to thank Paul Strike of the Salisbury District Hospital Research and Development Support Unit for help with the statistical analysis.


arrow
Footnotes
 
Funding: this work was supported by the Leukaemia Research Fund.

Authorship and Disclosures

LC designed and performed research, analyzed data and wrote the first draft of the paper; GPD, AHI, EDC, RKMP and DMS performed research; KHO, NCPC and CJH contributed to the analysis of the data; FMR designed and performed research, and analyzed data. All the authors contributed to the final draft of the paper. The authors reported no potential conflicts of interest.

Received for publication May 8, 2009. Revision received June 11, 2009. Accepted for publication June 29, 2009.


arrow
References
TOP
 ABSTRACT
 Introduction
 Design and Methods
 Results
 Discussion
 References
 
  1. Kyle RA, Therneau TM, Rajkumar SV, Offord JR, Larson DR, Plevak MF, et al. A long-term study of prognosis in monoclonal gammopathy of undetermined significance. N Engl J Med 2002;346:564–9.[Abstract/Free Full Text]
  2. Kyle RA, Rajkumar SV. Monoclonal gammopathy of undetermined significance. Br J Haematol 2006;134:573–89.[CrossRef][Web of Science][Medline]
  3. Kyle RA, Remstein ED, Therneau TM, Dispenzieri A, Kurtin PJ, Hodnefield JM, et al. Clinical course and prognosis of smoldering (asymptomatic) multiple myeloma. N Engl J Med 2007;356:2582–90.[Abstract/Free Full Text]
  4. Kyle RA. "Benign" monoclonal gammopathy–after 20 to 35 years of follow-up. Mayo Clin Proc 1993;68:26–36.[Web of Science][Medline]
  5. Kyle RA, Rajkumar SV. Monoclonal gammopathies of undetermined significance. Hematol Oncol Clin North Am 1999;13:1181–202.[CrossRef][Web of Science][Medline]
  6. Avet-Loiseau H, Li JY, Facon T, Brigaudeau C, Morineau N, Maloisel F, et al. High incidence of translocations t(11;14)(q13;q32) and t(4;14) (p16;q32) in patients with plasma cell malignancies. Cancer Res 1998;58:5640–5.[Abstract/Free Full Text]
  7. Fonseca R, Bailey RJ, Ahmann GJ, Rajkumar SV, Hoyer JD, Lust JA, et al. Genomic abnormalities in monoclonal gammopathy of undetermined significance. Blood 2002;100:1417–24.[Abstract/Free Full Text]
  8. Harrison CJ, Mazzullo H, Ross FM, Cheung KL, Gerrard G, Harewood L, et al. Translocations of 14q32 and deletions of 13q14 are common chromosomal abnormalities in systemic amyloidosis. Br J Haematol 2002;117:427–35.[CrossRef][Web of Science][Medline]
  9. Chng WJ, Van Wier SA, Ahmann GJ, Winkler JM, Jalal SM, Bergsagel PL, et al. A validated FISH trisomy index demonstrates the hyperdiploid and nonhyperdiploid dichotomy in MGUS. Blood 2005;106:2156–61.[Abstract/Free Full Text]
  10. Avet-Loiseau H, Facon T, Daviet A, Godon C, Rapp MJ, Harousseau JL, et al. 14q32 translocations and monosomy 13 observed in monoclonal gammopathy of undetermined significance delineate a multistep process for the oncogenesis of multiple myeloma. Intergroupe Francophone du Myelome. Cancer Res 1999;59:4546–50.[Abstract/Free Full Text]
  11. Avet-Loiseau H, Facon T, Grosbois B, Magrangeas F, Rapp MJ, Harousseau JL, et al. Oncogenesis of multiple myeloma: 14q32 and 13q chromosomal abnormalities are not randomly distributed, but correlate with natural history, immunological features, and clinical presentation. Blood 2002;99:2185–91.[Abstract/Free Full Text]
  12. Konigsberg R, Ackermann J, Kaufmann H, Zojer N, Urbauer E, Kromer E, et al. Deletions of chromosome 13q in monoclonal gammopathy of undetermined significance. Leukemia 2000;14:1975–9.[CrossRef][Web of Science][Medline]
  13. Avet-Louseau H, Daviet A, Sauner S, Bataille R. Chromosome 13 abnormalities in multiple myeloma are mostly monosomy 13. Br J Haematol 2000;111:1116–7.[CrossRef][Web of Science][Medline]
  14. Fonseca R, Oken MM, Harrington D, Bailey RJ, Van Wier SA, Henderson KJ, et al. Deletions of chromosome 13 in multiple myeloma identified by interphase FISH usually denote large deletions of the q arm or monosomy. Leukemia 2001;15:981–6.[CrossRef][Web of Science][Medline]
  15. Fonseca R, Barlogie B, Bataille R, Bastard C, Bergsagel PL, Chesi M, et al. Genetics and cytogenetics of multiple myeloma: a workshop report. Cancer Res 2004;64:1546–58.[Abstract/Free Full Text]
  16. Avet-Loiseau H, Attal M, Moreau P, Charbonnel C, Garban F, Hulin C, et al. Genetic abnormalities and survival in multiple myeloma: the experience of the Intergroupe Francophone du Myelome. Blood 2007;109:3489–95.[Abstract/Free Full Text]
  17. Chng WJ, Glebov O, Bergsagel PL, Kuehl WM. Genetic events in the pathogenesis of multiple myeloma. Best Pract Res Clin Haematol 2007;20:571–96.[Medline]
  18. Durie BG. Staging and kinetics of multiple myeloma. Semin Oncol 1986;13:300–9.[Web of Science][Medline]
  19. Ross FM, Ibrahim AH, Vilain-Holmes A, Winfield MO, Chiecchio L, Protheroe RK, et al. Age has a profound effect on the incidence and significance of chromosome abnormalities in myeloma. Leukemia 2005;19:1634–42.[CrossRef][Web of Science][Medline]
  20. Chiecchio L, Protheroe RK, Ibrahim AH, Cheung KL, Rudduck C, Dagrada GP, et al. Deletion of chromosome 13 detected by conventional cytogenetics is a critical prognostic factor in myeloma. Leukemia 2006;20:1610–7.[CrossRef][Web of Science][Medline]
  21. Wuilleme S, Robillard N, Lode L, Magrangeas F, Beris H, Harousseau JL, et al. Ploidy, as detected by fluorescence in situ hybridization, defines different subgroups in multiple myeloma. Leukemia 2005;19:275–8.[CrossRef][Web of Science][Medline]
  22. Brousseau M, Leleu X, Gerard J, Gastinne T, Godon A, Genevieve F, et al. Hyperdiploidy is a common finding in monoclonal gammopathy of undetermined significance and monosomy 13 is restricted to these hyperdiploid patients. Clin Cancer Res 2007;13:6026–31.[Abstract/Free Full Text]
  23. Bergsagel PL, Kuehl WM. Molecular pathogenesis and a consequent classification of multiple myeloma. J Clin Oncol 2005;23:6333–8.[Abstract/Free Full Text]
  24. Zhan F, Huang Y, Colla S, Stewart JP, Hanamura I, Gupta S, et al. The molecular classification of multiple myeloma. Blood 2006;108:2020–8.[Abstract/Free Full Text]
  25. Bochtler T, Hegenbart U, Cremer FW, Heiss C, Benner A, Hose D, et al. Evaluation of the cytogenetic aberration pattern in amyloid light chain amyloidosis as compared with monoclonal gammopathy of undetermined significance reveals common pathways of karyotypic instability. Blood 2008;111:4700–5.[Abstract/Free Full Text]




This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Google Scholar
Right arrow Articles by Chiecchio, L.
PubMed
Right arrow PubMed Citation
Right arrow Articles by Chiecchio, L.