EORTC1527/JCOG1609INT/ESSO02: Diffusion-weighted magnetic resonance imaging (DW-MRI) assessment of initially unresectable liver metastasis to improve surgical planning (DREAM)—Primary analysis.

K Kozo Kataoka (Division of Lower GI, Department of Gastroenterological Surgery, Hyogo Medical University, Nishinomiya-Shi, Japan) M Murielle E. Mauer (European Organisation for Research and Treatment of Cancer (EORTC) Headquarters, Brussels, Belgium) M Manabu Shiozawa S Sandrine Marreaud (European Organisation for Research and Treatment of Cancer (EORTC) Headquarters, Brussels, Belgium) Y Yoji Kishi J Jedelyn Cabrieto (Eurpean Organization for Research and Treatment of Cancer, Brussels, Belgium) H Hiroaki Onaya (Department of Diagnostic and Interventional Radiology, Aichi Cancer Center Hospital, Nagoya, Japan) M Michel Pierre Ducreux (Université Paris Saclay, Villejuif, France) T Takeshi Suto (Yamagata Prefectural Central Hospital, Yamagata-Shi, Japan) H Hyunseon Kang (Department of Abdominal Imaging, The University of Texas MD Anderson Cancer Center, Houston, TX) N Nobuhisa Matsuhashi (Department of Gastroenterological Surgery, Gifu University Graduate School of Medicine, Gifu, Japan) A Alice Fung (School of Medicine, Department of Diagnostic Radiology, Laboratory Medicine, Knight Diagnostic Laboratories, Oregon Health & Science University Knight Cancer Institute, Portland, OR) M Masayoshi Yasui (Osaka International Cancer Institute, Osaka, Japan) M Michel Rivoire T Toru Tonooka (Chiba Cancer Center, Chiba, Japan) R Roberto Troisi (Federico II University, Naples, Italy) K Kenichi Nakamura (National Cancer Center Hospital, Tokyo, Japan) S Stefan Staettner (Salzkammergutklinikum, Vöcklabruck, Austria) Y Yukihide Kanemitsu S Serge Evrard (Institut Bergonie, Universite de Bordeaux, Bordeaux, France)

Abstract

257 Background: Disappearing liver metastases (DLMs) diagnosed on post-chemotherapy (Cx) computed tomography (CT) is a favorable prognostic factor in patients (pts) with colorectal liver metastases (CRLM). However, the optimal treatment of DLMs - whether they should be resected or left behind - is controversial. This is a prospective, multi-centred, international study examining the added value of MRI (DWI, T1/T2 and contrast-enhanced) to that of CT alone in accurate assessment of the viability of DLMs. Methods: Pts with initially unresectable CRLM downstaged to a planned liver resection after Cx were enrolled, based on the obligatory decision of a multidisciplinary team. Pts were imaged by both CT and MRI at baseline and presurgical timepoints. DLMs were defined as disappeared lesions diagnosed by CT alone, while confirmed DLMs (cDLMs) were defined as lesions that disappeared on both CT and MRI. cDLMs were either resected or followed-up for 2 years if not resected. All imaging scans were collected centrally for quality assurance. The primary endpoint was the negative predictive value (NPV) of MRI and CT in confirming the status of cDLMs using either pathological complete response or the absence of a local recurrence at the site of cDLMs during the 2 year follow up. The study was aimed at excluding a NPV ≤0.85 with a 1-sided alfa of 5% and power of 90% under the alternative that the NPV ≥0.95. The planned sample size was 92 evaluable (resected or left behind) cDLMs, assuming a within-patient correlation between cDLMs of 0.2 and an average number of 2 cDLMs per pt. Results: 233 pts were registered at 22 participating centres, and 112 were enrolled for analysis. A median of 8 cycles of Cx was delivered, and pts had a median of 7 CRLMs at baseline. A total of 203 cDLMs were identified while the number of DLMs diagnosed by CT was 296. Of these, 152 cDLMs and 227 DLMs, respectively, were evaluable according to the imaging protocol. Intraoperative ultrasound was performed for 195 cDLMs and, of these, 59 (30.2%) were still detected. The rate of R0/R1 resection was 95.5%. The NPV of evaluable cDLMs either resected or left behind was 62.5 % (95/152, 95% CI:50.8-74.2), which was lower than the prespecified threshold. The NPV of DLMs was 52.9% (119/227, 95% CI:42.7, 63.0). The NPV of resected cDLMs, and those left behind were 56.8% (50/88, 95% CI: 44.2, 69.5) and 70.3% (45/64, 95% CI: 48.6 -92.0), respectively. For DLMs, the NPV of resected DLMs and those left behind were 45.6% (72/158, 95% CI: 35.4-55.7) and 69.6% (48/69, 95% CI: 47.7-91.5), respectively. Conclusions: For pts with initially unresectable CRLM, cDLMs diagnosed by both CT and MRI do not correspond to tumor viability, even after highly effective chemotherapy. Ongoing survival analysis (to be presented at the annual meeting) may impact the treatment strategy of pts with DLMs. Clinical trial information: NCT02781935 .

Article Details

Volume / Issue Vol. 43, Issue 4_suppl
Published February 01, 2025
Pages 257-257
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (20)

K

Kozo Kataoka

Division of Lower GI, Department of Gastroenterological Surgery, Hyogo Medical University, Nishinomiya-Shi, Japan

M

Murielle E. Mauer

European Organisation for Research and Treatment of Cancer (EORTC) Headquarters, Brussels, Belgium

M

Manabu Shiozawa

S

Sandrine Marreaud

European Organisation for Research and Treatment of Cancer (EORTC) Headquarters, Brussels, Belgium

Y

Yoji Kishi

J

Jedelyn Cabrieto

Eurpean Organization for Research and Treatment of Cancer, Brussels, Belgium

H

Hiroaki Onaya

Department of Diagnostic and Interventional Radiology, Aichi Cancer Center Hospital, Nagoya, Japan

M

Michel Pierre Ducreux

Université Paris Saclay, Villejuif, France

T

Takeshi Suto

Yamagata Prefectural Central Hospital, Yamagata-Shi, Japan

H

Hyunseon Kang

Department of Abdominal Imaging, The University of Texas MD Anderson Cancer Center, Houston, TX

N

Nobuhisa Matsuhashi

Department of Gastroenterological Surgery, Gifu University Graduate School of Medicine, Gifu, Japan

A

Alice Fung

School of Medicine, Department of Diagnostic Radiology, Laboratory Medicine, Knight Diagnostic Laboratories, Oregon Health & Science University Knight Cancer Institute, Portland, OR

M

Masayoshi Yasui

Osaka International Cancer Institute, Osaka, Japan

M

Michel Rivoire

T

Toru Tonooka

Chiba Cancer Center, Chiba, Japan

R

Roberto Troisi

Federico II University, Naples, Italy

K

Kenichi Nakamura

National Cancer Center Hospital, Tokyo, Japan

S

Stefan Staettner

Salzkammergutklinikum, Vöcklabruck, Austria

Y

Yukihide Kanemitsu

S

Serge Evrard

Institut Bergonie, Universite de Bordeaux, Bordeaux, France