Integrative Cancer Therapies (Nov 2022)

The Effect of Black Cohosh on Ki67 expression and Tumor Volume: A Pilot Study of Ductal Carcinoma in Situ Patients

  • Amelia A. Trant MD,
  • Anees Chagpar MD, MBA, MPH, FACS, FRCS(C),
  • Wei Wei PhD,
  • Veronique Neumeister MD,
  • David Rimm MD, PhD,
  • Karen Stavris RN,
  • Bonnie Lurie RN,
  • Courtney Frederick RN,
  • Liva Andrejeva MD,
  • Madhavi Raghu MD,
  • Brigid Killelea MD, MPH, FACS,
  • Nina Horowitz MD, FACS,
  • Donald Lannin MD,
  • Elspeth Knill-Selby APRN,
  • Tracy Sturrock APRN,
  • Erin Hofstatter MD

DOI
https://doi.org/10.1177/15347354221137290
Journal volume & issue
Vol. 21

Abstract

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Background: Black cohosh (BC) ( Cimicifuga racemosa ) may prevent and treat breast cancer through anti-proliferative, pro-apoptotic, anti-estrogenic, and anti-inflammatory effects. This study sought to evaluate the effect of BC on tumor cellular proliferation, measured by Ki67 expression, in a pre-operative window trial of ductal carcinoma in situ (DCIS) patients. Methods: Patients were treated pre-operatively for 2 to 6 weeks with BC extract. Eligible subjects were those who had DCIS on core biopsy. Ki67 was measured using automated quantitative immunofluorescence (AQUA) pre/post-operatively. Ki67, tumor volume, and hormone changes were assessed with 2-sided Wilcoxon signed-rank tests, α = .05. Results: Thirty-one patients were treated for an average of 24.5 days (median 25; range 15-36). Ki67 decreased non-significantly (n = 26; P = .20; median pre-treatment 1280, post-treatment 859; range pre-treatment 175-7438, post-treatment 162-3370). Tumor volume, estradiol, and FSH did not change significantly. No grade 3 or 4 adverse events were reported. Conclusions: BC use showed no significant impact on cellular proliferation, tumor volume, or invasive disease upgrade rates in DCIS patients. It was well-tolerated, with no observed significant toxicities. Further study is needed to elucidate BC’s role in breast cancer treatment and prevention. ClinicalTrials.gov Identifier: NCT01628536 https://clinicaltrials.gov/ct2/show/NCT01628536