Treatment-Related Toxicity Using Prostate-Only Versus Prostate and Pelvic Lymph Node Intensity-Modulated Radiation Therapy: A National Population-Based Study.


Journal

Journal of clinical oncology : official journal of the American Society of Clinical Oncology
ISSN: 1527-7755
Titre abrégé: J Clin Oncol
Pays: United States
ID NLM: 8309333

Informations de publication

Date de publication:
20 07 2019
Historique:
pubmed: 5 6 2019
medline: 20 5 2020
entrez: 5 6 2019
Statut: ppublish

Résumé

There is a debate about the effectiveness and toxicity of pelvic lymph node (PLN) irradiation for the treatment of men with high-risk prostate cancer. This study compared the toxicity of intensity-modulated radiation therapy (IMRT) to the prostate and the pelvic lymph nodes (PPLN-IMRT) with prostate-only IMRT (PO-IMRT). Patients with high-risk localized or locally advanced prostate cancer treated with IMRT in the English National Health Service between 2010 and 2013 were identified by using data from the Cancer Registry, the National Radiotherapy Dataset, and Hospital Episode Statistics, an administrative database of all hospital admissions. Follow-up was available up to December 31, 2015. Validated indicators were used to identify patients with severe toxicity according to the presence of both a procedure code and diagnostic code in patient Hospital Episode Statistics records. A competing risks regression analysis, with adjustment for patient and tumor characteristics, estimated subdistribution hazard ratios (sHRs) by comparing GI and genitourinary (GU) complications for PPLN-IMRT versus PO-IMRT. Three-year cumulative incidence in the PPLN-IMRT (n = 780) and PO-IMRT (n = 3,065) groups was 14% for both groups for GI toxicity, and 9% and 8% for GU toxicity, respectively. Patients receiving PPLN-IMRT and PO-IMRT had similar levels of severe GI (adjusted sHR, 1.00; 95% CI, 0.80 to 1.24; Including PLNs in radiation fields for high-risk or locally advanced prostate cancer is not associated with increased GI or GU toxicity at 3 years. Additional follow-up is required to answer questions about its impact on late GU toxicity. Results from ongoing trials will provide insight into the anticancer effectiveness of PLN irradiation.

Identifiants

pubmed: 31163009
doi: 10.1200/JCO.18.02237
pmc: PMC6641671
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1828-1835

Subventions

Organisme : Department of Health
ID : DRF-2018-11-ST2-036
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/S020470/1
Pays : United Kingdom

Commentaires et corrections

Type : CommentIn

Références

BMJ. 2016 Mar 02;352:i851
pubmed: 26936410
Acta Oncol. 2014 Oct;53(10):1380-9
pubmed: 24844918
Int J Radiat Oncol Biol Phys. 2011 Sep 1;81(1):23-8
pubmed: 20832182
Int J Radiat Oncol Biol Phys. 2017 Dec 1;99(5):1253-1260
pubmed: 28974414
JAMA. 2012 Apr 18;307(15):1611-20
pubmed: 22511689
Radiat Oncol J. 2013 Dec;31(4):199-205
pubmed: 24501707
Cancer Med. 2014 Apr;3(2):397-405
pubmed: 24519910
Int J Radiat Oncol Biol Phys. 2009 Dec 1;75(5):1344-9
pubmed: 19464821
Int J Radiat Oncol Biol Phys. 2017 Dec 1;99(5):1234-1242
pubmed: 28939224
JAMA Intern Med. 2013 Jun 24;173(12):1136-43
pubmed: 23689844
Int J Radiat Oncol Biol Phys. 2017 Dec 1;99(5):1261-1270
pubmed: 28964586
BMC Cancer. 2015 Nov 07;15:868
pubmed: 26547188
Prostate Cancer Prostatic Dis. 2018 Jun;21(2):269-276
pubmed: 29520019
Int J Radiat Oncol Biol Phys. 1988 Dec;15(6):1307-16
pubmed: 3058656
Int J Radiat Oncol Biol Phys. 2007 Nov 1;69(3):646-55
pubmed: 17531401
ACR Open Rheumatol. 2019 Aug 19;1(8):493-498
pubmed: 31777830
Int J Radiat Oncol Biol Phys. 2011 Dec 1;81(5):e721-6
pubmed: 21277100
Br J Surg. 2010 May;97(5):772-81
pubmed: 20306528
Lancet. 2004 May 22;363(9422):1728-31
pubmed: 15158638
Lancet Oncol. 2018 Nov;19(11):1504-1515
pubmed: 30316827
Int J Radiat Oncol Biol Phys. 2006 Nov 1;66(3):647-53
pubmed: 17011443
J Clin Oncol. 2007 Dec 1;25(34):5366-73
pubmed: 18048817

Auteurs

Matthew G Parry (MG)

1 London School of Hygiene and Tropical Medicine, London, United Kingdom.
2 Royal College of Surgeons of England, London, United Kingdom.

Arunan Sujenthiran (A)

2 Royal College of Surgeons of England, London, United Kingdom.

Thomas E Cowling (TE)

1 London School of Hygiene and Tropical Medicine, London, United Kingdom.

Julie Nossiter (J)

2 Royal College of Surgeons of England, London, United Kingdom.

Paul Cathcart (P)

3 Guy's and St Thomas' National Health Service (NHS) Foundation Trust, London, United Kingdom.

Noel W Clarke (NW)

4 The Christie and Salford Royal NHS Foundation Trusts, Manchester, United Kingdom.

Heather Payne (H)

5 University College London Hospitals, London, United Kingdom.

Jan van der Meulen (J)

1 London School of Hygiene and Tropical Medicine, London, United Kingdom.

Ajay Aggarwal (A)

3 Guy's and St Thomas' National Health Service (NHS) Foundation Trust, London, United Kingdom.
6 King's College London, London, United Kingdom.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH