Lingfeng TANG, Xiujie SHU, Ping YAN, et al. Influencing factors and efficacy prediction of neoadjuvant chemotherapy for ER positive breast cancer[J]. Journal of Third Military Medical University, 2020, 43(23): 2341-2349.
DOI:
Lingfeng TANG, Xiujie SHU, Ping YAN, et al. Influencing factors and efficacy prediction of neoadjuvant chemotherapy for ER positive breast cancer[J]. Journal of Third Military Medical University, 2020, 43(23): 2341-2349. DOI: 10.16016/j.1000-5404.202007121.
Influencing factors and efficacy prediction of neoadjuvant chemotherapy for ER positive breast cancer
To investigate the influencing factors of neoadjuvant chemotherapy (NAC) in estrogen receptor (ER) positive breast cancer and establish a prediction model of NAC efficacy.
Methods
2
A total of 321 ER positive breast cancer patients who received NAC treatment for 4 cycles followed by surgical treatment in our department from 2015 to 2018 were enrolled in this study. According to the efficacy evaluation criteria of solid tumors
the patients who achieved complete response (CR) or partial response (PR) after NAC were assigned into effective group
while those with stable disease (SD) and progressive disease (PD) into ineffective group. The differences of clinical and pathological parameters were retrospectively analyzed and compared between the 2 groups. Univariate and multivariate logistic regression analyses were applied to screen out the significant influencing factors. R Language was employed to establish the prediction models of NAC efficacy and pathological CR (pCR) rate of ER positive breast cancer patients. Then the prediction ability of the prediction models was evaluated by receiver operating characteristic (ROC) curve and correction curve.
Results
2
The overall effective rate of NAC and pCR were 75.39% and 15.26%
respectively
in the patients with ER positive breast cancer. Significant differences were seen in age
menstrual status
maximum tumor diameter
clinical node stage (cN)
tumor blood supply
and ER and Ki-67 expression levels and chemotherapy regimen between the 2 groups (
P
<
0.05). Logistic analysis showed that cN
tumor blood supply
ER and Ki-67 expression levels were related to the efficacy of NAC (
P
<
0.05)
while the rate of pCR after NAC was related to the maximal tumor diameter
tumor blood supply
and ER and Ki-67 expression levels (
P
<
0.05). The nomograms of predicting NAC efficacy and pCR in ER positive breast cancer patients were constructed with significant inde
pendent influencing factors. The area under ROC curve (AUC) of NAC Effectiveness Prediction Model for ER positive breast cancer patients was 0.785
and the cut-off value was (0.696
0.760)
and with calibration curve coinciding well with the reference standard. The AUC of pCR prediction model was 0.829 and the cut-off value was (0.673
0.857)
and the 2 curves were slightly biased.
Conclusion
2
Tumor blood supply
cN
ER and Ki-67 expression levels are the independent factors of NAC efficacy in ER positive breast cancer patients. The patients with axillary lymph node metastasis
low ER expression
high Ki-67 expression and good blood supply of tumor can achieve the best efficacy of NAC. Tumor maximal diameter
tumor blood supply
ER and Ki-67 expression levels are independent factors of pCR after NAC. The patients with small tumor
low expression of ER
high expression of Ki-67 and good blood supply of tumor have the highest probability of pCR after NAC. The established nomogram can primarily evaluate the benefit and probability of pCR in these patients.
关键词
Keywords
references
MIEOG J S D, VAN DER HAGE J A, VAN DE VELDE C J H. Neoadjuvant chemotherapy for operable breast cancer[J]. Br J Surg, 2007, 94(10): 1189-1200. DOI:10.1002/bjs.5894.
BEVERS T B, ANDERSON B O, BONACCIO E, et al . NCCN clinical practice guidelines in oncology: breast cancer screening and diagnosis[J ] . J Natl Compr Cancer Netw, 2009, 7(10): 1060. DOI: 10.6004/jnccn.2009.0070.
LIU N, MA T J, ZHI W G. The role of molecular classification of breast cancer in the efficacy and prognosis prediction of neoadjuvant chemotherapy[J].J Mod Oncol, 2017, 25(10):1564-1568. DOI: 10.3969/j.issn.1672-4992.2017.10.013.
LUO Y X, MA J, LIU Y G, et al . The application of diffusion weighted imaging and dynamic enhanced MRI in evaluation of response of different molecular types of breast cancer to neoadjuvant chemotherapy[J ] . J Med Imaging, 2019, 29(6): 962-968.
ADLER D D, CARSON P L, RUBIN J M, et al . Doppler ultrasound color flow imaging in the study of breast cancer: preliminary findings[J ] . Ultrasound Med Biol, 1990, 16(6): 553-559. DOI:10.1016/0301-5629(90)90020-d.
EISENHAUER E A, THERASSE P, BOGAERTS J, et al . New response evaluation criteria in solid tumours: Revised RECIST guideline (version 1.1)[J ] . Eur J Cancer, 2009, 45(2): 228-247. DOI:10.1016/j.ejca.2008.10.026.
FLUSS R, FARAGGI D, REISER B. Estimation of the Youden Index and its associated cutoff point[J]. Biom J, 2005, 47(4): 458-472. DOI:10.1002/bimj.200410135.
PEROU C M, SØRLIE T, EISEN M B, et al . Molecular portraits of human breast tumours[J ] . Nature, 2000, 406(6797): 747-752. DOI:10.1038/35021093.
HOUSSAMI N, MACASKILL P, VON MINCKWITZ G, et al . Meta-analysis of the association of breast cancer subtype and pathologic complete response to neoadjuvant chemotherapy[J ] . Eur J Cancer, 2012, 48(18): 3342-3354. DOI:10.1016/j.ejca.2012.05.023.
WANG J, SANG D, XU B, et al . Value of breast cancer molecular subtypes and Ki-67 expression for the prediction of efficacy and prognosis of neoadjuvant chemotherapy in a Chinese population[J ] . Medicine (Baltimore), 2016, 95(18): e3518. DOI:10.1097/md.0000000000003518.
CHOU H H, KUO W L, YU C C, et al . Impact of age on pathological complete response and locoregional recurrence in locally advanced breast cancer after neoadjuvant chemotherapy[J ] . Biomed J, 2019, 42(1): 66-74. DOI:10.1016/j.bj.2018.10.007.
LEE Y J, SHIN Y I, KIM J, et al . Abstract P2-16-25: Young age breast cancer who achieve pathologic complete response after neoadjuvant chemotherapy display excellent outcome than older age breast cancers[J ] . Cancer Res, 2020, 80(4 Supplement): P2-16-25. DOI:10.1158/1538-7445.sabcs19-p2-16-25.
ZHANG W, LAI M L, YANG S H, et al . Neoadjuvant chemotherapy effect and influencing factors on Luminal B breast cancer[J ] . Guangdong Med J, 2017, 38(22): 3426-3429, 3432.
LUO Q Q, HUANG J B, WU Y T, et al . Tidal chemotherapy in premenopausal patients with hormone receptor positive breast cancer[J ] . Med Hypotheses, 2017, 102: 4-7. DOI:10.1016/j.mehy.2017.03.003.
CHOI H J, RYU J M, KIM I, et al . Nomogram for accurate prediction of breast and axillary pathologic response after neoadjuvant chemotherapy in node positive patients with breast cancer[J ] . Ann Surg Treat Res, 2019, 96(4): 169- 176. DOI:10.4174/astr.2019.96.4.169.
ZHANG F, HUANG M, ZHOU H, et al . A nomogram to predict pathologic complete response of neoadjuvant chemotherapy in triple-negative breast cancer based on simple blood indicators[J ] . Ann Oncol, 2019, 30: v92. DOI:10.1093/annonc/mdz240.096.
HWANG H W, JUNG H, HYEON J, et al . A nomogram to predict pathologic complete response (pCR) and the value of tumor-infiltrating lymphocytes (TILs) for prediction of response to neoadjuvant chemotherapy (NAC) in breast cancer patients[J ] . Breast Cancer Res Treat, 2019, 173(2): 255-266. DOI:10.1007/s10549-018-4981-x.
PENG Y, CHEN R, QU F, et al . Low pretreatment lymphocyte/monocyte ratio is associated with the better efficacy of neoadjuvant chemotherapy in breast cancer patients[J ] . Cancer Biol Ther, 2020, 21(2): 189-196. DOI:10.1080/15384047.2019.1680057.
GRAZIANO V, GRASSADONIA A, IEZZI L, et al . Combination of peripheral neutrophil-to-lymphocyte ratio and platelet-to-lymphocyte ratio is predictive of pathological complete response after neoadjuvant chemotherapy in breast cancer patients[J ] . Breast, 2019, 44: 33-38. DOI:10.1016/j.breast.2018.12.014.
CUELLO-LÓPEZ J, FIDALGO-ZAPATA A, LÓPEZ-AGUDELO L, et al . Platelet-to-lymphocyte ratio as a predictive factor of complete pathologic response to neoadjuvant chemotherapy in breast cancer[J ] . PLoS ONE, 2018, 13(11): e0207224. DOI:10.1371/journal.pone.0207224.
ZOU S W, HAN Y F, WANG B H. The value of automatic breast full-volume imaging combined with color Doppler blood flow imaging in evaluating the effect of neoadjuvant chemotherapy for breast cancer[J]. Chin J Rural Med Pharm, 2019, 26(10): 54-55.
WANG T F. The diagnostic value of color Doppler flow imaging combined with ultrasound elastography for the efficacy of neoadjuvant chemotherapy for breast cancer[J]. Chin J Rural Med Pharm, 2018, 25(20):48-49. DOI: 10.19542/j.cnki.1006-5180.002143.
HUANG M, WANG S Q, FENG N N, et al . Significance of ABVS combined with CDFI in the evaluation of efficacy of neoadjuvant chemotherapy for breast cancer[J ] . Chin J Clin Oncol Rehabilit, 2017, 24(5): 570-574.
SUETA A, YAMAMOTO Y, HAYASHI M, et al . Clinical significance of pretherapeutic Ki-67 as a predictive parameter for response to neoadjuvant chemotherapy in breast cancer: is it equally useful across tumor subtypes?[J ] . Surgery, 2014, 155(5): 927-935. DOI:10.1016/j.surg.2014.01.009.
KONG L N. The relationship between the expression of ER and claudin6 and the sensitivity of luminal A breast cancer to anthracycline[D]. Shenyang: China Medical University, 2018.
SPRING L M, GUPTA A, REYNOLDS K L, et al . Neoadjuvant endocrine therapy for estrogen receptor-positive breast cancer: A systematic review and meta-analysis[J ] . JAMA Oncol, 2016, 2(11):1477-1486.DOI: 10.1001/jamaoncol.2016.1897.
HURVITZ S A, MARTIN M, SYMMANS W F, et al . Neoadjuvant trastuzumab, pertuzumab, and chemotherapy versus trastuzumab emtansine plus pertuzumab in patients with HER2-positive breast cancer (KRISTINE): a randomised, open-label, multicentre, phase 3 trial[J ] . Lancet Oncol, 2018, 19(1): 115-126. DOI:10.1016/s1470-2045(17)30716-7.
Correlation of types of residual tumor with expressions of ER, PR and HER-2 after neoadjuvant chemotherapy in breast cancer
Infiltrating characteristics of breast cancer after neoadjuvant chemotherapy: whole breast serial subsection observation
Effect of neoadjuvant chemotherapy on Survivin, p53 expression in breast cancer
A novel estrogen receptor expression stratification (low/moderate/high) based on Chinese population provides more accurate prognosis prediction for HR+/HER2- early breast cancer patients
Sulfasalazine antagonizes boosted metastasis of breast cancer induced by ionizing radiation
Related Author
王姝姝
张毅
齐晓伟
陈庆秋
姜军
张毅
周艳
郭美琴
Related Institution
Department of Breast and Thyroid Surgery, First Affiliated Hospital, Army Medical University (Third Military Medical University)
State Key Laboratory of Trauma, Burns and Combined Injury, Department of Anti-Radiation Medicine, Chongqing Engineering Research Center for Nanomedicine, Institute of Combined Injury, Faculty of Military Preventive Medicine, Army Medical University (Third Military Medical University)
Department of Breast and Thyroid Surgery, the Second Affiliated Hospital of Chongqing Medical University
Department of Environmental Health, College of Military Preventive Medicine, Army Medical University (Third Military Medical University)
Institute of Toxicology, College of Military Preventive Medicine, Army Medical University (Third Military Medical University)