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Hypofractionated vs Conventionally Fractionated Postmastectomy Radiation After Implant-Based Reconstruction: A Randomized Clinical Trial.
Wong, Julia S; Uno, Hajime; Tramontano, Angela C; Fisher, Lauren; Pellegrini, Catherine V; Abel, Gregory A; Burstein, Harold J; Chun, Yoon S; King, Tari A; Schrag, Deborah; Winer, Eric; Bellon, Jennifer R; Cheney, Matthew D; Hardenbergh, Patricia; Ho, Alice; Horst, Kathleen C; Kim, Janice N; Leonard, Kara-Lynne; Moran, Meena S; Park, Catherine C; Recht, Abram; Soto, Daniel E; Shiloh, Ron Y; Stinson, Susan F; Snyder, Kurt M; Taghian, Alphonse G; Warren, Laura E; Wright, Jean L; Punglia, Rinaa S.
Affiliation
  • Wong JS; Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Uno H; Harvard Medical School, Boston, Massachusetts.
  • Tramontano AC; Brigham and Women's Hospital, Boston, Massachusetts.
  • Fisher L; Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Pellegrini CV; Harvard Medical School, Boston, Massachusetts.
  • Abel GA; Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Burstein HJ; Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Chun YS; Dana-Farber Cancer Institute, Boston, Massachusetts.
  • King TA; Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Schrag D; Harvard Medical School, Boston, Massachusetts.
  • Winer E; Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Bellon JR; Harvard Medical School, Boston, Massachusetts.
  • Cheney MD; Brigham and Women's Hospital, Boston, Massachusetts.
  • Hardenbergh P; Harvard Medical School, Boston, Massachusetts.
  • Ho A; Brigham and Women's Hospital, Boston, Massachusetts.
  • Horst KC; Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Kim JN; Harvard Medical School, Boston, Massachusetts.
  • Leonard KL; Brigham and Women's Hospital, Boston, Massachusetts.
  • Moran MS; Memorial Sloan Kettering Cancer Center, New York, New York.
  • Park CC; Yale Cancer Center, New Haven, Connecticut.
  • Recht A; Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Soto DE; Harvard Medical School, Boston, Massachusetts.
  • Shiloh RY; Brigham and Women's Hospital, Boston, Massachusetts.
  • Stinson SF; Maine Medical Center, Portland, Maine.
  • Snyder KM; Vail Health, Vail, Colorado.
  • Taghian AG; Duke University Medical Center, Durham, North Carolina.
  • Warren LE; Stanford University School of Medicine, Stanford, California.
  • Wright JL; Fred Hutchinson Cancer Center/UW Medicine, Seattle, Washington.
  • Punglia RS; Warren Alpert Medical School of Brown University, Providence, Rhode Island.
JAMA Oncol ; 2024 Aug 08.
Article in En | MEDLINE | ID: mdl-39115975
ABSTRACT
Importance Postmastectomy radiation therapy (PMRT) improves local-regional disease control and patient survival. Hypofractionation (HF) regimens have comparable efficacy and complication rates with improved quality of life compared with conventional fractionation (CF) schedules. However, the use of HF after mastectomy in patients undergoing breast reconstruction has not been prospectively examined.

Objective:

To compare HF and CF PMRT outcomes after implant-based reconstruction. Design, Setting, and

Participants:

This randomized clinical trial assessed patients 18 years or older undergoing mastectomy and immediate expander or implant reconstruction for breast cancer (Tis, TX, or T1-3) and unilateral PMRT from March 8, 2018, to November 3, 2021 (median [range] follow-up, 40.4 [15.4-63.0] months), at 16 US cancer centers or hospitals. Analyses were conducted between September and December 2023.

Interventions:

Patients were randomized 11 to HF or CF PMRT. Chest wall doses were 4256 cGy for 16 fractions for HF and 5000 cGy for 25 fractions for CF. Chest wall toxic effects were defined as a grade 3 or higher adverse event. Main Outcomes and

Measures:

The primary outcome was the change in physical well-being (PWB) domain of the Functional Assessment of Cancer Therapy-Breast (FACT-B) quality-of-life assessment tool at 6 months after starting PMRT, controlling for age. Secondary outcomes included toxic effects and cancer recurrence.

Results:

Of 400 women (201 in the CF arm and 199 in the HF arm; median [range] age, 47 [23-79] years), 330 patients had PWB scores at baseline and at 6 months. There was no difference in the change in PWB between the study arms (estimate, 0.13; 95% CI, -0.86 to 1.11; P = .80), but there was a significant interaction between age group and study arm (P = .03 for interaction). Patients younger than 45 years had higher 6-month absolute PWB scores if treated with HF rather than CF regimens (23.6 [95% CI, 22.7-24.6] vs 22.0 [95% CI, 20.7-23.3]; P = .047) and reported being less bothered by adverse effects (mean [SD], 3.0 [0.9] in the HF arm and 2.6 [1.2] in the CF arm; P = .02) or nausea (mean [SD], 3.8 [0.4] in the HF arm and 3.6 [0.8] in the CF arm; P = .04). In the as-treated cohort, there were 23 distant (11 in the HF arm and 12 in the CF arm) and 2 local-regional (1 in the HF arm and 1 in the CF arm) recurrences. Chest wall toxic effects occurred in 39 patients (20 in the HF arm and 19 in the CF arm) at a median (IQR) of 7.2 (1.8-12.9) months. Fractionation was not associated with chest wall toxic effects on multivariate analysis (HF arm hazard ratio, 1.02; 95% CI, 0.52-2.00; P = .95). Fewer patients undergoing HF vs CF regimens had a treatment break (5 [2.7%] vs 15 [7.7%]; P = .03) or required unpaid time off from work (17 [8.5%] vs 34 [16.9%]; P = .02). Conclusions and Relevance In this randomized clinical trial, the HF regimen did not significantly improve change in PWB compared with the CF regimen. These data add to the increasing experience with HF PMRT in patients with implant-based reconstruction. Trial Registration ClinicalTrials.gov Identifier NCT03422003.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: JAMA Oncol Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: JAMA Oncol Year: 2024 Document type: Article