Second malignancies in patients with Hodgkin’s Lymphoma: Half a century of experience

Purpose: Therapeutic improvements for Hodgkin’s Lymphoma (HL) has resulted in excellent survival outcomes. Thus, patients are increasing susceptible to developing secondary malignancy (SM) a feared iatrogenic complication. Materials & Methods: We evaluated the SM risk in a cohort of patients...

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Main Authors: Bouthaina Shbib Dabaja, David Boyce-Fappiano, Wenli Dong, Ethan Damron, Penny Fang, Jill Gunther, Maria A. Rodriguez, Paolo Strati, Raphael Steiner, Ranjit Nair, Hun Lee, Zeinab Abou Yehia, Ferial Shihadeh, Chelsea Pinnix, Andrea K. Ng
Format: Article
Language:English
Published: Elsevier 2022-07-01
Series:Clinical and Translational Radiation Oncology
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2405630822000349
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author Bouthaina Shbib Dabaja
David Boyce-Fappiano
Wenli Dong
Ethan Damron
Penny Fang
Jill Gunther
Maria A. Rodriguez
Paolo Strati
Raphael Steiner
Ranjit Nair
Hun Lee
Zeinab Abou Yehia
Ferial Shihadeh
Chelsea Pinnix
Andrea K. Ng
author_facet Bouthaina Shbib Dabaja
David Boyce-Fappiano
Wenli Dong
Ethan Damron
Penny Fang
Jill Gunther
Maria A. Rodriguez
Paolo Strati
Raphael Steiner
Ranjit Nair
Hun Lee
Zeinab Abou Yehia
Ferial Shihadeh
Chelsea Pinnix
Andrea K. Ng
author_sort Bouthaina Shbib Dabaja
collection DOAJ
description Purpose: Therapeutic improvements for Hodgkin’s Lymphoma (HL) has resulted in excellent survival outcomes. Thus, patients are increasing susceptible to developing secondary malignancy (SM) a feared iatrogenic complication. Materials &amp; Methods: We evaluated the SM risk in a cohort of patients with HL treated over a 50-year period. In total, 1653 patients were treated for HL from 1956 to 2009 at a tertiary-cancer-center. A cumulative incidence function was used to quantify SM risk and the Fine and Gray competing risk model was used to identify disease and treatment related correlates. Results: Two-hundred-ninety patients (19%) developed SMs. Paradoxically, SM risk was higher in the modern era with 20-year cumulative incidence rates of 11.1%, 11.9%, 17% and 21.8%, for patients treated <1970, 1971–1986, 1986–1995 and 1996–2009, respectively. We hypothesized that the disproportionately high rate of early deaths in the early era may skew the assessment of SM risks, a much-delayed event. When the analysis was restricted to patients with early-stage favorable HL treated >1980, we found a reversal of the trend, especially on the risk of solid tumor, with a hazard ratio of 0.57 (p = 0.0651) in patients treated after 1996. Conclusion: Our findings highlight the limitations of comparing the risk of a late event between groups with disparate rates of early deaths, despite the use of a competing risk model. When partially corrected for, patients treated in the more recent time period experienced a lower solid tumor risk.
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spelling doaj.art-a4338188d5c948ccbd8d7d5d7a1b48692022-12-22T02:37:06ZengElsevierClinical and Translational Radiation Oncology2405-63082022-07-01356469Second malignancies in patients with Hodgkin’s Lymphoma: Half a century of experienceBouthaina Shbib Dabaja0David Boyce-Fappiano1Wenli Dong2Ethan Damron3Penny Fang4Jill Gunther5Maria A. Rodriguez6Paolo Strati7Raphael Steiner8Ranjit Nair9Hun Lee10Zeinab Abou Yehia11Ferial Shihadeh12Chelsea Pinnix13Andrea K. Ng14Departments of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA; Corresponding author at: Department of Radiation Oncology, Division of Radiation Oncology Incident Commander, University of Texas MD Anderson Cancer Center, Director of Research of the International Lymphoma Radiation Oncology Group (ILROG), 1515 Holcombe Blvd., Houston, TX 77030, USA.Departments of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USADepartments of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX, USADepartments of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USADepartments of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USADepartments of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USADepartments of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX, USADepartments of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX, USADepartments of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX, USADepartments of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX, USADepartments of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX, USADepartment of Radiation Oncology, Rutgers Robertwood Johnson Medical Center, Houston, TX, USADepartments of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USADepartments of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USADepartment of Radiation Oncology, Dana-Farber/Brigham and Women’s Cancer Center, Harvard Medical School, Houston, TX, USAPurpose: Therapeutic improvements for Hodgkin’s Lymphoma (HL) has resulted in excellent survival outcomes. Thus, patients are increasing susceptible to developing secondary malignancy (SM) a feared iatrogenic complication. Materials &amp; Methods: We evaluated the SM risk in a cohort of patients with HL treated over a 50-year period. In total, 1653 patients were treated for HL from 1956 to 2009 at a tertiary-cancer-center. A cumulative incidence function was used to quantify SM risk and the Fine and Gray competing risk model was used to identify disease and treatment related correlates. Results: Two-hundred-ninety patients (19%) developed SMs. Paradoxically, SM risk was higher in the modern era with 20-year cumulative incidence rates of 11.1%, 11.9%, 17% and 21.8%, for patients treated <1970, 1971–1986, 1986–1995 and 1996–2009, respectively. We hypothesized that the disproportionately high rate of early deaths in the early era may skew the assessment of SM risks, a much-delayed event. When the analysis was restricted to patients with early-stage favorable HL treated >1980, we found a reversal of the trend, especially on the risk of solid tumor, with a hazard ratio of 0.57 (p = 0.0651) in patients treated after 1996. Conclusion: Our findings highlight the limitations of comparing the risk of a late event between groups with disparate rates of early deaths, despite the use of a competing risk model. When partially corrected for, patients treated in the more recent time period experienced a lower solid tumor risk.http://www.sciencedirect.com/science/article/pii/S2405630822000349Hodgkin's LymphomaRadiationSecondary MalignancyToxicity
spellingShingle Bouthaina Shbib Dabaja
David Boyce-Fappiano
Wenli Dong
Ethan Damron
Penny Fang
Jill Gunther
Maria A. Rodriguez
Paolo Strati
Raphael Steiner
Ranjit Nair
Hun Lee
Zeinab Abou Yehia
Ferial Shihadeh
Chelsea Pinnix
Andrea K. Ng
Second malignancies in patients with Hodgkin’s Lymphoma: Half a century of experience
Clinical and Translational Radiation Oncology
Hodgkin's Lymphoma
Radiation
Secondary Malignancy
Toxicity
title Second malignancies in patients with Hodgkin’s Lymphoma: Half a century of experience
title_full Second malignancies in patients with Hodgkin’s Lymphoma: Half a century of experience
title_fullStr Second malignancies in patients with Hodgkin’s Lymphoma: Half a century of experience
title_full_unstemmed Second malignancies in patients with Hodgkin’s Lymphoma: Half a century of experience
title_short Second malignancies in patients with Hodgkin’s Lymphoma: Half a century of experience
title_sort second malignancies in patients with hodgkin s lymphoma half a century of experience
topic Hodgkin's Lymphoma
Radiation
Secondary Malignancy
Toxicity
url http://www.sciencedirect.com/science/article/pii/S2405630822000349
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