TY - JOUR
T1 - Multicenter study of zoledronic acid administration in non-small-cell lung cancer patients with bone metastasis
T2 - Thoracic oncology research group (TORG) 1017
AU - Nakahara, Yoshiro
AU - Hosomi, Yukio
AU - Shibuya, Masahiko
AU - Mitsufuji, Hisashi
AU - Katagiri, Masato
AU - Naoki, Katsuhiko
AU - Soejima, Kenzo
AU - Nogami, Naoyuki
AU - Nagase, Seisuke
AU - Nishikawa, Masanori
AU - Minato, Koichi
AU - Takiguchi, Yuichi
AU - Seki, Nobuhiko
AU - Yamada, Kouzo
AU - Seto, Takashi
AU - Okamoto, Hiroaki
N1 - Publisher Copyright:
© 2019 Molecular and Clinical Oncology. All rights reserved.
PY - 2019/10
Y1 - 2019/10
N2 - Skeletal-related events (SREs) may occur at the time of first diagnosis in 20-30% of lung cancer patients with bone metastases. Several clinical trials have shown that zoledronic acid (ZA) is effective for decreasing SREs. The main objective of the present study was to discuss clinical data of ZA and compare the frequency of SREs with previous reports. All patients with non-small-cell lung cancer (NSCLC) with metastatic bone disease who were administered ZA at least twice between January 2008 and December 2009 were eligible for inclusion in the study. In total, 198 consecutive patients were identified. The median duration of ZA administration was 106 days [95% confidence interval (CI), 92-133 days], and the median number of ZA administrations was 4 (range, 2-41). The median time to first SRE in patients who experienced SRE following ZA treatment was 202 days (95% CI, 156-264 days). Among the 78 patients who had already experienced SRE prior to ZA treatment, 35 (45%) experienced SRE subsequently after starting ZA treatment. On the other hand, among the 120 patients without a history of SRE before starting ZA treatment, 42 (35%) experienced SRE after the start of ZA administration (P=0.16). No osteonecrosis of the jaw (ONJ) was reported in any of the patients. The present study revealed that ZA had a certain level of efficacy regardless of the presence or absence of prior SREs. However, the duration of ZA therapy was short in this study; further accumulation of data on the long-term prognosis and incidence rates of ONJ and other late complications of ZA therapy seems to be particularly important.
AB - Skeletal-related events (SREs) may occur at the time of first diagnosis in 20-30% of lung cancer patients with bone metastases. Several clinical trials have shown that zoledronic acid (ZA) is effective for decreasing SREs. The main objective of the present study was to discuss clinical data of ZA and compare the frequency of SREs with previous reports. All patients with non-small-cell lung cancer (NSCLC) with metastatic bone disease who were administered ZA at least twice between January 2008 and December 2009 were eligible for inclusion in the study. In total, 198 consecutive patients were identified. The median duration of ZA administration was 106 days [95% confidence interval (CI), 92-133 days], and the median number of ZA administrations was 4 (range, 2-41). The median time to first SRE in patients who experienced SRE following ZA treatment was 202 days (95% CI, 156-264 days). Among the 78 patients who had already experienced SRE prior to ZA treatment, 35 (45%) experienced SRE subsequently after starting ZA treatment. On the other hand, among the 120 patients without a history of SRE before starting ZA treatment, 42 (35%) experienced SRE after the start of ZA administration (P=0.16). No osteonecrosis of the jaw (ONJ) was reported in any of the patients. The present study revealed that ZA had a certain level of efficacy regardless of the presence or absence of prior SREs. However, the duration of ZA therapy was short in this study; further accumulation of data on the long-term prognosis and incidence rates of ONJ and other late complications of ZA therapy seems to be particularly important.
KW - bone metastases
KW - non-small-cell lung cancer
KW - zoledronic acid
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UR - http://www.scopus.com/inward/citedby.url?scp=85073393413&partnerID=8YFLogxK
U2 - 10.3892/mco.2019.1903
DO - 10.3892/mco.2019.1903
M3 - Article
AN - SCOPUS:85073393413
SN - 2049-9450
VL - 11
SP - 349
EP - 353
JO - Molecular and Clinical Oncology
JF - Molecular and Clinical Oncology
IS - 4
ER -