Ramucirumab Plus Docetaxel for Patients with Non-small cell Lung Cancer with Brain Metastases: A Multicenter, Open-Label Single-Arm Phase II Trial.


Journal

The oncologist
ISSN: 1549-490X
Titre abrégé: Oncologist
Pays: England
ID NLM: 9607837

Informations de publication

Date de publication:
02 06 2023
Historique:
received: 12 10 2022
accepted: 03 01 2023
medline: 8 6 2023
pubmed: 14 4 2023
entrez: 13 4 2023
Statut: ppublish

Résumé

Ramucirumab plus docetaxel combination therapy (DOC/RAM) for advanced non-small cell lung cancer (NSCLC) achieves favorable outcomes; however, efficacy and safety for patients with brain metastases are still unclear. Eligible patients included those with advanced NSCLC with measurable asymptomatic brain metastases that progressed after chemotherapy. Patients were intravenously administered ramucirumab (10 mg/kg) and docetaxel (60 mg/m2) every 21-day cycle. Due to difficulties in accumulating the planned 65 participants, enrollment was terminated early when 25 patients were enrolled. Primary endpoint: Median progression-free survival (PFS) was 3.9 months (95% CI, 1.8-5.3). Secondary endpoints: Median intracranial progression-free survival was 4.6 months (95% CI, 2.5-5.9); median overall survival was 20.9 months (95% CI, 6.6-not possible to estimate); objective response rate was 20% (95% CI, 6.8-40.7); disease control rate was 68% (95% CI, 46.5-85.1). The most common grade 3 or higher toxicities were neutropenia in 10 patients (40%). Neither intracranial hemorrhage nor grade 5 adverse events were observed. Patients with higher serum soluble vascular endothelial growth factor receptor 2 concentrations at the start of treatment had slightly longer PFS. No clinical concerns were identified with DOC/RAM for NSCLC with brain metastases in this study. Further investigation with a larger sample size is needed to determine the tolerability and safety of these populations (Trial Identifiers: University Hospital Medical Information Network in Japan [UMIN000024551] and Japan Registry of Clinical Trials [jRCTs071180048]).

Sections du résumé

BACKGROUND
Ramucirumab plus docetaxel combination therapy (DOC/RAM) for advanced non-small cell lung cancer (NSCLC) achieves favorable outcomes; however, efficacy and safety for patients with brain metastases are still unclear.
METHODS
Eligible patients included those with advanced NSCLC with measurable asymptomatic brain metastases that progressed after chemotherapy. Patients were intravenously administered ramucirumab (10 mg/kg) and docetaxel (60 mg/m2) every 21-day cycle.
RESULTS
Due to difficulties in accumulating the planned 65 participants, enrollment was terminated early when 25 patients were enrolled. Primary endpoint: Median progression-free survival (PFS) was 3.9 months (95% CI, 1.8-5.3). Secondary endpoints: Median intracranial progression-free survival was 4.6 months (95% CI, 2.5-5.9); median overall survival was 20.9 months (95% CI, 6.6-not possible to estimate); objective response rate was 20% (95% CI, 6.8-40.7); disease control rate was 68% (95% CI, 46.5-85.1). The most common grade 3 or higher toxicities were neutropenia in 10 patients (40%). Neither intracranial hemorrhage nor grade 5 adverse events were observed. Patients with higher serum soluble vascular endothelial growth factor receptor 2 concentrations at the start of treatment had slightly longer PFS.
CONCLUSION
No clinical concerns were identified with DOC/RAM for NSCLC with brain metastases in this study. Further investigation with a larger sample size is needed to determine the tolerability and safety of these populations (Trial Identifiers: University Hospital Medical Information Network in Japan [UMIN000024551] and Japan Registry of Clinical Trials [jRCTs071180048]).

Identifiants

pubmed: 37053467
pii: 7117810
doi: 10.1093/oncolo/oyad013
pmc: PMC10243767
doi:

Substances chimiques

Docetaxel 15H5577CQD
Vascular Endothelial Growth Factor A 0

Banques de données

UMIN-CTR
['UMIN000024551']
JPRN
['jRCTs071180048']

Types de publication

Clinical Trial, Phase II Multicenter Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

551-e454

Informations de copyright

© The Author(s) 2023. Published by Oxford University Press.

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Auteurs

Keiko Tanimura (K)

Department of Pulmonary Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan.

Junji Uchino (J)

Department of Pulmonary Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan.

Hideharu Kimura (H)

Department of Respiratory Medicine, Kanazawa University Hospital, Kanazawa, Japan.

Osamu Hiranuma (O)

Department of Respiratory Medicine, Otsu City Hospital, Otsu, Japan.

Yusuke Chihara (Y)

Department of Respiratory Medicine, Uji-Tokushukai Medical Center, Uji, Japan.

Shigeru Tanzawa (S)

Division of Medical Oncology, Department of Internal Medicine, Teikyo University Hospital, Tokyo, Japan.

Chieko Takumi (C)

Department of Respiratory Medicine, Japanese Red Cross Kyoto Daiichi Hospital, Kyoto, Japan.

Toshiyuki Kita (T)

Department of Respiratory Medicine, National Hospital Organization, Kanazawa Medical Center, Kanazawa, Japan.

Koji Inoue (K)

Department of Respiratory Medicine, Kitakyushu Municipal Medical Center, Kitakyushu, Japan.

Koichi Minato (K)

Division of Respiratory Medicine, Gunma Prefectural Cancer Center, Ota, Japan.

Shinnosuke Takemoto (S)

Department of Respiratory Medicine, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.

Akira Nakao (A)

Department of Respiratory Medicine, Fukuoka University Hospital, Fukuoka, Japan.

Kenichi Yoshimura (K)

Future Medical Center, Hiroshima University Hospital, Hiroshima, Japan.

Koichi Takayama (K)

Department of Pulmonary Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan.

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