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A morphometric study of bone marrow angiogenesis in hairy cell leukaemia with clinicopathological correlations
Author(s) -
Korkolopoulou Penelope,
Gribabis Despina A.,
Kavantzas Nikolaos,
Angelopoulou Maria K.,
Siakantaris Marina P.,
Patsouris Efstratios,
Androulaki Athina,
Thymara Irene,
Kokoris Styliani I.,
Kyrtsonis Maria C.,
Kittas Christos,
Pangalis Gerassimos A.
Publication year - 2003
Publication title -
british journal of haematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.907
H-Index - 186
eISSN - 1365-2141
pISSN - 0007-1048
DOI - 10.1046/j.1365-2141.2003.04527.x
Subject(s) - bone marrow , angiogenesis , microvessel , cd34 , pathology , univariate analysis , medicine , concomitant , immunohistochemistry , biology , multivariate analysis , stem cell , genetics
Summary. Bone marrow angiogenesis has recently been implicated in the pathophysiology and course of various haematological malignancies. Little is known, however, about the significance of this phenomenon in hairy cell leukaemia (HCL). We evaluated various morphometric characteristics of microvessels, highlighted by means of anti‐CD34 immunohistochemistry, in the bone marrow of 44 patients with typical HCL, before and after treatment with interferon‐α (IFN‐α). Overall, bone marrow from 103 HCL patients and 20 controls was examined. Microvessel density (MVD) and several size‐ and shape‐related parameters were quantified in the region of most intense vascularization using image analysis. MVD, size‐related parameters and the percentage of branching microvessels were higher in HCL than in controls. Likewise, perimeter counts were higher in partial/non‐responders than in complete responders. Achievement of complete response was accompanied by smaller calibre microvessels. IFN‐α induced a decrease in MVD and branching values in cases with diffuse marrow involvement. In univariate analysis, progression‐free survival was adversely affected by MVD, branching and major axis length. Multivariate analysis indicated that MVD/branching independently affected progression‐free survival and the likelihood of complete response. Our data suggest that the generation of bone marrow microvessels indicated an increased risk of progression and IFN‐α treatment failure in HCL. Furthermore, the prognostic significance of angiogenesis requires the concomitant assessment of MVD and the complexity of the microvascular network.