| Literature DB >> 33976381 |
Makoto Murata1, Seitaro Terakura2, Atsushi Wake3, Kotaro Miyao4, Kazuhiro Ikegame5, Naoyuki Uchida6, Keisuke Kataoka7, Toshihiro Miyamoto8, Makoto Onizuka9, Tetsuya Eto10, Noriko Doki11, Shuichi Ota12, Maho Sato13, Yoshiko Hashii14, Tatsuo Ichinohe15, Takahiro Fukuda16, Yoshiko Atsuta17,18, Shinichiro Okamoto7, Takanori Teshima19.
Abstract
Temcell is a cryopreserved, human bone marrow-derived mesenchymal stem cell (MSC) product approved for the treatment of patients of all ages with acute graft-versus-host disease (GVHD). Initial experience with Temcell in a real-world setting from a cellular therapy registry in Japan is presented. A total of 381 consecutive patients were enrolled since its approval in 2016. The median cell number infused was 2.00 × 106/kg. The most common number of infusions was 8 in 100 patients. Of the 306 evaluable patients, the overall response rate (ORR) on day 28 after the start of MSC therapy was 56%. Of the 151 evaluable patients who received it as second-line therapy following first-line steroid therapy for classic acute GVHD, the ORR was 61%. Liver involvement of GVHD and ≥14 days from first-line steroid therapy to second-line MSC therapy was associated with a lower ORR. Day 28 ORR, patient age, GVHD grade, GVHD organ involvement, and a number of GVHD therapies before MSC therapy were associated with nonrelapse mortality. Overall survival at 6 months in 381 patients was 40%. This study suggests that Temcell is one of the treatment options for steroid-refractory acute GVHD until a new treatment with survival benefit is developed.Entities:
Mesh:
Substances:
Year: 2021 PMID: 33976381 DOI: 10.1038/s41409-021-01304-y
Source DB: PubMed Journal: Bone Marrow Transplant ISSN: 0268-3369 Impact factor: 5.483