Dose-Finding Study of a CEA-Targeting Agent, SGM-101, for Intraoperative Fluorescence Imaging of Colorectal Cancer.


Journal

Annals of surgical oncology
ISSN: 1534-4681
Titre abrégé: Ann Surg Oncol
Pays: United States
ID NLM: 9420840

Informations de publication

Date de publication:
Mar 2021
Historique:
received: 24 02 2020
accepted: 09 08 2020
pubmed: 10 10 2020
medline: 11 5 2021
entrez: 9 10 2020
Statut: ppublish

Résumé

Carcinoembryonic antigen is overexpressed in colorectal cancer (CRC), making it an optimal target for fluorescence imaging. A phase I/II study was designed to determine the optimal imaging dose of SGM-101 for intraoperative fluorescence imaging of primary and recurrent CRC. Patients were included and received a single dose of SGM-101 at least 24 h before surgery. Patients who received routine anticancer therapy (i.e., radiotherapy or chemotherapy) also were eligible. A dedicated near-infrared imaging system was used for real-time fluorescence imaging during surgery. Safety assessments were performed and SGM-101 efficacy was evaluated per dose level to determine the most optimal imaging dose. Thirty-seven patients with CRC were included in the analysis. Fluorescence was visible in all primary and recurrent tumors. In seven patients, no fluorescence was seen; all were confirmed as pathological complete responses after neoadjuvant therapy. Two tumors showed false-positive fluorescence. In the 37 patients, a total of 97 lesions were excised. The highest mean intraoperative tumor-to-background ratio (TBR) of 1.9 (p = 0.019) was seen in the 10-mg dose. This dose showed a sensitivity of 96%, specificity of 63%, and negative predictive value of 94%. Nine patients (24%) had a surgical plan alteration based on fluorescence, with additional malignant lesions detected in six patients. The optimal imaging dose was established at 10 mg 4 days before surgery. The results accentuate the potential of SGM-101 and designated a promising base for the multinational phase III study, which enrolled the first patients in June 2019.

Sections du résumé

BACKGROUND BACKGROUND
Carcinoembryonic antigen is overexpressed in colorectal cancer (CRC), making it an optimal target for fluorescence imaging. A phase I/II study was designed to determine the optimal imaging dose of SGM-101 for intraoperative fluorescence imaging of primary and recurrent CRC.
METHODS METHODS
Patients were included and received a single dose of SGM-101 at least 24 h before surgery. Patients who received routine anticancer therapy (i.e., radiotherapy or chemotherapy) also were eligible. A dedicated near-infrared imaging system was used for real-time fluorescence imaging during surgery. Safety assessments were performed and SGM-101 efficacy was evaluated per dose level to determine the most optimal imaging dose.
RESULTS RESULTS
Thirty-seven patients with CRC were included in the analysis. Fluorescence was visible in all primary and recurrent tumors. In seven patients, no fluorescence was seen; all were confirmed as pathological complete responses after neoadjuvant therapy. Two tumors showed false-positive fluorescence. In the 37 patients, a total of 97 lesions were excised. The highest mean intraoperative tumor-to-background ratio (TBR) of 1.9 (p = 0.019) was seen in the 10-mg dose. This dose showed a sensitivity of 96%, specificity of 63%, and negative predictive value of 94%. Nine patients (24%) had a surgical plan alteration based on fluorescence, with additional malignant lesions detected in six patients.
CONCLUSIONS CONCLUSIONS
The optimal imaging dose was established at 10 mg 4 days before surgery. The results accentuate the potential of SGM-101 and designated a promising base for the multinational phase III study, which enrolled the first patients in June 2019.

Identifiants

pubmed: 33034788
doi: 10.1245/s10434-020-09069-2
pii: 10.1245/s10434-020-09069-2
pmc: PMC7892528
doi:

Substances chimiques

Carcinoembryonic Antigen 0

Types de publication

Clinical Trial, Phase I Clinical Trial, Phase II Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1832-1844

Références

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pubmed: 2946403

Auteurs

Kim S de Valk (KS)

Centre for Human Drug Research, Leiden, The Netherlands.
Department of Surgery, Leiden University Medical Center, Leiden, The Netherlands.

Marion M Deken (MM)

Department of Surgery, Leiden University Medical Center, Leiden, The Netherlands.

Dennis P Schaap (DP)

Department of Surgery, Catharina Hospital Eindhoven, Eindhoven, The Netherlands.

Ruben P Meijer (RP)

Centre for Human Drug Research, Leiden, The Netherlands.
Department of Surgery, Leiden University Medical Center, Leiden, The Netherlands.

Leonora S Boogerd (LS)

Department of Surgery, Leiden University Medical Center, Leiden, The Netherlands.

Charlotte E Hoogstins (CE)

Centre for Human Drug Research, Leiden, The Netherlands.
Department of Surgery, Leiden University Medical Center, Leiden, The Netherlands.

Maxime J van der Valk (MJ)

Department of Surgery, Leiden University Medical Center, Leiden, The Netherlands.

Ingrid M Kamerling (IM)

Centre for Human Drug Research, Leiden, The Netherlands.

Shadhvi S Bhairosingh (SS)

Department of Surgery, Leiden University Medical Center, Leiden, The Netherlands.

Bérénice Framery (B)

SurgiMab, Montpellier, France.

Denise E Hilling (DE)

Department of Surgery, Leiden University Medical Center, Leiden, The Netherlands.

Koen C Peeters (KC)

Department of Surgery, Leiden University Medical Center, Leiden, The Netherlands.

Fabian A Holman (FA)

Department of Surgery, Leiden University Medical Center, Leiden, The Netherlands.

Miranda Kusters (M)

Department of Surgery, Amsterdam University Medical Center, Amsterdam, The Netherlands.

Harm J Rutten (HJ)

Department of Surgery, Catharina Hospital Eindhoven, Eindhoven, The Netherlands.

Françoise Cailler (F)

SurgiMab, Montpellier, France.

Jacobus Burggraaf (J)

Centre for Human Drug Research, Leiden, The Netherlands.

Alexander L Vahrmeijer (AL)

Department of Surgery, Leiden University Medical Center, Leiden, The Netherlands. a.l.vahrmeijer@lumc.nl.

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