Your browser doesn't support javascript.
loading
MRD at the end of induction and EFS in T-cell lymphoblastic lymphoma: Children's Oncology Group trial AALL1231.
Hayashi, Robert J; Hermiston, Michelle L; Wood, Brent L; Teachey, David T; Devidas, Meenakshi; Chen, Zhiguo; Annett, Robert D; Asselin, Barbara L; August, Keith; Cho, Steve; Dunsmore, Kimberly P; Freedman, Jason Lawrence; Galardy, Paul J; Harker-Murray, Paul; Horton, Terzah M; Jaju, Alok; Lam, Allison; Messinger, Yoav H; Miles, Rodney R; Okada, Maki; Patel, Samir; Schafer, Eric S; Schechter, Tal; Shimano, Kristin A; Singh, Neelam; Steele, Amii; Sulis, Maria L; Vargas, Sarah L; Winter, Stuart S; Wood, Charlotte; Zweidler-McKay, Patrick A; Loh, Mignon L; Hunger, Stephen P; Raetz, Elizabeth A; Bollard, Catherine M; Allen, Carl E.
Afiliação
  • Hayashi RJ; Division of Pediatric Hematology/Oncology, Department of Pediatrics, Washington University School of Medicine, St. Louis, MO.
  • Hermiston ML; Pediatric Hematology Oncology, University of California, San Francisco, San Francisco, CA.
  • Wood BL; Department of Pathology and Laboratory Medicine, Children's Hospital Los Angeles, Los Angeles, CA.
  • Teachey DT; Division of Pediatric Oncology, Department of Pediatrics, Center for Childhood Cancer Research, Children's Hospital of Philadelphia and Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Devidas M; Department of Global Pediatric Medicine, St. Jude Children's Research Hospital, Memphis, TN.
  • Chen Z; Department of Biostatistics, University of Florida, Gainesville, FL.
  • Annett RD; Department of Pediatrics, University of New Mexico, Albuquerque, NM.
  • Asselin BL; Division of Pediatric Hematology/Oncology, Department of Pediatrics, Golisano Children's Hospital, University of Rochester, Rochester, NY.
  • August K; Division of Pediatric Hematology/Oncology, Department of Pediatrics, Children's Mercy Kansas City, Kansas City, MO.
  • Cho S; Division of Nuclear Medicine and Molecular Imaging, Department of Radiology, Wisconsin Institute for Medical Research, Madison, WI.
  • Dunsmore KP; Department of Pediatrics, Virginia Tech Carilion School of Medicine, Roanoke, VA.
  • Freedman JL; Division of Oncology, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA.
  • Galardy PJ; Department of Pediatric Hematology and Oncology, Mayo Clinic, Rochester, MN.
  • Harker-Murray P; Division of Pediatric Hematology/Oncology, Department of Pediatrics, Midwest Children's Cancer Center, Milwaukee, WI.
  • Horton TM; Division of Pediatric Hematology/Oncology, Department of Pediatrics, Texas Children's Cancer Center, Baylor College of Medicine, Houston, TX.
  • Jaju A; Division of Pediatric Radiology, Department of Radiology, Lurie Children's Hospital, Chicago, IL.
  • Lam A; Miller Children's and Women's Hospital, Long Beach, CA.
  • Messinger YH; Division of Pediatric Hematology/Oncology, Department of Pediatrics, Children's Hospitals and Clinics of Minnesota, Minneapolis, MN.
  • Miles RR; Division of Hematopathology, Department of Pathology, ARUP Institute for Clinical and Experimental Pathology, University of Utah, Primary Children's Hospital, Salt Lake City, UT.
  • Okada M; Division of Radiation Oncology, Department of Oncology, University of Alberta-Stollery Children's Hospital, Edmonton, AB, Canada.
  • Patel S; Division of Radiation Oncology, Department of Oncology, University of Alberta-Stollery Children's Hospital, Edmonton, AB, Canada.
  • Schafer ES; Division of Pediatric Hematology/Oncology, Department of Pediatrics, Baylor College of Medicine, Texas Children's Hospital, Houston, TX.
  • Schechter T; Division of Hematology/Oncology, Department of Pediatrics, University of Toronto, The Hospital for Sick Children, Toronto, ON, Canada.
  • Shimano KA; Department of Pediatrics, University of California Benioff Children's Hospital, San Francisco, CA.
  • Singh N; Michigan State University Clinical Center, Lansing, MI.
  • Steele A; Division of Pediatric Hematology/Oncology, Department of Pediatrics, Carolinas Medical Center/Levine Cancer Institute, Charlotte, NC.
  • Sulis ML; Department of Pediatrics, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Vargas SL; Division of Pediatric Hematology/Oncology, Department of Pediatrics, Children's Oncology Group, Monrovia, CA.
  • Winter SS; Division of Pediatric Hematology/Oncology, Department of Pediatrics, Research Institute and Cancer and Blood Disorders Program, Children's Minnesota, Minneapolis, MN.
  • Wood C; Department of Biostatistics, Children's Oncology Group Data Center, Gainesville, FL.
  • Zweidler-McKay PA; ImmunoGen, Inc, Waltham, MA.
  • Loh ML; Division of Pediatric Hematology/Oncology, Department of Pediatrics, University of Washington, Seattle, WA.
  • Hunger SP; Division of Pediatric Oncology, Department of Pediatrics, Center for Childhood Cancer Research, Children's Hospital of Philadelphia and Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Raetz EA; Division of Pediatric Hematology and Oncology, Stephen D. Hassenfeld Children's Center for Cancer and Blood Disorders, NYU Langone Health, New York, NY.
  • Bollard CM; Division of Blood and Bone Marrow Transplantation, Department of Pediatrics, Center for Cancer and Immunology Research, Children's National Medical Center, Washington, DC.
  • Allen CE; Division of Pediatric Hematology/Oncology, Department of Pediatrics, Baylor College of Medicine, Texas Children's Hospital, Houston, TX.
Blood ; 143(20): 2053-2058, 2024 May 16.
Article em En | MEDLINE | ID: mdl-38457359
ABSTRACT
ABSTRACT Defining prognostic variables in T-lymphoblastic lymphoma (T-LL) remains a challenge. AALL1231 was a Children's Oncology Group phase 3 clinical trial for newly diagnosed patients with T acute lymphoblastic leukemia or T-LL, randomizing children and young adults to a modified augmented Berlin-Frankfurt-Münster backbone to receive standard therapy (arm A) or with addition of bortezomib (arm B). Optional bone marrow samples to assess minimal residual disease (MRD) at the end of induction (EOI) were collected in T-LL analyzed to assess the correlation of MRD at the EOI to event-free survival (EFS). Eighty-six (41%) of the 209 patients with T-LL accrued to this trial submitted samples for MRD assessment. Patients with MRD <0.1% (n = 75) at EOI had a superior 4-year EFS vs those with MRD ≥0.1% (n = 11) (89.0% ± 4.4% vs 63.6% ± 17.2%; P = .025). Overall survival did not significantly differ between the 2 groups. Cox regression for EFS using arm A as a reference demonstrated that MRD EOI ≥0.1% was associated with a greater risk of inferior outcome (hazard ratio, 3.73; 95% confidence interval, 1.12-12.40; P = .032), which was independent of treatment arm assignment. Consideration to incorporate MRD at EOI into future trials will help establish its value in defining risk groups. CT# NCT02112916.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Neoplasia Residual / Leucemia-Linfoma Linfoblástico de Células T Precursoras Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Neoplasia Residual / Leucemia-Linfoma Linfoblástico de Células T Precursoras Idioma: En Ano de publicação: 2024 Tipo de documento: Article