Pretransplantation Inflammatory and Nutritional Status in Elderly Allogeneic Hematopoietic Stem Cell Transplantation: Prognostic Value of C-Reactive Protein-to-Albumin Ratio
•Biomarkers were compared in elderly patients undergoing allogeneic HSCT.•C-reactive protein-to-albumin ratio (CAR) was the most useful prognostic indicator for HSCT in elderly patients.•CAR is a powerful patient-related risk factor independent of HCT-CI score. There are no clear criteria for select...
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Published in | Transplantation and cellular therapy Vol. 30; no. 4; pp. 400.e1 - 400.e9 |
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Main Authors | , , , , , , , , , , , , , , , , , , |
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Language | English |
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Elsevier Inc
01.04.2024
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Abstract | •Biomarkers were compared in elderly patients undergoing allogeneic HSCT.•C-reactive protein-to-albumin ratio (CAR) was the most useful prognostic indicator for HSCT in elderly patients.•CAR is a powerful patient-related risk factor independent of HCT-CI score.
There are no clear criteria for selecting elderly patients with hematologic malignancies eligible for allogeneic hematopoietic stem cell transplantation (HSCT). This study aimed to evaluate inflammatory and nutritional status biomarkers as prognostic indicators of allogeneic HSCT in elderly patients. We compared the prognostic effects of 4 representative pretransplantation biomarkers: C-reactive protein-to-albumin ratio (CAR), Glasgow Prognostic Score (GPS), prognostic nutritional index (PNI), and albumin-to-globulin ratio (AGR). A total of 143 patients age ≥60 years who underwent their first allogeneic HSCT for a hematologic malignancy were enrolled between 2010 and 2020 in our single-center cohort. The median patient age was 65 years (range, 60 to 72 years). Pretransplantation high CAR, high GPS, and low PNI scores were associated with poor overall survival (OS), but the AGR was not associated with OS. Among the 4 biomarkers, CAR stratified OS most significantly (P < .001). Multivariate analyses identified only high CAR as an independent prognostic factor associated with OS (hazard ratio [HR], 1.98; P = .031) and showed that a Hematopoietic Cell Transplantation-Specific Comorbidity Index (HCT-CI) score ≥3 also was associated with OS (HR, 2.04; P = .012). High CAR was correlated with poor performance status, male sex, and high Disease Risk Index, but not with high HCT-CI score. When the patients were stratified into 3 groups according to a composite risk assessment using CAR and HCT-CI, the 3-year OS decreased significantly with increasing scores (82.8%, 50.3%, and 27.0%, respectively; P < .0001). In conclusion, CAR is the most useful prognostic indicator among the inflammatory and nutritional status biomarkers for allogeneic HSCT in elderly patients. Inflammatory and nutritional status in the elderly may be important prognostic factors for allogeneic HSCT independent of HCT-CI score. |
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AbstractList | There are no clear criteria for selecting elderly patients with hematologic malignancies eligible for allogeneic hematopoietic stem cell transplantation (HSCT). This study aimed to evaluate inflammatory and nutritional status biomarkers as prognostic indicators of allogeneic HSCT in elderly patients. We compared the prognostic effects of 4 representative pretransplantation biomarkers: C-reactive protein-to-albumin ratio (CAR), Glasgow Prognostic Score (GPS), prognostic nutritional index (PNI), and albumin-to-globulin ratio (AGR). A total of 143 patients age ≥60 years who underwent their first allogeneic HSCT for a hematologic malignancy were enrolled between 2010 and 2020 in our single-center cohort. The median patient age was 65 years (range, 60 to 72 years). Pretransplantation high CAR, high GPS, and low PNI scores were associated with poor overall survival (OS), but the AGR was not associated with OS. Among the 4 biomarkers, CAR stratified OS most significantly (P < .001). Multivariate analyses identified only high CAR as an independent prognostic factor associated with OS (hazard ratio [HR], 1.98; P = .031) and showed that a Hematopoietic Cell Transplantation-Specific Comorbidity Index (HCT-CI) score ≥3 also was associated with OS (HR, 2.04; P = .012). High CAR was correlated with poor performance status, male sex, and high Disease Risk Index, but not with high HCT-CI score. When the patients were stratified into 3 groups according to a composite risk assessment using CAR and HCT-CI, the 3-year OS decreased significantly with increasing scores (82.8%, 50.3%, and 27.0%, respectively; P < .0001). In conclusion, CAR is the most useful prognostic indicator among the inflammatory and nutritional status biomarkers for allogeneic HSCT in elderly patients. Inflammatory and nutritional status in the elderly may be important prognostic factors for allogeneic HSCT independent of HCT-CI score. There are no clear criteria for selecting elderly patients with hematologic malignancies eligible for allogeneic hematopoietic stem cell transplantation (HSCT). This study aimed to evaluate inflammatory and nutritional status biomarkers as prognostic indicators of allogeneic HSCT in elderly patients. We compared the prognostic effects of 4 representative pretransplantation biomarkers: C-reactive protein-to-albumin ratio (CAR), Glasgow Prognostic Score (GPS), prognostic nutritional index (PNI), and albumin-to-globulin ratio (AGR). A total of 143 patients age ≥60 years who underwent their first allogeneic HSCT for a hematologic malignancy were enrolled between 2010 and 2020 in our single-center cohort. The median patient age was 65 years (range, 60 to 72 years). Pretransplantation high CAR, high GPS, and low PNI scores were associated with poor overall survival (OS), but the AGR was not associated with OS. Among the 4 biomarkers, CAR stratified OS most significantly (P < .001). Multivariate analyses identified only high CAR as an independent prognostic factor associated with OS (hazard ratio [HR], 1.98; P = .031) and showed that a Hematopoietic Cell Transplantation-Specific Comorbidity Index (HCT-CI) score ≥3 also was associated with OS (HR, 2.04; P = .012). High CAR was correlated with poor performance status, male sex, and high Disease Risk Index, but not with high HCT-CI score. When the patients were stratified into 3 groups according to a composite risk assessment using CAR and HCT-CI, the 3-year OS decreased significantly with increasing scores (82.8%, 50.3%, and 27.0%, respectively; P < .0001). In conclusion, CAR is the most useful prognostic indicator among the inflammatory and nutritional status biomarkers for allogeneic HSCT in elderly patients. Inflammatory and nutritional status in the elderly may be important prognostic factors for allogeneic HSCT independent of HCT-CI score.There are no clear criteria for selecting elderly patients with hematologic malignancies eligible for allogeneic hematopoietic stem cell transplantation (HSCT). This study aimed to evaluate inflammatory and nutritional status biomarkers as prognostic indicators of allogeneic HSCT in elderly patients. We compared the prognostic effects of 4 representative pretransplantation biomarkers: C-reactive protein-to-albumin ratio (CAR), Glasgow Prognostic Score (GPS), prognostic nutritional index (PNI), and albumin-to-globulin ratio (AGR). A total of 143 patients age ≥60 years who underwent their first allogeneic HSCT for a hematologic malignancy were enrolled between 2010 and 2020 in our single-center cohort. The median patient age was 65 years (range, 60 to 72 years). Pretransplantation high CAR, high GPS, and low PNI scores were associated with poor overall survival (OS), but the AGR was not associated with OS. Among the 4 biomarkers, CAR stratified OS most significantly (P < .001). Multivariate analyses identified only high CAR as an independent prognostic factor associated with OS (hazard ratio [HR], 1.98; P = .031) and showed that a Hematopoietic Cell Transplantation-Specific Comorbidity Index (HCT-CI) score ≥3 also was associated with OS (HR, 2.04; P = .012). High CAR was correlated with poor performance status, male sex, and high Disease Risk Index, but not with high HCT-CI score. When the patients were stratified into 3 groups according to a composite risk assessment using CAR and HCT-CI, the 3-year OS decreased significantly with increasing scores (82.8%, 50.3%, and 27.0%, respectively; P < .0001). In conclusion, CAR is the most useful prognostic indicator among the inflammatory and nutritional status biomarkers for allogeneic HSCT in elderly patients. Inflammatory and nutritional status in the elderly may be important prognostic factors for allogeneic HSCT independent of HCT-CI score. •Biomarkers were compared in elderly patients undergoing allogeneic HSCT.•C-reactive protein-to-albumin ratio (CAR) was the most useful prognostic indicator for HSCT in elderly patients.•CAR is a powerful patient-related risk factor independent of HCT-CI score. There are no clear criteria for selecting elderly patients with hematologic malignancies eligible for allogeneic hematopoietic stem cell transplantation (HSCT). This study aimed to evaluate inflammatory and nutritional status biomarkers as prognostic indicators of allogeneic HSCT in elderly patients. We compared the prognostic effects of 4 representative pretransplantation biomarkers: C-reactive protein-to-albumin ratio (CAR), Glasgow Prognostic Score (GPS), prognostic nutritional index (PNI), and albumin-to-globulin ratio (AGR). A total of 143 patients age ≥60 years who underwent their first allogeneic HSCT for a hematologic malignancy were enrolled between 2010 and 2020 in our single-center cohort. The median patient age was 65 years (range, 60 to 72 years). Pretransplantation high CAR, high GPS, and low PNI scores were associated with poor overall survival (OS), but the AGR was not associated with OS. Among the 4 biomarkers, CAR stratified OS most significantly (P < .001). Multivariate analyses identified only high CAR as an independent prognostic factor associated with OS (hazard ratio [HR], 1.98; P = .031) and showed that a Hematopoietic Cell Transplantation-Specific Comorbidity Index (HCT-CI) score ≥3 also was associated with OS (HR, 2.04; P = .012). High CAR was correlated with poor performance status, male sex, and high Disease Risk Index, but not with high HCT-CI score. When the patients were stratified into 3 groups according to a composite risk assessment using CAR and HCT-CI, the 3-year OS decreased significantly with increasing scores (82.8%, 50.3%, and 27.0%, respectively; P < .0001). In conclusion, CAR is the most useful prognostic indicator among the inflammatory and nutritional status biomarkers for allogeneic HSCT in elderly patients. Inflammatory and nutritional status in the elderly may be important prognostic factors for allogeneic HSCT independent of HCT-CI score. |
Author | Inoue, Yasuyuki Sato, Shuku Hashimoto, Chizuko Hirasawa, Akira Ishiyama, Taijiro Ishii, Ryuji Tanaka, Masatsugu Suzuki, Takahiro Kanamori, Heiwa Nakajima, Hideaki Tachibana, Takayoshi Kabasawa, Nobuyuki Yamamoto, Koh Miyazaki, Takuya Izumi, Akihiko Fujimaki, Katsumichi Tamai, Yotaro Suzuki, Taisei Michishita, Yusuke |
Author_xml | – sequence: 1 givenname: Takuya orcidid: 0000-0003-1884-4757 surname: Miyazaki fullname: Miyazaki, Takuya email: takuya_m@yokohama-cu.ac.jp organization: Department of Hematology, Kanagawa Cancer Center, Yokohama, Japan – sequence: 2 givenname: Takayoshi surname: Tachibana fullname: Tachibana, Takayoshi organization: Department of Hematology, Kanagawa Cancer Center, Yokohama, Japan – sequence: 3 givenname: Taisei surname: Suzuki fullname: Suzuki, Taisei organization: Department of Hematology, Kanagawa Cancer Center, Yokohama, Japan – sequence: 4 givenname: Akihiko surname: Izumi fullname: Izumi, Akihiko organization: Department of Hematology, Kanagawa Cancer Center, Yokohama, Japan – sequence: 5 givenname: Katsumichi surname: Fujimaki fullname: Fujimaki, Katsumichi organization: Department of Hematology, Fujisawa City Hospital, Fujisawa, Japan – sequence: 6 givenname: Shuku surname: Sato fullname: Sato, Shuku organization: Department of Hematology, Shonan Kamakura General Hospital, Kamakura, Japan – sequence: 7 givenname: Yotaro orcidid: 0000-0003-4013-1737 surname: Tamai fullname: Tamai, Yotaro organization: Department of Hematology, Shonan Kamakura General Hospital, Kamakura, Japan – sequence: 8 givenname: Yusuke surname: Michishita fullname: Michishita, Yusuke organization: Department of Hematology, Kitasato University School of Medicine, Sagamihara, Japan – sequence: 9 givenname: Takahiro orcidid: 0000-0002-8438-2186 surname: Suzuki fullname: Suzuki, Takahiro organization: Department of Hematology, Kitasato University School of Medicine, Sagamihara, Japan – sequence: 10 givenname: Ryuji surname: Ishii fullname: Ishii, Ryuji organization: Division of Hematology, Japan Community Health Care Organization Sagamino Hospital, Sagamihara, Japan – sequence: 11 givenname: Akira surname: Hirasawa fullname: Hirasawa, Akira organization: Department of Hematology, Yokohama Rosai Hospital, Yokohama, Japan – sequence: 12 givenname: Chizuko surname: Hashimoto fullname: Hashimoto, Chizuko organization: Department of Hematology/Oncology, Yamato Municipal Hospital, Yamato, Japan – sequence: 13 givenname: Nobuyuki surname: Kabasawa fullname: Kabasawa, Nobuyuki organization: Division of Hematology, Department of Medicine, Showa University Fujigaoka Hospital, Yokohama, Japan – sequence: 14 givenname: Yasuyuki surname: Inoue fullname: Inoue, Yasuyuki organization: Department of Hematology, St. Marianna University Yokohama City Seibu Hospital, Yokohama, Japan – sequence: 15 givenname: Taijiro surname: Ishiyama fullname: Ishiyama, Taijiro organization: Department of Hematology, Yokohama Tsurugamine Hospital, Yokohama, Japan – sequence: 16 givenname: Koh surname: Yamamoto fullname: Yamamoto, Koh organization: Department of Hematology, Yokohama City Minato Red Cross Hospital, Yokohama, Japan – sequence: 17 givenname: Heiwa surname: Kanamori fullname: Kanamori, Heiwa organization: Department of Hematology, Kanagawa Cancer Center, Yokohama, Japan – sequence: 18 givenname: Masatsugu orcidid: 0000-0001-8814-230X surname: Tanaka fullname: Tanaka, Masatsugu organization: Department of Hematology, Kanagawa Cancer Center, Yokohama, Japan – sequence: 19 givenname: Hideaki orcidid: 0000-0002-8967-4954 surname: Nakajima fullname: Nakajima, Hideaki organization: Department of Hematology and Clinical Immunology, Yokohama City University School of Medicine, Yokohama, Japan |
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Keywords | Elderly transplantation Prognostic factor Allogeneic hematopoietic stem cell transplantation C-reactive protein-to-albumin ratio Inflammation and nutrition |
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Snippet | •Biomarkers were compared in elderly patients undergoing allogeneic HSCT.•C-reactive protein-to-albumin ratio (CAR) was the most useful prognostic indicator... There are no clear criteria for selecting elderly patients with hematologic malignancies eligible for allogeneic hematopoietic stem cell transplantation... |
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SubjectTerms | Aged Allogeneic hematopoietic stem cell transplantation Biomarkers C-Reactive Protein - analysis C-Reactive Protein - chemistry C-reactive protein-to-albumin ratio Elderly transplantation Hematologic Neoplasms - therapy Hematopoietic Stem Cell Transplantation - adverse effects Humans Inflammation - diagnosis Inflammation and nutrition Nutritional Status Prognosis Prognostic factor Retrospective Studies Serum Albumin - analysis Serum Albumin - chemistry Transplantation, Homologous - adverse effects |
Title | Pretransplantation Inflammatory and Nutritional Status in Elderly Allogeneic Hematopoietic Stem Cell Transplantation: Prognostic Value of C-Reactive Protein-to-Albumin Ratio |
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