Pauline Huang1, Renee Cattell1, Meghan Moriarty1, Kwan Chen1, Lev Bangiyev1, Cliff Bernstein1, Jules Cohen1, Lea Baer1, Dinko Franceschi1, Haifang Li1, and Tim Duong1
1Radiology, Renaissance School of Medicine, Stony Brook, NY, United States
Synopsis
In breast cancer, lymph node status is highly related to prognosis. We evaluated
the use of MRI of axillary lymph nodes (aLNs) to detect metastasis in pre-chemo
breast cancer with PET as reference standard. For 4 readers scoring on
T1-weighted DCE and T2-weighted MRI, the AUC, sensitivity, specificity and accuracy
ranged from 0.73-0.85, 64%-83%, 54-91%, and 67-79%, respectively. Readers
showed significant agreement (Spearman’s Rho 0.35-0.65). Though improvement is needed, this approach presents a
less invasive method of assessing all aLNs and avoiding their unnecessary removal.
Introduction
The majority of the lymphatic fluid in breasts pass
through the axillary lymph nodes (aLNs), making them critical in staging and
treatment planning of breast cancer. Presence of nodal metastases decreases survival
and increases likelihood of treatment failure [1, 2]. The current standard for nodal staging for breast cancer patients includes needle
biopsy pre neoadjuvant chemotherapy (NAC) and sentinel lymph node biopsy (SLNB)
or full dissection post NAC. Only a small amount of tissue can be sampled in
the biopsy and the majority of nodes removed in SLNB are negative [3], suggesting that better screening methods are
needed.
MRI can 3D visualize all axillary lymph nodes in situ
but aLNs are small and often clustered together, making cross-validation of MRI
detection of nodal metastasis with pathology difficult.
Two recent studies on FDG-PET have shown it can reliably detect and locate aLN metastasis in the whole breast with high accuracy (79 to 88%) [4, 5]. However, FDG-PET requires injection of a radiotracer
and is generally not indicated for breast cancer patients at this stage, except
where metastasis is suspected.
In this study we evaluate the use of
MRI for radiological nodal staging of individual aLNs in breast cancer with PET as a
reference standard. Methods
120 unilateral
breast cancer patients from 2011-2017 were found, of which 55 had pre NAC MRI and PET/CT. We identified 149 aLNs of which 69 (46%) showed FDG-PET
hypermetabolism. FDG PET/CT and MRI data were
acquired within 2 weeks of each other (average 6 days). Exclusion criteria were inadequate
visibility in the axillary region on MRI or evidence of biopsy needle tracts and
biopsy clips on MRI.
Standard post-contrast MRI were obtained
on a 1.5T GE clinical MRI scanner (Signa, GE Healthcare) using an eight-channel
breast array coil (GE Liberty 9000). Standard 18FDG-PET/CT was
obtained on a Biograph-40 PET-CT scanner (Siemens Medical System) with
40-detector row helical CT scanner.
Based on anatomical landmarks, the same nodes on the
MRI and PET/CT were reliably identified for determination of disease in the
aLNs.
Each aLN on MRI and PET/CT images were independently scored in a blinded manner as 0, 1, 2, and 3 representing no,
low, moderate, and high likelihood of cancer in the aLNs. aLNs on MRI were
considered abnormal if there was absence of fatty hilum, cortical thickening or
cortical enlargement. aLNs on PET were considered abnormal if they were
hyperintense relative to background tissue as evaluated by a nuclear medicine radiologist.
MRI staging (scoring) was performed by one experienced radiologist and three radiologist trainees. Sensitivity,
specificity, accuracy and area under the ROC curve were calculated. Results
Figure 1 shows the typical MRI and PET scores as 0, 1, 2,
and 3 as no, low, moderate, and high likelihood of cancer in the aLNs.
Representative scoring of diseased and non-diseased nodes of are shown in Figure 2. The typical MRI characteristics of normal nodes were thin
cortex, prominent fatty hilum, and small in size, whereas the typical MRI
characteristics of abnormal nodes thickened and irregular cortex, absence of
fatty hilum, rounded shape, and enlargement. The PET characteristics of normal
nodes is no significant
18FDG-PET activity relative to background whereas abnormal nodes
showed high 18FDG-PET activity.
Figure 3 shows the performance of MRI staging for 4
readers. Reader 1 was an experienced radiologist with some additional training
on aLN MRI. Reader 4 was an experienced trainee with specific
training on aLN MRI. Reader 2 and 3 were less experienced trainees who received
some training. Overall, AUC ranged from 0.85 to 0.73 depending on experience. Training
was done by showing readers images of normal and abnormal nodes with known pathology results and testing on new images. Figure 4 Shows significant correlation between readers (Spearman’s Rho 0.35-0.65).
Figure 5 shows the aLN
volume versus PET scoring and aLN volume versus MRI scoring. aLN volumes
increased with increasing PET and MRI scores. However, volume was not the only factor
used in scoring. Discussion
There was good agreement between MRI
and PET scores and the accuracy of the MRI scores are consistent with a few MRI studies
assessing metastasis in the aLNs.
Previously, He et al. assessed 1,242
aLN MRI and morphological features alone resulted in AUC, sensitivity and
specificity ranging from 0.69 to 0.89, 51.5% to 83.6% and 68.4% to 86.3%,
respectively [6].
Other studies showed an MRI
sensitivity of 82.0% and negative predictive value (NPV) of 82.6%[7].
In particular, DCE-MRI
had a lower median sensitivity (60.0%) and NPV (80.0%) compared to non-enhanced
T1-weighted and T2-weighted MRI sequences (88.4-94.7%), and diffusion-weighted
imaging (84.2-90.6%) [7], possibly due to enhancement obscuring lymph node architecture. Our study using T1-weighted DCE and T2-weighted images from a
standardized breast protocol compares favorably with these studies.Conclusion
MRI
radiological scoring of aLNs provides accurate staging of aLNs, although
improvement is needed to visualize and evaluate aLNs more consistently. A benefit of using MRI is that it is less invasive and is capable of assessing lymph nodes located deep beneath the skin. aLN data is available from standard breast MRI and doesn't disrupt regular clinical workflow. Improvement of this technique can minimize unnecessary SLNB.Acknowledgements
No acknowledgement found.References
1. Carter, C.L., C. Allen,
and D.E. Henson, Relation of tumor size,
lymph node status, and survival in 24,740 breast cancer cases. Cancer,
1989. 63(1): p. 181-7.
2. Nemoto, T., et al., Management
and survival of female breast cancer: results of a national survey by the
American College of Surgeons. Cancer, 1980. 45(12): p. 2917-24.
3. Kim, T., A.E. Giuliano, and G.H. Lyman, Lymphatic mapping and sentinel lymph node biopsy in early-stage breast
carcinoma: a metaanalysis. Cancer, 2006. 106(1): p. 4-16.
4. Mori, M., et al., Diagnostic
performance of time-of-flight PET/CT for evaluating nodal metastasis of the
axilla in breast cancer. Nucl Med Commun, 2019. 40(9): p. 958-964.
5. Orsaria, P., et al., Evaluation
of the Usefulness of FDG-PET/CT for Nodal Staging of Breast Cancer.
Anticancer Res, 2018. 38(12): p.
6639-6652.
6. He, N., et al., A new,
preoperative, MRI-based scoring system for diagnosing malignant axillary lymph nodes
in women evaluated for breast cancer. Eur J Radiol, 2012. 81(10): p. 2602-12.
7. Kuijs, V.J., et al., The
role of MRI in axillary lymph node imaging in breast cancer patients: a
systematic review. Insights Imaging, 2015. 6(2): p. 203-15.