PMID- 15614146 OWN - NLM STAT- MEDLINE DCOM- 20050131 LR - 20190713 IS - 0041-1337 (Print) IS - 0041-1337 (Linking) VI - 78 IP - 12 DP - 2004 Dec 27 TI - Reduced-intensity allogeneic hematopoietic stem-cell transplantation as an immunotherapy for metastatic colorectal cancer. PG - 1740-6 AB - BACKGROUND: Allogeneic stem-cell transplantation (allo-SCT) can induce curative graft-versus-leukemia reactions for hematologic malignancies through allogeneic immunity. Because the gastrointestinal tract is a target of graft-versus-host disease (GvHD), colorectal cancer might be a candidate for allo-SCT. METHODS: Four patients with metastatic colorectal cancer underwent reduced-intensity stem-cell transplantation (RIST) in the National Cancer Center Hospital between July 2002 and February 2003. Three patients received transplants from an human leukocyte antigen (HLA)-identical related donor, and the remaining patient received selected CD34-positive cells from a two-loci HLA-mismatched donor. The basis of preparative regimen was busulfan 4 mg/kg for 2 days and fludarabine 25 mg/kg for 6 days. RESULTS: All the patients tolerated the preparative regimen and achieved engraftment without significant toxicities. All developed acute or chronic GvHD. Although serum levels of CA19-9 and carcinoembryonic antigen were transiently elevated after RIST in all the patients, the levels subsequently decreased below the levels from before RIST in all but one patient. Three had measurable lesions before RIST, one achieved partial response, and the others stable disease, which was durable for 120 and 60 days. Three patients died; the causes of death were progressive disease, GvHD, and accident. Postmortem examination was obtained for two patients; in one patient, the peritoneal metastatic lesions macroscopically disappeared, and in the other patient, the supraclavicular lymph node disappeared while the other measurable lesions remained stable. CONCLUSIONS: All the patients showed some evidence suggesting the presence of a graft-versus-tumor effect for colorectal cancer, which should be confirmed in a future prospective trial. FAU - Kojima, Rie AU - Kojima R AD - Hematopoietic Stem Cell Transplant Unit, the National Cancer Center Hospital, Tokyo, Japan. FAU - Kami, Masahiro AU - Kami M FAU - Hori, Akiko AU - Hori A FAU - Murashige, Naoko AU - Murashige N FAU - Ohnishi, Mutsuko AU - Ohnishi M FAU - Kim, Sung-Won AU - Kim SW FAU - Hamaki, Tamae AU - Hamaki T FAU - Kishi, Yukiko AU - Kishi Y FAU - Tsutsumi, Yutaka AU - Tsutsumi Y FAU - Masauzi, Nobuo AU - Masauzi N FAU - Heike, Yuji AU - Heike Y FAU - Mori, Shin-Ichiro AU - Mori S FAU - Kobayashi, Kazuhiko AU - Kobayashi K FAU - Masuo, Shigeru AU - Masuo S FAU - Tanosaki, Ryuji AU - Tanosaki R FAU - Takaue, Yoichi AU - Takaue Y LA - eng PT - Case Reports PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - United States TA - Transplantation JT - Transplantation JID - 0132144 RN - 0 (CA-19-9 Antigen) RN - 0 (Carcinoembryonic Antigen) SB - IM MH - Adult MH - CA-19-9 Antigen/blood MH - Carcinoembryonic Antigen/blood MH - Colorectal Neoplasms/immunology/*pathology/*surgery/therapy MH - Female MH - Graft vs Host Disease/etiology MH - *Graft vs Tumor Effect MH - *Hematopoietic Stem Cell Transplantation/adverse effects MH - Humans MH - *Immunotherapy MH - Liver Neoplasms/secondary/surgery MH - Lung Neoplasms/secondary/surgery MH - Male MH - Middle Aged MH - Peritoneal Neoplasms/secondary/surgery MH - Time Factors MH - Tomography, X-Ray Computed MH - Transplantation, Homologous MH - Treatment Outcome EDAT- 2004/12/23 09:00 MHDA- 2005/02/03 09:00 CRDT- 2004/12/23 09:00 PHST- 2004/12/23 09:00 [pubmed] PHST- 2005/02/03 09:00 [medline] PHST- 2004/12/23 09:00 [entrez] AID - 00007890-200412270-00009 [pii] AID - 10.1097/01.tp.0000146194.36297.4e [doi] PST - ppublish SO - Transplantation. 2004 Dec 27;78(12):1740-6. doi: 10.1097/01.tp.0000146194.36297.4e.