High risk CLL pts get allogeneic hematopoietic stem cell transplantation (allo-SCT).
Major cause of allo-SCT failure is relapse or disease progression.
No standard treatment available and prognosis of failed allo-SCT pts unknown.
Retrospective intention-to-treat analysis between 1998 and 2012 at MD Anderson Cancer Center.
73 pts with CLL (n=40, 55%) or Richter's transformation (RT, n=33, 45%) who failed or progressed after median of 7 months (range 0-85 months).
63 received non-myeloablative conditioning and 32 received donor lymphocyte infusion (DLI).
68 (93%) received salvage therapy.
Median of 2 treatment regimens (range 0 - 8) administered.
Most common salvage treatment regimens: rituximab (R): R-HyperCVAD (n=24, 33%), OFAR (n=13, 18%), FCR, FBR, PCR, BR (n=24, 33%), thalidomide or lenalidomide (n=21, 29%), alemtuzumab with or without chemotherapy (n=12, 16%), Bruton's Tyrosine Kinase (BTK) inhibitor (n=5, 7%).
Last follow up: 26 pts (36%) alive.
Median overall survival (OS) was 33 months (95% CI, 27– 39) and 60% of the pts were alive 2 years from time of progression.
Median OS high-risk CLL or RT from time of allo-SCT failure/progression: 33 months.
Longest OS in pts who attained CR after first salvage treatment.
OS of pts treated with BTK inhibitors not reached.
No treatment modality appeared superior.
BTK inhibitors likely to prove superior.
CR after salvage is important prognostic marker.