Myelodysplastic syndrome (MDS) is a bone marrow failure disorder characterized by intractable cytopenia and dysplastic hematological changes. MDS has a varied clinical course, with some patients remaining asymptomatic with mild cytopenia for a long time, while others show progressive leukemia a short time after the diagnosis. Allogeneic hematopoietic cell transplantation (*1) is considered the only curative treatment.
A research group led by Assistant Professor Takaaki Konuma in the Department of Hematology/Oncology, the Hospital of the Institute of Medical Science, the University of Tokyo (IMSUT Hospital) has demonstrated a graft-versus-tumor (GVT) effect (*2) of a previously unknown/novel allogeneic hematopoietic cell transplantation in MDS patients. In addition, they succeeded in identifying a category of patients for whom the GVT effect was identified. These results used data from 3119 MDS patients aged 16 to 70 who are registered at the Japanese Data Center for Hematopoietic Cell Transplantation (JDCHCT).
These results were published online in Clinical Cancer Research, a journal of the American Association for Cancer Research on September 7.
Graft-versus-tumor effect associated with limited chronic GVHD alone improved survival in high-risk MDS
According to Assistant Professor Konuma, the research group retrospectively evaluated the impact of acute and chronic graft-versus-host disease (GVHD) (*3) on transplant outcomes for a large cohort of adult patients with a low-risk (n = 1193) or high-risk (n = 1926) of myelodysplastic syndrome (MDS).
Their study demonstrated that for patients with a low-risk of MDS, acute and chronic GVHD at any grade or severity did not improve overall mortality, relapse, or non-relapse mortality (NRM). For patients with a high-risk of MDS, the favorable effect of limited chronic GVHD on disease relapse was associated with a decrease in overall mortality; however, the favorable effects of grade III–IV acute GVHD, or extensive chronic GVHD on disease relapse were offset by increased NRM.
Importantly, the graft-versus-tumor effect associated with limited chronic GVHD alone improved survival in those at high-risk of MDS. This GVT associated GVHD could be the explanation for the fact that excessive immune reactions, as they become clinically visible with severe GVHD, ultimately have negative effects.
For details of the research, please see the paper.
Here is Press release.
Assistant Professor Konuma described the research as “a large-scale clinical study targeting improved treatment of MDS and development of cancer immunotherapy.".
Their study demonstrated that for patients with a low-risk of MDS, acute and chronic GVHD at any grade or severity did not improve overall mortality, relapse, or non-relapse mortality (NRM). For patients with a high-risk of MDS, the favorable effect of limited chronic GVHD on disease relapse was associated with a decrease in overall mortality; however, the favorable effects of grade III–IV acute GVHD, or extensive chronic GVHD on disease relapse were offset by increased NRM.
Importantly, the graft-versus-tumor effect associated with limited chronic GVHD alone improved survival in those at high-risk of MDS. This GVT associated GVHD could be the explanation for the fact that excessive immune reactions, as they become clinically visible with severe GVHD, ultimately have negative effects.
For details of the research, please see the paper.
Here is Press release.
Assistant Professor Konuma described the research as “a large-scale clinical study targeting improved treatment of MDS and development of cancer immunotherapy.".
Forest plots for hazard ratios (HR) of overall mortality, relapse, and non-relapse mortality by grade of acute GVHD in low-risk MDS (a) and high-risk MDS (b). Forest plots for hazard ratios (HR) of overall mortality, relapse, and non-relapse mortality by grade of chronic GVHD in low-risk MDS (c) and high-risk MDS (d).
Research Notes
(*1) Allogeneic hematopoietic cell transplantation
The treatment of recipients with irradiation and/or high-dose chemotherapy followed by the infusion of cells containing haematopoietic stem and progenitor cells, such as bone marrow, cytokine-mobilized peripheral blood or umbilical cord blood. It also can mediate graftversustumour (GVT) effects in which donorderived immune cells attack the host tumours, along with irradiation and/or high-dose chemotherapy for host tumors.
(*2) Graft-versus-tumor (GVT) effect
A phenomenon in which malignant host cells are attacked by donor immune cells. Clinically, it is augmented in patients with graft-versus-host disease.
(*3) Graft-versus-host disease (GVHD)
A complication mediated by host alloantigen- activated donor T cells attacking the normal tissues of the host after allogeneic hematopoietic cell transplantation.
The treatment of recipients with irradiation and/or high-dose chemotherapy followed by the infusion of cells containing haematopoietic stem and progenitor cells, such as bone marrow, cytokine-mobilized peripheral blood or umbilical cord blood. It also can mediate graftversustumour (GVT) effects in which donorderived immune cells attack the host tumours, along with irradiation and/or high-dose chemotherapy for host tumors.
(*2) Graft-versus-tumor (GVT) effect
A phenomenon in which malignant host cells are attacked by donor immune cells. Clinically, it is augmented in patients with graft-versus-host disease.
(*3) Graft-versus-host disease (GVHD)
A complication mediated by host alloantigen- activated donor T cells attacking the normal tissues of the host after allogeneic hematopoietic cell transplantation.
About the research
1) Journal Article
Takaaki Konuma*, Ken Ishiyama, Aiko Igarashi, Naoyuki Uchida, Yukiyasu Ozawa, Takahiro Fukuda, Yasunori Ueda, Ken-ichi Matsuoka, Takehiko Mori, Yuta Katayama, Makoto Onizuka, Tatsuo Ichinohe, and Yoshiko Atsuta; for the Adult Myelodysplastic Syndrome Working Group of the Japan Society for Hematopoietic Cell Transplantation. “Effects of acute and chronic graft-versus-myelodysplastic syndrome on long-term outcomes following allogeneic hematopoietic cell transplantation” Clinical Cancer Research．
*Correspondence.
*Correspondence.
DOI: 10.1158/1078-0432.CCR-20-1104
2) Publication Journal
Clinical Cancer Research, a journal of the American Association for Cancer Research
