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. 2012 Aug 5;2012:945950. doi: 10.1155/2012/945950

Table 1.

Studies on rituximab-based chemotherapy that investigated both HCV reactivation and hepatic flares.

   Coppola et al., 2012 [40] Ennishi et al., 2010 [36] Marignani et al., 2011 [39] Pitini et al., 2010 [38] Tsutsumi et al., 2009 [37]
Type of study Observational prospective Multicentre retrospective Observational retrospective Observational prospective Observational prospective
Disease LNH, CLL LNH (DLBCL) LNH LNH (DLBCL, FL) LNH (DLBCL)
Number of cases 8 34 3 10 4
Treatment R-CHOP in 5 R- and P-based R-CHOP RCHOP R-CHOP in 1
R-FC in 1 chemotherapy R-CHO in 2
CP and then R-FC R-THP-CO in 1
in 1
FC in 1
With HCV reactivation, number of cases: 7 34 2 10 4
 During CT 7 34 0 10 4
 After CT 0 0 2 0 0
With hepatic flare, number of cases: 7 The available datum (27%) refers to flares observed in 131 patients, of whom only 34 were followed up for HCV RNA 2 10 3
 During CT 7 0 10 3
 After CT 0 2 0 0

NHL: non-Hodgkin lymphoma; DLBCL: diffuse large B-cell lymphoma; FL: follicular lymphoma; CLL: chronic lymphocytic leukaemia; R-CHO: rituximab, cyclophosphamide, doxorubicin, vincristine; RFC: rituximab, fludarabine, and cyclophosphamide; CP: cyclophosphamide, prednisone; FC: fludarabine and cyclophosphamide; R-THPCOP: rituximab, pirarubicin (tetrahydropyranyl-adriamicin [TPH] ) cyclophosphamid, vincristine without prednisone.