Prognostic role of serum beta 2-microglobulin in Hodgkin's disease. 1993

M A Dimopoulos, and F Cabanillas, and J J Lee, and F Swan, and L Fuller, and P K Allen, and F B Hagemeister
Department of Hematology, M.D. Anderson Cancer Center, Houston, TX 77030.

OBJECTIVE To evaluate the role of serum beta 2-microglobulin (beta 2M) in the prognosis of patients with Hodgkin's disease. METHODS One hundred sixty previously untreated patients with Hodgkin's disease had serum beta 2M levels determined before initiation of treatment. Serum beta 2M was tested for its correlation with known prognostic factors for patients with Hodgkin's disease. These variables, including beta 2M, were correlated with complete remission (CR) rate and time to treatment failure (TTF). Univariate and multivariate analyses were performed. RESULTS Serum beta 2M levels greater than 2.5 mg/L were found in 29% of patients. Such elevation was more common in patients with more advanced-stage disease. Elevated serum beta 2M was an independent and powerful factor in the prediction of lower response rate and shorter TTF. Its impact appeared to be more significant in patients with advanced disease. CONCLUSIONS Serum beta 2M appears to correlate with tumor stage in patients with Hodgkin's disease and elevated serum levels of this polypeptide predict a less favorable prognosis.

UI MeSH Term Description Entries
D008297 Male Males
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D011379 Prognosis A prediction of the probable outcome of a disease based on a individual's condition and the usual course of the disease as seen in similar situations. Prognostic Factor,Prognostic Factors,Factor, Prognostic,Factors, Prognostic,Prognoses
D005260 Female Females
D006689 Hodgkin Disease A malignant disease characterized by progressive enlargement of the lymph nodes, spleen, and general lymphoid tissue. In the classical variant, giant usually multinucleate Hodgkin's and REED-STERNBERG CELLS are present; in the nodular lymphocyte predominant variant, lymphocytic and histiocytic cells are seen. Granuloma, Hodgkin,Granuloma, Malignant,Hodgkin Lymphoma,Lymphogranuloma, Malignant,Granuloma, Hodgkin's,Granuloma, Hodgkins,Hodgkin Lymphoma, Adult,Hodgkin's Disease,Hodgkin's Lymphoma,Hodgkins Disease,Lymphocyte Depletion Hodgkin's Lymphoma,Lymphocyte-Rich Classical Hodgkin's Lymphoma,Mixed Cellularity Hodgkin's Lymphoma,Nodular Lymphocyte-Predominant Hodgkin's Lymphoma,Nodular Sclerosing Hodgkin's Lymphoma,Adult Hodgkin Lymphoma,Disease, Hodgkin,Disease, Hodgkin's,Disease, Hodgkins,Hodgkin Granuloma,Hodgkin's Granuloma,Hodgkins Granuloma,Hodgkins Lymphoma,Lymphocyte Rich Classical Hodgkin's Lymphoma,Lymphogranulomas, Malignant,Lymphoma, Hodgkin,Lymphoma, Hodgkin's,Malignant Granuloma,Malignant Granulomas,Malignant Lymphogranuloma,Malignant Lymphogranulomas,Nodular Lymphocyte Predominant Hodgkin's Lymphoma
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D001613 beta 2-Microglobulin An 11-kDa protein associated with the outer membrane of many cells including LYMPHOCYTES. It is the small subunit of MHC CLASS I MOLECULES. Association with beta 2-microglobulin is generally required for the transport of class I heavy chains from the endoplasmic reticulum to the cell surface. Beta 2-microglobulin is present in small amounts in serum, CEREBROSPINAL FLUID, and urine of healthy individuals, and to a much greater degree in the urine and plasma of patients with tubular PROTEINURIA, renal failure, or kidney transplants. Thymotaxin,beta 2 Microglobulin

Related Publications

M A Dimopoulos, and F Cabanillas, and J J Lee, and F Swan, and L Fuller, and P K Allen, and F B Hagemeister
March 1983, European journal of cancer & clinical oncology,
M A Dimopoulos, and F Cabanillas, and J J Lee, and F Swan, and L Fuller, and P K Allen, and F B Hagemeister
July 2002, Haematologica,
M A Dimopoulos, and F Cabanillas, and J J Lee, and F Swan, and L Fuller, and P K Allen, and F B Hagemeister
August 1992, Lancet (London, England),
M A Dimopoulos, and F Cabanillas, and J J Lee, and F Swan, and L Fuller, and P K Allen, and F B Hagemeister
August 1992, Lancet (London, England),
M A Dimopoulos, and F Cabanillas, and J J Lee, and F Swan, and L Fuller, and P K Allen, and F B Hagemeister
August 1992, Lancet (London, England),
M A Dimopoulos, and F Cabanillas, and J J Lee, and F Swan, and L Fuller, and P K Allen, and F B Hagemeister
April 1993, British journal of cancer,
M A Dimopoulos, and F Cabanillas, and J J Lee, and F Swan, and L Fuller, and P K Allen, and F B Hagemeister
May 1979, European journal of cancer,
M A Dimopoulos, and F Cabanillas, and J J Lee, and F Swan, and L Fuller, and P K Allen, and F B Hagemeister
September 1986, Mayo Clinic proceedings,
M A Dimopoulos, and F Cabanillas, and J J Lee, and F Swan, and L Fuller, and P K Allen, and F B Hagemeister
October 1992, Leukemia,
M A Dimopoulos, and F Cabanillas, and J J Lee, and F Swan, and L Fuller, and P K Allen, and F B Hagemeister
January 1991, Hematological oncology,
Copied contents to your clipboard!