Dosimetric and therapeutic effectiveness of high-dose-rate radionuclide sources in breast cancer brachytherapy: A systematic review.

BrachytherapySep 16, 2026 (epub)

Tsige Gebremariam, Teweldebrhan Gebru, Brhanu Tsegaye et al.

✦ AI-curated · Sources linked

In 30 seconds

This systematic review compared dosimetric properties and therapeutic evidence for ¹⁹²Ir, ⁶⁰Co, and ¹⁶⁹Yb in high-dose-rate breast cancer brachytherapy. Sixteen studies were included, spanning clinical trials, retrospective cohorts, and simulation studies. Dose rate constants were similar across sources (approximately 1.08-1.20 cGy·h⁻¹·U⁻¹), but dose gradients and tissue penetration differed. ¹⁹²Ir had the most extensive clinical validation, with reported local control rates exceeding 90%; evidence for ⁶⁰Co was limited, and ¹⁶⁹Yb evidence was confined to dosimetric and Monte Carlo investigations.

Key findings

  • Dose rate constants were similar among radionuclides, at approximately 1.08-1.20 cGy·h⁻¹·U⁻¹.
  • ¹⁶⁹Yb showed the steepest dose fall-off and superior organ-at-risk sparing in dosimetric analyses.
  • ¹⁹²Ir had the strongest clinical evidence, with local control rates exceeding 90%.
  • Clinical evidence was limited for ⁶⁰Co and absent for ¹⁶⁹Yb, whose evidence was restricted to dosimetric and Monte Carlo studies.

Why it matters

Radionuclide choice can affect dose distribution, tissue penetration, and organ-at-risk exposure, while the depth of clinical evidence differs substantially between sources. The review highlights that dosimetric advantages do not by themselves establish clinical benefit, particularly for ¹⁶⁹Yb. Distinguishing established outcomes from planning-based findings is important when interpreting comparisons and considering treatment objectives.

What to keep in mind

Clinical outcome evidence was limited for ⁶⁰Co and unavailable for ¹⁶⁹Yb; the review reports that ¹⁶⁹Yb evidence was restricted to dosimetric and Monte Carlo investigations.

Source

Published in Brachytherapy. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

ShareTelegramLinkedIn

AI-generated summaries may contain errors or omissions. Verify clinically important information with the original publication.

More in Oncology (Medical)

Want this personalized?

Stop searching the literature. Choose what you follow and xxcode will build your personalized medical digest.

  • Your specialties
  • Your filters and thresholds
  • Clinical Research + Case Reports, tuned separately
  • Automatic weekly delivery
  • Audio and text

Prefer listening? Personalized audio digests are available with Pro.

Stay updated for free

Get the 3 most interesting publications in one specialty each week.

Weekly email. Unsubscribe anytime.