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Incidence and prognostic impact of other cancers in a population of long-term survivors of chronic lymphocytic leukemia.
Falchi, L; Vitale, C; Keating, M J; Lerner, S; Wang, X; Elhor Gbito, K Y; Strom, S; Wierda, W G; Ferrajoli, A.
Affiliation
  • Falchi L; Department of Leukemia.
  • Vitale C; Department of Leukemia.
  • Keating MJ; Department of Leukemia.
  • Lerner S; Department of Leukemia.
  • Wang X; Department of Biostatistics.
  • Elhor Gbito KY; Department of Epidemiology, The University of Texas MD Anderson Cancer Center, Houston, USA.
  • Strom S; Department of Epidemiology, The University of Texas MD Anderson Cancer Center, Houston, USA.
  • Wierda WG; Department of Leukemia.
  • Ferrajoli A; Department of Leukemia. Electronic address: aferrajo@mdanderson.org.
Ann Oncol ; 27(6): 1100-1106, 2016 06.
Article in En | MEDLINE | ID: mdl-26912560
ABSTRACT

BACKGROUND:

Information on the impact of other cancers (OCs) in long-term survivors (LTSs) of chronic lymphocytic leukemia (CLL) is limited. PATIENTS AND

METHODS:

Patients with CLL who survived >10 years were defined as LTSs of CLL. We calculated standardized incidence ratios (SIRs) to compare the incidence of OC in LTS of CLL versus the general population. A multivariable model was used to identify independent predictors of OC. Overall survival was analyzed as a function of the presence of OC.

RESULTS:

Among 797 LTSs of CLL, the cumulative frequency of OC was 36%, similar between 570 patients (72%) who required treatment for CLL (TRT) and 227 (28%) who remained untreated (UT). The most common OC in both groups was non-melanoma skin cancer, followed by prostate cancer, breast cancer, melanoma, lung cancer, and leukemia in TRT patients, and by prostate cancer, breast cancer, melanoma, lung cancer, and gastrointestinal tumors in the UT group. The SIR for all OC was 1.2 (P = 0.034). It was higher in males (SIR 1.31; P = 0.013) and patients <60 years (SIR 1.27; P = 0.027). A higher SIR was shown for secondary leukemia, melanoma, and head-and-neck cancers, whereas a lower SIR was found for gastrointestinal and bladder cancers. Independent predictors of OC development were advanced age, male gender, and lower platelets. The survival of patients with OC was 16.2 months and that of patients without OC 22.9 years.

CONCLUSIONS:

LTSs of CLL have an increased incidence of OC compared with the general population. CLL therapy is not a risk factor for OC in LTSs of CLL. The presence of an OC in these patients may be associated with shorter survival.
Subject(s)
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prognosis / Leukemia, Lymphocytic, Chronic, B-Cell / Neoplasms, Second Primary / Cancer Survivors Type of study: Etiology_studies / Incidence_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Ann Oncol Journal subject: NEOPLASIAS Year: 2016 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prognosis / Leukemia, Lymphocytic, Chronic, B-Cell / Neoplasms, Second Primary / Cancer Survivors Type of study: Etiology_studies / Incidence_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Ann Oncol Journal subject: NEOPLASIAS Year: 2016 Type: Article