Chemosensitivity to doxorubicin of ER-positive/HER2-negative breast cancers with high 21-gene recurrence score: A study based on in vitro chemoresponse assay

被引:14
作者
Ahn, Sung Gwe [1 ]
Bae, Soong June [1 ]
Yoon, Changik [1 ]
Cha, Yoon Jin [2 ]
Lee, Hak Woo [1 ]
Lee, Seung Ah [3 ]
Jeong, Joon [1 ]
机构
[1] Yonsei Univ, Gangnam Severance Hosp, Dept Surg, Coll Med, Seoul, South Korea
[2] Yonsei Univ, Gangnam Severance Hosp, Dept Pathol, Coll Med, Seoul, South Korea
[3] CHA Univ, Dept Surg, CHA Bundang Med Ctr, Seongnam, South Korea
关键词
CLINICAL-PRACTICE; GENE-EXPRESSION; THERAPY; WOMEN; CHEMOTHERAPY; DECISIONS;
D O I
10.1371/journal.pone.0187679
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Aim The 21-gene recurrence score (RS) predicts a clinical benefit of chemotherapy for individuals with ER-positive/HER2-negative breast cancer. Using in vitro chemoresponse assay, we compared the chemosensitivity according to RS in these patients. Method Among the patients with Oncotype Dx assay, we identified 63 patients who had chemotherapy response assays to doxorubicin based on adenosine triphosphate. The degree of chemosensitivity to doxorubicin was translated into the cell death rate (CDR). The RS was also dichotomized with a cutoff of 26. Results Of 63 patients, 34 (54%), 17 (27%), and 12 patients (19%) had a low, intermediate, and high RS, respectively. The mean CDR differed significantly according to categorized RS, with 17.3 10.8 in the low RS group vs. 23.6 16.3 in the intermediate RS group vs. 28.8 12.6 in the high RS group (P=0.024, One-way ANOVA test). The mean CDR was significantly higher in the higher RS (26>) group compared with the lower RS (<26) group (P=0.025, the Student's t-test), as well as in the high RS (>30) group compared with the low RS (<18) group (P=0.012, the Student's t-test). Also, continuous RS and CDR correlated positively (Pearson's R =0.337; P =0.007). High RS demonstrated the odds ratio (OR =26.33; 95% CI =1.69-410.0) for predicting tumors with chemosensitivity on the multivariate analysis. Conclusions The chemosensitivity measured by in vitro chemoresponse assay was different according to the RS. Our findings support that tumors with high RS has the chemosensitivity even though they are luminal/HER2-negative tumors.
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页数:9
相关论文
共 17 条
[11]   A multigene assay to predict recurrence of tamoxifen-treated, node-negative breast cancer [J].
Paik, S ;
Shak, S ;
Tang, G ;
Kim, C ;
Baker, J ;
Cronin, M ;
Baehner, FL ;
Walker, MG ;
Watson, D ;
Park, T ;
Hiller, W ;
Fisher, ER ;
Wickerham, DL ;
Bryant, J ;
Wolmark, N .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 351 (27) :2817-2826
[12]   Gene expression and benefit of chemotherapy in women with node-negative, estrogen receptor-positive breast cancer [J].
Paik, Soonmyung ;
Tang, Gong ;
Shak, Steven ;
Kim, Chungyeul ;
Baker, Joffre ;
Kim, Wanseop ;
Cronin, Maureen ;
Baehner, Frederick L. ;
Watson, Drew ;
Bryant, John ;
Costantino, Joseph P. ;
Geyer, Charles E., Jr. ;
Wickerham, D. Lawrence ;
Wolmark, Norman .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (23) :3726-3734
[13]   Outcome of ATP-based tumor chemosensitivity assay directed chemotherapy in heavily pre-treated recurrent ovarian carcinoma [J].
Sharma, S ;
Neale, MH ;
Di Nicolantonio, F ;
Knight, LA ;
Whitehouse, PA ;
Mercer, SJ ;
Higgins, BR ;
Lamont, A ;
Osborne, R ;
Hindley, AC ;
Kurbacher, CM ;
Cree, IA .
BMC CANCER, 2003, 3 (1)
[14]  
Soran Atilla, 2016, Breast Dis, V36, P65, DOI 10.3233/BD-150199
[15]   Prospective Validation of a 21-Gene Expression Assay in Breast Cancer [J].
Sparano, J. A. ;
Gray, R. J. ;
Makower, D. F. ;
Pritchard, K. I. ;
Albain, K. S. ;
Hayes, D. F. ;
Geyer, C. E., Jr. ;
Dees, E. C. ;
Perez, E. A. ;
Olson, J. A., Jr. ;
Zujewski, J. A. ;
Lively, T. ;
Badve, S. S. ;
Saphner, T. J. ;
Wagner, L. I. ;
Whelan, T. J. ;
Ellis, M. J. ;
Paik, S. ;
Wood, W. C. ;
Ravdin, P. ;
Keane, M. M. ;
Gomez Moreno, H. L. ;
Reddy, P. S. ;
Goggins, T. F. ;
Mayer, I. A. ;
Brufsky, A. M. ;
Toppmeyer, D. L. ;
Kaklamani, V. G. ;
Atkins, J. N. ;
Berenberg, J. L. ;
Sledge, G. W. .
NEW ENGLAND JOURNAL OF MEDICINE, 2015, 373 (21) :2005-2014
[16]  
Sparano JA, 2008, J CLIN ONCOL, V26, P721, DOI 10.1200/JCO.2008.16.7528
[17]   Paclitaxel, bevacizumab, and everolimus/placebo as first-line treatment for patients with metastatic HER2-negative breast cancer: a randomized placebo-controlled phase II trial of the Sarah Cannon Research Institute [J].
Yardley, Denise A. ;
Bosserman, Linda D. ;
O'Shaughnessy, Joyce A. ;
Harwin, William N. ;
Morgan, Susan K. ;
Priego, Victor M. ;
Peacock, Nancy W. ;
Bass, J. David ;
Burris, Howard A., III ;
Hainsworth, John D. .
BREAST CANCER RESEARCH AND TREATMENT, 2015, 154 (01) :89-97