Impact of docetaxel plus ramucirumab on metastatic site in previously treated patients with non-small cell lung cancer: a multicenter retrospective study.


Journal

Translational lung cancer research
ISSN: 2218-6751
Titre abrégé: Transl Lung Cancer Res
Pays: China
ID NLM: 101646875

Informations de publication

Date de publication:
Apr 2021
Historique:
entrez: 20 5 2021
pubmed: 21 5 2021
medline: 21 5 2021
Statut: ppublish

Résumé

Docetaxel (DOC) plus ramucirumab (RAM) has been recommended as an optimal therapy for previously treated patients with non-small cell lung cancer (NSCLC). In a clinical setting, there are few reports about DOC plus RAM, therefore its effect on factors such as Eastern Cooperative Oncology Group (ECOG) performance status (PS) and metastatic sites is still unknown. We recruited NSCLC patients who received DOC plus RAM in four medical facilities in Japan from June 2016 to March 2020. We retrospectively investigated the overall response rate (ORR), disease control rate (DCR), and progression-free survival (PFS) of DOC plus RAM and conducted univariate and multivariate analyses using PFS as a dependent factor. Patients were followed up until June 30, 2020. A total of 237 patients were consecutively enrolled. For all patients, the ORR, DCR, and median PFS were 25.2%, 63.9%, and 4.5 months, respectively. The ORR and DCR for malignant pleural effusion (MPE), lung metastasis, and liver metastasis were 7.7% and 53.8%, 30.3% and 77.5%, and 48.6% and 71.4%, respectively. In the multivariate analysis, MPE, lung metastasis, and liver metastasis were not prognostic factors for poor PFS. However, ECOG-PS 2 or more [hazard ratio (HR): 1.66, 95% confidence interval (CI): 1.14-2.40, P=0.008] and brain metastasis (HR: 1.71, 95% CI: 1.23-2.37, P=0.001) were significant and independent factors associated with shorter PFS. DOC plus RAM could be an optimal therapy for previous treated NSCLC patients with lung and liver metastasis, and furthermore, should be used carefully for patients with poor ECOG-PS or brain metastasis. Docetaxel and ramucirumab; non-small cell lung cancer (NSCLC); metastatic site; poor performance status.

Sections du résumé

BACKGROUND BACKGROUND
Docetaxel (DOC) plus ramucirumab (RAM) has been recommended as an optimal therapy for previously treated patients with non-small cell lung cancer (NSCLC). In a clinical setting, there are few reports about DOC plus RAM, therefore its effect on factors such as Eastern Cooperative Oncology Group (ECOG) performance status (PS) and metastatic sites is still unknown.
METHODS METHODS
We recruited NSCLC patients who received DOC plus RAM in four medical facilities in Japan from June 2016 to March 2020. We retrospectively investigated the overall response rate (ORR), disease control rate (DCR), and progression-free survival (PFS) of DOC plus RAM and conducted univariate and multivariate analyses using PFS as a dependent factor. Patients were followed up until June 30, 2020.
RESULTS RESULTS
A total of 237 patients were consecutively enrolled. For all patients, the ORR, DCR, and median PFS were 25.2%, 63.9%, and 4.5 months, respectively. The ORR and DCR for malignant pleural effusion (MPE), lung metastasis, and liver metastasis were 7.7% and 53.8%, 30.3% and 77.5%, and 48.6% and 71.4%, respectively. In the multivariate analysis, MPE, lung metastasis, and liver metastasis were not prognostic factors for poor PFS. However, ECOG-PS 2 or more [hazard ratio (HR): 1.66, 95% confidence interval (CI): 1.14-2.40, P=0.008] and brain metastasis (HR: 1.71, 95% CI: 1.23-2.37, P=0.001) were significant and independent factors associated with shorter PFS.
CONCLUSIONS CONCLUSIONS
DOC plus RAM could be an optimal therapy for previous treated NSCLC patients with lung and liver metastasis, and furthermore, should be used carefully for patients with poor ECOG-PS or brain metastasis.
KEYWORDS BACKGROUND
Docetaxel and ramucirumab; non-small cell lung cancer (NSCLC); metastatic site; poor performance status.

Identifiants

pubmed: 34012781
doi: 10.21037/tlcr-20-1263
pii: tlcr-10-04-1642
pmc: PMC8107751
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1642-1652

Informations de copyright

2021 Translational Lung Cancer Research. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/tlcr-20-1263). AT reports personal fees from Chugai Pharmaceutical, grants and personal fees from AstraZeneka, personal fees from Boehringer Ingelheim, grants and personal fees from Ono Pharmaceutical, grants and personal fees from Bristol-Myers Squibb, personal fees from MSD, personal fees from Taiho, personal fees from Pfizer, personal fees from Eli Lilly, personal fees from Kissei, outside the submitted work. S.A reports grants and personal fees from AstraZeneca, grants and non-financial support from F. Hoffmann-La Roche, grants and personal fees from Ono, grants and personal fees from Taiho, grants and personal fees from Boehringer Ingelheim, grants and personal fees from Pfizer, grants and personal fees from Bristol-Myers Squibb, personal fees from Hisamitsu, grants and personal fees from MSD, grants and personal fees from Eli Lilly, grants and personal fees from Chugai, personal fees from Kyowa Hakko Kirin, grants and personal fees from Merck, outside the submitted work. MT reports grants and personal fees from Boehringer Ingelheim, grants and personal fees from Ono Pharmaceutical, grants and personal fees from Bristol-Myers Squibb, personal fees from Chugai Pharmaceutical, personal fees from AstraZeneca, personal fees from Taiho Pharmaceutical, personal fees from Eli Lilly, personal fees from Asahi Kasei Pharmaceutical, personal fees from MSD, outside the submitted work. HS reports personal fees from Chugai Pharmaceutical, personal fees from MSD, personal fees from AstraZeneca, outside the submitted work. TH reports grants and personal fees from Ono Pharmaceutical Co. Ltd, grants and personal fees from Lilly Japan Co. Ltd, grants and personal fees from AstraZeneca Co. Ltd, grants and personal fees from Taiho Pharmaceutical Co. Ltd, grants and personal fees from Chugai Pharmaceutical Co. Ltd., grants from Merck Serono Co. Ltd., grants from Boehringer Ingelheim, grants and personal fees from MSD Oncology Co. Ltd, outside the submitted work. The other authors have no conflicts of interest to declare.

Références

Pathol Res Pract. 2018 Aug;214(8):1136-1141
pubmed: 29935812
J Thorac Oncol. 2012 Oct;7(10):1485-9
pubmed: 22982649
N Engl J Med. 2018 Nov 22;379(21):2040-2051
pubmed: 30280635
CA Cancer J Clin. 2012 Jan-Feb;62(1):10-29
pubmed: 22237781
Chin J Cancer Res. 2014 Dec;26(6):669-77
pubmed: 25561764
Clin Cancer Res. 2004 Sep 15;10(18 Pt 1):6222-30
pubmed: 15448011
J Clin Oncol. 2000 May;18(10):2095-103
pubmed: 10811675
Cancer Res. 2010 Nov 1;70(21):8357-67
pubmed: 20978198
Arch Pathol Lab Med. 2000 Jul;124(7):1061-5
pubmed: 10888784
Lung Cancer. 2011 Sep;73(3):338-44
pubmed: 21296449
Cancer Cell. 2002 Oct;2(4):289-300
pubmed: 12398893
Cancer Chemother Pharmacol. 2013 Feb;71(2):457-61
pubmed: 23178954
N Engl J Med. 2018 Jun 14;378(24):2288-2301
pubmed: 29863955
J Thorac Oncol. 2010 Jan;5(1):110-6
pubmed: 20035187
Lancet Oncol. 2019 Feb;20(2):282-296
pubmed: 30665869
Eur J Cancer. 2009 Jan;45(2):228-47
pubmed: 19097774
Am J Pathol. 2006 Feb;168(2):639-48
pubmed: 16436677
Cancer. 2006 Apr 1;106(7):1624-33
pubmed: 16518827
Future Oncol. 2019 Aug;15(23):2699-2706
pubmed: 31282758
BMC Cancer. 2020 Dec 3;20(1):1185
pubmed: 33272262
Cancer Chemother Pharmacol. 2008 Aug;62(3):551-7
pubmed: 18064462
Mol Clin Oncol. 2015 Mar;3(2):415-419
pubmed: 25798278
Thorac Cancer. 2019 Apr;10(4):775-781
pubmed: 30809973
Clin Exp Metastasis. 2020 Feb;37(1):199-207
pubmed: 31768815
N Engl J Med. 2020 Jan 2;382(1):41-50
pubmed: 31751012
Ann Thorac Surg. 1996 Jul;62(1):246-50
pubmed: 8678651
Med Oncol. 2013;30(3):676
pubmed: 23925664
Genes Cancer. 2011 Dec;2(12):1097-105
pubmed: 22866201
J Gastrointestin Liver Dis. 2007 Dec;16(4):373-7
pubmed: 18193117
Lancet. 2014 Aug 23;384(9944):665-73
pubmed: 24933332
Thorac Cancer. 2020 Jun;11(6):1559-1565
pubmed: 32291896
Pharmacol Res. 2018 Oct;136:97-107
pubmed: 30170190
J Oncol Pract. 2019 Oct;15(10):e878-e887
pubmed: 31509482
Oncotarget. 2016 Aug 16;7(33):53245-53253
pubmed: 27449299
Crit Rev Oncol Hematol. 2014 Jun;90(3):190-9
pubmed: 24434034
N Engl J Med. 2018 May 31;378(22):2078-2092
pubmed: 29658856
Clin Cancer Res. 1997 Jan;3(1):47-50
pubmed: 9815536
Anticancer Res. 2019 Sep;39(9):4987-4993
pubmed: 31519605
Thorac Cancer. 2020 Feb;11(2):389-393
pubmed: 31851428
Cancer. 2000 May 15;88(10):2239-45
pubmed: 10820344
Transl Lung Cancer Res. 2019 Aug;8(4):450-460
pubmed: 31555518
J Clin Oncol. 2006 Aug 1;24(22):3657-63
pubmed: 16877734
J Clin Oncol. 2004 May 1;22(9):1589-97
pubmed: 15117980

Auteurs

Kinnosuke Matsumoto (K)

Department of Internal Medicine, National Hospital Organization Kinki-Chuo Chest Medical Center, Osaka, Japan.

Akihiro Tamiya (A)

Department of Internal Medicine, National Hospital Organization Kinki-Chuo Chest Medical Center, Osaka, Japan.

Yoshinobu Matsuda (Y)

Department of Internal Medicine, National Hospital Organization Kinki-Chuo Chest Medical Center, Osaka, Japan.

Yoshihiko Taniguchi (Y)

Department of Internal Medicine, National Hospital Organization Kinki-Chuo Chest Medical Center, Osaka, Japan.

Shinji Atagi (S)

Clinical Research Center, National Hospital Organization Kinki-Chuo Chest Medical Center, Osaka, Japan.

Hayato Kawachi (H)

Department of Respiratory Medicine, Osaka International Cancer Institute, Osaka, Japan.

Motohiro Tamiya (M)

Department of Respiratory Medicine, Osaka International Cancer Institute, Osaka, Japan.

Satoshi Tanizaki (S)

Department of Respiratory Medicine, Osaka General Medical Center, Osaka, Japan.

Junji Uchida (J)

Department of Respiratory Medicine, Osaka General Medical Center, Osaka, Japan.

Kiyonobu Ueno (K)

Department of Respiratory Medicine, Osaka General Medical Center, Osaka, Japan.

Takafumi Yanase (T)

Department of Respiratory Medicine, Osaka Prefectural Medical Center for Respiratory and Allergic Disease, Osaka, Japan.

Hidekazu Suzuki (H)

Department of Respiratory Medicine, Osaka Prefectural Medical Center for Respiratory and Allergic Disease, Osaka, Japan.

Tomonori Hirashima (T)

Department of Respiratory Medicine, Osaka Prefectural Medical Center for Respiratory and Allergic Disease, Osaka, Japan.

Classifications MeSH