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Clinical Trials |
The Wistar Institute [S. V., A. C., D. S.], The University of Pennsylvania Cancer Center [D. L. P., S. L. L., L. S., M. K., K. D., E. A. S.], and The Fox Chase Cancer Center [M. H. T.], Philadelphia, Pennsylvania 19104
The
human cytotoxic T-cell line TALL-104 displays antitumor effects in
animals with implanted and spontaneous malignancies. A Phase I trial
was conducted to determine toxicity of TALL-104 cell therapy in women
with metastatic refractory breast cancer. Fifteen patients with
metastatic infiltrating ductal (n = 12), lobular
(n = 2), or medullary (n = 1)
carcinoma received escalating doses of lethally irradiated TALL-104
cells (three patients/group received 106, 3 x
106, 107, 3 x 107, and
108 cells/kg) for 5 consecutive days (induction course).
Patients without progressive disease received monthly maintenance 2-day
infusions at the same dose level. Mild grade I/II toxicity developed in
11 patients regardless of cell dose. One grade IV toxicity consequent
to hepatic tumor necrosis occurred in a patient given 108
cells/kg, 3 weeks after the induction course. Nine patients progressed
within 1 month from induction, and five patients had stable disease for
26 months. One patient (at 3 x 107/kg) had
improvement of liver metastases and ascites, and a second patient (at
106/kg) experienced a dramatic relief in bone pain.
Increases in blood natural killer cell activity and levels of IFN-
,
interleukin-10, and activation markers (soluble interleukin-2 receptor
and soluble intercellular adhesion molecule-1) were often seen.
Only one patient developed anti-HLA class I antibody responses against
TALL-104 cells; specific CTL activity developed in three patients
during induction and in four patients during the maintenance boosts. In
conclusion, TALL-104 cells were well tolerated by patients with
metastatic breast cancer at the doses and regimen tested. The clinical
responses observed in this preliminary trial demonstrate that further
investigation of TALL-104 cell therapy is warranted.
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