High remission rate in T-cell prolymphocytic leukemia with CAMPATH-1H.

@article{Dearden2001HighRR,
  title={High remission rate in T-cell prolymphocytic leukemia with CAMPATH-1H.},
  author={Claire Dearden and Estella Matutes and Bruno Cazin and Geir Erland Tj{\o}nnfjord and Ant{\'o}nio Parreira and Benet Nomdedeu and Pietro Leoni and Fiona J. Clark and Deepti H Radia and Saad M. B. Rassam and Tony Roques and Nicolas Ketterer and Vasantha Brito‐Babapulle and M. J. S. Dyer and Daniel Catovsky},
  journal={Blood},
  year={2001},
  volume={98 6},
  pages={
          1721-6
        }
}
T-cell prolymphocytic leukemia (T-PLL) is a chemotherapy-resistant malignancy with a median survival of 7.5 months. Preliminary results indicated a high remission induction rate with the human CD52 antibody, CAMPATH-1H. This study reports results in 39 patients with T-PLL treated with CAMPATH-1H between March 1993 and May 2000. All but 2 patients had received prior therapy with a variety of agents, including 30 with pentostatin; none achieved complete remission (CR). CAMPATH-1H (30 mg) was… 

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References

SHOWING 1-10 OF 21 REFERENCES

Treatment of T-cell prolymphocytic leukemia with human CD52 antibody.

  • R. PawsonM. Dyer D. Catovsky
  • Medicine, Biology
    Journal of clinical oncology : official journal of the American Society of Clinical Oncology
  • 1997
CAMPATH-1H alone is not sufficient for long-term remissions, and the role of autologous stem-cell transplantation needs further investigation, but it represents a significant improvement over other types of therapy.

The role of pentostatin in the treatment of T-cell malignancies: analysis of response rate in 145 patients according to disease subtype.

It is concluded that DCF is effective as a single agent in T-PLL, Sézary syndrome, and LGL leukemia, but has low activity in other T-cell disorders.

Phase II multicenter study of human CD52 antibody in previously treated chronic lymphocytic leukemia. European Study Group of CAMPATH-1H Treatment in Chronic Lymphocytic Leukemia.

  • A. OsterborgM. Dyer H. Mellstedt
  • Medicine, Biology
    Journal of clinical oncology : official journal of the American Society of Clinical Oncology
  • 1997
CAMPATH-1H had significant activity in patients with advanced and chemotherapy-resistant CLL, and the most pronounced effects were noted in blood, bone marrow, and spleen.

Indolent course as a relatively frequent presentation in T‐prolymphocytic leukaemia

T‐PLL may start as an indolent disease similar to that reported in ataxia telangectasia, and in this rare genetic disorder, some patients develop stable T‐cell clones which progress toward T‐P LL‐like leukaemia.

In vivo CAMPATH-1H prevents graft-versus-host disease following nonmyeloablative stem cell transplantation.

This study demonstrates that this nonmyeloablative preparative regimen is associated with durable engraftment, minimal toxicity, and low incidence of GVHD.

REMISSION INDUCTION IN NON-HODGKIN LYMPHOMA WITH RESHAPED HUMAN MONOCLONAL ANTIBODY CAMPATH-1H

Treatment of T prolymphocytic leukemia with allogeneic bone marrow transplantation

A 47-year-old male with refractory T-PLL who was treated with high-dose chemoradiotherapy and allogeneic bone marrow transplantation from an HLA-matched sibling achieves complete remission and remains in remission 3 years after the transplant.

In vivo‘Purging’ of residual disease in CLL with Campath‐1H

Treatment with Campath‐1H may be of value in eradicating residual disease in CLL and may facilitate high‐dose therapy in young patients.

Clinical and laboratory features of 78 cases of T-prolymphocytic leukemia.

The clinical course was progressive with a median survival of 7.5 months and the response rate increased to 58% in patients with a CD4+ CD8- phenotype, and a subgroup of patients may benefit from deoxycoformycin.