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Sökning: WFRF:(Jerkeman Mats) > Lenalidomide-bendam...

Lenalidomide-bendamustine-rituximab in patients older than 65 years with untreated mantle cell lymphoma

Albertsson-Lindblad, Alexandra (författare)
Skane Univ Hosp, Dept Oncol, SE-22185 Lund, Sweden.
Kolstad, Arne (författare)
Oslo Univ Hosp, Dept Oncol, Oslo, Norway.
Laurell, Anna (författare)
Univ Uppsala Hosp, Dept Oncol, Uppsala, Sweden.
visa fler...
Raty, Riikka (författare)
Helsinki Univ Hosp, Dept Hematol, Helsinki, Finland.
Gronbaek, Kirsten (författare)
Rigshosp, Dept Hematol, Copenhagen, Denmark.
Sundberg, Jan (författare)
Skane Univ Hosp, Dept Oncol, SE-22185 Lund, Sweden.
Pedersen, Lone Bredo (författare)
Rigshosp, Dept Hematol, Copenhagen, Denmark.
Ralfkiaer, Elisabeth (författare)
Rigshosp, Dept Pathol, Copenhagen, Denmark.
Karjalainen-Lindsberg, Marja-Liisa (författare)
Univ Helsinki, Cent Hosp, Dept Pathol, Helsinki, Finland.
Sundström, Christer (författare)
Uppsala universitet,Klinisk och experimentell patologi,Department of Pathology, Uppsala University Hospital, Uppsala, Sweden; and.,Rose-Marie Amini
Ehinger, Mats (författare)
Univ Lund Hosp, Dept Pathol Cytol, Lund, Sweden.
Geisler, Christian (författare)
Rigshosp, Dept Hematol, Copenhagen, Denmark.
Jerkeman, Mats (författare)
Skane Univ Hosp, Dept Oncol, SE-22185 Lund, Sweden.
visa färre...
Skane Univ Hosp, Dept Oncol, SE-22185 Lund, Sweden Oslo Univ Hosp, Dept Oncol, Oslo, Norway. (creator_code:org_t)
American Society of Hematology, 2016
2016
Engelska.
Ingår i: Blood. - : American Society of Hematology. - 0006-4971 .- 1528-0020. ; 128:14, s. 1814-1820
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • For elderly patients with mantle cell lymphoma (MCL), there is no defined standard therapy. In this multicenter, open-label phase 1/2 trial, we evaluated the addition of lenalidomide (LEN) to rituximab-bendamustine (R-B) as first-line treatment for elderly patients with MCL. Patients >65 years with untreated MCL, stages II-IV were eligible for inclusion. Primary end points were maximally tolerable dose (MTD) of LEN and progression-free survival (PFS). Patients received 6 cycles every four weeks of L-B-R (L D1-14, B 90 mg/m(2) IV, days 1-2 and R 375 mg/m(2) IV, day 1) followed by single LEN (days 1-21, every four weeks, cycles 7-13). Fifty-one patients (median age 71 years) were enrolled from 2009 to 2013. In phase 1, the MTD of LEN was defined as 10 mg in cycles 2 through 6, and omitted in cycle 1. After 6 cycles, the complete remission rate (CRR) was 64%, and 36% were MRD negative. At a median follow-up time of 31 months, median PFS was 42 months and 3-year overall survival was 73%. Infection was the most common nonhematologic grade 3 to 5 event and occurred in 21 (42%) patients. Opportunistic infections occurred in 3 patients: 2 Pneumocystis carinii pneumonia and 1 cytomegalovirus retinitis. Second primary malignancies (SPM) were observed in 8 patients (16%). LEN could safely be combined with R-B when added from the second cycle in patients with MCL, and was associated with a high rate of CR and molecular remission. However, we observed a high degree of severe infections and an unexpected high number of SPMs, which may limit its use. This trial is registered at www.Clinicaltrials.gov as #NCT00963534.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Hematologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Hematology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Klinisk laboratoriemedicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Clinical Laboratory Medicine (hsv//eng)

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Patologi
Pathology

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