As a different entity of diffuse large B-cell lymphoma (DLBCL) according to the current World Health Organization classification, 1 primary mediastinal large B-cell lymphoma (PMBL) is different from DLBCL in terms of clinical, immunohistochemical and genetic features. 2 Despite a remarkable advance with first-line treatment of PMBL patients in the rituximab era, 3 , 4 , 5 , 6 , 7 10–30% of patients still experience progression or relapse. Although patients with relapsed or refractory PMBL are often treated with high-dose therapy followed by autologous stem cell transplantation (HDT/ASCT) after salvage treatment, the progression-free survival (PFS) at 5 years of 27% is unsatisfactory compared with DLBCL in the pre-rituximab era. 8 , 9 , 10 Moreover, information regarding outcomes after HDT/ASCT for relapsed or refractory PMBL is limited in the rituximab era. Therefore, clarifying the current role of HDT/ASCT is vital to establish the optimal treatment strategy.
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Aoki et al. (2015) studied this question.
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