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1 not after each of 4 cycles of induction and consolidation chemotherapy.
2 d the benefit of cyclosporine (CsA) added to consolidation chemotherapy.
3 er ATRA maintenance or observation following consolidation chemotherapy.
4 who had been receiving radiation therapy and consolidation chemotherapy.
5 l [CI], 18% to 42%) in patients receiving no consolidation chemotherapy, 22% (95% CI, 17% to 28%) in
6 evaluated molecular response after induction/consolidation chemotherapy according to standardized met
8 vant chemotherapy with intrathecal thiotepa, consolidation chemotherapy, and autologous stem-cell res
9 erapy, autologous stem-cell transplantation, consolidation chemotherapy, and maintenance with interfe
11 ogeneic SCT, autologous transplantation, and consolidation chemotherapy are considered of equivalent
12 arm, and patients in this arm received less consolidation chemotherapy as a result of higher inducti
13 s bone marrow transplantation with intensive consolidation chemotherapy as treatments for children wi
16 rs administered after induction and possibly consolidation chemotherapy can shorten the duration of n
17 ompared randomized assignment with intensive consolidation chemotherapy (CC) or autologous bone marro
18 and safety of bortezomib in combination with consolidation chemotherapy consisting of intermediate-do
19 stable disease received two 21-day cycles of consolidation chemotherapy consisting of paclitaxel 200
21 ith high-dose DAT and the addition of CsA to consolidation chemotherapy did not prolong the durations
23 sting the addition of GO to induction and/or consolidation chemotherapy in untreated younger patients
26 of 254 patients who completed induction and consolidation chemotherapy on CALGB 9720 were randomly a
27 e/cytarabine combination, followed by either consolidation chemotherapy or allogeneic stem cell trans
31 2 weeks after chemoradiation, two cycles of consolidation chemotherapy separated by 3 weeks were giv
32 2 and Total Therapy 3 that applied post-HDT consolidation chemotherapy (suggesting possible post-HDT
33 Remitting patients received one course of consolidation chemotherapy that included DNR with or wit
34 ection, postoperative radiation therapy, and consolidation chemotherapy (three courses of cyclophosph
36 nts with AML receiving uniform induction and consolidation chemotherapy, we demonstrate that the time
37 first complete remission after induction and consolidation chemotherapy were randomly assigned to no
39 as a slightly higher death rate in CR during consolidation chemotherapy with ADE (9%) than with DAT (
40 remission (CR) received up to two courses of consolidation chemotherapy with cytarabine 2 gm/m(2) on
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