Assessment of Radiation Doses Delivered to Organs at Risk Among Patients With Early-Stage Favorable Hodgkin Lymphoma Treated With Contemporary Radiation Therapy.


Journal

JAMA network open
ISSN: 2574-3805
Titre abrégé: JAMA Netw Open
Pays: United States
ID NLM: 101729235

Informations de publication

Date de publication:
01 09 2020
Historique:
entrez: 29 9 2020
pubmed: 30 9 2020
medline: 7 1 2021
Statut: epublish

Résumé

Response-adapted randomized trials have used positron emission tomography-computed tomography to attempt to identify patients with early-stage favorable Hodgkin lymphoma (ESFHL) who could be treated with doxorubicin, bleomycin, vinblastine, and dacarbazine (ABVD) without radiation therapy (RT). While maximal efficacy is demonstrated with combined modality therapy, RT is often omitted in fear of late adverse effects; however, the application of modern RT could limit these toxic effects. To determine the radiation doses delivered to organs at risk with modern involved-site RT among patients with ESFHL treated with 20 Gy after 2 cycles of ABVD. This case series included 42 adult patients with ESFHL (according to the German Hodgkin Study Group criteria) who were treated between 2010 and 2019, achieved complete response by positron emission tomography-computed tomography (1-3 on 5-point scale) following 2 cycles of ABVD, and then received consolidative RT. The study was conducted at a single comprehensive cancer center. 2 cycles of chemotherapy followed by 20-Gy involved-site RT. The medical records of patients with ESFHL were examined. Organs at risk were contoured, and doses were calculated. Progression-free survival, defined from date of diagnosis to disease progression, relapse, or death, and overall survival were estimated using the Kaplan-Meier method. The cohort comprised 42 patients with ESFHL (median [range] age at diagnosis, 35 [18-74] years; 18 [43%] women; 24 [57%] with stage II disease). At a median follow-up of 44.6 (95% CI, 27.6-61.6) months, the 3-year progression-free survival and overall survival rates were 91.2% (95% CI, 74.9%-97.1%) and 97.0% (95% CI, 80.4%-99.6%), respectively. The mean heart dose was less than 5 Gy (mean, 0.8 Gy; SD, 1.5 Gy; range, 0-4.8 Gy) in all patients. The mean (SD) breast dose for both breasts was 0.1 (0.2) Gy (left breast range, 0-1.0 Gy; right breast range, 0-0.9 Gy). In this study, combined modality therapy with 2 cycles of ABVD and 20 Gy for ESFHL was highly effective and avoided excess doses to organs at risk, which may limit long-term toxic effects.

Identifiants

pubmed: 32990738
pii: 2770978
doi: 10.1001/jamanetworkopen.2020.13935
pmc: PMC7525355
doi:

Substances chimiques

Bleomycin 11056-06-7
Vinblastine 5V9KLZ54CY
Dacarbazine 7GR28W0FJI
Doxorubicin 80168379AG

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2013935

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Auteurs

Chelsea C Pinnix (CC)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston.

Jillian R Gunther (JR)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston.

Penny Fang (P)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston.

Mikaela E Bankston (ME)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston.

Sarah A Milgrom (SA)

Department of Radiation Oncology, University of Colorado, Denver.

David Boyce (D)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston.

Hun Ju Lee (HJ)

Department of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston.

Ranjit Nair (R)

Department of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston.

Raphael Steiner (R)

Department of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston.

Paolo Strati (P)

Department of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston.

Sairah Ahmed (S)

Department of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston.

Swaminathan P Iyer (SP)

Department of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston.

Jason Westin (J)

Department of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston.

Simrit Parmar (S)

Department of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston.

M Alma Rodriguez (MA)

Department of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston.

Loretta Nastoupil (L)

Department of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston.

Sattva Neelapu (S)

Department of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston.

Christopher Flowers (C)

Department of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston.

Bouthaina S Dabaja (BS)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston.

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Classifications MeSH