scholarly journals High Prevalence of Bone Marrow Involvement and Advanced Disease in Saudi Patients Diagnosed With Hodgkin Lymphoma

Cureus ◽  
2021 ◽  
Author(s):  
Musa F Alzahrani ◽  
Mohammed B Alkahil ◽  
Abdulaziz A Alhusainy ◽  
Abdulmohsen K Alangari ◽  
Mohammed N Almania ◽  
...  
Blood ◽  
2014 ◽  
Vol 124 (21) ◽  
pp. 5361-5361
Author(s):  
Moyosore M. Suleiman ◽  
Ankit Mangla ◽  
Hussein Hamad ◽  
Romy Thekekkara ◽  
Kalid Adab ◽  
...  

Abstract Introduction: The incidence of bone marrow involvement (BMI) in patients diagnosed with Hodgkin Lymphoma (HL) is relatively low varying from 4-14% in different series occurring mainly in patients with advanced disease (stage III-IV). Ann Arbor staging system with Cotswolds modification in 1989 recommend staging bone marrow in patients with clinical stage III-IV and stage II patients with adverse risk features. It’s utility is now questionable and no longer recommended by many authors as it does not alter the way patients are managed. The advent of 18F-fluoro-2 –deoxy-D-glucose positive emission tomography (FDG-PET) scan use in the staging of patients has improved the prediction of possible bone marrow involvement obviating further the need for bone marrow biopsy. While BMI is said to be an independent prognostic factor in the survival of patient with HL, more studies have shown that BMI alone in patients with Stage IV disease does not influence survival or freedom from disease progression. Because staging bone marrow biopsy (BMB) use in HL varies from one institution to another, we performed a retrospective review in our institution in order to determine its incidence, risk factors and effect in the management of patients. Methods: We performed a retrospective search in John H Stroger, Jr. Hospital database of patients with HL seen from 2004 to 2013. 237 adult (18yr and above) patients were screened. 185 patients had BMB done as part of work up. Results: BMI was detected in 21%(38 of 185) of patients who had BMB as part of work up. M:F ratio was 2.5:1. Mean age was 39.8 +/- 11.5yrs. 51%(95 of 185) of patients who had BMB had advanced disease. 94%(33 out of 35) of patients with BMI had advanced disease prior to BMB. 3 patients with BMI were incompletely staged. Advanced disease was significantly more likely to be associated with BMI than early stage disease (OR 20.2 95% CI 4.6-87.6 p=0.0001). Less than 1%(2 out of 78) of patients with early stage disease were upstaged .The 2 patients that were upstaged had Stage IIB disease prior to BMB.38%(14 of 37) of patients with BMI were HIV positive which was higher compared to 12%(16 of 129) of patients without BMI that were HIV positive (OR 5.8 95% CI 2.4-14.0 p=0.0001). 5 of 38 patients with BMI had staging FDG-PET and all showed positivity in the skeletal system. Patients with BMI in our review were managed with 6-8cycles of chemotherapy (CT)-Adriamycin, Bleomycin, Vinblastine and Dacarbazine regimen (ABVD). 5 cases were relapsed disease. 4 of these patients with relapsed disease received Platinum/Gemcitabine regimen and one patient received Mechlorethamine, Vincristine, Procarbazine and Prednisone regimen (MOPP). Radiation Therapy (RT) was part of the management in 4 patients done for cord compression (2), bulky mediastinal disease (1) and for residual disease after chemotherapy (1). Conclusions: The incidence of BMI was high in our retrospective review compared to other series, however majority of involvement were in patients with advanced disease as in most series. Patients were rarely upstaged from early stage to advanced stage with bone marrow biopsy. This occurred in less than 1% in our retrospective review. Staging FDG-PET although done in few of our patients with BMI was predictive. Management of these patients was not significantly altered based on BMI. They were managed mainly with CT. RT needed in some of these patients was justified (cord compression, and bulky mediastinal disease). RT for residual disease is not a standard of care. Risks factors identified for BMI includes advanced disease and associated HIV infection. BMB does not alter patient management and its sole prognostic significance in patients with stage IV disease is controversial. It is therefore not necessary in the staging of newly diagnosed patients with HL. Disclosures No relevant conflicts of interest to declare.


Author(s):  
Dominic Kaddu-Mulindwa ◽  
Bettina Altmann ◽  
Gerhard Held ◽  
Stephanie Angel ◽  
Stephan Stilgenbauer ◽  
...  

Abstract Purpose Fluorine-18 fluorodeoxyglucose positron emission tomography combined with computed tomography (FDG PET/CT) is the standard for staging aggressive non-Hodgkin lymphoma (NHL). Limited data from prospective studies is available to determine whether initial staging by FDG PET/CT provides treatment-relevant information of bone marrow (BM) involvement (BMI) and thus could spare BM biopsy (BMB). Methods Patients from PETAL (NCT00554164) and OPTIMAL>60 (NCT01478542) with aggressive B-cell NHL initially staged by FDG PET/CT and BMB were included in this pooled analysis. The reference standard to confirm BMI included a positive BMB and/or FDG PET/CT confirmed by targeted biopsy, complementary imaging (CT or magnetic resonance imaging), or concurrent disappearance of focal FDG-avid BM lesions with other lymphoma manifestations during immunochemotherapy. Results Among 930 patients, BMI was detected by BMB in 85 (prevalence 9%) and by FDG PET/CT in 185 (20%) cases, for a total of 221 cases (24%). All 185 PET-positive cases were true positive, and 709 of 745 PET-negative cases were true negative. For BMB and FDG PET/CT, sensitivity was 38% (95% confidence interval [CI]: 32–45%) and 84% (CI: 78–88%), specificity 100% (CI: 99–100%) and 100% (CI: 99–100%), positive predictive value 100% (CI: 96–100%) and 100% (CI: 98–100%), and negative predictive value 84% (CI: 81–86%) and 95% (CI: 93–97%), respectively. In all of the 36 PET-negative cases with confirmed BMI patients had other adverse factors according to IPI that precluded a change of standard treatment. Thus, the BMB would not have influenced the patient management. Conclusion In patients with aggressive B-cell NHL, routine BMB provides no critical staging information compared to FDG PET/CT and could therefore be omitted. Trial registration NCT00554164 and NCT01478542


2016 ◽  
Vol 37 (1) ◽  
pp. 23-29 ◽  
Author(s):  
Hugo J.A. Adams ◽  
John M.H. de Klerk ◽  
Rob Fijnheer ◽  
Ben G.F. Heggelman ◽  
Stefan V. Dubois ◽  
...  

2003 ◽  
Vol 28 (8) ◽  
pp. 674-676 ◽  
Author(s):  
Stephen B. Chiang ◽  
Alan Rebenstock ◽  
Liang Guan ◽  
Abass Alavi ◽  
Hongming Zhuang

Blood ◽  
2016 ◽  
Vol 128 (22) ◽  
pp. 5370-5370 ◽  
Author(s):  
Ankit Mangla ◽  
Muhammad Umair Mushtaq ◽  
Rohit Kumar ◽  
Nikki Agarwal ◽  
Sibgha Gull Chaudhary ◽  
...  

Abstract Background: The utility of bone marrow biopsy (BMB) in patients with Hodgkin lymphoma (HL) has been a controversial topic. Clinical stage 4 (CS4) has been shown to be an independent poor prognostic marker and is also included in the International Prognostic Scoring (IPS) index for predicting both progression-free survival (PFS) and overall survival (OS). The current guidelines still recommend performing a BMB in patients with stage IIB (with unfavorable risk factors), III and IV HL, mainly for staging purposes. Though bone marrow involvement (BMI) upstages the HL to stage IV, the prognostic significance of BMI remains unclear. The study was aimed to determine the prognostic significance of BMI in underserved patients with HL and to determine the prognostic importance of other blood parameters. Methods: The study was conducted at John H. Stroger Hospital of Cook County, an inner city tertiary care hospital providing care to the underserved population of Chicago. Charts of 241 patients diagnosed with HL were screened from tumor registry. Patients with incomplete charts were not included in the study. Socio-demographic, clinical and pathologic factors were recorded at the time of diagnosis. For comparative purpose, CS4 disease did not include patients with BMI. Kaplan-Meier and bivariate analyses were performed. Cox regression analyses were conducted to explore predictors of OS and PFS. Hazard ratios (HR) with 95% confidence intervals (CI) were obtained. Results: The study included 192 patients of which 41% were Afro-Americans, 34% were Hispanics and 21% were Caucasians. Median age was 34 years with 25.5% patients being older than 45 years and 68% patients being women. Seventeen percent patients were positive for HIV. Nodular sclerosis was the most common histologic subtype (55%), bulky disease was recorded in 19% patients and 61.5% patients had B-symptoms. CS4 disease was seen in 12% patients while 28% patients were stage III, 47% were stage II and 13% were stage I. Single-site BMB was done in 96% patients. BMB was positive for involvement with HL in 19% patients (n=37). Out of these 37 patients, 84% (n=31) had advanced stage (III & IV) HL. BMI was seen in 5% patients with early-stage HL (stages I-II) and 41% patients with advanced-stage HL. Median IPS score was 2 (range 0-6). Median values for clinical factors were: hemoglobin-11.8 g/dL, platelets 314.5 x103/uL, leukocytes 8.3 x103/uL, neutrophils 6x103/uL, lymphocytes 1.2 x103/uL and albumin 3.7 g/dL. Mean OS was 143 months (95% CI 126-160) with 5-year OS of 89%. Significant correlates of OS included: age 45 years or older (HR 2.83, 95%CI 1.25-6.43, P =0.013), HIV (HR 2.80, 95%CI 1.19-6.61, P =0.019), nodular sclerosistype (HR 0.29, 95%CI 0.12-0.71, P =0.006), CS4 disease (HR 3.05, 95%CI 1.20-7.77, P =0.019), BM positive for involvement with HL (HR 5.76, 95%CI 2.56-12.98, P <0.001), IPS score (HR 1.57, 95%CI 1.20-2.06, P =0.001), hemoglobin <10.5 g/dL (HR 3.57, 95%CI 1.56-8.19, P =0.003), platelets <150 x103/uL (HR 5.32, 95%CI 2.19-12.96, P <0.001) and lymphocytes <0.6 x103/uL (HR 2.97, 95%CI 1.21-7.28, P =0.017). Gender, albumin level, leukocytosis (>15 x103/uL) and relative lymphopenia (<8%) did not have a significant association with OS. When adjusted for CS4 disease, BMI remained an independent predictor of OS (HR 2.17, 95%CI 1.04-4.55, P =0.039). Mean PFS was 105 months (95% CI 97-117) with 5-year PFS of 78%. BMI (HR 2.38, 95%CI 1.21-4.67, P =0.012), albumin level (HR 0.71, 95%CI 0.53-0.94, P =0.017) and albumin-globulin ratio (HR 0.41, 95%CI 0.18-0.93, P =0.032) predicted PFS. None of the other factors had a significant association with PFS. BMI had inverse association with OS (mean OS 97.5 months vs. 164 months, P <0.001; 5-year OS 70% vs. 93.5%, P<0.001) and PFS (mean PFS 74 months vs. 112 months, P = 0.004; 5-year PFS 65% vs. 81%, P=0.030). Conclusion: BMI in HL indicates disseminated disease. Our study shows that BMI in patients with HL has a significant inverse relation with OS and PFS, independent of stage. Our data indicates that in patients with HL important prognostic information can be achieved by demonstrating BMI and it should be considered for inclusion in the IPS score. The rate of BMI is higher in our cohort, for both early and advanced stage HL, when compared with literature and maybe a limitation of our retrospective study. However our results still warrant that long term prospective studies should be designed to explore the prognostic significance of BMI. Disclosures No relevant conflicts of interest to declare.


2019 ◽  
Vol 7 (2) ◽  
pp. 95-100
Author(s):  
Ali ESER ◽  
Funda PEPEDİL TANRIKULU ◽  
Aslıhan SEZGİN ◽  
Ayşe Tülin TUĞLULAR

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