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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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1410207 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% k5 S3 c" O4 t$ o0 ?% z
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 & V! O, l5 ^; ~
+ Author Affiliations
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" ?. P# g% S' z% d1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
* O; e( J! O% m; t. a2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan . N, a$ U# v6 A; j) }& y: [
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan + l' Z& k. N4 i0 I7 f
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan # c3 M' V3 z1 _3 Q
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan 1 D: G/ n, ~8 Q9 I! a9 r/ c, H* }( l
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan , v' v: c7 M7 Z2 X3 f
7Kinki University School of Medicine, Osaka 589-8511, Japan ; W5 M8 v# q* b( J
8Izumi Municipal Hospital, Osaka 594-0071, Japan 6 H/ H' J0 L- C# M9 k0 z
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan 8 u% j* |3 o4 u) @
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 K- H4 K- y& o+ L; X  y; g
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.
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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 0 U# C' s- Y, V; K# r  z

6 U2 D" C7 K) ~+ G6 p/ pAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
) H$ b. H" t& [+ m6 F5 w" M' P- U2 m3 G- V# _; ~+ U4 X
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
1 m" ^1 \- X! E4 n. o5 |: B! H# H2 l6 i) @1 h" E
Published online on: Thursday, December 1, 2011 ! s* a0 Z+ I2 s2 j5 i
# B" H% B- j" A
Doi: 10.3892/ol.2011.507
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Pages: 405-410 3 y& v/ K4 F0 p4 y& o8 A
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Abstract:) V' V" D% B, z* Y' p( Q$ d1 S
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 population
3 o- ^+ o% I  G! vF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
* E2 R, i! E+ O/ j: S+ Author Affiliations8 N, M/ |* }) e, I  m6 {4 L9 O) T: c
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
4 x9 }& v7 h1 _2Department of Thoracic Surgery, Kyoto University, Kyoto
* I# V* e* n+ Q  h6 L4 J/ q. ^3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
$ Y6 e/ B$ J7 W8 O# |&#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
1 W' r) Z6 ?  O! O5 R5 LReceived September 3, 2010.
# k, [/ ?5 V: I: h" e" A; ZRevision received November 11, 2010.
. ~  M: s! u" Z* `Accepted November 17, 2010. - j. u2 a' W+ Z, l7 K0 D6 n, @
Abstract4 S) U5 s3 {! `! [$ [5 c: z& V' T
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.
& ~1 I5 ]6 {/ |/ x1 ^* P: pPatients 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. % P- \0 a0 p( K2 o- R$ |" z. b5 b# [
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. % G8 _& q- F- c6 w
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. " o7 p" ~0 E2 f$ f6 [( i; H
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。
8 I. R. C5 A3 d5 _# n* R) U# N/ Y& g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- @7 W& k1 J: S2 c  w' K2 q# J3 H( B& r
http://clinicaltrials.gov/ct2/show/NCT01523587$ U5 Y2 n1 K3 a# W( v2 [

1 [# w8 I- j5 A: o& [8 o1 z! ^BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC5 z$ d: E% C9 ]* P# e  J! s# S
http://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 7 Z7 f' f) k& ?- D/ x  m7 m
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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。
7 R) c  ]9 s/ r8 h) |  S) A( p) c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
  ?" k) b3 H1 _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。
& I& q! r: p: H% y6 |3 H, F  u% ^至今为止,未出 ...

% _) A' @- g+ [' T没有副作用是第一追求,效果显著是第二追求。
: {3 m1 c; A9 R2 T( q4 p6 |  _不错。

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