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我父亲肺鳞癌的治疗贴(2014年3月1日驾鹤西去)

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1207275 1620 老马 发表于 2011-10-27 08:05:18 | 置顶 |
老马  博士一年级 发表于 2012-4-27 18:50:42 | 显示全部楼层 来自: 浙江温州
Pooled Analysis of S-1 Trials in Non-Small Cell Lung Cancer According to Histological Type
$ l5 _, E" P" m$ eNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
6 o6 A% a7 }0 q7 P& L& A" t+ Author Affiliations
" J" v9 U. K4 Q( M  t" c2 I3 _" g; h4 D& d
1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan $ [4 K# |7 a( y; B
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
4 Q* X) F1 N" z; M% t3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan & W8 ^. f. @7 C& \2 }6 m2 b  a
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan # e) T8 w+ M2 O9 d" W
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
# a* K' ]5 b) X: q! c. ^& F6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
/ I9 d. j% f+ L7Kinki University School of Medicine, Osaka 589-8511, Japan ! ^3 E6 }: b: l
8Izumi Municipal Hospital, Osaka 594-0071, Japan
1 t9 K' h- i1 ]: R. E5 }9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan 7 ^+ g- X' q4 g. ?) k
Correspondence to: Nobuyuki Yamamoto, Division of Thoracic Oncology, Shizuoka Cancer Center, 1007 Shimonagakubo, Nagaizumi-cho, Sunto-gun, Shizuoka 411-8777, Japan. Tel: +81 559895222, Fax: +81 559895783, e-mail: n.yamamoto@scchr.jp ) q& j6 Y2 C) n
AbstractBackground: The antimetabolic agent S-1 inhibits thymidylate synthase similar to pemetrexed, but through a different mechanism of action. Whether the antitumour activity of S-1 depends on histological type remains unclear. We analysed pooled data from 2 phase II clinical studies of cisplatin and S-1 in patients with previously untreated advanced non-small cell lung cancer. Patients and Methods: We comprised 110 patients with stage IIIB or IV non–small cell lung cancer. Univariate and multivariate analyses were performed to determine the effects of histological type on progression-free survival and response rates. Results: On pooled analysis of the data, according to histological type, median progression-free survival was 3.8 months in patients with squamous cell carcinoma and 4.4 months in those with non-squamous cell carcinoma. Both analyses showed that progression-free survival and response rate did not differ significantly. Conclusion: Unlike molecular targeted agents and pemetrexed, a combination of cisplatin and S-1 may be no difference in response according to histological type. ! i& ?" A# `" {! d7 z% `2 W

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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:52:43 | 显示全部楼层 来自: 浙江温州
S-1 monotherapy for previously treated non-small cell lung cancer: A retrospective analysis by age and histopathological type   e- [- F8 v6 M
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Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
3 W" J6 ~4 J, f
& V+ j/ o% X1 F8 n& IAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  2 f; y( D/ [& u, n+ ^
5 {: W5 I- n% I1 u2 t  Y; F
Published online on: Thursday, December 1, 2011
8 Q; @0 V+ [9 |. e$ Q1 l4 O+ j
: O# f4 X3 P0 q, |* n& ^' W4 CDoi: 10.3892/ol.2011.507
$ @6 W' ]4 {; \" D% A. B2 h9 O" M' n/ R, q6 s/ l
Pages: 405-410
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Abstract:) Q$ V! p# I) \) s5 J& b- |0 C/ W7 w, b! x
S-1, an oral fluoropyrimidine derivative, has been approved for the treatment of non-small cell lung cancer (NSCLC) in Japan. In the present study, the efficacy and safety of S-1 monotherapy for elderly patients with previously treated NSCLC were retrospectively evaluated, and the efficacy of S-1 monotherapy was compared by histopathological type. This retrospective study included 54 patients with advanced or recurrent NSCLC who had received S-1 monotherapy following the failure of previous chemotherapy regimens at our institutes. Patient outcomes were compared based on their age and histopathological type. S-1 was administered orally, twice daily, while the duration and interval were modified according to the medical condition of each patient. The default delivery schedule, the mean number of S-1 cycles, did not differ significantly between the two age groups (<70 and ≥70 years). The rate of therapy discontinuation, schedule modification or dose reduction due to intolerable toxicities or patient refusal was relatively frequent in the older group (40.7 and 55.6% for ages <70 and ≥70 years, respectively; p=0.414), and the incidence of grade 3 anemia was relatively high in the older group (3.7 and 18.5%, respectively; p=0.192). The response rates (13.0 and 4.8%, respectively; p=0.609) and disease control rates (39.1 and 33.3%, respectively; p=0.761) did not differ significantly between the two age groups. According to histopathological type, the disease control rate was significantly higher in adenocarcinoma (57.9%) compared to non-adenocarcinoma (20.0%, p=0.013). Thus, S-1 monotherapy may be equally effective and tolerated in patients <70 years and those ≥70 years. Additionally, adenocarcinoma may have a higher disease control rate than non-adenocarcinoma.1 N8 b& C" h) ]& V  T8 g2 y
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:57:27 | 显示全部楼层 来自: 浙江温州
Thymidylate synthase (TS) gene expression in primary lung cancer patients: a large-scale study in Japanese population
$ R% u# ]. e! h. B& }8 mF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
4 c3 c$ m5 V& R: a- l+ Author Affiliations% t  b; w$ j8 T5 P( d
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu ! P6 q0 s% @# u" B
2Department of Thoracic Surgery, Kyoto University, Kyoto
4 W2 I- a# K, r8 a' z7 r% ?, |3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan $ l4 ~, N7 J0 a/ ?8 |$ q# w
&#8629;*Correspondence to: Dr F. Tanaka, Second Department of Surgery, University of Environmental and Occupational Health, 1-1 Isegaoka, Yahata-nishi, Kitakakyushu, 807-8555, Japan. Tel: +81-93-891-7442; Fax: +81-93-692-4004; E-mail: ftanaka@med.uoeh-u.ac.jp 8 b# {; Q1 D3 R
Received September 3, 2010.
$ X1 W- B* f# M1 x7 NRevision received November 11, 2010.
% `. a" X3 A8 `: H. o; BAccepted November 17, 2010.
0 m" Q2 N# t' Q& T& m8 IAbstract
% K- \6 f3 q. e; G: i1 E' EBackground: Previous small-sized studies showed lower thymidylate synthase (TS) expression in adenocarcinoma of the lung, which may explain higher antitumor activity of TS-inhibiting agents such as pemetrexed.
9 l/ ]* r7 `1 k. E! c$ bPatients and methods: To quantitatively measure TS gene expression in a large-scale Japanese population (n = 2621) with primary lung cancer, laser-captured microdissected sections were cut from primary tumors, surrounding normal lung tissues and involved nodes. 2 A/ U: n& s, C
Results: TS gene expression level in primary tumor was significantly higher than that in normal lung tissue (mean TS/β-actin, 3.4 and 1.0, respectively; P < 0.01), and TS gene expression level was further higher in involved node (mean TS/β-actin, 7.7; P < 0.01). Analyses of TS gene expression levels in primary tumor according to histologic cell type revealed that small-cell carcinoma showed highest TS expression (mean TS/β-actin, 13.8) and that squamous cell carcinoma showed higher TS expression as compared with adenocarcinoma (mean TS/β-actin, 4.3 and 2.3, respectively; P < 0.01); TS gene expression was significantly increased along with a decrease in the grade of tumor cell differentiation. There was no significant difference in TS gene expression according to any other patient characteristics including tumor progression.
4 p6 X* v  |# }& b( sConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. 4 C5 U& e8 E- h! i4 @- F) m
个人公众号:treeofhope
走在异乡  高中一年级 发表于 2012-4-28 00:30:22 | 显示全部楼层 来自: 四川成都
一直关注老马的帖子,前方的指明灯。祝福你爸好疗效
累计签到:1 天
连续签到:1 天
[LV.1]初来乍到
baiselianyi  初中二年级 发表于 2012-4-28 10:24:44 | 显示全部楼层 来自: 浙江台州
一直得到老马帮助,祝福老马爸爸
老马  博士一年级 发表于 2012-4-28 18:00:37 | 显示全部楼层 来自: 浙江温州
26日吃了12片地米(0.75mg一片),27日吃了22片地米(0.75mg 一片),28日吃了12片地米(0.75mg一片),都分二次吃。
0 p6 O/ g1 H" }9 n; P) }今天为止没有任何反应,每天吃VC,VB2,还有漱口水,就怕口腔溃疡。
个人公众号:treeofhope
bishop_cn  大学一年级 发表于 2012-4-28 23:16:11 | 显示全部楼层 来自: 中国
副作用如何,单药反应很小吧?
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老马  博士一年级 发表于 2012-4-29 00:20:00 | 显示全部楼层 来自: 浙江温州
LUX-Lung 8: A Phase III Trial of Afatinib (BIBW 2992) Versus Erlotinib for the Treatment of Squamous Cell Lung Cancer After at Least One Prior Platinum Based Chemotherapy
- T& g2 u! j& o* U3 ~0 }( t0 Nhttp://clinicaltrials.gov/ct2/show/NCT01523587. v  X( C' J# \9 o' {
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
2 b) T7 [. ?8 G; E% |" Jhttp://clinicaltrials.gov/ct2/show/NCT01156545
个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-29 20:53:58 | 显示全部楼层 来自: 浙江温州
本帖最后由 老马 于 2012-4-30 09:33 编辑
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从4月24日开始到4月28日,打了5天的舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。
3 Q! o. y1 v; ?, t" r5 ^% j$ K! z至今为止,未出现化疗副作用。
个人公众号:treeofhope
英雄武松  大学四年级 发表于 2012-4-30 01:37:05 | 显示全部楼层 来自: 哈萨克斯坦

2 G$ i, N7 y% G! I5 c3 U没有副作用是第一追求,效果显著是第二追求。
1 H$ r* {. P. K$ I7 p不错。

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