We read with interest the recent report of the NHL13 randomized trial, which evaluated a 2-year rituximab maintenance program versus no further treatment in patients with diffuse large B-cell lymphoma (DLBCL; n=662) or follicular lymphoma grade 3b (n=21), who had achieved a complete remission (CR) or CR unconfirmed (CRu) with 4-8 cycles of CHOP or similar chemotherapy and 8 rituximab applications.1 Overall, NHL13 was a "negative" trial: the 3-year event-free survival (EFS) was 80.4% in the rituximab maintenance arm versus 76.5% in the observation arm (P=0.14), while 3-year overall survival (OS) remained unchanged (92.0% vs. 90.4%). However, subgroup analysis revealed very interesting findings. Although rituximab maintenance did not work in females at all and toxicity was higher, males enjoyed a statistically and numerically significant benefit with a 3-year EFS of 84.1% versus 74.4% for rituximab maintenance versus observation (P=0.03), and a 3-year progression-free survival (PFS) of 89.0% versus 77.6% (P=0.006), but again with no impact on OS. Indeed, rituximab maintenance might have overcome the reduced exposure of elderly males to rituximab due to its faster clearance,2 similarly to what was observed in the SEXIE-R trial, where higher rituximab doses in induction obscured the adverse significance of male sex.3 A closer look at Figure 3 1 also reveals that a potential benefit from rituximab maintenance was more prominent in good risk patients according to most International Prognostic Index (IPI) factors (stage I/II, performance status 0-1, low LDH, <2 extranodal sites). As a result, low IPI risk males had the best outcomes. A notable exception to this "rule" was the observation that the 74 patients with bone marrow (BM) involvement (approx. 10% of the total number of patients), a feature associated with adverse prognosis, gained the most significant benefit from rituximab maintenance compared to any other patient subgroup (hazard ratio 0.31, 95%CI: 0.13-0.71, P=0.006 vs. a hazard ratio of 0.90, 95%CI: 0.64-1.26, P=0.53 for patients without BM involvement).Bone marrow involvement is observed in 13%-20% of patients with DLBCL.4-8 Bone marrow can be infiltrated by large cells in slightly more than 50% of these cases. 4,7,8 This "concordant" BM involvement is independently associated with poor PFS and OS 4,7,8 and a higher rate of primary refractory disease.7 In the remaining DLBCL patients with involved BM, the infiltration is due to the presence of small cells, resulting in "discordant" histology between the primary (nodal or extranodal) site and BM. Such cases of BM involvement are not independently associated with prognosis 4,7,8 and may reflect the presence of an underlying lowgrade lymphoma component, which is usually, but not always, of follicle-center cell origin.9 Such small cell BM populations are often, although not invariably, 9 clonally related to the original neoplastic DLBCL cell, and may potentially lead to a subsequent relapse that pursues a course resembling more to that of an indolent follicul...