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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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1252742 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- o1 s* A! S2 M5 L5 [
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 3 ~) b* i; X3 S' l2 V& r
+ Author Affiliations
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* T- k/ j7 H' D: I- e/ @2 L5 u+ G! A1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
7 p2 d; l5 H) f) }2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
8 H4 b2 O1 n8 k) Z$ b6 K+ W3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 2 x, r* [. F( y! @: c
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
8 K  q$ }& W1 ~2 a2 h5 m# C# I5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan 5 d% e: B+ e: ~6 n) |8 h
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan ; B0 R" n5 k. b* R+ x: H
7Kinki University School of Medicine, Osaka 589-8511, Japan
1 j$ E3 X& x1 H; w! I  ?8Izumi Municipal Hospital, Osaka 594-0071, Japan
  b. r4 j; L* a' `# E. A9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
5 @9 W' E: E/ eCorrespondence 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 9 e; N! ?. z1 B/ ~. b. l- K, 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. ) X1 h! N. g$ @0 {
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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 - X' M3 P: o' L' A$ J* N
5 o4 _5 w3 {: a
Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
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Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  4 ?1 ?0 ^& j& E0 o( r3 l
7 Q2 q( K5 E2 A2 d
Published online on: Thursday, December 1, 2011
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/ `# s: O! \/ b. F$ t( ~Doi: 10.3892/ol.2011.507 2 J& b, @  k- g8 r

" q4 B5 ?0 z' ~2 [, h  c* r; dPages: 405-410
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Abstract:9 P  k# M7 N# j/ g
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 population5 \/ Y0 Q3 Z8 ?4 d
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
! J% M" ?5 d; w$ W# a0 @+ Author Affiliations+ ?4 z# j% y3 f
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
# J& ^5 b5 c- ^4 T2Department of Thoracic Surgery, Kyoto University, Kyoto
+ m' N$ i5 E' R: F1 K3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
$ ~0 \# G+ }. Q. R1 M&#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 / \& j/ O% j) p) X
Received September 3, 2010. . A& n9 j! S; v; t
Revision received November 11, 2010.
0 J$ l- ?6 o5 m7 T, GAccepted November 17, 2010.
" D7 F, @+ f$ D, Y5 r6 u5 jAbstract
+ g% J* r3 w! o. x& [% hBackground: 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.
* Q% F: i/ g! F7 h. Y" fPatients 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.
5 b, p, G  k* x/ q2 h' NResults: 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. 5 f! G3 b% K5 Q# X4 B
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study.
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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。/ F9 {: z6 `; U) a! _! J4 O
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* f/ M- R% D* b" I6 w3 ?3 ?# S
http://clinicaltrials.gov/ct2/show/NCT01523587& S: C% ~) W, c+ X

" ^: `% }4 G6 y* ^& n; hBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC/ }. e# d$ l) O4 Z% e! T1 ?
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 ; A9 R0 ?! |6 X( \

# w% m- a. f0 {0 ?& ^2 m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。
+ m& f: }! e# }3 C. \, U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 # P1 [1 S( }( R0 N# X
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 t5 r" B" E% p8 ^5 G. @. w: r
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。6 _4 C: Y1 ^  X0 O+ U7 X* P% r  K
不错。

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