Does external beam radiation boost to pelvic lymph nodes improve outcomes in patients with locally advanced cervical cancer?


Journal

BMC cancer
ISSN: 1471-2407
Titre abrégé: BMC Cancer
Pays: England
ID NLM: 100967800

Informations de publication

Date de publication:
25 Apr 2019
Historique:
received: 15 07 2018
accepted: 09 04 2019
entrez: 27 4 2019
pubmed: 27 4 2019
medline: 16 8 2019
Statut: epublish

Résumé

Current recommendation for locally advanced cervical cancer includes pelvic external beam radiation therapy (EBRT) with concurrent chemotherapy followed by brachytherapy. Involvement of pelvic lymph nodes is an important prognostic factor in locally advanced cervical cancer and recurrence commonly occurs despite definitive treatment. To date, there is no standard guideline on whether an EBRT boost should be applied to involved pelvic lymph nodes. Our study aims to assess if pelvic EBRT boost would reduce recurrence, benefit survival, and affect associated toxicities. We conducted a retrospective review of locally advanced cervical cancer cases treated with definitive treatment at our institution. Involvement of pelvic lymph nodes were assessed on CT, MRI (> 10 mm or suspicious features) or PET scan (SUVmax > 2.5). EBRT dose ranged from 45 to 50.4 Gy with nodal boost ranging from 3.6-19.8 Gy. Between 2008 to 2015, 139 patients with locally advanced cervical cancer underwent treatment. Sixty-seven patients had positive pelvic lymph nodes, of which 53.7% received a nodal boost. Five-year recurrence free survival was 48.6% with vs. 64.5% without nodal boost (P = 0.169) and 5-year overall survival in those with positive pelvic lymph nodes was 74.3% with vs. 80.6% without nodal boost (P = 0.143). There was no significant difference in toxicity with nodal boost. EBRT boost to pelvic lymph nodes does not reduce recurrence or improve survival in locally advanced cervical cancer with lymph node involvement at diagnosis.

Sections du résumé

BACKGROUND BACKGROUND
Current recommendation for locally advanced cervical cancer includes pelvic external beam radiation therapy (EBRT) with concurrent chemotherapy followed by brachytherapy. Involvement of pelvic lymph nodes is an important prognostic factor in locally advanced cervical cancer and recurrence commonly occurs despite definitive treatment. To date, there is no standard guideline on whether an EBRT boost should be applied to involved pelvic lymph nodes. Our study aims to assess if pelvic EBRT boost would reduce recurrence, benefit survival, and affect associated toxicities.
METHODS METHODS
We conducted a retrospective review of locally advanced cervical cancer cases treated with definitive treatment at our institution. Involvement of pelvic lymph nodes were assessed on CT, MRI (> 10 mm or suspicious features) or PET scan (SUVmax > 2.5). EBRT dose ranged from 45 to 50.4 Gy with nodal boost ranging from 3.6-19.8 Gy.
RESULTS RESULTS
Between 2008 to 2015, 139 patients with locally advanced cervical cancer underwent treatment. Sixty-seven patients had positive pelvic lymph nodes, of which 53.7% received a nodal boost. Five-year recurrence free survival was 48.6% with vs. 64.5% without nodal boost (P = 0.169) and 5-year overall survival in those with positive pelvic lymph nodes was 74.3% with vs. 80.6% without nodal boost (P = 0.143). There was no significant difference in toxicity with nodal boost.
CONCLUSIONS CONCLUSIONS
EBRT boost to pelvic lymph nodes does not reduce recurrence or improve survival in locally advanced cervical cancer with lymph node involvement at diagnosis.

Identifiants

pubmed: 31023261
doi: 10.1186/s12885-019-5594-4
pii: 10.1186/s12885-019-5594-4
pmc: PMC6485109
doi:

Types de publication

Journal Article

Langues

eng

Pagination

385

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Auteurs

Caryn Wujanto (C)

Department of Radiation Oncology, National University Cancer Institute, National University Hospital, NUHS Tower Block Level 7, Singapore, 119228, Singapore. caryn.wujanto@mohh.com.sg.

Bok Ai Choo (BA)

Department of Radiation Oncology, National University Cancer Institute, National University Hospital, NUHS Tower Block Level 7, Singapore, 119228, Singapore.

David Tan (D)

Department of Medical Oncology, National University Cancer Institute, National University Hospital, NUHS Tower Block, Level 7, Singapore, 119228, Singapore.

Arunachalam Ilancheran (A)

Division of Gynaecologic Oncology, National University Cancer Institute, National University Hospital, NUHS Tower Block, Level 12, Singapore, 119228, Singapore.

Joseph Ng (J)

Division of Gynaecologic Oncology, National University Cancer Institute, National University Hospital, NUHS Tower Block, Level 12, Singapore, 119228, Singapore.

Jeffrey J H Low (JJH)

Division of Gynaecologic Oncology, National University Cancer Institute, National University Hospital, NUHS Tower Block, Level 12, Singapore, 119228, Singapore.

Liang Shen (L)

Biostatistics Unit, Yong Loo Lin School of Medicine, National University of Singapore, 21 Lower Kent Ridge Road, Singapore, 119077, Singapore.

Johann Tang (J)

Department of Radiation Oncology, National University Cancer Institute, National University Hospital, NUHS Tower Block Level 7, Singapore, 119228, Singapore.

Vicky Koh (V)

Department of Radiation Oncology, National University Cancer Institute, National University Hospital, NUHS Tower Block Level 7, Singapore, 119228, Singapore.

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Classifications MeSH