A Retrospective Study Investigating the Safety and Efficacy of Nanoliposomal Irinotecan in Elderly Patients with Unresectable Pancreatic Cancer

被引:1
|
作者
Ikoma, Tatsuki [1 ,2 ]
Matsumoto, Toshihiko [1 ]
Boku, Shogen [1 ]
Yasuda, Tomoyo [1 ]
Masuda, Masataka [3 ]
Ito, Takashi [3 ]
Nakamaru, Koh [3 ]
Yamaki, So [4 ]
Nakayama, Shinji [3 ]
Hashimoto, Daisuke [4 ]
Yamamoto, Tomohisa [4 ]
Shibata, Nobuhiro [1 ]
Ikeura, Tsukasa [3 ]
Naganuma, Makoto [3 ]
Satoi, Sohei [4 ,5 ]
Kurata, Takayasu [1 ,2 ]
机构
[1] Kansai Med Univ Hosp, Canc Treatment Ctr, 2-3-1 Shinmachi, Osaka 5731191, Japan
[2] Kansai Med Univ, Dept Thorac Oncol, 2-3-1 Shinmachi, Osaka 5731191, Japan
[3] Kansai Med Univ, Dept Gastroenterol, 2-3-1 Shinmachi, Osaka 5731191, Japan
[4] Kansai Med Univ, Dept Surg, 2-3-1 Shinmachi, Osaka 5731191, Japan
[5] Univ Colorado, Div Surg Oncol, Anschutz Med Campus, Aurora, CO 80045 USA
关键词
nanoliposomal irinotecan (nal-IRI); pancreatic cancer; elderly patients; nutritional status; HEPATOCELLULAR-CARCINOMA; NAB-PACLITAXEL; GEMCITABINE;
D O I
10.3390/jcm12103477
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Although nanoliposomal irinotecan combined with 5-fluorouracil and leucovorin (nal-IRI+5-FU/LV) has been used to treat first-line resistant unresectable pancreatic cancer, the efficacy and safety data among the elderly remain limited. We retrospectively analyzed clinical outcomes among elderly patients. Patients treated with nal-IRI+5-FU/LV were assigned to the elderly (=75 years) and non-elderly (<75 years) groups. Herein, 85 patients received nal-IRI+5-FU/LV, with 32 assigned to the elderly group. Patient characteristics in the elderly and non-elderly groups were as follows: age: 78.5 (75-88)/71 (48-74), male: 17/32 (53%/60%), performance status (ECOG) 0:9/20 (28%/38%), nal-IRI+5-FU/LV in second line: 23/24 (72%/45%), respectively. A significantly high number of elderly patients exhibited aggravated kidney and hepatic functions. Median overall survival (OS) and progression-free survival (PFS) in the elderly group vs. non-elderly group were 9.4 months vs. 9.9 months (hazard ratio (HR) 1.51, 95% confidence interval (CI) 0.85-2.67, p = 0.16) and 3.4 months vs. 3.7 months (HR 1.41, 95% CI 0.86-2.32, p = 0.17). Both groups exhibited a similar incidence of efficacy and adverse events. There were no significant differences in OS and PFS between groups. We analyzed the C-reactive protein/albumin ratio (CAR) and neutrophil/lymphocyte ratio (NLR) as indicators that could determine eligibility for nal-IRI+5-FU/LV. The median CAR and NLR scores in the ineligible group were 1.17 and 4.23 (p < 0.001 and p = 0.018, respectively). Elderly patients with worse CAR and NLR score could be deemed ineligible for nal-IRI+5-FU/LV.
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页数:10
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