Low RNA disruption during neoadjuvant chemotherapy predicts pathologic complete response absence in patients with breast cancer.
Marina Elena CazzanigaFoluso AdemuyiwaThierry PetitJoke TioDaniele GeneraliEva Ciruelos GilNadia CalifarettiBrigitte PoirierAntonio ArdizzoiaArnd HoenigBenno LexMarie-Ange Mouret-ReynierDagmar GieseckeNicolas IsambertRicardo MasettiLacey D PitreDenise WrobelPaule AugereauManuela MilaniSara RaskChristine SolbachLaura PritzkerSanaa NoubirAmadeo M ParissentiMaureen E TrudeauPublished in: JNCI cancer spectrum (2024)
In previously reported retrospective studies, high tumor RNA disruption during neoadjuvant chemotherapy predicted for post-treatment pathologic complete response (pCR) and improved disease-free survival at definitive surgery for primary early breast cancer. The BREVITY (Breast Cancer Response Evaluation for Individualized Therapy) prospective clinical trial (NCT03524430) seeks to validate these prior findings. Here we report training set (Phase I) findings, including determination of RNA disruption index (RDI) cut points for outcome prediction in the subsequent validation set (Phase II; 454 patients). In 80 patients of the training set, maximum tumor RDI values for biopsies obtained during neoadjuvant chemotherapy were significantly higher in pCR responders than in patients without pCR post-treatment (P = .008). Moreover, maximum tumor RDI values ≤3.7 during treatment predicted for a lack of pCR at surgery (negative predictive value = 93.3%). These findings support the prospect that on-treatment tumor RNA disruption assessments may effectively predict post-surgery outcome, possibly permitting treatment optimization.
Keyphrases
- neoadjuvant chemotherapy
- locally advanced
- clinical trial
- end stage renal disease
- lymph node
- ejection fraction
- minimally invasive
- newly diagnosed
- phase ii
- sentinel lymph node
- prognostic factors
- coronary artery bypass
- radiation therapy
- rectal cancer
- randomized controlled trial
- acute coronary syndrome
- young adults
- early stage
- mesenchymal stem cells
- bone marrow
- coronary artery disease
- molecularly imprinted
- replacement therapy
- virtual reality
- tandem mass spectrometry
- simultaneous determination