TY - JOUR
T1 - Diffuse large B-cell lymphoma
T2 - Experience from a tertiary care center in North India
AU - Khera, Rohan
AU - Jain, Snigdha
AU - Kumar, Lalit
AU - Thulkar, S.
AU - Vijayraghwan, M.
AU - Dawar, R.
N1 - Funding Information:
Immediately after the publication of the report of the Royal Commission on Medical Education, in April 1968, Morris wrote to the chairmen of the Council of the Society of MOsH,49 of the meeting of the SAMOs,50of the Committee of the Society for Social Medicine (SSM)51 and of the Scottish Association of Medical Administrators (SAMA)52 and the chief medical officers of the Ministry of Health and the Scottish Home and Health Department inviting them or their representatives to a meeting at the London School of Hygiene and Tropical Medicine to consider the recommendation of the Royal Commission quoted at the beginning of this paper.
PY - 2010/6
Y1 - 2010/6
N2 - Limited information is available from developing countries regarding clinico-pathological presentation of diffuse large B-cell lymphoma (DLBCL). We undertook a retrospective case record study to determine the clinicolaboratory characteristics, treatment outcomes, and prognostic factors for DLBCL and additionally analyzed percentage distribution and patient characteristics for other major subtypes of non-Hodgkin's lymphoma (NHL). DLBCL, constituting 59.3% of all NHL cases, was the predominant subtype. For DLBCL, males:females ratio was 2.7:1 and the median age at presentation was 47 years. Lymphadenopathy was present in 57% patients and B symptoms in 56.7%. A total of 49.3% of patients had Ann Arbor Stage IV disease. Significant differences were observed between favorable (international prognostic index [IPI]-0, 1, and 2) and unfavorable prognosis groups (IPI-3, 4, and 5) with regards to mean hemoglobin levels (P\0.005), platelet counts (P\0.05), serum albumin levels (P\0.05), and erythrocyte sedimentation rates (P\0.005), thereby suggesting their role as prognostic markers in our population. The median event free survival was 32 months (95% CI: 0-92 months) and the median overall survival was 47 months (95% CI: 3-100 months). Among total NHL, the earlier age of onset, male dominant sex ratio, and higher frequency of B symptoms sets apart NHL in Indian population from that in the developed countries.
AB - Limited information is available from developing countries regarding clinico-pathological presentation of diffuse large B-cell lymphoma (DLBCL). We undertook a retrospective case record study to determine the clinicolaboratory characteristics, treatment outcomes, and prognostic factors for DLBCL and additionally analyzed percentage distribution and patient characteristics for other major subtypes of non-Hodgkin's lymphoma (NHL). DLBCL, constituting 59.3% of all NHL cases, was the predominant subtype. For DLBCL, males:females ratio was 2.7:1 and the median age at presentation was 47 years. Lymphadenopathy was present in 57% patients and B symptoms in 56.7%. A total of 49.3% of patients had Ann Arbor Stage IV disease. Significant differences were observed between favorable (international prognostic index [IPI]-0, 1, and 2) and unfavorable prognosis groups (IPI-3, 4, and 5) with regards to mean hemoglobin levels (P\0.005), platelet counts (P\0.05), serum albumin levels (P\0.05), and erythrocyte sedimentation rates (P\0.005), thereby suggesting their role as prognostic markers in our population. The median event free survival was 32 months (95% CI: 0-92 months) and the median overall survival was 47 months (95% CI: 3-100 months). Among total NHL, the earlier age of onset, male dominant sex ratio, and higher frequency of B symptoms sets apart NHL in Indian population from that in the developed countries.
KW - Diffuse large B-cell lymphoma
KW - India
KW - Lymphoma
KW - Non-Hodgkin's lymphoma
KW - Prognostic factors
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U2 - 10.1007/s12032-009-9211-2
DO - 10.1007/s12032-009-9211-2
M3 - Article
C2 - 19350421
AN - SCOPUS:77956906938
SN - 1357-0560
VL - 27
SP - 310
EP - 318
JO - Medical Oncology
JF - Medical Oncology
IS - 2
ER -