Survival disparities for second primary malignancies diagnosed among childhood cancer survivors: A population‐based assessment
Background Curative therapy places childhood cancer survivors at increased risk for second primary malignancies (SPMs). However, there have been few population‐based attempts to characterize differences between outcomes of SPMs in childhood cancer survivors and outcomes of first primary malignancies...
Gespeichert in:
Veröffentlicht in: | Cancer 2019-10, Vol.125 (20), p.3623-3630 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Background
Curative therapy places childhood cancer survivors at increased risk for second primary malignancies (SPMs). However, there have been few population‐based attempts to characterize differences between outcomes of SPMs in childhood cancer survivors and outcomes of first primary malignancies (FPMs).
Methods
Clinical and demographic information about childhood cancer survivors who developed SPMs and individuals with comparable FPMs was extracted from the Surveillance, Epidemiology, and End Results program. Hazard ratios (HRs) and 95% confidence intervals (CIs) were estimated with Cox proportional hazards models comparing the overall survival (OS) of individuals with and without a history of childhood cancer. OS was evaluated both overall and for specific cancers diagnosed in 50 or more childhood cancer survivors. Models accounted for potential confounders, including sex, race, age, treatment decade, histology, and disease stage.
Results
Compared with individuals with FPMs (n = 1,332,203), childhood cancer survivors (n = 1409) with an SPM experienced poorer OS (HR, 1.86; 95% CI, 1.72‐2.02) after the study had accounted for cancer type, age, sex, race, and decade of diagnosis. A history of childhood cancer remained a poor prognostic factor for all specific cancers evaluated, including breast cancer (HR, 2.07; 95% CI, 1.63‐2.62), thyroid cancer (HR, 3.59; 95% CI, 2.08‐6.19), acute myeloid leukemia (HR, 2.38; 95% CI, 1.87‐3.05), brain cancer (HR, 2.09; 95% CI, 1.72‐2.55), melanoma (HR, 2.57; 95% CI, 1.55‐4.27), bone cancer (HR, 1.88; 95% CI, 1.37‐2.57), and soft‐tissue sarcoma (HR, 2.44; 95% CI, 1.78‐3.33).
Conclusions
Compared with individuals without a prior cancer diagnosis, survivors of childhood cancer with an SPM experienced inferior outcomes. Survival disparities were observed for the most frequent SPMs diagnosed in childhood cancer survivors.
Compared with individuals without a prior cancer diagnosis, survivors of childhood cancer with a second primary malignancy experience inferior outcomes. These disparities in overall survival are observed across cancer types, therapeutic exposures, and clinical factors. |
---|---|
ISSN: | 0008-543X 1097-0142 |
DOI: | 10.1002/cncr.32356 |