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Copyright ©The Author(s) 2021.
World J Clin Oncol. Oct 24, 2021; 12(10): 882-896
Published online Oct 24, 2021. doi: 10.5306/wjco.v12.i10.882
Table 2 Clinical efficacy of lenalidomide single-agent in T-cell lymphomas
Ref.Patient, nStudy designTreatmentHistology (number of patients)ORRCR rateMedian PFSMedian DORMedian OS
Ishida et al[44], 201626Multicenter phase II25 mg continuously until progression or unacceptable toxicityATLL (26)42%19%3.8 moNR20.3 mo
Querfeld et al[52], 201432Multicenter phase II25 mg for 21 d of a 28-d cycle; initial dose was reduced to 10 mg, with the possibility of increasing by 5 mg every cycle, until a maximum of 25 mg, until progression or up to 2 yr for SD or PR, while patients in CR received two additional cyclesTotal evaluable (29)28%/8 mo10 mo43 mo
Mycosis fungoides (19)36.8%
Sézary syndrome (13)15.4%
Zinzani et al[56], 201110Phase II, bi-centric25 mg for 21 d of a 28-d cycle for 4 cycles as induction phase; After the 4th cycle, patients who achieved at least a SD continued for other eight cycles as maintenancePTCL-NOS (10)30%30%NA13 moNA
Morschhauser et al[51], 201354Multicenter phase II25 mg on d 1-21 of a 28-d cycle, until progression or unacceptable toxicity, for a maximum of 2 yrTotal evaluable (54)22%11%2.5 mo (4.6 mo in AITL)3.6 moNA
AITL (26)31%15%
PTCL-NOS (20)20%NA
CTCL (3)NANA
ALCL (3)NANA
Cutaneous ALCL (1)NANA
Extranodal NK/T-cell, nasal type (1)NANA
Toumishey et al[57], 201539Multicenter phase II25 mg daily on d 1-21 of a 28-d cycle, until progression or unacceptable toxicityTotal evaluable (39)26%7.7%4 mo13 mo12 mo
ALCL (10)10%/
AITL (9)33%11.1%
PTCL-NOS (14)43%14.3%
Other (6)//