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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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1392131 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 Type4 Z5 [* {8 s$ q3 @: C5 ?1 [+ B
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 3 C1 u- P- M2 `/ d/ V/ v
+ Author Affiliations2 W3 b: j, a; }' V6 z6 T/ d, w

$ N$ m7 d9 O6 q+ C& X5 E1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
, i% J; T2 G" B4 s$ [0 }2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan ! F% j# E8 e- k2 w5 b
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan , f5 r7 q7 J4 z- N
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan " W2 b: y( I6 X7 D1 i8 v9 R0 c
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
- Q* r5 W$ J3 o- q+ o' U6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
" S9 }3 n$ h9 F$ r3 e+ Z7Kinki University School of Medicine, Osaka 589-8511, Japan   y% O/ r9 \+ I# @' ?6 b
8Izumi Municipal Hospital, Osaka 594-0071, Japan * C- d, N  U1 J1 q- `9 ^) f
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
, i0 w  T- X! CCorrespondence 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
& f6 s# X4 I& H& E: z0 Y  {# kAbstractBackground: 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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! K! R# ?3 x. L( {- C, eAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato . @& x9 f* N% u6 ]- {, X

& F( `9 y- e2 m0 w- f/ [# sAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan    J* a2 Q$ ?7 |# K. w7 C' ^

3 S) [$ X! o  Z/ U" gPublished online on: Thursday, December 1, 2011 3 r+ Y" n+ X* B4 o, M

5 m! ]. l# T! c- A/ R5 M2 p, nDoi: 10.3892/ol.2011.507
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+ G) x- t2 v/ `- ?& E9 a! mPages: 405-410 . L: J3 d; \5 q) F6 }' }1 x
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Abstract:. \7 Z* ]( E0 i" p" ]7 p0 i, x; [$ @
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.5 _; A% R7 o$ W

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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* I2 Z0 ?% \, }
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 & D5 y- V! P0 y6 t! D7 |# Q3 j
+ Author Affiliations
5 w- z# `0 F' t2 c, c; V/ x1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
) G5 V1 i3 W7 t. k* ]4 J# V2Department of Thoracic Surgery, Kyoto University, Kyoto
9 w6 _: `* @& C7 I3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan 5 o* ], X% M' y
&#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
; |5 U1 y! P( k- I, Y8 fReceived September 3, 2010.
% S8 _3 f1 U0 ]/ ?- H% URevision received November 11, 2010.
& m/ h' P9 W# {Accepted November 17, 2010. ) X, ]% _% t/ x$ l* p6 _1 {! ]# a
Abstract
4 }9 w$ f# v- G$ r+ [) I; nBackground: 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.
6 A0 i7 ?/ U: E. R) n9 i( T# QPatients 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. 2 A2 U* ]- t9 I
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.
- l7 M2 ^6 F) iConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. 1 Z4 B7 \% B6 e2 ]0 o# G* ^
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。
/ J) @* ?2 i- h9 w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; Y0 ~) ]/ a5 j9 w, z9 r: f) M% o
http://clinicaltrials.gov/ct2/show/NCT01523587
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
# n) Q0 W$ l9 W7 R0 n) bhttp://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
. i6 Z+ @6 [9 S& S  o( h, P) H$ e7 x& J5 ]
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。( W! M$ _  V4 @6 t& B4 \
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
" h+ J. ?- V9 [0 Y' D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。  _; b# L+ p- f% q1 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。
8 m- Z7 n. ~" u+ H, K不错。

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