Cellular immune therapy for refractory cancers: Novel therapeutic strategies

Karen K. Ballen, Gerald Colvin, Bimalangshu R. Dey, David Porter, Peter Westervelt, Thomas R. Spitzer, Peter J. Quesenberry

Research output: Contribution to journalReview articlepeer-review

14 Scopus citations

Abstract

Objective. Allogeneic stem cell transplantation is curative for certain cancers, but the high doses of chemotherapy and radiotherapy may lead to toxicity. This review summarizes the field of cellular immune therapy using very-low-dose conditioning for refractory cancers. Methods. In our initial study, we treated 25 patients with refractory cancers with 100 cGy total body irradiation followed by allogeneic, nonmobilized peripheral blood cells. Eighteen patients received sibling and seven patients received unrelated cord blood stem cells. Results. None of the 13 patients with solid tumors achieved donor chimerism or had a sustained response. Twelve patients with hematologic malignancies were treated, 1 received a cord blood transplant and 11 received sibling donor cells. Nine of these 11 patients achieved donor chimerism, ranging from 5% to 100%. Four patients had sustained complete remission of their cancers. The patients who received cord blood transplants did not respond. Development of chimerism correlated with total previous myelotoxic chemotherapy (p < 0.001). We review additional studies in this area, including data in the haploidentical and unrelated donor setting. The data presented comprises studies performed at the four institutions represented by the authors, and a review of other pertinent studies in this area. Conclusions. Cellular immune therapy is an emerging application of transplantation therapy, which may be appropriate for refractory cancers. New studies in solid tumors, and with alternative donors, will expand the application of this new and promising treatment.

Original languageEnglish
Pages (from-to)1427-1435
Number of pages9
JournalExperimental Hematology
Volume33
Issue number12
DOIs
StatePublished - Dec 2005

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