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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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1399823 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 Type6 F! R  L! X$ p
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
. M7 t, ^" x; Y+ Author Affiliations
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; A: s1 D" H( q' `  K1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan & T; v. `5 A5 a, S2 W! A
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
8 k. }: N" y5 m7 S' K7 n3 t3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan   r1 N$ W/ l" i, Z  ]. T
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
. d+ x$ A$ J& q2 V- P; n6 {5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
/ R; }  J3 s6 h7 ?/ A: ?( G6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan ( Q" d* L! y. S
7Kinki University School of Medicine, Osaka 589-8511, Japan ( h/ R" s9 P( m3 z$ b6 g4 e: C
8Izumi Municipal Hospital, Osaka 594-0071, Japan " l% O" m- @: {* l4 q5 R+ Q/ X0 j
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan * m( o  M' p" e/ j! |
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
% [: c1 r% B; U5 k( n# GAbstractBackground: 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. 5 F% x( q7 Q* c7 M* L
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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
* K; F1 @( O3 M6 i9 ?; c9 P) u+ O5 {* P( p! `' C! _
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
0 ^3 d& G' L5 F( k1 P# s1 O% ?4 a$ ^4 O3 G2 P, K# e7 x
Published online on: Thursday, December 1, 2011 + R  l6 G" p5 H& W4 {7 a# D

9 g3 ^8 V$ V+ y5 h1 o) Q' F0 BDoi: 10.3892/ol.2011.507 7 s# Y+ N7 f; q! }( U) r0 K& Z$ ^

/ x5 K+ p" ^! t9 z) M# k5 N0 e/ @Pages: 405-410 - ]8 D! d! m, Q9 |# f; v, z- {" u) E
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Abstract:# I" ]9 w' F$ c& a  @8 r4 c
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.  \) p3 j7 U/ Z6 s5 K( p$ C
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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 population0 z: I9 ]- S$ r9 s) [. w0 k
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 ( ^) ?' R3 ~& w2 G* I7 k' W
+ Author Affiliations# ?: _! F' p& o
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
# h7 Q& y" e% @8 O2 p2Department of Thoracic Surgery, Kyoto University, Kyoto 1 Q, P8 c( w& t  {/ T  ~' g
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan . w  x5 `. S* H% {1 ?
&#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 # h6 Y2 V2 S7 T- [) a6 m
Received September 3, 2010. / c6 Z1 n/ ~" W3 E% M1 Z
Revision received November 11, 2010.
- I! f- R# c# [/ q: _/ N, Z3 PAccepted November 17, 2010. , H, L6 V6 ~1 O  M+ I4 H' F
Abstract
# s+ R  @. g( H1 s( y8 w! R. GBackground: 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.
+ r; e7 D  ?. Q, A9 t2 ?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.
$ n$ @. z. c( D" w+ @* A# jResults: 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. ( Y; g1 j- 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。8 C  ~/ t, s, `0 E' ^1 ^
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
) K1 g8 j' l6 V) K; I. c. mhttp://clinicaltrials.gov/ct2/show/NCT01523587
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" @7 @% [7 C: a, g7 s8 zBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
' |4 `$ Q* p. Z/ E2 Thttp://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 ; }1 A3 J1 ?: m4 Z/ f

+ t) i9 d8 }5 s$ e% N* _4 f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。9 ]( L' l" G5 \4 B; M
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
! B  Z0 A. G( o; b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。: z6 Y8 S. [6 J- p; u8 ]5 e
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。, r0 j' M. \. V+ M0 U
不错。

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