Monitoring bony metastases response with diffusion MRI

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Monitoring bony metastases response with diffusion MRI Anwar Padhani MD Mount Vernon Hospital Cancer Centre London, UK

Objectives To illustrate the potential of whole body DWI in the therapy response assessment of bone metastases To illustrate that there are 4 patterns of response when signal intensity and ADC values are evaluated To provide advice on how to use WB-DWI in conjunction with anatomic MRI to successfully gauge bone marrow therapy response Kwee TC, et al. Whole-body diffusion-weighted MRI. Eur J Radiol 2009; 70:409 417 Padhani AD, Koh DM, Collins D. Whole body diffusion MR imaging in cancer current status and research directions. Radiology in press Padhani AR & Koh DM. Diffusion MRI for monitoring of treatment response. MRI ClinN Am 2011; 19: 181-209 Padhani AR & Gogbashian A. Bony metastases -assessing response to therapy with whole body diffusion MRI. Cancer Imaging 2011; - in press

Monitoring bone therapy response Symptoms assessments (analgesic requirements) and development of skeletal related events are markers of therapeutic efficacy in clinical c trials Serum markers are not useful for therapy response for the majority of tumors that metastasize to bone Serum PSA: not reliable in late stage hormone-refractory refractory prostate disease; flare phenomenon in responding patients* CA15-3: moderate sensitivity for metastatic disease (60-65%); 65%); flare reaction in responding breast cancer patients** Serum/urinary markers of osteoblastic and osteoclastic activity monitor bone response NOT tumor response Circulating tumor cells (CTCs) are emerging as strong response biomarkers b for breast, colorectal and prostate cancers *Scher HI et al. JCO 2008; 26:1148-59 **Duffy MJ. Clin Chem 2006; 52:345-51 51

Evaluating bony disease by MRI: combining sequences into whole body examinations T1-weighted spin-echo, T2-weighted (FS) & STIR Cellular and water content T2*-weighted GRE (IP/OP) Fat:waterratio and susceptibility induced by trabecular bone Dynamic contrast enhanced MRI Vascularisation Ultrashort TE (UTE) Trabecular bone structure DW-MRI Perfusion, cell density, fat and water content * Schaefer JF, et al. Total-body MR-imaging in oncology. Eur Radiol.. 2006; 16(9):2000-15. 15. * Schmidt GP, et al. Whole-body MRI for the staging and follow-up of patients with metastasis. Eur J Radiol 2009; 70: 393 400

Whole body DWI for metastasis detection Widespread availability Better than CT scans and bone scans for lytic bony disease Also provides information about soft tissue disease Advantages No ionizing radiation No injections of isotopes or contrast medium Quick to perform & read Quantitative At a glance assessments Improves whole body MRI performance Kwee TC, et al. Whole-body diffusion-weighted MRI. EurJ Radiol 2009; 70: 409 417 417

WB-DWI sub-protocol (STIR for FS total 25mins) Scouts; T1W/STIR Whole body b50 b900 4 stations; 50 slices, 5mm; b50, b900 Coils surface FOV (cm) 380 Rectangular (%) 100 Acquisition matrix 128i Scan % 80 Slices 50 Thickness/gap 5/0 Z-axis coverage (cm) 25 TR (ms) 9000 TE (ms) min ( 67) TI (ms) 180 Half scan factor 6/8i b-values 50, 900 NE 6 Bandwidth (Hz/pix pix) 1628 Scan time/station (mins( mins) 6.15

Normal bone marrow pattern Normal adult BM distribution established by 25 yo Yellow bone marrow: 10-20% water, fat cells ( SI) Red bone marrow: 40-60% water & more cells ( SI) Variable red BM atrophy and trabecular bone loss after 40 yo(> ) Increase in yellow bone marrow Normal adult BM distribution

Non-linear (paradoxical) relationship between ADC & bone marrow cellularity Yellow (fatty) marrow low SI & ADC - Low water content & cellularity - Fat acts as a barrier to water diffusion repelling water - Low perfusion Red bone marrow higher SI & ADC - More cells and water -Less big fat cells & more small cells - Higher perfusion Tumor & BM hyperplasia highest SI but variable ADC -Highest water content & cellularity within restricted bone marrow space - Highest perfusion

Assessing WB-DWI response to Rx Changes in tumor burden/volume Changes in signal intensity on high b-value b images Reflects changes in water diffusivity and water content Changes in ADC values Objective evaluations of water diffusivity Amenable to numerical analysis Heterogeneity assessments are made possible Histogram & pixel map analyses (parametric response maps)

Multiple Myeloma cyclophosphamide, dexamethasone, thalidomide (CDT) and bortezomib Biological processes involved in therapy induced changes in DWI 25/Mar/10 2/Dec/10 Prior Current Hamstra DA, et al, J Clin Oncol 2007: 25:4104-4109

WB-DWI Metastatic bone disease: not responding to therapy New areas of focal abnormal signal intensity Increasing extent (becoming confluent) and intensity of lesions For BM disease ADC values can, or (heterogeneous; but remains below thresholds)!

Signal intensity changes in non-response 11-3-10 10 8-6-10 8-9-10 b800 b800 b800 47 yo F metastatic breast cancer 1 st Taxanes/APD then Letrozole

Increases in tumour volume & ADC values with progression 51 yo F metastatic breast cancer Bone and liver disease Pre and post Taxanes/ APD/ Herceptin Bone tumor volume 29.3 179.2 cm 3 ADC 780 930 μm 2 /s

DW-MRI and cellularity in bone marrow Disease progression can cause modest increases, stable or slight decreases in ADC ADC Non- effective Rx Yellow marrow 10% H 2 0 Red marrow 40-60% H 2 0 Hyperplastic/moderate tumour infiltration 60-80% H 2 0 Dense malignant infiltration >80% H 2 0 Signal intensity on high b-value b images

BM hyperplasia: increased SI but stable ADC 40 F post-partum, left mastectomy and axillary nodal dissection Rx adjuvant chemotherapy with G-CSF support PRIOR 30-July 2010 10-December-2010 ADC 920 ± 266 920 ± 211 µm 2 /s CURRENT

Myeloma progression 11 SI & ADC th 11-Jan-10 STIR 11-Jan -10 T1W 1-April-10 Jan 1-April-10 1st April b800 ADC 900 µm2/s 11th Jan 1st April 725 µm2/s 62M Multiple Myeloma Rx Bortezomib

Variable changes in ADC in non- responders (stable + progression) 26 patients with metastatic prostate cancer Chemotherapy 100 lesions 33 in responders 59 in progressors 8 stable Limits of reproducibility of normal BM ± 86 µm 2 /s Courtesy of C. Messiou, Royal Marsden Hospital, London Change in ADC (µm 2 /s) Change in ADC (um2/s) 1200 1000 800 600 400 200 0-200 -400-600 Responders Progressors Stable patients Limits of reproducibility Messiou C, et al. Assessing response in bone metastases in prostate cancer with diffusion weighted MRI. Eur Radiol 2011 ahead of print

WB-DWI Bony disease responding to therapy Decrease in volume of focal abnormal signal intensity Signal intensity changes generally decrease but occasionally unchanged/increase if there is a strong inflammatory response ADC values : marked increases

Breast cancer (triple negative) Rx GemCarbo + APD (bisphosphonate) 29-July July-2010 01-Oct Oct-2010 T1W T2W+FS WB-DWI b900 T1W T2W+FS WB-DWI b900 Decreases in DW-MRI is due to a combination of changes in tissue water content and cellularity

Breast cancer (triple negative) Rx GemCarbo + APD (bisphosphonate) 37F perimenopausal 29-July July-2010 01-Oct Oct-2010 Triple negative, metastatic breast cancer Rx GemCarbo plus APD b900 Diffuse increase in ADC values ADC 883 1905 μm 2 /s Cut-off values: 650 & 1500 μm 2 /s ADC Prior Current

Decreasing cellularity Effective Rx ADC Non- effective Rx Yellow marrow 10% H 2 0 Red marrow 40-60% H 2 0 Hyperplastic/moderate tumour infiltration 60-80% H 2 0 Dense malignant infiltration >80% H 2 0 Signal intensity on high b-value b images

Breast cancer Rx Capecitabine (3 cycles) + APD 21-Jan Jan-2011 04-April April-2011 T1W T2W+FS b900 T1W T2W+FS b900

Breast cancer Rx capcitabine + APD ADC 21-Jan Jan-2011 04-April April-2011 41F postmenopausal Metastatic breast cancer - asymptomatic (before and during Rx) Rx cepcitabine (3 cycles) plus APD Signal intensity is unchanged but marked increase in ADC values ADC mean 900 to 1500 μm 2 /s b900 Cut-off values: 650 & 1500 μm 2 /s Prior Current

Decreasing cellularity Effective Rx Necrosis (T2-shine through) ADC Non- effective Rx Yellow marrow 10% H 2 0 Red marrow 40-60% H 2 0 Hyperplastic/moderate tumour infiltration 60-80% H 2 0 Dense malignant infiltration >80% H 2 0 Signal intensity on high b-value b images

Progression with bisphosphonates response with docetaxel + bisphosphonates 5/Jan/10 6/Apr/10 30/Jul/10 28/Oct/10 1/Mar/11 Response with GemCarbo+bisphosphonates relapse after stopping Rx 23/Jul/10 1/Oct/10 15/Dec/10 8/Feb/11 20/Apr/11

Proposed response criteria of BM lesions EARLY after starting cytotoxic Rx SI on high b- value images ADC in relation cut-off Biological inference and response assessment Most pixels <cut-off Persistent hypercellularity no evidence of response Most pixels >cut-off Necrosis, T2-shine through evidence of response Most pixels >cut-off Hypocellularity evidence of response Most pixels <cut-off Possible sclerotic or fibrotic reaction indeterminate for response ADC change needs to be judged in relation to cut-off values defined from untreated patients examined using the same imaging protocol. This is likely to be tumor t type dependent. Criteria may not apply to non-cytotoxic therapies. The timeline for the applicability of these criteria are undefined Padhani AR & Gogbashian A. Bony metastases -assessing response to therapy with whole body diffusion MRI. Cancer Imaging 2011; - in press

Some outstanding R&D questions It is not clear what proportion of tumor cells have to be killed for ADC changes to become detectable by DW-MRI Does the mechanism of cell death affect DW-MRI appearances? What is the reproducibility of WB-DWI ADC estimates (that is, how much of measured change can be considered real? What factors affect the measurement reproducibility? Essential information for the development of WB-DWI as a pharmacodynamic biomarker for use in drug trials How much change in ADC results in patient benefit (improvements in symptoms and survival) for the variety of available therapies? Essential information for the development of WB-DWI as a tool for personalized medicine Padhani AR, Koh DM & Collins D. Whole body diffusion MRI in cancer -current status & research directions.. Radiology - in press

WB-DWI is a SI based tool for Take home points DWI is a SI based tool for bone marrow lesion detection and therapy response Lytic bone deposits are better seen than sclerotic lesions Non-linear (paradoxical) relationship between ADC & bone marrow signal intensity Disease progression causes heterogeneous changes in ADC Response assessments larger ADC increases WB-DWI should always be interpreted with conventional imaging findings WB-DWI has not yet been proven to impact meaningful health outcomes in patients with metastatic bone disease Padhani AR & Gogbashian A. Bony metastases -assessing response to therapy with whole body diffusion MRI. Cancer Imaging 2011; - in press