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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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1110423 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* I5 _6 S0 s  b. ]4 q1 Q# G
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
% r$ B3 j6 m5 n" Y  ]3 b: b+ Author Affiliations/ Q, f0 H5 n( a& _

5 B% y* a/ V0 d, G, V5 x8 M1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
1 l! D( w9 [: @0 {$ u) g1 ]- |9 `. j2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
* A# J3 j, u2 n  M3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan * _: d$ P# F0 k) ^( p
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
9 |# w9 Z9 c" M& k; c: f5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan , w( N9 D0 A  _7 U- H4 `
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
; u6 O; L( O( @1 h1 \  }7Kinki University School of Medicine, Osaka 589-8511, Japan
: B9 ?" [' z: V4 M8Izumi Municipal Hospital, Osaka 594-0071, Japan
! R: C+ `7 m1 w7 u3 {( J  u- s+ _  i9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
- _- H3 y/ I9 M+ N9 ?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
5 F5 X6 @' F4 B# EAbstractBackground: 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 ' A' [6 Z3 ?8 j$ M

$ o! ^0 _. d" w" nAffiliations: 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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$ o6 m( D; m; N* n3 X( g! o' JPublished online on: Thursday, December 1, 2011
. V! \+ ^9 f! S: ~9 L( n- {! F3 N/ d! c% K3 X3 Z3 V! K3 B- A
Doi: 10.3892/ol.2011.507 + m- N1 [" {( l5 h/ }( Y
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Pages: 405-410 3 b6 k# d7 w6 H/ g
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Abstract:5 U' h) c6 F1 E6 ^$ n5 j0 O7 I
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.
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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 population6 K3 l: s0 ?/ V) Z
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
* S5 K; `( w: I: V; B2 O+ Author Affiliations
9 M; E2 O" b; G. K" y1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
+ h" g( ]+ B% ~7 y5 A% D; P2Department of Thoracic Surgery, Kyoto University, Kyoto
4 c; Y2 a% k2 W) E1 h3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
$ T( g6 a" _9 f1 Y. ]- x) f&#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
2 i) w0 F4 v/ m( BReceived September 3, 2010. % l0 f5 S) ?' J+ V' m: Q
Revision received November 11, 2010. ( Z4 ]3 ]3 c) j# R4 x3 G" O- [
Accepted November 17, 2010.
+ s6 j5 S( U1 e% ^Abstract) l9 T9 g7 g* e
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.
0 w+ E' E" C" z2 O4 K" P7 dPatients 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.
8 C0 i. a, b" M$ ZResults: 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. * I  S) O6 ?3 G1 y
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. " A# J( Z" A3 h: A& P4 G$ U  `  ~
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。+ G! {& y2 T$ }
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
8 L4 h( H- [" @; Z" x5 ?/ q* Phttp://clinicaltrials.gov/ct2/show/NCT015235876 D& o+ h/ C( H* A5 x$ c$ B
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
& ^, P( a' X+ Q8 G& khttp://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。
  f9 C. d" X4 s! g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 $ l: y& k& Q. V/ L! K
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。
4 Y+ J, ~. M+ @8 ?/ R7 Z至今为止,未出 ...

9 f) b7 |* b5 v  y; F0 l' u! @没有副作用是第一追求,效果显著是第二追求。% m, ^3 {+ ~6 `! q8 t7 @+ Y) `4 G/ S
不错。

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