Clinical Course of Breast Cancer Patients With Complete Pathologic Primary Tumor and Axillary Lymph Node Response to Doxorubicin-Based Neoadjuvant Chemotherapy

American Society of Clinical Oncology (ASCO) - Tập 17 Số 2 - Trang 460-460 - 1999
Henry M. Kuerer1, Lisa A. Newman1, Terry L. Smith1, Fred C. Ames1, Kelly K. Hunt1, Kapil Dhingra1, Richard L. Theriault1, Gurpreet Singh1, Susan M. Binkley1, Nour Sneige1, Thomas A. Buchholz1, Merrick I. Ross1, Marsha D. McNeese1, Aman U. Buzdar1, Gabriel N. Hortobágyi1, S. Eva Singletary1
1From the Departments of Surgical Oncology, Biomathematics, Breast Medical Oncology, Pathology, and Radiation Oncology, University of Texas M.D. Anderson Cancer Center, Houston, TX.

Tóm tắt

PURPOSE: To assess patient and tumor characteristics associated with a complete pathologic response (pCR) in both the breast and axillary lymph node specimens and the outcome of patients found to have a pCR after neoadjuvant chemotherapy for locally advanced breast cancer (LABC). PATIENTS AND METHODS: Three hundred seventy-two LABC patients received treatment in two prospective neoadjuvant trials using four cycles of doxorubicin-containing chemotherapy. Patients had a total mastectomy with axillary dissection or segmental mastectomy and axillary dissection followed by four or more cycles of additional chemotherapy. Patients then received irradiation treatment of the chest-wall or breast and regional lymphatics. Median follow-up was 58 months (range, 8 to 99 months). RESULTS: The initial nodal status, age, and stage distribution of patients with a pCR were not significantly different from those of patients with less than a pCR (P > .05). Patients with a pCR had initial tumors that were more likely to be estrogen receptor (ER)–negative (P < .01), and anaplastic (P = .01) but of smaller size (P < .01) than those of patients with less than a pCR. Upon multivariate analysis, the effects of ER status and nuclear grade were independent of initial tumor size. Sixteen percent of the patients in this study (n = 60) had a pathologic complete primary tumor response. Twelve percent of patients (n = 43) had no microscopic evidence of invasive cancer in their breast and axillary specimens. A pathologic complete primary tumor response was predictive of a complete axillary lymph node response (P < .01). The 5-year overall and disease-free survival rates were significantly higher in the group who had a pCR (89% and 87%, respectively) than in the group who had less than a pCR (64% and 58%, respectively; P < .01). CONCLUSION: Neoadjuvant chemotherapy has the capacity to completely clear the breast and axillary lymph nodes of invasive tumor before surgery. Patients with LABC who have a pCR in the breast and axillary nodes have a significantly improved disease-free survival rate. However, a pCR does not entirely eliminate recurrence. Further efforts should focus on elucidating the molecular mechanisms associated with this response.

Từ khóa


Tài liệu tham khảo

10.1007/BF00253147

10.1002/1097-0142(19830301)51:5<763::AID-CNCR2820510502>3.0.CO;2-C

Lippman ME, Sorace RA, Bagley CS, et al: Treatment of locally advanced breast cancer using primary induction chemotherapy with hormonal synchronization followed by radiation therapy with or without debulking surgery. NCI Monogr 1:156,1986-159,

Scholl SM, Fourquet A, Asselain B, et al: Neoadjuvant versus adjuvant chemotherapy in premenopausal patients with tumours considered too large for breast conserving surgery: Preliminary results of a randomised trial: S6. Eur J Cancer 5:645,1994-652,

10.1200/JCO.1997.15.7.2483

Feldman DL, Hortobagyi GN, Buzdar AU, et al: Pathologic assessment of response to induction chemotherapy in breast cancer. Cancer Res 46:2578,1986-2581,

Kaplan EL, Meier P: Nonparametric estimation from incomplete observations. J Am Stat Assoc 185:1457,1958-1481,

Mantel N: Evaluation of survival data and two row rank order statistics arising in its consideration. Cancer Chemother Rep 50:163,1966-170,

10.1002/1097-0142(19940115)73:2<362::AID-CNCR2820730221>3.0.CO;2-L

10.1200/JCO.1995.13.3.547

Brain E, Garrino C, Misset JL, et al: Long-term prognostic and predictive factors in 107 stage II/III breast cancer patients treated with anthracycline-based neoadjuvant chemotherapy. Br J Cancer 79:1360,1997-1367,

10.1002/(SICI)1097-0142(19980201)82:3<503::AID-CNCR12>3.0.CO;2-5

10.1200/JCO.1998.16.1.93

McCready DR, Hortobagyi GN, Kau SW, et al: The prognostic significance of lymph node metastases after preoperative chemotherapy for locally advanced breast cancer. Arch Surg 124:21,1985-25,

10.1016/0360-3016(85)90028-8

10.3109/07357909809039761

10.1200/JCO.1995.13.12.2886

10.1200/JCO.1995.13.5.1152

10.1002/1097-0142(19881215)62:12<2507::AID-CNCR2820621210>3.0.CO;2-D

10.1007/BF01806351

10.1200/JCO.1998.16.1.107

10.1016/0167-8140(92)90263-T

10.1111/j.1524-4741.1995.tb00225.x

10.7326/0003-4819-94-2-218

10.1056/NEJM197806012982203

10.1093/jnci/82.19.1539

10.1093/oxfordjournals.annonc.a057953

10.1016/S0140-6736(98)03301-7

10.1002/1097-0142(19870501)59:9<1554::AID-CNCR2820590904>3.0.CO;2-B

10.1016/0046-8177(93)90246-D

10.1093/jnci/81.18.1383

10.1002/cyto.990160202

10.1002/gcc.2870100403

Teixeira MR, Pandis N, Bardi G, et al: Karyotypic comparisons of multiple tumorous and macroscopically normal surrounding tissue samples from patients with breast cancer. Cancer Res 56:855,1996-859,

Kuukasjärvi T, Karhu R, Tanner M, et al: Genetic heterogeneity and clonal evolution underlying development of asynchronous metastasis in human breast cancer. Cancer Res 57:1597,1997-1604,

Resnick JM, Sneige N, Kemp BL, et al: p53 and c-erbB-2 expression and response to preoperative chemotherapy in locally advanced breast carcinoma. Breast Dis 8:149,1995-158,

10.1002/(SICI)1097-0142(19960115)77:2<292::AID-CNCR11>3.0.CO;2-X

Makris A, Powles TJ, Dowsett M, et al: Prediction of response to neoadjuvant chemoendocrine therapy in primary breast carcinomas. Clin Cancer Res 3:593,1997-600,