Chronic lymphocytic leukaemia is the most common
leukaemia in adults, and it remains an incurable malignancy with conventional
chemoimmunotherapy. A middle-aged gentleman who was diagnosed with high-risk
chronic lymphocytic leukaemia (CLL), Rai stage IV, Binet C with del(17p) and
del(13q) underwent allogeneic haematopoeitic stem cell transplantation
(allo-HSCT) from a human leukocyte antigen (HLA) identical sister. Allogeneic
haematopoeitic stem cell transplantation remains the only treatment with curative
potential but is associated with high non-relapsed mortality (NRM). The patient
developed extensive skin, oral, and liver chronic graft versus host disease
(GVHD) and required tacrolimus, mycophenolate mofetil (MMF), and prednisolone.
In seventh month after allo-HSCT, the patient presented with systemic symptoms,
right cervical lymphadenopathy, splenomegaly, marked pancytopaenia, and
elevated lactate dehydrogenase (LDH). Bone marrow study, immunophenotyping
(IP), chromosome analysis, and PET-CT scan confirmed relapsed CLL with no
evidence of Richter’s transformation or posttransplant lymphoproliferative
disease (PTLD). Withdrawal of immunosuppressant (IS) worsened cutaneous and
liver GVHD. Chemotherapy was not a suitable treatment option in view of immunodeficiency.
The patient underwent extracorporeal photopheresis (ECP) therapy eventually for
extensive chronic GVHD, and the IS were gradually tapered to the minimal
effective dose. The relapsed CLL was treated successfully with oral venetoclax
accessible via a compassionate drug program. This case highlights challenges in
managing relapsed CLL and loss of graft-versus-leukaemia (GVL) effect despite
extensive chronic GVHD. Venetoclax is an effective and well-tolerated oral novel
agent for relapsed CLL after allo-HSCT. In conclusion, this study achieved an
excellent outcome when treating a patient with relapsed CLL after allo-HSCT
using oral venetoclax and concomitant ECP therapy for extensive chronic GVHD.
Venetoclax is a well-tolerated oral novel agent and long-term follow-up is
important to ensure the disease achieves a sustained complete remission.
Author (s) Details
Ching Soon Teoh
Haematology Unit, Department of Internal Medicine,
Hospital Pulau Pinang, Jalan Residensi, 10990 Georgetown, Penang, Malaysia.
Ai Sim Goh
Haematology
Unit, Department of Internal Medicine, Hospital Pulau Pinang, Jalan Residensi,
10990 Georgetown, Penang, Malaysia.
Please
see the book :- https://doi.org/10.9734/bpi/rudhr/v9/337
No comments:
Post a Comment