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1 her risk of Waldenstrom macroglobulinemia, a low-grade lymphoma.
2 ombination for patients with advanced-stage, low-grade lymphoma.
3 nged survival in some patients with advanced low-grade lymphoma.
4 tologous hematopoietic rescue for follicular low-grade lymphoma.
5 dered dependable in evaluating patients with low-grade lymphoma.
6 nd site sensitivity was 32% in patients with low-grade lymphoma.
7 ive against chronic lymphocytic leukemia and low-grade lymphomas.
8 mation was lower than that observed in other low-grade lymphomas.
9 tential for combination with other agents in low-grade lymphomas.
12 or DLBCL/PMBCL, 63% (95% CI, 25% to 92%) for low-grade lymphoma, and 50% (95% CI, 16% to 84%) for CLL
13 ariant exhibits the clinical attributes of a low-grade lymphoma; and (3) the poor survival rates of p
17 A large fraction of patients with stage I-II low-grade lymphoma attain long-term disease-free surviva
18 strom macroglobulinemia (WM) is an incurable low-grade lymphoma characterized by bone marrow (BM) inv
19 um-67-citrate appears relatively nonavid for low-grade lymphoma compared to 201Tl and is statisticall
21 ic immunophenotyping study when performed in low-grade lymphomas correlates with marrow involvement.
25 , the role of bone marrow transplantation in low-grade lymphomas has been limited by the usual indole
26 sibling bone marrow transplants in advanced low-grade lymphoma in an observational study of 113 pati
27 l and is statistically inferior in detecting low-grade lymphoma in comparison to its ability to detec
28 nation in patients with previously untreated low-grade lymphoma is cyclophosphamide 1, 000 mg/m(2) da
29 ithin the abdomen, since gallium avidity for low-grade lymphoma is low and gastrointestinal excretion
31 ogical appearance and a resemblance to other low-grade lymphomas, many of which grow slowly, this lym
32 l salvage therapy for relapsed follicular or low-grade lymphomas now includes monoclonal antibody the
34 201Tl and 67Ga sensitivity in patients with low-grade lymphoma on a site basis was statistically sig
35 r, relatively small numbers of patients with low grade lymphoma or chronic lymphocytic leukemia have
37 ent against chronic lymphocytic leukemia and low-grade lymphoma, produces synergistic cytotoxicity ag
38 tive evidence that any treatment of advanced low-grade lymphoma prolongs survival, although the use o
41 e cohort used for MIPI-b development (German Low-Grade Lymphoma Study Group [GLSG] 1996 and GLSG2000)
42 munochemotherapy (151 patients from a German Low-Grade Lymphoma Study Group [GLSG] trial and 107 pati
43 treated within phase 3 trials of the German Low-Grade Lymphoma Study Group, were comparatively analy
44 was found to be statistically more avid for low-grade lymphoma than for intermediate, high or Hodgki
45 leukemia, chronic lymphocytic leukemia, and low-grade lymphomas that are not intrinsically very aggr
53 l or 67Ga is dependable in the evaluation of low-grade lymphoma within the abdomen, since gallium avi