Definitive hyperfractionated, accelerated proton reirradiation for patients with pelvic malignancies.

Anal cancer Proton beam radiation Proton re-irradiation Rectal cancer Recurrent cancer

Journal

Clinical and translational radiation oncology
ISSN: 2405-6308
Titre abrégé: Clin Transl Radiat Oncol
Pays: Ireland
ID NLM: 101713416

Informations de publication

Date de publication:
Nov 2019
Historique:
received: 24 06 2019
revised: 23 08 2019
accepted: 26 08 2019
entrez: 14 9 2019
pubmed: 14 9 2019
medline: 14 9 2019
Statut: epublish

Résumé

Pelvic reirradiation (re-RT) presents challenges due to concerns for late toxicity to tissues-at-risk including pelvic bone marrow (PBM). We routinely utilize a hyperfractionated, accelerated re-RT for recurrent rectal or anal cancer in the setting of prior radiation. We hypothesized that proton beam radiation (PBR) is uniquely suited to limit doses to pelvic non-target tissues better than photon-based approaches. All patients who received hyperfractionated, accelerated PBR re-RT to the pelvis from 2007 to 2017 were identified. Re-RT was delivered twice daily with a 6 h minimum interfraction interval at 1.5 Gray Relative Biological Effectiveness (Gy(RBE)) per fraction to a total dose of 39-45 Gy(RBE). Concurrent chemotherapy was given to all patients. Comparison photon plans were generated for dosimetric analysis. Dosimetric parameters compared using a matched-pair analysis and the Wilcoxon signed-rank test. Survival analysis was performed Kaplan Meier curves. Fifteen patients were identified, with a median prior pelvic RT dose of 50.4 Gy (range 25-80 Gy). Median time between the initial RT and PBRT re-RT was 4.7 years (range 1.0-36.1 years). In comparison to corresponding photon re-RT plans, PBR re-RT plans had lower mean PBM dose, and lower volume of PBM getting 5 Gy, 10 Gy, 20 Gy, and 30 Gy (p < 0.001, p < 0.001, p < 0.001, and p = 0.033, respectively).With median 13.9 months follow-up after PBR re-RT, five patients had developed local recurrences, and four patients had developed distant metastases. One-year overall survival following PBR re-RT was 67.5% and one-year progression free survival was 58.7%. No patients developed acute or late Grade 4 toxicity. PBR re-RT affords improved sparing of PBM compared with photon-based re-RT. Clinically, PBR re-RT is well-tolerated. However, given modest control rates with definitive re-RT without subsequent surgical resection, a multidisciplinary approach should be favored in this setting when feasible.

Identifiants

pubmed: 31517071
doi: 10.1016/j.ctro.2019.08.004
pii: S2405-6308(19)30092-8
pmc: PMC6734102
doi:

Types de publication

Journal Article

Langues

eng

Pagination

59-65

Subventions

Organisme : NCI NIH HHS
ID : K07 CA211804
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA016672
Pays : United States

Déclaration de conflit d'intérêts

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

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Auteurs

Shalini Moningi (S)

Division of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.

Ethan B Ludmir (EB)

Division of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.

Praveen Polamraju (P)

School of Medicine, University of Texas Medical Branch, Galveston, TX, United States.

Tyler Williamson (T)

Division of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.

Marcella M Melkun (MM)

Division of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.

Joseph D Herman (JD)

Division of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.

Sunil Krishnan (S)

Division of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.

Eugene J Koay (EJ)

Division of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.

Albert C Koong (AC)

Division of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.

Bruce D Minsky (BD)

Division of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.

Grace L Smith (GL)

Division of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.

Cullen Taniguchi (C)

Division of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.

Prajnan Das (P)

Division of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.

Emma B Holliday (EB)

Division of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.

Classifications MeSH