Hyaluronic Acid Spacer for Hypofractionated Prostate Radiation Therapy: A Randomized Clinical Trial.


Journal

JAMA oncology
ISSN: 2374-2445
Titre abrégé: JAMA Oncol
Pays: United States
ID NLM: 101652861

Informations de publication

Date de publication:
01 04 2023
Historique:
medline: 24 4 2023
pubmed: 10 2 2023
entrez: 9 2 2023
Statut: ppublish

Résumé

Hypofractionated radiation therapy (RT) for prostate cancer has been associated with greater acute grade 2 gastrointestinal (GI) toxic effects compared with conventionally fractionated RT. To evaluate whether a hyaluronic acid rectal spacer could (1) improve rectal dosimetry and (2) affect acute grade 2 or higher GI toxic effects for hypofractionated RT. This randomized clinical trial was conducted from March 2020 to June 2021 among 12 centers within the US, Australia, and Spain, with a 6-month follow-up. Adult patients with biopsy-proven, T1 to T2 prostate cancer with a Gleason score 7 or less and prostate-specific antigen level of 20 ng/mL or less (to convert to μg/L, multiply by 1) were blinded to the treatment arms. Of the 260 consented patients, 201 patients (77.3%) were randomized (2:1) to the presence or absence of the spacer. Patients were stratified by intended 4-month androgen deprivation therapy use and erectile quality. For the primary outcome, we hypothesized that more than 70% of patients in the spacer group would achieve a 25% or greater reduction in the rectal volume receiving 54 Gy (V54). For the secondary outcome, we hypothesized that the spacer group would have noninferior acute (within 3 months) grade 2 or higher GI toxic effects compared with the control group, with a margin of 10%. Of the 201 randomized patients, 8 (4.0%) were Asian, 26 (12.9%) Black, 42 (20.9%) Hispanic or Latino, and 153 (76.1%) White; the mean (SD) age for the spacer group was 68.6 (7.2) years and 68.4 (7.3) years for the control group. For the primary outcome, 131 of 133 (98.5%; 95% CI, 94.7%-99.8%) patients in the spacer group experienced a 25% or greater reduction in rectum V54, which was greater than the minimally acceptable 70% (P < .001). The mean (SD) reduction was 85.0% (20.9%). For the secondary outcome, 4 of 136 patients (2.9%) in the spacer group and 9 of 65 patients (13.8%) in the control group experienced acute grade 2 or higher GI toxic effects (difference, -10.9%; 95% 1-sided upper confidence limit, -3.5; P = .01). The trial results suggest that rectal spacing with hyaluronic acid improved rectal dosimetry and reduced acute grade 2 or higher GI toxic effects. Rectal spacing should potentially be considered for minimizing the risk of acute grade 2 or higher toxic effects for hypofractionated RT. ClinicalTrials.gov Identifier: NCT04189913.

Identifiants

pubmed: 36757690
pii: 2801296
doi: 10.1001/jamaoncol.2022.7592
pmc: PMC9912169
doi:

Substances chimiques

Hyaluronic Acid 9004-61-9
Androgen Antagonists 0

Banques de données

ClinicalTrials.gov
['NCT04189913']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

511-518

Auteurs

Neil F Mariados (NF)

Cancer Care of Western New York, Buffalo, New York.

Peter F Orio (PF)

Brigham and Women's Hospital, Boston, Massachusetts.
Dana Farber Cancer Institute, Boston, Massachusetts.

Zvi Schiffman (Z)

Houston Metro Urology, Houston, Texas.

Thanh John Van (TJ)

Houston Metro Urology, Houston, Texas.

Alexander Engelman (A)

Florida Urology Partners, Tampa, Florida.

Rizwan Nurani (R)

Western Radiation Oncology, Campbell, California.
Interventional Radiation Oncology of California, Campbell.

Steven M Kurtzman (SM)

Western Radiation Oncology, Campbell, California.

Escarlata Lopez (E)

Vithas La Milagrosa Hospital, Calle de Modesto Lafuente, Madrid, Spain.

Michael Chao (M)

Ringwood Private Hospital, East Victoria, Australia.

Thomas P Boike (TP)

GenesisCare, Troy, Michigan.

Alvaro A Martinez (AA)

GenesisCare, Troy, Michigan.

Glen Gejerman (G)

New Jersey Urology, Saddle Brook, New Jersey.

John Lederer (J)

The Cancer Center of Hawaii, Honolulu.

John E Sylvester (JE)

GenesisCare, Lakewood Ranch, Florida.

Gregory Bell (G)

Austin Cancer Center, Austin, Texas.

Douglas Rivera (D)

Austin Cancer Center, Austin, Texas.

Neal Shore (N)

Carolina Urologic Research Center, Myrtle Beach, South Carolina.

Katie Miller (K)

M Squared Associates, New York, New York.

Boris Sinayuk (B)

Rhode Island Medical Imaging, Warwick, Rhode Island.

Michael L Steinberg (ML)

University of California, Los Angeles.

Daniel A Low (DA)

University of California, Los Angeles.

Amar U Kishan (AU)

University of California, Los Angeles.

Martin T King (MT)

Brigham and Women's Hospital, Boston, Massachusetts.
Dana Farber Cancer Institute, Boston, Massachusetts.

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Classifications MeSH