scholarly journals Role of computed tomography texture analysis using dual-energy-based bone marrow imaging for multiple myeloma characterization: comparison with histology and established serologic parameters

Author(s):  
Christian Philipp Reinert ◽  
Eva Krieg ◽  
Michael Esser ◽  
Konstantin Nikolaou ◽  
Hans Bösmüller ◽  
...  

Abstract Objective To identify textural features on dual-energy CT (DECT)–based bone marrow images in myeloma which correlate with serum markers of myeloma activity and the degree of medullary involvement. Methods A total of 110 patients (63.0 ± 11.0 years, 51 female) who underwent unenhanced whole-body DECT between September 2015 and February 2019 were retrospectively included, which was approved by our institutional ethics committee with a waiver of the informed consent requirement. All patients had current hematologic laboratory tests. Using DECT post-processing, non-calcium bone marrow images were reconstructed. The vertebral bodies T10–L5 were segmented for quantification of textural features, which were compared with serologic parameters and myeloma stages by the Mann-Whitney U test. In a subgroup of 56/110 patients with current bone marrow biopsies, textural features were correlated with the degree of bone marrow infiltration. Results First-order features were higher in patients with advanced stage of myeloma (p < .02), whereas the 2nd-order “gray-level co-occurrence matrix (GLCM) cluster prominence” was lower (p < .04). In patients with elevated serum-free light chains (SFLC) or kappa/lambda SFLC ratio above 1.56, the “entropy” and 2nd-order GLCM features were lower (p < .03). The degree of bone marrow infiltration correlated with 1st-order features (e.g., “uniformity”; rP = 0.49; p < .0001), whereas “entropy” and 2nd-order GLCM features were negatively correlated (e.g., “difference entropy”; rP = − 0.54; p < .0001). Conclusions CT textural features applied on non-calcium bone marrow images correlate well with myeloma-related serologic parameters and histology showing a more uniform tissue structure and higher attenuation with increasing medullary infiltration and could therefore be used as additional imaging biomarkers for non-invasive assessment of medullary involvement. Key Points • Texture analysis applied on dual-energy reconstructed non-calcium bone marrow images provides information about marrow structure and attenuation. • Myeloma-related serologic parameters and the degree of myeloma cell infiltration correlate with 1st- and 2nd-order features which could be useful as additional imaging biomarkers for non-invasive assessment of medullary involvement.

Blood ◽  
2021 ◽  
Vol 138 (Supplement 1) ◽  
pp. 3997-3997
Author(s):  
Michael Laurence Langsen ◽  
Jerry Thwin Wong ◽  
Maximilian Merz ◽  
Brian Yu ◽  
Hemn Mohammadpour ◽  
...  

Abstract Introduction: Osteolytic bone disease represents a severe clinical presentation of multiple myeloma (MM), as MM cells infiltrate the bone marrow throughout the skeleton, forming tumors, activating bone-resorbing osteoclasts, and impeding bone-depositing osteoblast activity. The extent of osteolytic lesions encompassing the skeleton influences the severity of disease for patients, with severe lesions leading to skeletal-related events (SREs). MM cell infiltration into the bone marrow gradually increases with disease progression; however, the distribution of myeloma cells within the bone and marrow is heterogenous. Standard of care imaging modalities used to monitor the number, size, and extent of bone destruction of lesions include whole-body magnetic resonance imaging (MRI), whole-body low-dose computed tomography (CT), and positron emission tomography with CT (PET/CT). With the use of computational methodologies, imaging textural features can be calculated from PET. In this prospective study, we aim to find PET textural features that will correlate with histological evaluation of myeloma cell infiltration patterns of osteolytic lesions and un-guided bone marrow biopsies in MM patients. Patients and Methods: 40 patients were enrolled in this prospective study with either newly diagnosed multiple myeloma (n=16, 40%) or relapse/refractory multiple myeloma (n= 24, 60%). Whole-body PET/CT imaging was performed on all patients as part of MM standard of care, after which CT-guided biopsies were taken from patient osteolytic lesions identified by imaging and in bone marrow biopsies. 68 biopsies were evaluated by an expert hematopathologist, of which 59 had analyzable imaging studies in the respective areas. Myeloma cell infiltration patterns in all biopsies were classified as interstitial (n=23, 41.8%), nodular (n=19, 34.6%), or packed (n=13, 23.6%), as described by Andrulis et al. (2014). PET lesion and bone marrow segmentation was performed on the Medical Imaging Interaction Toolkit (MITK) and 72 textural features were calculated using the PyRadiomics extension (van Griethuysen et al. 2017) for 3D Slicer 4.11 (Fedorov et al. 2012). PET quantitative features were calculated using the PET IndiC extension from 3D Slicer (QIICR (2015b)). Statistical analysis was performed via GraphPad Prism 9 (GraphPad Software, San Diego, California USA) and the Radiomics Analysis with R (RadAR, Benelli et al. 2020) package in the RStudio environment (RStudio Team (2020). RStudio: Integrated Development for R. RStudio, PBC, Boston, MA). Results: Lesion biopsy samples predominantly favored packed infiltration pattern (53.6%) over interstitial (21.4%) or nodular (25%), while staging/follow-up bone marrow biopsies predominantly favored interstitial or nodular patterns (47.5% and 35.0%, respectively) compared to packed (22.5%). Two-way analysis of variance (ANOVA) tests was performed to compare imaging features between biopsy infiltration patterns and also between disease status of patients. The first order uniformity (p&lt;0.05) was able to discern between interstitial, nodular, or packed infiltration for all biopsies and textural features from the Gray Level Co-Occurrence Matrix (GLCM) Correlation and Joint Entropy were accurately able to discern between interstitial and either nodular or packed infiltration patterns for all biopsies (p&lt;0.01). Within lesion biopsies specifically (n=25), first order uniformity, kurtosis, skewness, and textural features Joint Entropy and Dependence Non-Uniformity could discern between MM cell infiltration patterns (p&lt;0.05). PET quantitative SUV statistics did not show any significant separation between infiltration patterns. First order, textural, and PET SUV quantitative features could not distinguish disease status of the patient. Conclusions: In this preliminary study, we demonstrate a correlation between textural imaging features and pathological findings within the bone marrow and osteolytic lesions of MM patients. This correlation illustrates a potential link between computational imaging features to predict pathological findings in patients with MM. Further expansion of this study with genomic, flow cytometry, and multimodality imaging data could lead to the generation of computational modeling of the pathophysiology of osteolytic lesions in MM and a reduction in the need for invasive bone marrow and lesion biopsies. Figure 1 Figure 1. Disclosures Merz: Takeda: Honoraria; onkowissen.de: Honoraria; Amgen: Honoraria; BMS: Honoraria; Celgene: Honoraria; Sanofi: Honoraria; Janssen: Honoraria; GSK: Honoraria; Hexal: Honoraria. McCarthy: Janssen: Honoraria, Membership on an entity's Board of Directors or advisory committees; Bluebird: Honoraria, Membership on an entity's Board of Directors or advisory committees; Bristol Myers Squibb: Honoraria, Membership on an entity's Board of Directors or advisory committees; Juno: Honoraria, Membership on an entity's Board of Directors or advisory committees; Karyopharm: Honoraria, Membership on an entity's Board of Directors or advisory committees; Celgene: Honoraria, Membership on an entity's Board of Directors or advisory committees; Magenta Therapeutics: Honoraria, Membership on an entity's Board of Directors or advisory committees; Oncopeptides: Honoraria, Membership on an entity's Board of Directors or advisory committees; Takeda: Honoraria, Membership on an entity's Board of Directors or advisory committees. Hillengass: Beijing Life Oasis Public Service Center: Speakers Bureau; Oncopeptides: Membership on an entity's Board of Directors or advisory committees; Axxess Network: Membership on an entity's Board of Directors or advisory committees; Beijing Medical Award Foundation: Speakers Bureau; Adaptive: Membership on an entity's Board of Directors or advisory committees; Bristol Myers Squibb: Membership on an entity's Board of Directors or advisory committees; Skyline: Membership on an entity's Board of Directors or advisory committees; GlaxoSmithKline: Membership on an entity's Board of Directors or advisory committees; Sanofi: Membership on an entity's Board of Directors or advisory committees; Oncotracker: Membership on an entity's Board of Directors or advisory committees; Curio Science: Speakers Bureau.


Blood ◽  
2004 ◽  
Vol 104 (11) ◽  
pp. 4800-4800
Author(s):  
Achille Ambrosetti ◽  
Roberta Zanotti ◽  
Marco Chilosi ◽  
Flavia Zanetti ◽  
Maurizio Lestani ◽  
...  

Abstract New biological prognostic factors have been developed over the last years with the aim of predicting at presentation the heterogeneous clinical course of B chronic lymphocytic leukaemia (B-CLL) and of planning a risk-adapted treatment strategy. Among them ZAP-70 expression on leukemic cells as evaluated by molecular analysis or flow cytometry, initially proposed as surrogate of IgVH mutational status, appears a strong prognostic marker in B-CLL. However the optimal methodological approach to immunophenotipical demonstration of ZAP-70 expression as still matter of debate. We evaluated the cytoplasmic expression of ZAP-70 protein in leukemic cells by immunohistochemical method on bone marrow trephine biopsies taken at diagnosis of 84 patients with B-CLL. We used a mouse anti-human monoclonal antibody to ZAP-70 (clone 2F3.2, 1/200, Upstate, Lake Placid NY) with a polymeric labelling two-step method (Dako cytomation EnVision+, HRP). The results were correlated with age, sex, Binet stage, pattern of bone marrow infiltration, survival and clinical outcome. They were 54 males (64%), aged 34 to 80 years (median 62.5). At presentation 69 (82%) were Binet stage A, 9 (11%) stage B and 6 (7%) stage C. Among the 60 survivors, the median follow-up period from diagnosis was 78.5 months (range 22 – 236 months) Thirty-nine cases (46%) of B-CLL patients had cytoplasmic expression of ZAP-70. This group of patients presented higher percentage of advanced Binet stage (B–C) (p= 0.001). The ZAP-70 positivity was significantly related to inferior OS (55% vs 90% at 7 years)(HR 4.67 CI 1.95–11.14) and PFS (15% vs 57% at 7 years) (HR 5.52 CI 2.57–11.86), confirmed in multivariate analysis. ZAP-70 expression was correlated to poorer outcome also when we evaluated only the 69 stage A patients and the 56 cases with non-diffuse bone marrow infiltration, whereas in patients with diffuse pattern ZAP-70 expression had no prognostic significance. In conclusion, immunohistological detection of ZAP-70 on bone marrow samples at diagnosis appears a useful methodological approach to identify patients with different prognosis in B-CLL.


Blood ◽  
2011 ◽  
Vol 118 (21) ◽  
pp. 4617-4617
Author(s):  
Deepa Ranjani Jayakody Arachchillage ◽  
Samuel Moses ◽  
Stephen O'Brien ◽  
Tobias Menne ◽  
Peter Carey ◽  
...  

Abstract Abstract 4617 We report 3 patients who developed Haemophagocytic Lymphohistiocytosis (HLH) following treatment with Fludarabine/Cyclophosphamide (FC) chemotherapy for Chronic Lymphocytic Leukaemia (CLL). Acquired (secondary) HLH is more frequent than primary (familial) HLH and usually described in patients with an underlying immune disorder. Acquired HLH in association with haematological malignancies is well recognised. The most commonly reported associations in adults are NK/T and peripheral T cell lymphomas. There is only one previous published case report of HLH in association with CLL as a direct trigger for development of HLH where the patient developed HLH one month after FC therapy and died in spite of treatment with the HLH 2004 protocol. Our 3 patients were diagnosed with HLH using standard diagnostic criteria, fulfilling at least 5 out of 8 clinical/laboratory criteria (Table 1). There was no evidence of haemophagocytosis in the bone marrow of any of these patients prior to treatment with FC. Two patients are still alive while the other died one month after diagnosis.Table 1Patient 1Patient 2Patient 3Fever+++Splenomegaly (cm)181719Haemoglobin (g/dl)10.39.07.3Platelets (× 109/l)116319Neutrophils (× 109/l)0.81.020.6Haemophagocytosis in bone marrow+++Ferritin (ug/l)165009342>100000Triglycerides (0.5–1.7 mmol/l)1.7 mmol/l1.9 mmol/l1.8 mmo/lFibrinogen level(2.1–4.8 g/l)0.6 g/l2.0 g/l1.0 g/lDecreased/absent NK cell activityNot assessedNot assessedNot assessedSoluble CD25Not assessedNot assessedNot assessed Each had been treated with FC before they developed HLH and 2 of them had received previous treatment with chlorambucil. All 3 patients were extensively investigated for infective causes that may be associated with HLH. Multiple blood, urine and sputum cultures were negative for bacteria, fungi, mycobacteria and parasites. Polymerase chain reaction (PCR) studies for cytomegalovirus, Epstein Barr virus, herpes simplex virus, human herpes virus-6 and parvovirus B19 were all negative initially in all 3 patients. Patient 2 developed immunosuppression related HHV-6 reactivation while he was undergoing treatment with HLH 2004. This responded to brief treatment with Foscarnet. All 3 patients were treated with empirical intravenous antibiotics for neutropenic sepsis and subsequently administered antifungal therapy due to prolonged fever not responding to antibiotics. All had whole body Computerised Tomography (CT) scans looking for any evidence of infection. CT scans in each case showed splenomegaly and minor adenopathy in the abdomen and chest with no evidence of infection. Bone marrow biopsies from all 3 patients showed appearances of haemophagocytosis but no significant residual infiltration with CLL. The time interval from treatment with FC to the development of HLH ranged from 1 month to 6 months (Table 2). Patient 1 died 4 weeks following the diagnosis of HLH in spite of treatment according to HLH 2004. The remaining 2 patients are still alive and undergoing treatment as per HLH 2004. Patient 2 has been worked up for allogenic bone marrow transplant (alloBMT) as part of HLH 2004. The other patient is being treated with chemotherapy alone due to age and other co morbidity factors precluding consideration for alloBMT.Table 2:Patient 1Patient 2Patient 3Age655774SexmalemalefemaleDate of first diagnosis of CLL09/05/200931/07/200605/06/2001Previous treatmentChlorambucilNoneChlorambucilTime of treatment with FC15/09/2009 To 28/06/201003/01/2009 to 09/10/2009 and 04/04/201104/03/2010 To 10/11/2010Number of FC cycles88 and 1(FC +Rituximab)6Date of diagnosis of HLH05/01/201115/05/201106/05/2011Current statusDied on 05/02/2011Undergoing treatment with HLH2004 and awaiting alloBMTUndergoing treatment with HLH2004 To our knowledge, this is the first case series of CLL patients who developed HLH in direct association with FC treatment without evidence of an underlying infective aetiology. Therefore in CLL patients presenting with cytopenias and fever, HLH should be considered early and diagnostic tests performed. This complication of treated CLL may be more common with FC than treatment with Chlorambucil alone, with which it had not previously been reported. Disclosures: No relevant conflicts of interest to declare.


2019 ◽  
Vol 98 (6) ◽  
pp. 2652-2661
Author(s):  
S. Schallier ◽  
C. Li ◽  
J. Lesuisse ◽  
G.P.J. Janssens ◽  
N. Everaert ◽  
...  

1993 ◽  
Vol 11 (2) ◽  
pp. 294-303 ◽  
Author(s):  
M A Schwartz ◽  
D R Lovett ◽  
A Redner ◽  
R D Finn ◽  
M C Graham ◽  
...  

PURPOSE Mouse monoclonal antibody (mAb) M195 (anti-CD33) is reactive with most myeloid leukemia cells, monocytes, and hematopoietic progenitors, but not with other hematopoietic cells or stem cells nor with nonhematopoietic human tissues. A therapeutic dose-escalation study of M195 labeled with iodine 131 was conducted in patients with relapsed or refractory myeloid leukemias. METHODS Twenty-four patients (16 relapsed or refractory acute myeloid leukemias, five blastic myelodysplastic syndromes [MDS], two chemotherapy-related secondary leukemias, and one blastic chronic myelogenous leukemia [CML]), including seven who had failed to respond to prior bone marrow transplantation (BMT), received from 50 mCi/m2 to 210 mCi/m2 of 131I-M195 in divided doses. RESULTS In 22 patients, whole-body gamma-imaging demonstrated marked uptake of antibody into all areas of bone marrow. Twenty-three patients (96%) demonstrated decreases in peripheral-blood cell counts, with decreased percentage of bone marrow blasts seen in 83% of cases. Eighty-nine percent of bone marrow biopsies examined quantitatively demonstrated substantial decreases in the number of blasts, with greater than 99% of blasts killed in some patients. The two cases that failed to demonstrate leukemic cytoreduction occurred in the first two dose levels. For 131I doses of 135 mCi/m2 or greater, pancytopenia was profound and lasted for at least 12 days. Eight patients had sufficient marrow cytoreduction to proceed to BMT. Three of these achieved marrow remission, one of 6+, and one of 9 months' duration. Two patients in blastic phase temporarily reverted to their original myelodysplastic states. Thirty-seven percent of assessable patients developed human anti-mouse antibody (HAMA). In two patients with HAMA who were re-treated, plasma 131I-M195 levels could not be maintained and no therapeutic effect resulted. Significant nonhematologic toxicity (hepatic) was seen in one patient and the maximum-tolerated dose (MTD) was not reached. CONCLUSION These data suggest that safe leukemic cytoreduction can be achieved with 131I-M195 even in multiply relapsed or chemotherapy-refractory leukemias. This agent may be useful as part of a preparative regimen for BMT.


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