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Title:
Bendamustine and rituximab (BR) versus dexamethasone, rituximab, and cyclophosphamide (DRC) in patients with Waldenström macroglobulinemia | Annals of Hematology
Description:
The treatment approaches for Waldenstrom macroglobulinemia (WM) are largely based upon information from single-arm phase II trials, without comparative data. We compared the efficacy of two commonly used regimens in routine practice (bendamustine-rituximab (BR) and dexamethasone, rituximab plus cyclophosphamide (DRC)) and evaluated their activity with respect to the patients’ MYD88L265P mutation status. Of 160 consecutive patients, 60 received BR (43 with relapsed/refractory WM) and 100 received DRC (50 had relapsed/refractory WM). In the treatment-naïve setting, overall response rate (ORR) was 93% with BR versus 96% with DRC (p = 0.55). Two-year progression-free survival (PFS) with BR and DRC was 88 and 61%, respectively (p = 0.07). In salvage setting, ORR was 95% with BR versus 87% with DRC, p = 0.45; median PFS with BR was 58 versus 32 months with DRC (2-year PFS was 66 versus 53%; p = 0.08). Median disease-specific survival was not reached with BR versus 166 months with DRC (p = 0.51). The time-to-event endpoints and depth of response were independent of the MYD88 mutation status. Grade ≥ 3 adverse events of both regimens were comparable. A trend for longer PFS was observed with BR although the regimens have comparable toxicities. The activity of BR and DRC appears to be unaffected by patients’ MYD88 mutation status.
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article, pubmed, macroglobulinemia, google, scholar, cas, rituximab, research, patients, waldenstroms, treon, versus, bendamustine, waldenstrom, received, institution, study, drc, treatment, lymphoma, oncol, data, myd, therapy, celgene, cyclophosphamide, ansell, kyle, kapoor, phase, castillo, clin, gertz, mayo, funding, kumar, morra, patterson, hunter, ibrutinib, usa, privacy, cookies, content, information, hematology, dexamethasone, waldenström, paludo, lacy,
Topics {✒️}
median disease-specific survival year progression-free survival month download article/chapter b-cell lymphoproliferative disorders relapsed indolent b-cell targeted genomic instability lymphoplasmacytic lymphoma access owen rg full article pdf mantle-cell lymphomas privacy choices/manage cookies myd88 mutation status waldenstrom macroglobulinemia/lymphoplasmacytic lymphomas front-line treatment regimens jama oncology 3 rummel mj received research funding phase iii study chronic lymphocytic leukemia article annals received research support clinical trial participation european economic area clinico-pathological profile tertiary care centre intermittent oral chlorambucil ohio lexi-comp adverse events v4 ethnic/racial minority ighv gene features institutional review board bristol-myers squibb leuk lymphoma 56 risk-adapted therapy conditions privacy policy consensus panel recommendations prashant kapoor year updated results article paludo mantle cell article log drug information handbook vith international workshop eighth international workshop 5th international workshop castillo jj accepting optional cookies clin lymphoma 5 chanan-khan aa common terminology criteria
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- Jimenez R, Zhang B, Joffe S, Nilsson M, Rivera L, Mutchler J, Lathan C, Paulk ME, Prigerson HG (2013) Clinical trial participation among ethnic/racial minority and majority patients with advanced cancer: what factors most influence enrollment?
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headline:Bendamustine and rituximab (BR) versus dexamethasone, rituximab, and cyclophosphamide (DRC) in patients with Waldenström macroglobulinemia
description:The treatment approaches for Waldenstrom macroglobulinemia (WM) are largely based upon information from single-arm phase II trials, without comparative data. We compared the efficacy of two commonly used regimens in routine practice (bendamustine-rituximab (BR) and dexamethasone, rituximab plus cyclophosphamide (DRC)) and evaluated their activity with respect to the patients’ MYD88L265P mutation status. Of 160 consecutive patients, 60 received BR (43 with relapsed/refractory WM) and 100 received DRC (50 had relapsed/refractory WM). In the treatment-naïve setting, overall response rate (ORR) was 93% with BR versus 96% with DRC (p = 0.55). Two-year progression-free survival (PFS) with BR and DRC was 88 and 61%, respectively (p = 0.07). In salvage setting, ORR was 95% with BR versus 87% with DRC, p = 0.45; median PFS with BR was 58 versus 32 months with DRC (2-year PFS was 66 versus 53%; p = 0.08). Median disease-specific survival was not reached with BR versus 166 months with DRC (p = 0.51). The time-to-event endpoints and depth of response were independent of the MYD88 mutation status. Grade ≥ 3 adverse events of both regimens were comparable. A trend for longer PFS was observed with BR although the regimens have comparable toxicities. The activity of BR and DRC appears to be unaffected by patients’ MYD88 mutation status.
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headline:Bendamustine and rituximab (BR) versus dexamethasone, rituximab, and cyclophosphamide (DRC) in patients with Waldenström macroglobulinemia
description:The treatment approaches for Waldenstrom macroglobulinemia (WM) are largely based upon information from single-arm phase II trials, without comparative data. We compared the efficacy of two commonly used regimens in routine practice (bendamustine-rituximab (BR) and dexamethasone, rituximab plus cyclophosphamide (DRC)) and evaluated their activity with respect to the patients’ MYD88L265P mutation status. Of 160 consecutive patients, 60 received BR (43 with relapsed/refractory WM) and 100 received DRC (50 had relapsed/refractory WM). In the treatment-naïve setting, overall response rate (ORR) was 93% with BR versus 96% with DRC (p = 0.55). Two-year progression-free survival (PFS) with BR and DRC was 88 and 61%, respectively (p = 0.07). In salvage setting, ORR was 95% with BR versus 87% with DRC, p = 0.45; median PFS with BR was 58 versus 32 months with DRC (2-year PFS was 66 versus 53%; p = 0.08). Median disease-specific survival was not reached with BR versus 166 months with DRC (p = 0.51). The time-to-event endpoints and depth of response were independent of the MYD88 mutation status. Grade ≥ 3 adverse events of both regimens were comparable. A trend for longer PFS was observed with BR although the regimens have comparable toxicities. The activity of BR and DRC appears to be unaffected by patients’ MYD88 mutation status.
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name:Division of Hematology, Mayo Clinic, Rochester, USA
type:PostalAddress
type:Organization
name:S. Vincent Rajkumar
affiliation:
name:Mayo Clinic
address:
name:Division of Hematology, Mayo Clinic, Rochester, USA
type:PostalAddress
type:Organization
name:Morie A. Gertz
affiliation:
name:Mayo Clinic
address:
name:Division of Hematology, Mayo Clinic, Rochester, USA
type:PostalAddress
type:Organization
name:Prashant Kapoor
affiliation:
name:Mayo Clinic
address:
name:Division of Hematology, Mayo Clinic, Rochester, USA
type:PostalAddress
type:Organization
email:[email protected]
PostalAddress:
name:Division of Hematology, Mayo Clinic, Rochester, USA
name:Department of Internal Medicine, Mayo Clinic, Rochester, USA
name:Division of Hematology, Mayo Clinic, Jacksonville, USA
name:Division of Hematology, Mayo Clinic, Rochester, USA
name:Division of Hematology, Mayo Clinic, Rochester, USA
name:Division of Hematology, Mayo Clinic, Jacksonville, USA
name:Division of Hematopathology, Mayo Clinic, Rochester, USA
name:Division of Hematology, Mayo Clinic, Rochester, USA
name:Division of Hematology, Mayo Clinic, Scottsdale, USA
name:Division of Hematology, Mayo Clinic, Rochester, USA
name:Division of Hematology, Mayo Clinic, Rochester, USA
name:Division of Hematology, Mayo Clinic, Rochester, USA
name:Division of Hematology, Mayo Clinic, Rochester, USA
name:Division of Hematology, Mayo Clinic, Rochester, USA
name:Division of Hematology, Mayo Clinic, Rochester, USA
name:Division of Hematology, Mayo Clinic, Rochester, USA
name:Division of Hematology, Mayo Clinic, Rochester, USA
name:Division of Hematology, Mayo Clinic, Rochester, USA
name:Division of Hematology, Mayo Clinic, Rochester, USA
name:Division of Hematology, Mayo Clinic, Rochester, USA
name:Division of Hematology, Mayo Clinic, Rochester, USA
name:Division of Hematology, Mayo Clinic, Rochester, USA
name:Division of Hematology, Mayo Clinic, Rochester, USA
name:Division of Hematology, Mayo Clinic, Rochester, USA
name:Division of Hematology, Mayo Clinic, Rochester, USA
name:Division of Hematology, Mayo Clinic, Rochester, USA
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