Multicenter Cohort Study to Assess the Association between Changes on Imaging and Outcome after Regorafenib Treatment (KSCC1603).


Journal

Oncology
ISSN: 1423-0232
Titre abrégé: Oncology
Pays: Switzerland
ID NLM: 0135054

Informations de publication

Date de publication:
2020
Historique:
received: 10 03 2020
accepted: 25 03 2020
pubmed: 9 7 2020
medline: 21 10 2020
entrez: 9 7 2020
Statut: ppublish

Résumé

Molecular targeted drugs having angiogenesis-inhibiting properties allow the induction of necrosis inside tumors. We retrospectively investigated the relationship between changes on imaging associated with regorafenib (REGO) and treatment outcomes using real-world data. The eligibility criteria included an ECOG PS of 0-1, a starting dose of 120 or 160 mg/day of REGO, and a duration of treatment of at least 35 days. Regarding changes on imaging, cavitation in lung lesions (CLL), morphologic response of liver lesions (MRL), and change of liver metastasis density (CLD) were evaluated. We finally screened 671 cases, and 226 cases were eligible. In total, 172 and 145 patients had lung and liver metastases, respectively. Among the patients with lung metastasis, CLL was found in 69 patients (40.0%). The median progression-free survival (PFS) of the patients with and those without CLL was 3.2 and 2.4 months, respectively (hazard ratio [HR] = 0.758; 95% confidence interval [CI]: 0.529-1.087), and the median overall survival (OS) of these groups was 10.5 and 8.9 months, respectively (HR = 0.862; 95% CI: 0.579-1.285). MRL and CLD of liver metastasis were analyzed in 145 and 90 patients, respectively. The median OS with and without MRL was 8.9 and 8.2 months, respectively, whereas the median OS with and without CLD was 11.6 and 7.7 months, respectively (HR = 0.523; 95% CI: 0.275-0.992). CLL may predict PFS but not OS among patients with lung metastasis. CLD was predictive of favorable outcomes for REGO in patients with liver metastasis.

Sections du résumé

BACKGROUND BACKGROUND
Molecular targeted drugs having angiogenesis-inhibiting properties allow the induction of necrosis inside tumors. We retrospectively investigated the relationship between changes on imaging associated with regorafenib (REGO) and treatment outcomes using real-world data.
PATIENTS AND METHODS METHODS
The eligibility criteria included an ECOG PS of 0-1, a starting dose of 120 or 160 mg/day of REGO, and a duration of treatment of at least 35 days. Regarding changes on imaging, cavitation in lung lesions (CLL), morphologic response of liver lesions (MRL), and change of liver metastasis density (CLD) were evaluated.
RESULTS RESULTS
We finally screened 671 cases, and 226 cases were eligible. In total, 172 and 145 patients had lung and liver metastases, respectively. Among the patients with lung metastasis, CLL was found in 69 patients (40.0%). The median progression-free survival (PFS) of the patients with and those without CLL was 3.2 and 2.4 months, respectively (hazard ratio [HR] = 0.758; 95% confidence interval [CI]: 0.529-1.087), and the median overall survival (OS) of these groups was 10.5 and 8.9 months, respectively (HR = 0.862; 95% CI: 0.579-1.285). MRL and CLD of liver metastasis were analyzed in 145 and 90 patients, respectively. The median OS with and without MRL was 8.9 and 8.2 months, respectively, whereas the median OS with and without CLD was 11.6 and 7.7 months, respectively (HR = 0.523; 95% CI: 0.275-0.992).
CONCLUSION CONCLUSIONS
CLL may predict PFS but not OS among patients with lung metastasis. CLD was predictive of favorable outcomes for REGO in patients with liver metastasis.

Identifiants

pubmed: 32640458
pii: 000507814
doi: 10.1159/000507814
doi:

Substances chimiques

Phenylurea Compounds 0
Protein Kinase Inhibitors 0
Pyridines 0
regorafenib 24T2A1DOYB

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

719-726

Informations de copyright

© 2020 S. Karger AG, Basel.

Auteurs

Eiji Oki (E)

Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan, okieiji@surg2.med.kyushu-u.ac.jp.

Masahiro Kawahira (M)

Shizuoka Cancer Center, Mishima, Japan.

Tetsuya Kusumoto (T)

Kyushu Medical Center, Fukuoka, Japan.

Satoshi Yuki (S)

Department of Gastroenterology and Hepatology, Hokkaido University Hospital, Sapporo, Japan.

Kazuteru Hatanaka (K)

Hakodate Municipal Hospital, Hakodate, Japan.

Yoshimitsu Kobayashi (Y)

Kushiro Rosai Hospital, Kushiro, Japan.

Akihiro Nishie (A)

Department of Clinical Radiology, Kyushu University, Fukuoka, Japan.

Satoshi Kawanami (S)

Department of Clinical Radiology, Kyushu University, Fukuoka, Japan.

Akitaka Makiyama (A)

JCHO Kyushu Hospital, Kitakyushu, Japan.

Hiroshi Saeki (H)

Gunma University, Gunma, Japan.

Sanae Sakamoto (S)

Kyushu Study Group of Clinical Cancer, Fukuoka, Japan.

Yoshito Komatsu (Y)

Department of Gastroenterology and Hepatology, Hokkaido University Hospital, Sapporo, Japan.

Mototsugu Shimokawa (M)

Yamaguchi University, Yamaguchi, Japan.

Masaki Mori (M)

Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan.

Taito Esaki (T)

National Hospital Organization Kyushu Cancer Center, Fukuoka, Japan.

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Classifications MeSH