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Published on: July 20, 2016
High remission rate in T-cell prolymphocytic leukemia with CAMPATH-1H
C E Dearden1, E Matutes, B Cazin
1Royal Marsden NHS Trust, London, United Kingdom. claire.dearden@ccmail.stgh-tr.sthames.nhs.uk
Blood
|September 6, 2001
Summary
The human CD52 antibody, CAMPATH-1H, shows significant effectiveness in treating T-cell prolymphocytic leukemia (T-PLL), a difficult chemotherapy-resistant cancer. This therapy achieved high remission rates and prolonged survival in patients, warranting further investigation with stem cell transplantation.
Area of Science:
- Hematology
- Oncology
- Immunotherapy
Background:
- T-cell prolymphocytic leukemia (T-PLL) is an aggressive hematologic malignancy.
- T-PLL exhibits resistance to conventional chemotherapy, leading to poor prognoses.
- The human CD52 antibody, CAMPATH-1H, was investigated for its therapeutic potential in T-PLL.
Observation:
- Thirty-nine patients with T-PLL, most with prior treatment failures, received CAMPATH-1H.
- CAMPATH-1H was administered intravenously three times weekly until maximal response.
- Prior therapies, including pentostatin, had not resulted in complete remission for most patients.
Findings:
- An overall response rate of 76% was observed, with 60% achieving complete remission (CR) and 16% partial remission (PR).
- Responses were durable, with a median disease-free interval of 7 months.
- Survival was significantly improved in patients achieving CR compared to PR or no response.
Implications:
- CAMPATH-1H demonstrates considerable efficacy as a treatment for T-cell prolymphocytic leukemia.
- Stem cell transplantation may serve as a valuable consolidation strategy following CAMPATH-1H therapy.
- Further studies are warranted to explore the combined use of CAMPATH-1H and stem cell transplantation in T-PLL management.

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