INCIDENCE OF NODAL AND DISTANT METASTASIS AND THEIR CORRELATION WITH PRIMARY BREAST TUMOR SIZE ON PRE-THERAPY FDG PET/CT IMAGING

Nosheen Ftima, Sidra Zaman, Areeba Zaman, Naeem Pasha, Unaiza UZ Zaman, Rabia Tahseen, Anamta UZ Zaman, Maseeh Uz Zaman

Abstract


 

Background:  In patients with breast cancer, it is thought that the risk of developing metastases increases monotonically with tumor size, because the larger the cancer at diagnosis, the more cells are available to metastasize with increase disease specific mortality. Purpose of this study was to evaluate relation between primary tumor size and metastases (nodal and non-nodal) using baseline FDG PET/CT.  Material and Methods:  We recruited 214 consecutive breast cancer patients who were referred for FDG PET/CT imaging for initial staging. Patients were categorized in to four groups based on primary tumor size (T1: ≤ 2 cm; T2: >2 cm and ≤ 5 cm; T3: > 5 cm; T4: any size involving chest wall or skin). For each group we determined ipsilateral axillary nodal, extra-axillary (including contralateral axillary) nodal, visceral and skeletal metastases seen on FDG PET/CT imaging. Results: 37/214 patients had T1 tumor and found to have 15% axillary, 47% extra-axillary, 11% visceral and 04% skeletal metastases. 104/214 patients had T2 tumor and found to have 21% axillary, 45% extra-axillary, 19% visceral and 11% skeletal metastases. 34/214 patients had T3 tumor and found to have 26% axillary, 47% extra-axillary, 53% visceral and 08% skeletal metastases. 29/214 patients had T4 tumor and found to have 45% axillary, 69% extra-axillary, 55% visceral and 06% skeletal metastases. On regression analysis, highest positive linear correlation was found for ipsilateral nodal metastasis (r = 0.945; significant p-value) followed by visceral (r = 0.941) and extra-axillary nodal (r = 0.772), metastases. No significant correlation was found between primary tumor size and skeletal metastasis (r= 0.129). Conclusions: We found a linear correlation between primary tumor size and presence of metastases to nodes (highest for ipsilateral nodes) and viscera and favoring the conventional linear model. However, no linear correlation was found between presence of skeletal metastases and primary breast tumor size.

Key Words: Breast cancer; tumor size; nodal metastasis; distant metastasis; linear model

 


Full Text:

PDF

References


. Jemal A, Bray F, Ferlay J, Ward E, Forman D. Global cancer statistics. CA Cancer J Clin 2011; 61: 69-90.

Carter CL, Allen C, Henson DE. Relation of tumor size, lymph node status, and survival in 24,740 breast cancer cases. Cancer 1989; 63:181.

Michaelson JS, Silverstein M, Wyatt J, Weber G, Moore R, Halpern E, et al. Predicting the survival of patients with breast carcinoma using tumor size. Cancer 2002; 95:713–23.

. Laura S, Coombs N, Ung O, Boyages J. Tumour size as a predictor of axillary node metastases in patients with breast cancer. ANZ J Surg 2006; 76:1002–06

. Yu KD, Jiang YZ, Chen S, Cao Z, Wu J, Shen Z, et al. Effect of large tumor size on cancer-specific mortality in node-negative breast cancer. Mayo Clin Proc 2012; 87:1171–80

. Zheng YZ, Wang L, Hu X, Shao ZM. Effect of tumor size on breast cancer-specific survival stratified by joint hormone receptor status in a SEER population-based study. Oncotarget 2015; 6:22985–95

. Victoria Sopik, Steven A. Narod. The relationship between tumour size, nodal status and distant metastases: on the origins of breast cancer. Breast Cancer Research and Treatment 2018; 170:647–656 (https://doi.org/10.1007/s10549-018-4796-9)

. Boellaard R, Bolton RD, Oyen WJ, Giammarile F, Tatsch K, Eschner W, et al. FDG PET/CT: EANM procedure guidelines for tumour imaging: version 2.0. Eur J Nucl Med Mol Imaging 2015; 42, 328–54.

. Yu KD, Jiang YZ, Shao ZM. Difference between observed and expected number of involved lymph nodes reflects the metastatic potential of breast cancer independent to intrinsic subtype. Oncotarget 2015; 6:16686–97

. Weigelt B, Peterse JL, van‘t Veer LJ. Breast cancer metastasis: markers and models. Nat Rev Cancer 2005; 5:591–602

. Orang E, Marzony ET, Afsharfard A. Predictive Role of Tumor Size in Breast Cancer with Axillary Lymph Node Involvement - Can Size of Primary Tumor be used to Omit an Unnecessary Axillary Lymph Node Dissection? Asian Pac J Cancer Prev 2013; 14(2):717-22 (https://doi.org/10.7314/APJCP.2013.14.2.717)

. Ali B, Mubarik F, Zahid N, Sattar AK. Clinicopathologic Features Predictive of Distant Metastasis in Patients Diagnosed With Invasive Breast Cancer. JCO Global Oncol 2020; 6:1346-51

. Xiao W, Zheng S, Yang A, Zhang X, Zou Y, Tang H, et al. Breast cancer subtypes and the risk of distant metastasis at initial diagnosis: a population-based study. Cancer Manag Res. 2018 Nov 5;10:5329-5338.

. Hosseini H, Obradović MM, Hoffmann M, Kathryn LH, Soledad MS, Werner-Klein M, et al. Early dissemination seeds metastasis in breast cancer. Nature 2016; 22;540(7634):552-558 (https ://doi.org/10.1038/natur e2078 5)

Rhim AD, Mirek ET, Aiello NM et al (2012) EMT and dissemination

precede pancreatic tumor formation. Cell 148:349–361

. Sottoriva A, Kang H, Ma Z, Graham TA, Salomon M, Zhao J, et al. A big bang model of human colorectal tumor growth. Nat Genet 2015; 47:209–16

. Werner-Klein M, Scheitler S, Hoffmann M, Isabelle Hodak, Klaus Dietz, Petra Lehnert et al. Genetic alterations driving metastatic colony formation are acquired outside of the primary tumour in melanoma. Nat Commun 2018; 9:595


Refbacks

  • There are currently no refbacks.


© Copyright PJR 2008-