Abstract
Background:
The aim of the study was to evaluate the feasibility and efficacy of a non-myeloablative regimen to achieve complete donor chimerism after stem cell transplantation (SCT) in patients with metastatic solid tumors.
Patients and methods:
Seven patients with renal cell carcinoma (RCC), 3 with colorectal carcinoma and 1 with soft tissue sarcoma received an allogeneic SCT after fludarabine (90 mg/m2) and TBI 200 cGy.
Results:
At day 30, median donor chimerism was 94%. Regression of tumor metastases has been observed in 1 patient with RCC. Overall, 8 patients (73%) died from progressive disease (median progression-free survival 3.7 months) and 1 (9%) from treatment-related complications; 2 patients were alive 152 and 862 days after transplantation.
Conclusions:
Our preliminary results suggest that non-myeloablative SCT for metastatic solid tumors is feasible, although may lead to durable responses in a minority of patients. Careful patient selection seems to be mandatory in this transplant setting.
MeSH terms
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Adenocarcinoma / secondary
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Adenocarcinoma / surgery
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Adult
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Aged
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Carcinoma, Renal Cell / secondary
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Carcinoma, Renal Cell / surgery
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Colonic Neoplasms / pathology
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Colonic Neoplasms / surgery
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Feasibility Studies
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Female
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Graft Survival
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Graft vs Host Disease / epidemiology
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Graft vs Host Disease / etiology
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Graft vs Host Disease / prevention & control
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Graft vs Tumor Effect
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Humans
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Immunosuppressive Agents / therapeutic use
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Kidney Neoplasms / surgery
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Male
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Middle Aged
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Neoplasm Metastasis
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Neoplasms / surgery*
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Peripheral Blood Stem Cell Transplantation / adverse effects
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Peripheral Blood Stem Cell Transplantation / statistics & numerical data*
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Postoperative Complications
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Rectal Neoplasms / pathology
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Rectal Neoplasms / surgery
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Sarcoma / secondary
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Sarcoma / surgery
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Survival Analysis
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Transplantation Conditioning / methods*
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Transplantation, Homologous / adverse effects
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Transplantation, Homologous / statistics & numerical data
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Vidarabine / administration & dosage
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Vidarabine / analogs & derivatives*
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Whole-Body Irradiation*
Substances
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Immunosuppressive Agents
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Vidarabine
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fludarabine