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  1. Article ; Online: Establishing Cost-Effective Allocation of Proton Therapy for Patients With Mediastinal Hodgkin Lymphoma.

    Mailhot Vega, Raymond B / Mohammadi, Homan / Patel, Samir I / Holtzman, Adam L / Lockney, Natalie A / Lynch, James W / Bansal, Manisha M / Liang, Xiaoying / Slayton, William B / Parsons, Susan K / Hoppe, Bradford S / Mendenhall, Nancy P

    International journal of radiation oncology, biology, physics

    2021  Volume 112, Issue 1, Page(s) 158–166

    Abstract: Purpose: For curative treatment of Hodgkin lymphoma, radiation therapy benefit must be weighed against toxicity. Although more costly, proton radiation therapy reduces dose to healthy tissue, potentially improving the therapeutic ratio compared with ... ...

    Abstract Purpose: For curative treatment of Hodgkin lymphoma, radiation therapy benefit must be weighed against toxicity. Although more costly, proton radiation therapy reduces dose to healthy tissue, potentially improving the therapeutic ratio compared with photons. We sought to determine the cost-effectiveness of proton versus photon therapy for mediastinal Hodgkin lymphoma (MHL) based on reduced heart disease.
    Methods and materials: Our model approach was 2-fold: (1) Use patient-level dosimetric information for a cost-effectiveness analysis using a Markov cohort model. (2) Use population-based data to develop guidelines for policymakers to determine thresholds of proton therapy favorability for a given photon dose. The HD14 trial informed relapse risk; coronary heart disease risk was informed by the Framingham risk calculator modified by the mean heart dose (MHD) from radiation. Sensitivity analyses assessed model robustness and identified the most influential model assumptions. A 30-year-old adult with MHL was the base case using 30.6-Gy proton therapy versus photon intensity modulated radiation therapy.
    Results: Proton therapy was not cost-effective in the base case for male ($129,000/ quality-adjusted life years [QALYs]) or female patients ($196,000/QALY). A 5-Gy MHD decrease was associated with proton therapy incremental cost-effectiveness ratio <$100,000/QALY in 40% of scenarios. The hazard ratio associating MHD and heart disease was the most influential clinical parameter.
    Conclusions: Proton therapy may be cost-effective a select minority of patients with MHL based on age, sex, and MHD reduction. We present guidance for clinicians using MHD to aid decision-making for radiation therapy modality.
    MeSH term(s) Adult ; Cost-Benefit Analysis ; Female ; Hodgkin Disease/radiotherapy ; Humans ; Male ; Neoplasm Recurrence, Local/etiology ; Proton Therapy/adverse effects ; Proton Therapy/methods ; Quality-Adjusted Life Years
    Language English
    Publishing date 2021-08-02
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 197614-x
    ISSN 1879-355X ; 0360-3016
    ISSN (online) 1879-355X
    ISSN 0360-3016
    DOI 10.1016/j.ijrobp.2021.07.1711
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Children's Oncology Group Trial AALL1231: A Phase III Clinical Trial Testing Bortezomib in Newly Diagnosed T-Cell Acute Lymphoblastic Leukemia and Lymphoma.

    Teachey, David T / Devidas, Meenakshi / Wood, Brent L / Chen, Zhiguo / Hayashi, Robert J / Hermiston, Michelle L / Annett, Robert D / Archer, J Hunter / Asselin, Barbara L / August, Keith J / Cho, Steve Y / Dunsmore, Kimberly P / Fisher, Brian T / Freedman, Jason L / Galardy, Paul J / Harker-Murray, Paul / Horton, Terzah M / Jaju, Alok I / Lam, Allison /
    Messinger, Yoav H / Miles, Rodney R / Okada, Maki / Patel, Samir I / Schafer, Eric S / Schechter, Tal / Singh, Neelam / Steele, Amii C / Sulis, Maria Luisa / Vargas, Sarah L / Winter, Stuart S / Wood, Charlotte / Zweidler-McKay, Patrick / Bollard, Catherine M / Loh, Mignon L / Hunger, Stephen P / Raetz, Elizabeth A

    Journal of clinical oncology : official journal of the American Society of Clinical Oncology

    2022  Volume 40, Issue 19, Page(s) 2106–2118

    Abstract: Purpose: To improve the outcomes of patients with T-cell acute lymphoblastic leukemia (T-ALL) and lymphoblastic lymphoma (T-LL), the proteasome inhibitor bortezomib was examined in the Children's Oncology Group phase III clinical trial AALL1231, which ... ...

    Abstract Purpose: To improve the outcomes of patients with T-cell acute lymphoblastic leukemia (T-ALL) and lymphoblastic lymphoma (T-LL), the proteasome inhibitor bortezomib was examined in the Children's Oncology Group phase III clinical trial AALL1231, which also attempted to reduce the use of prophylactic cranial radiation (CRT) in newly diagnosed T-ALL.
    Patients and methods: Children and young adults with T-ALL/T-LL were randomly assigned to a modified augmented Berlin-Frankfurt-Münster chemotherapy regimen with/without bortezomib during induction and delayed intensification. Multiple modifications were made to the augmented Berlin-Frankfurt-Münster backbone used in the predecessor trial, AALL0434, including using dexamethasone instead of prednisone and adding two extra doses of pegaspargase in an attempt to eliminate CRT in most patients.
    Results: AALL1231 accrued 824 eligible and evaluable patients from 2014 to 2017. The 4-year event-free survival (EFS) and overall survival (OS) for arm A (no bortezomib) versus arm B (bortezomib) were 80.1% ± 2.3% versus 83.8% ± 2.1% (EFS,
    Conclusion: Patients with T-LL had significantly improved EFS and OS with bortezomib on the AALL1231 backbone. Systemic therapy intensification allowed elimination of CRT in more than 90% of patients with T-ALL without excess relapse.
    MeSH term(s) Antineoplastic Combined Chemotherapy Protocols/adverse effects ; Bortezomib/adverse effects ; Child ; Disease-Free Survival ; Humans ; Infant ; Lymphoma/drug therapy ; Precursor Cell Lymphoblastic Leukemia-Lymphoma/drug therapy ; Precursor T-Cell Lymphoblastic Leukemia-Lymphoma/drug therapy ; T-Lymphocytes ; Young Adult
    Chemical Substances Bortezomib (69G8BD63PP)
    Language English
    Publishing date 2022-03-10
    Publishing country United States
    Document type Clinical Trial, Phase III ; Journal Article ; Randomized Controlled Trial ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 604914-x
    ISSN 1527-7755 ; 0732-183X
    ISSN (online) 1527-7755
    ISSN 0732-183X
    DOI 10.1200/JCO.21.02678
    Database MEDical Literature Analysis and Retrieval System OnLINE

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