TY - JOUR
T1 - Low RNA disruption during neoadjuvant chemotherapy predicts pathologic complete response absence in patients with breast cancer
AU - Cazzaniga, Marina Elena
AU - Ademuyiwa, Foluso
AU - Petit, Thierry
AU - Tio, Joke
AU - Generali, Daniele
AU - Ciruelos, Eva M.
AU - Califaretti, Nadia
AU - Poirier, Brigitte
AU - Ardizzoia, Antonio
AU - Med, Arnd Hoenig
AU - Med, Benno Lex
AU - Mouret-Reynier, Marie Ange
AU - Med, Dagmar Giesecke
AU - Isambert, Nicolas
AU - Masetti, Ricardo
AU - Pitre, Lacey
AU - Med, Denise Wrobel
AU - Augereau, Paule
AU - Milani, Manuela
AU - Rask, Sara
AU - Med, Christine Solbach
AU - Pritzker, Laura
AU - Noubir, Sanaa
AU - Parissenti, Amadeo
AU - Trudeau, Maureen E.
N1 - Publisher Copyright:
© 2024 Oxford University Press. All rights reserved.
PY - 2024/1/1
Y1 - 2024/1/1
N2 - 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 ¼ .008). Moreover, maximum tumor RDI values ≤3.7 during treatment predicted for a lack of pCR at surgery (negative predictive value ¼ 93.3%). These findings support the prospect that on-treatment tumor RNA disruption assessments may effectively predict post-surgery outcome, possibly permitting treatment optimization.
AB - 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 ¼ .008). Moreover, maximum tumor RDI values ≤3.7 during treatment predicted for a lack of pCR at surgery (negative predictive value ¼ 93.3%). These findings support the prospect that on-treatment tumor RNA disruption assessments may effectively predict post-surgery outcome, possibly permitting treatment optimization.
UR - http://www.scopus.com/inward/record.url?scp=85182715665&partnerID=8YFLogxK
U2 - 10.1093/jncics/pkad107
DO - 10.1093/jncics/pkad107
M3 - Article
C2 - 38113421
AN - SCOPUS:85182715665
SN - 2515-5091
VL - 8
JO - JNCI Cancer Spectrum
JF - JNCI Cancer Spectrum
IS - 1
M1 - pkad107
ER -