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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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1131196 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( @6 N- C) m! |" X+ |
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 # _8 N1 N! j! U
+ Author Affiliations8 U4 z( r$ i8 N) N$ y8 b5 u

- o' Z, ^: Z  s1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
8 n- q* ]# d9 [" f8 u# g2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan $ c$ A$ ]' @5 g+ ^; {# M5 U- P. ^) V" q
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
9 F+ t, h  L0 u+ ~7 K  ?% p4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
* F3 d, \( \1 g$ ?6 p% S5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
; Y2 o& C9 \; ]1 N3 S6 v, h1 l6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
$ z% Q; l5 {- ?7 p- I7Kinki University School of Medicine, Osaka 589-8511, Japan 2 P2 J/ w: h, p: M$ v3 ]
8Izumi Municipal Hospital, Osaka 594-0071, Japan & T1 b( F' }7 W' ?; \9 n6 Y
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan / ~+ y3 u' S, g
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
, l; `4 o: z8 \: H9 yAbstractBackground: 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.
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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
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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 # `# f" ]# _* B% j

4 L' M8 N$ Q4 U( YAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
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Published online on: Thursday, December 1, 2011
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! W6 a+ w+ ^, d$ Q' j/ V7 tDoi: 10.3892/ol.2011.507 3 W- {; |# [7 S% ?) t

+ q; V9 n( _; {, w$ b8 G* ~Pages: 405-410 " O0 h8 Q3 z. u/ B7 K( n4 `4 P

3 i8 ?( n# B/ q7 g6 T) f8 p2 R( vAbstract:) Y- }' g4 H& {
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 B4 {9 u0 L# u7 K2 i  Y- D
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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
0 T3 C1 F2 D- ?; C' N" B; fF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
) L2 ^: O2 P- d0 o+ Author Affiliations
' F3 c$ `: r  u# U1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
. k  @+ B8 \7 r, w8 ^2Department of Thoracic Surgery, Kyoto University, Kyoto
6 @& e  W% i7 A& z+ N1 Y3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
) @& c0 b3 `1 m6 b* I+ O7 @&#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
0 }9 B& T& f/ E/ uReceived September 3, 2010.   C" L% e5 ^1 H
Revision received November 11, 2010. & \- p; N0 ^# y; g  `5 M, ?
Accepted November 17, 2010.
% H9 l; P* ]: FAbstract' }( @5 u# T( W- s
Background: 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. 3 |+ N, q' R* R/ o" W/ ]% m
Patients 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.
4 A* C( W5 {6 U( e7 _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. ! _. U& @% L* b, c0 `* `: E, I, K
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. 6 J; c4 Z0 t& Y& e; x$ H+ l1 X
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 w. y3 l4 O" U" P( c" h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" W" k2 b- W! E+ R- k
http://clinicaltrials.gov/ct2/show/NCT01523587
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) e" X" @9 P% I% V* YBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
# g2 R7 E  }' vhttp://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。
% o$ B" J) G& {  O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
老马 发表于 2012-4-29 20:53 1 d! K3 {% f: j( j3 s9 X& N
从4月24日开始到4月28日,打了5天的打了5天舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。+ Z' K& r0 ?' S- [
至今为止,未出 ...
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没有副作用是第一追求,效果显著是第二追求。, y/ l8 G- }/ c. @+ j" U
不错。

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