Literature DB >> 15663054

Neoadjuvant chemotherapy for locally advanced breast cancer results in alterations in preoperative tumor marker status.

G L Piper1, N A Patel, J A Patel, M B Malay, T B Julian.   

Abstract

Neoadjuvant therapy followed by breast-conserving surgery has become an acceptable option for patients with locally advanced breast cancer. Although a distinct survival benefit has not been demonstrated using this approach, several questions have been raised following such therapy including its effects on receptor status and tumor markers. The current study retrospectively reviews estrogen receptor (ER), progesterone receptor (PR), and HER2-neu status in 55 consecutive patients treated by neoadjuvant chemotherapy. Preoperative and postoperative tumor markers were available for 43 of the 55 patients (78%). The pathologic complete tumor response rate (pCR) for this group was 19 per cent (8/43). Of those patients who did not achieve a pCR (n = 35), a change in tumor markers was seen in 25.7 per cent (9/35) of patients. When compared to a control group not undergoing neoadjuvant therapy, a significantly higher percent change in marker expression was noted in the neoadjuvant group (25.7% vs 5.9%, P = 0.046). ER, PR, and HER2-neu status remain important prognostic indicators for breast cancer. Tumor markers are useful in planning adjuvant therapy regimens. In this review, nearly 19 per cent of patients achieved a pCR. In patients not achieving a pCR, one in four patients had at least one change in tumor marker status. This study demonstrates the importance of establishing receptor and marker status prior to neoadjuvant therapy, as many patients will achieve a pCR and make tumor analysis impossible. Postoperative marker studies should be performed given the possibility of a change in status. The clinical relevance of this data will require further long-term follow-up. Until such data becomes available, caution should be considered when basing adjuvant therapy regimens on preoperative tumor marker studies alone.

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Year:  2004        PMID: 15663054

Source DB:  PubMed          Journal:  Am Surg        ISSN: 0003-1348            Impact factor:   0.688


  6 in total

1.  Evaluation of biomarker changes after administration of various neoadjuvant chemotherapies in breast cancer.

Authors:  Guangchao Jin; Yu Han; Cun Liu; Liansheng Chen; Butong Ding; Shijin Xuan; Xianqiang Liu; Guohui Ma; Jun Gao; Xingsong Tian
Journal:  Int J Clin Exp Pathol       Date:  2015-01-01

2.  The effect of prolonged cold ischemia time on estrogen receptor immunohistochemistry in breast cancer.

Authors:  Xiaoxian Li; Michael T Deavers; Ming Guo; Ping Liu; Yun Gong; Constance T Albarracin; Lavinia P Middleton; Lei Huo
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3.  A case-control study of reproductive factors associated with subtypes of breast cancer in Northeast China.

Authors:  Peng Xing; Jiguang Li; Feng Jin
Journal:  Med Oncol       Date:  2009-09-23       Impact factor: 3.064

4.  Immunohistochemical expression of PTEN and phosphorylated Akt are not correlated with clinical outcome in breast cancer patients treated with trastuzumab-containing neo-adjuvant chemotherapy.

Authors:  Kan Yonemori; Koji Tsuta; Chikako Shimizu; Yutaka Hatanaka; Kaoru Hashizume; Makiko Ono; Tsutomu Kouno; Masashi Ando; Kenji Tamura; Noriyuki Katsumata; Tadashi Hasegawa; Takayuki Kinoshita; Yasuhiro Fujiwara
Journal:  Med Oncol       Date:  2008-11-18       Impact factor: 3.064

5.  High RBM3 expression is associated with an improved survival and oxaliplatin response in patients with metastatic colorectal cancer.

Authors:  Christina Siesing; Halfdan Sorbye; Anca Dragomir; Per Pfeiffer; Camilla Qvortrup; Fredrik Pontén; Karin Jirström; Bengt Glimelius; Jakob Eberhard
Journal:  PLoS One       Date:  2017-08-11       Impact factor: 3.240

6.  Combinational Treatment of Doxorubicin With Neoadjuvant Docetaxel for Different Subtypes of Patients With Breast Cancer.

Authors:  Ling-Cheng Wang; Ling-Sheng Wang; Ai-Xia Li; Zhen-Zong Shi; Ya-Qiong Li; Wei Huang; Shi-Man Chen; Fei Han; De-Qiang Zhu
Journal:  Technol Cancer Res Treat       Date:  2020 Jan-Dec
  6 in total

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