Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Multicenter Study
. 2017 Nov;6(11):2507-2514.
doi: 10.1002/cam4.1205. Epub 2017 Sep 27.

Bone marrow biopsy superiority over PET/CT in predicting progression-free survival in a homogeneously-treated cohort of diffuse large B-cell lymphoma

Affiliations
Multicenter Study

Bone marrow biopsy superiority over PET/CT in predicting progression-free survival in a homogeneously-treated cohort of diffuse large B-cell lymphoma

Tzu-Hua Chen-Liang et al. Cancer Med. 2017 Nov.

Abstract

Several studies have reported uneven results when evaluating the prognostic value of bone marrow biopsy (BMB) and PET/CT as part of the staging of diffuse large B-cell lymphoma (DLBCL). The heterogeneity of the inclusion criteria and not taking into account selection and collinearity biases in the analysis models might explain part of these discrepancies. To address this issue we have carried a retrospective multicenter study including 268 DLBCL patients with a BMB and a PET/CT available at diagnosis where we estimated both the prognosis impact and the diagnostic accuracy of each technique. Only patients treated with R-CHOP/21 as first line (n = 203) were included in the survival analysis. With a median follow-up of 25 months the estimated 3-year progression-free survival (PFS) and overall survival (OS) were 76.3% and 82.7% respectively. In a multivariate analysis designed to avoid a collinearity bias with IPI categories, BMB-BMI [bone marrow involvement](+) (HR: 3.6) and ECOG PS > 1 (HR: 2.9) were independently associated with a shorter PFS and three factors, age >60 years old (HR: 2.4), ECOG PS >1 (HR: 2.4), and abnormally elevated B2-microglobulin levels (HR: 2.2) were independently associated with a shorter OS. In our DLBCL cohort, treated with a uniform first-line chemotherapy regimen, BMI by BMB complemented performance status in predicting those patients with a higher risk for relapse or progression. In this cohort BMI by PET/CT could not independently predict a shorter PFS and/or OS.

Keywords: Bone marrow biopsy; PET/CT; diffuse large B-cell lymphoma; outcomes research.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Study flow diagram. Visual representation of the exclusion criteria (left) and chemotherapy regimens (right).
Figure 2
Figure 2
Kaplan–Meier estimates of PFS in R‐CHOP/21(N = 203), treated DLBCL according to BMI with PET/CT (A) or bone marrow biopsy (B). BMI, bone marrow involvement; BMB, bone marrow biopsy; PET/CT, positron emission tomography/computed tomography.

References

    1. El‐Najjar, I. , Barwick T., Avril N., and Montoto S.. 2012. The role of FDG‐PET and bone marrow examination in lymphoma staging. Ann. Oncol. 23(SUPPL. 10):2–4. - PubMed
    1. Conlan, M. G. , Bast M., Armitage J. O., and Weisenburger D. D.. 1990. Bone marrow involvement by non‐Hodgkin's lymphoma: the clinical significance of morphologic discordance between the lymph node and bone marrow. Nebraska Lymphoma Study Group. J. Clin. Oncol. 8:1163–1172. - PubMed
    1. Avigdor, A . 2013. Staging DLBCL: bone marrow biopsy or PET‐CT? Blood 122:4–5. - PubMed
    1. Adams, H. J. A. , and Kwee T. C.. 2016. Reply: The Need for Prudence required when using 18F‐FDG PET as reference standard for lymphoma detection. J. Nucl. Med. 58:1354–1355. - PubMed
    1. Adams, H. J. A. , and Kwee T. C.. 2015. Do not abandon the bone marrow biopsy yet in diffuse large B‐cell lymphoma. J. Clin. Oncol. 33:1217. - PubMed

Publication types

MeSH terms