TY - JOUR
T1 - PRECISE
T2 - Preoperative Radiation Therapy to Elicit Critical Immune Stimulating Effects—A Phase 2 Clinical Trial
AU - Shaitelman, Simona F.
AU - Le-Petross, Huong
AU - Raso, Maria G.
AU - Swanson, David M.
AU - Schalck, Aislyn P.
AU - Contreras, Alejandro
AU - Yang, Fei
AU - Muruganandham, Manickam
AU - Zhao, George Z.
AU - Sawakuchi, Gabriel O.
AU - Kim, Leonard H.
AU - Batra, Harsh
AU - Smith, Benjamin D.
AU - Stauder, Michael C.
AU - Woodward, Wendy A.
AU - Reddy, Jay P.
AU - Litton, Jennifer K.
AU - Thompson, Alastair
AU - Bedrosian, Isabelle
AU - Mittendorf, Elizabeth A.
N1 - Publisher Copyright:
© 2024 Elsevier Inc.
PY - 2025/1/1
Y1 - 2025/1/1
N2 - Purpose: Radiation therapy is an underinvestigated tool for priming the immune system in intact human breast cancers. We sought here to investigate if a preoperative radiation therapy boost delivered was associated with a significant change in tumor-infiltrating lymphocytes (TILs) in the tumor in estrogen receptor positive, HER2Neu nonamplified breast cancers. Methods and Materials: A total of 20 patients were enrolled in a phase 2 clinical trial and received either 7.5 Gy × 1 fraction or 2 Gy × 5 fractions, completed 6 to 8 days before surgery. Percent stromal TILs were evaluated on hematoxylin and eosin–stained samples. Short-term safety was assessed based on time to surgery, toxicities, and cosmesis up to 6 months after boost. Results: Stromal TIL increased 6 to 8 days after completion of boost radiation therapy (median 3.0 [IQR, 1.0-6.5]) before radiation therapy versus median 5.0 (IQR, 1.5-8.0) after radiation therapy, P = .0037. Zero grade ≥3 toxicities up to 6 months after boost were experienced. In all, 94% (16/17) patients with 6-month follow-up cosmetic assessment after breast conservation had good-excellent cosmesis by physician assessment. Conclusion: In this phase 2 trial, preoperative radiation therapy boost resulted in a short-term increase in stromal TIL with minimal toxicities. Preoperative breast radiation therapy appears to be safe and may be a feasible means for priming the tumor microenvironment.
AB - Purpose: Radiation therapy is an underinvestigated tool for priming the immune system in intact human breast cancers. We sought here to investigate if a preoperative radiation therapy boost delivered was associated with a significant change in tumor-infiltrating lymphocytes (TILs) in the tumor in estrogen receptor positive, HER2Neu nonamplified breast cancers. Methods and Materials: A total of 20 patients were enrolled in a phase 2 clinical trial and received either 7.5 Gy × 1 fraction or 2 Gy × 5 fractions, completed 6 to 8 days before surgery. Percent stromal TILs were evaluated on hematoxylin and eosin–stained samples. Short-term safety was assessed based on time to surgery, toxicities, and cosmesis up to 6 months after boost. Results: Stromal TIL increased 6 to 8 days after completion of boost radiation therapy (median 3.0 [IQR, 1.0-6.5]) before radiation therapy versus median 5.0 (IQR, 1.5-8.0) after radiation therapy, P = .0037. Zero grade ≥3 toxicities up to 6 months after boost were experienced. In all, 94% (16/17) patients with 6-month follow-up cosmetic assessment after breast conservation had good-excellent cosmesis by physician assessment. Conclusion: In this phase 2 trial, preoperative radiation therapy boost resulted in a short-term increase in stromal TIL with minimal toxicities. Preoperative breast radiation therapy appears to be safe and may be a feasible means for priming the tumor microenvironment.
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U2 - 10.1016/j.ijrobp.2024.08.008
DO - 10.1016/j.ijrobp.2024.08.008
M3 - Article
C2 - 39147206
AN - SCOPUS:85202970238
SN - 0360-3016
VL - 121
SP - 90
EP - 96
JO - International Journal of Radiation Oncology Biology Physics
JF - International Journal of Radiation Oncology Biology Physics
IS - 1
ER -