2012
DOI: 10.1016/s1470-2045(12)70481-3
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Conventional chemotherapy (CHOEP-14) with rituximab or high-dose chemotherapy (MegaCHOEP) with rituximab for young, high-risk patients with aggressive B-cell lymphoma: an open-label, randomised, phase 3 trial (DSHNHL 2002-1)

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Cited by 223 publications
(175 citation statements)
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“…5,6 One of the largest randomized trials incorporating ASCT conducted without positron emission tomography (PET) scans failed to show an obvious benefit of early dose-escalated sequential HDT. 7 Similar trials used a variety of study designs, and the value of treatment intensification remains unresolved; suffice to say that such treatment is feasible, but at the price of greater toxicity than that associated with the current standard treatment. A more individualized approach, such as interim PET-based risk stratification, would allow the selection of high-risk patients for treatment intensification, while at the same time avoiding unnecessary toxicity in patients destined to do well with R-CHOP alone.…”
Section: Introductionmentioning
confidence: 99%
“…5,6 One of the largest randomized trials incorporating ASCT conducted without positron emission tomography (PET) scans failed to show an obvious benefit of early dose-escalated sequential HDT. 7 Similar trials used a variety of study designs, and the value of treatment intensification remains unresolved; suffice to say that such treatment is feasible, but at the price of greater toxicity than that associated with the current standard treatment. A more individualized approach, such as interim PET-based risk stratification, would allow the selection of high-risk patients for treatment intensification, while at the same time avoiding unnecessary toxicity in patients destined to do well with R-CHOP alone.…”
Section: Introductionmentioning
confidence: 99%
“…15 The anti-CD20 monoclonal antibody rituximab used in combination with cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) chemotherapy is standard treatment for DLBCL. [16][17][18][19][20][21][22] However, there is a need to further improve treatment outcomes, as the 2-year PFS rate of a large populationbased analysis of R-CHOP was only 69%. 23 In a second SWOG study, the feasibility and safety of adding bevacizumab to R-CHOP (RA-CHOP) was explored in 13 patients with newly diagnosed DLBCL.…”
Section: Introductionmentioning
confidence: 99%
“…In aaIPI = 1, better survival has been demonstrated with the more intensive regimen rituximab-doxorubicin-cyclophosphamidevindesine-bleomycin-prednisone (R-ACVBP) than R-CHOP-without-irradiation (Recher et al, 2011). In aaIPI ≥ 2, rituximab was combined with CHOP-etoposide (R-CHOEP), which is now common in Europe, but not in North America, where R-CHOP is given to most patients (Armitage, 2012;Schmitz et al, 2012). Recent Scandinavian registry studies suggest that R-CHOEP is preferable to R-CHOP in younger high-risk patients (Gang et al, 2012;Wasterlid et al, 2015).…”
Section: Introductionmentioning
confidence: 99%