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Validation of a Post-Transplant Lymphoproliferative Disorder Risk Prediction Score and Derivation of a New Prediction Score Using a National Bone Marrow Transplant Registry Database.
Lee, Chien-Chang; Hsu, Tzu-Chun; Kuo, Chia-Chih; Liu, Michael A; Abdelfattah, Ahmed M; Chang, Chia-Na; Yao, Ming; Li, Chi-Cheng; Wu, Kang-Hsi; Chen, Tsung-Chih; Gau, Jyh-Pyng; Wang, Po-Nan; Liu, Yi-Chang; Chiou, Lun-Wei; Lee, Ming-Yang; Li, Sin-Syue; Chao, Tsu-Yi; Jou, Shiann-Tarng; Chang, Hsiu-Hao.
Afiliação
  • Lee CC; Department of Emergency Medicine, National Taiwan University Hospital, Taipei, Taiwan.
  • Hsu TC; Center of Intelligent Healthcare, National Taiwan University Hospital, Taipei, Taiwan.
  • Kuo CC; Department of Emergency Medicine, National Taiwan University Hospital, Taipei, Taiwan.
  • Liu MA; Department of Medicine, National Taiwan University Hospital, Taipei, Taiwan.
  • Abdelfattah AM; Department of Medicine, Warren Alpert Medical School of Brown University, Providence, Rhode Island, USA.
  • Chang CN; Information Services Department, Boston Children's Hospital, Boston, Massachusetts, USA.
  • Yao M; Department of Radiation Oncology, Taipei Municipal Wanfang Hospital, Taipei, Taiwan.
  • Li CC; Division of Hematology and Oncology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
  • Wu KH; Division of Pediatric Hematology and Oncology, China Medical University Children's Hospital, Taichung, Taiwan.
  • Chen TC; Division of Pediatric Hematology and Oncology, China Medical University Children's Hospital, Taichung, Taiwan.
  • Gau JP; Division of Hematology and Oncology, Department of Internal Medicine, Taichung Veterans General Hospital, Taichung, Taiwan.
  • Wang PN; Division of Hematology and Oncology, Department of Internal Medicine, Taipei Veterans General Hospital, Taipei, Taiwan.
  • Liu YC; Division of Hematology and Oncology, Department of Internal Medicine, Chang Gung Medical Foundation, Linkou Branch, Taoyuan, Taiwan.
  • Chiou LW; Division of Hematology and Oncology, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung, Taiwan.
  • Lee MY; Department of Hematology and Medical Oncology, Koo Foundation Sun Yat-Sen Cancer Center, Taipei, Taiwan.
  • Li SS; Division of Hematology and Oncology, Department of Internal Medicine, Ditmanson Medical Foundation Chiayi Christian Hospital, Chiayi, Taiwan.
  • Chao TY; Division of Hematology and Oncology, Department of Internal Medicine, National Cheng Kung University Hospital, Tainan, Taiwan.
  • Jou ST; Division of Hemato-Oncology, Department of Internal Medicine, Taipei Medical University-Shuang Ho Hospital, Taipei, Taiwan.
  • Chang HH; Department of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan.
Oncologist ; 26(11): e2034-e2041, 2021 11.
Article em En | MEDLINE | ID: mdl-34506688
ABSTRACT

BACKGROUND:

We externally validated Fujimoto's post-transplant lymphoproliferative disorder (PTLD) scoring system for risk prediction by using the Taiwan Blood and Marrow Transplant Registry Database (TBMTRD) and aimed to create a superior scoring system using machine learning methods. MATERIALS AND

METHODS:

Consecutive allogeneic hematopoietic cell transplant (HCT) recipients registered in the TBMTRD from 2009 to 2018 were included in this study. The Fujimoto PTLD score was calculated for each patient. The machine learning algorithm, least absolute shrinkage and selection operator (LASSO), was used to construct a new score system, which was validated using the fivefold cross-validation method.

RESULTS:

We identified 2,148 allogeneic HCT recipients, of which 57 (2.65%) developed PTLD in the TBMTRD. In this population, the probabilities for PTLD development by Fujimoto score at 5 years for patients in the low-, intermediate-, high-, and very-high-risk groups were 1.15%, 3.06%, 4.09%, and 8.97%, respectively. The score model had acceptable discrimination with a C-statistic of 0.65 and a near-perfect moderate calibration curve (HL test p = .81). Using LASSO regression analysis, a four-risk group model was constructed, and the new model showed better discrimination in the validation cohort when compared with The Fujimoto PTLD score (C-statistic 0.75 vs. 0.65).

CONCLUSION:

Our study demonstrated a more comprehensive model when compared with Fujimoto's PTLD scoring system, which included additional predictors identified through machine learning that may have enhanced discrimination. The widespread use of this promising tool for risk stratification of patients receiving HCT allows identification of high-risk patients that may benefit from preemptive treatment for PTLD. IMPLICATIONS FOR PRACTICE This study validated the Fujimoto score for the prediction of post-transplant lymphoproliferative disorder (PTLD) development following hematopoietic cell transplant (HCT) in an external, independent, and nationally representative population. This study also developed a more comprehensive model with enhanced discrimination for better risk stratification of patients receiving HCT, potentially changing clinical managements in certain risk groups. Previously unreported risk factors associated with the development of PTLD after HCT were identified using the machine learning algorithm, least absolute shrinkage and selection operator, including pre-HCT medical history of mechanical ventilation and the chemotherapy agents used in conditioning regimen.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transplante de Células-Tronco Hematopoéticas / Transtornos Linfoproliferativos Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transplante de Células-Tronco Hematopoéticas / Transtornos Linfoproliferativos Idioma: En Ano de publicação: 2021 Tipo de documento: Article