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Second primary acute lymphoblastic leukemia in adults: a SEER analysis of incidence and outcomes.
Swaika, Abhisek; Frank, Ryan D; Yang, Dongyun; Finn, Laura E; Jiang, Liuyan; Advani, Pooja; Chanan-Khan, Asher A; Ailawadhi, Sikander; Foran, James M.
  • Swaika A; Division of Hematology & Medical Oncology, Mayo Clinic, Jacksonville, Florida.
  • Frank RD; Mayo Clinic Cancer Center, Jacksonville, Florida.
  • Yang D; Division of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, Minnesota.
  • Finn LE; Department of Preventive Medicine, Norris Comprehensive Cancer Center, University of Southern California, Los Angeles, California.
  • Jiang L; Division of Hematology & Medical Oncology, Mayo Clinic, Jacksonville, Florida.
  • Advani P; Division of Hematopathology, Department of Pathology and Laboratory Medicine, Mayo Clinic, Jacksonville, Florida.
  • Chanan-Khan AA; Division of Hematology & Medical Oncology, Mayo Clinic, Jacksonville, Florida.
  • Ailawadhi S; Division of Hematology & Medical Oncology, Mayo Clinic, Jacksonville, Florida.
  • Foran JM; Mayo Clinic Cancer Center, Jacksonville, Florida.
Cancer Med ; 7(2): 499-507, 2018 02.
Article en En | MEDLINE | ID: mdl-29282894
ABSTRACT
We conducted a surveillance epidemiology and end results (SEER)-based analysis to describe the incidence and characteristics of second primary acute lymphoblastic leukemia (sALL) among adults (≥18 years) with a history of primary malignancies (1M). Standardized incidence ratios (SIRs) of sALL cases were calculated by site and 1M stage. We also evaluated the differences in 5-year sALL survival by age, site, and extent of 1M, latency of sALL after 1M, and evidence of underlying racial/ethnic disparity. We identified 10,956 patients with de-novo/primary acute lymphoblastic leukemia (1ALL) and 772 with sALL. Women (49.1% vs. 42.9%), white patients (72.0% vs. 59.5%), older patients (58.8% vs. 25.2%; age ≥65 years), and patients diagnosed between 2003 and 2012 (66.8% vs. 53.9%) had a higher proportion of sALL compared with 1ALL. There was a significantly inferior median 5-year survival for sALL patients compared to 1ALL (6 vs. 15 months; HR 1.20, 95% CI 1.10-1.31, P < 0.001). The median latency period was 60.0 months; the most common 1M among sALL patients were breast (17.9%) and prostate (17.4%). Patients with any 1M were at increased risk of developing sALL (SIR 1.76, 95% CI 1.58-1.95, P < 0.001). Hematological-1M sites had significantly higher SIRs (hematological-SIR 7.35; solid-SIR 1.33; P < 0.001). We observed a significant increase in sALL incidence after a 1M and a significantly worse 5-year survival with different demographic characteristics from 1ALL. There is a need to define appropriate screening methods for patients surviving their primary cancer.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Primarias Secundarias / Programa de VERF / Leucemia-Linfoma Linfoblástico de Células Precursoras Tipo de estudio: Incidence_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged País como asunto: America do norte Idioma: En Año: 2018 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Primarias Secundarias / Programa de VERF / Leucemia-Linfoma Linfoblástico de Células Precursoras Tipo de estudio: Incidence_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged País como asunto: America do norte Idioma: En Año: 2018 Tipo del documento: Article