Explore the Tumor Imaging Metrics Core

Overview

The Tumor Imaging Metrics Core (TIMC):

  • Makes reliable, quantitative, longitudinal measurements (such as RECIST, Lugano, RANO, standardized uptake value [SUV] etc.) of lesions from serial MRI, CT, PET, and PET/CT scan images
  • Presents results of analyses on a password protected secure web-based report
  • Provides an independent service, with verifiable measurement of treatment response for patients enrolled in cancer center trials
  • Serves as a centralized, computerized resource to facilitate efficient internal or external auditing

Reliable tracking of changes in lesion size or metabolism is essential for clinical trials that use radiological measurements as surrogate endpoints. The Tumor Metrics Core provides a service for managing these images, making measurements in a routine, reliable, and centralized way, and making results available to investigators efficiently.

Facilities & Equipment

Major Equipment:

  • HERMES workstation
  • Merge Healthcare eFilm workstation
  • Vitrea workstation

Services

  • Consultation services for image-based protocol and image analysis design
  • Image capture and management of multimodality scans from all DF/HCC institutions
  • Tumor measurements from scans of patients on clinical trials according to trial protocol
  • Web-based reporting of results with annotated images and results summary
  • Database management of radiological data for clinical trials
  • Quality Control:
    • For site review, the TIMC paradigm utilizes one central reader per radiologic exam (single read). The central reader will be randomly assigned and cannot be selected by trial staff based on site location.
    • A mediation process has been established in the instance that the central review is felt to be discordant with clinical assessment. Trial staff should file a request for mediation with the TIMC Help Desk (tumormetrics@partners.org) which will trigger a review by a blinded, independent reviewer at a site where the patient is not enrolled.
    • A randomly selected subset of imaging studies are reviewed by dedicated TIMC staff to ensure that documentation was made to justify discordance between central radiology and clinical reviews. Additionally, data are reviewed to ensure appropriate disease was selected at baseline and that follow-up assessments were rendered according to established criteria.
  • Radiology reviewer training:
    • Radiologists and Image Analysts are trained and certified as proficient in established response assessment criteria and clinical research principles.
  • Standardized lesion measurement:
    • Standardized, longitudinal image measurement of radiological scans for oncology clinical trials.

Fee Schedule

Included in the TIMC user fees are the following services; consultation with Trial PIs prior to trial initiation, image study capture from DF/HCC centers, image study archival for the length of the trial, tumor measurements as specified in the protocol, database management of measurement results and image snapshots, web-based results reporting and assistance with trial audits with respect to the image analysis components of the trial.

The TIMC offers consultative services to clinical trials investigators at no additional cost to DF/HCC investigators. The goal of the consultative service is to optimize clinical trials’ protocol design for imaging acquisition and analysis methods so that trials are established with appropriate and optimal imaging methods.

TIMC service fees (per scan). Updated September 2022
For sites outside of DF/HCC, other fees may apply.

Tumor Imaging Response Criteria

PI/Group sponsored

Industry sponsored  

RECIST 1.0 (Therasse, 2000) / RECIST 1.1 (Eisenhauer, 2009); Response Evaluation Criteria in Solid Tumors

$110

$330

mRECIST for HCC (Lencioni, 2010); Modified RECIST for Hepatocellular Carcinoma

$110

$330

Recurrence; Based on RECIST 1.1 definition of new disease

$110

$330

MDA Bone (Hamaoka et al., 2004) for bone metastases; MD Anderson Criteria

$110

$330

*IPCG (Abrey, 2005); International PCNSL Collaborative Group

$110

$330

MacDonald (MacDonald, 1990); For supratentorial malignant gliomas

$110

$330

WHO (Miller, 1979); World Health Organization

$110

$330

mRECIST for mesothelioma (Byrne MJ, 2004); Modified RECIST for mesothelioma

$140

$400

Lugano (Cheson, 2014), includes Deauville Score

$140

$400

iwCLL (Hallek, 2008/2018), includes spleen and liver measurements; International Workshop on Chronic Lymphocytic Leukemia

$140

$400

IWG (Cheson, 1999) or Revised IWG (Cheson, 2007); International Working Group for malignant lymphoma

$140

$400

IMWG (Durie, 2006 / Rajkumar, 2011 / Kumar, 2016); International Myeloma Working Group

$140

$400

IWWM (Owen, 2013 / Dimopoulos et al., 2014), includes spleen measurements; International Workshop for Waldenström Macroglobulinaemia

$140

$400

ATL (Tsukasaki et al., 2009), includes spleen and liver measurements; Adult T-cell Leukemia-Lymphoma

$140

$400

RECIL (Younes, 2017), includes spleen measurements and Deauville score; Response Evaluation Criteria in Lymphoma

$140

$400

INRC (Park, 2017); International Neuroblastoma Response Criteria

$140

$400

ISCL (Olsen, 2007) – includes liver and spleen measurements; International Society for Cutaneous Lymphoma

$140

$400

Choi (Choi et al., 2007) + RECIST 1.0 or 1.1

$140

$400

iRECIST (Seymour, 2017); RECIST for immunotherapy

$165

$500

imRECIST (Hodi, 2018); Immune-modified RECIST

$165

$500

irRC (Wolchock, 2009); Immune-related Response Criteria

$165

$500

3D Volume, for CNS tumors and NF, Maximum of two lesions

$165

$500

PCWG2 (Scher et al., 2008) or PCWG3 (Scher et al., 2016) + RECIST 1.0 or 1.1; Prostate Cancer Working Group 3

$165

$500

irRECIST (Nishino et al., 2013); Immune-related Response Evaluation Criteria in Solid Tumors

$165

$500

*LYRIC (Cheson, 2016), includes Deauville Score; Lymphoma Response to Immunomodulatory Therapy Criteria

$165

$500

EORTC (Young, 1999), maximum of five lesions; European Organisation for Research and Treatment of Cancer

$165

$500

PET-SUV Max

$165

$500

PERCIST (Oo, 2013); PET Response Criteria in Solid Tumors

$165

$500

*iRANO (Okada, 2015); Immuno-therapy Response Assessment in Neuro-Oncology

$165

$500

*RANO (Wen, 2010) for high-grade gliomas; Response Assessment in Neuro-Oncology

$165

$500

*RANO-BM (Lin, 2015) for brain metastases; Response Assessment in Neuro-Oncology

$165

$500

itRECIST (Goldmacher, 2020) for intratumoral immunotherapy

$200

$600

Dual Criteria (more than 1 criteria)

Please consult with TIMC as prices vary

 

*TIMC will provide radiographic assessment only.

Meet the Team

Core Co-Director: Gordon Harris, PhD (MGH)
Core Co-Director: Annick Van den Abbeele, MD (DFCI)

Core Manager:
Deanne Hobba
dhobba@partners.org

Research Fellows:

Carolina Jorge, MD
pjorge@mgh.harvard.edu

Niranjan Rachamreddy, MD
NRACHAMREDDY@mgh.harvard.edu

Nazmi Kurt, MD
nkurt@mgh.harvard.edu

Tagwa Idris, MD
TIDRIS@mgh.harvard.edu

Image Analyst Specialists:

Douglas Brown
douglas_brown@dfci.harvard.edu

Kimberly Ruiz
KMRUIZ@partners.org

Maegan Bergeron
MABERGERON@partners.org

Coordinators:

Nicole Pagliarulo
NPAGLIARULO@partners.org

Salina Clarke-Folger
SCLARKE-FOLGER@mgh.harvard.edu

Staff Assistant:

Habi Balde
HBALDE@partners.org