• 患者服务: 与癌共舞小助手
  • 微信号: yagw_help22

QQ登录

只需一步,快速开始

开启左侧

我父亲肺鳞癌的治疗贴(2014年3月1日驾鹤西去)

    [复制链接]
1227400 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. V  [: U6 m8 @* z
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
- f1 t6 _; M7 G  R1 j% [5 H+ Author Affiliations
8 R$ b' Z- {* ?  O. k- k5 X1 N3 p
. g7 U* W) d" A9 l: n3 h5 Q1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
7 ]; u' z% W# b) m2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
2 w3 V8 d0 w3 G- `" E! R( L3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 5 u6 @% J2 }2 ~. }- [4 E4 r- D
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan ; F% a$ W0 s2 Q4 @$ c* A) @: ]  A
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan : `- @2 V& a" U
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan + I% U: n/ {, v
7Kinki University School of Medicine, Osaka 589-8511, Japan # @/ o' u1 N" S( Y# f# K" w
8Izumi Municipal Hospital, Osaka 594-0071, Japan
& g' H$ w; x* p( X, L$ j1 ?$ T9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan & g' o) n9 z6 v7 U9 `( g$ J, J- s
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 + Q* Y& X- k$ y$ N+ p) f
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. 2 g# }- T5 s, d. V' F+ E$ S& }' q
% Y5 l! z; ?, j! `4 X3 `
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 5 y+ P: f! s7 I3 q
3 {. A1 Z& y6 Y. m
Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
0 `" b( o8 j! T. {% u8 E% i. T) \+ V# t# G4 r) S
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
, W6 w' |# O$ U2 [6 Q/ X
! f( o7 i* z5 c2 R- k9 DPublished online on: Thursday, December 1, 2011 ' U. f$ g$ Q+ g1 x7 C

, K: |" r2 m9 K3 eDoi: 10.3892/ol.2011.507 / _1 e% a- v2 V  H: f6 n+ M; ]
- j: y/ c" k9 J. y' d
Pages: 405-410
0 i) r. P: K- ~: l3 j0 Z( C# Y% n- Y/ {; X/ i! q* p+ C& m
Abstract:" C0 |0 \( \0 s5 f4 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 q+ Q7 r& ^0 M" B " j+ c( J% w+ V$ M1 M" y; n  o9 Q
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* M: b3 `6 Z1 b: E2 {' \% F
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
- K* t: h0 ?( M5 I, r+ \5 w+ Author Affiliations' W, O5 t7 \5 A1 G
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
* }- V- [4 O$ m7 o# X5 F* w& h5 H2Department of Thoracic Surgery, Kyoto University, Kyoto ) m2 l+ t. T$ f' F* k2 m$ j
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan % k* h; N  y# D0 Y. ^$ E
&#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 M! Y1 y* P2 W2 {! K0 RReceived September 3, 2010. 3 z; e) {2 |$ [+ j0 P1 k/ I
Revision received November 11, 2010. / d* K; v2 ^/ q# x$ I2 g
Accepted November 17, 2010. 8 ^" B- N+ K9 U8 _4 i/ N" C5 q
Abstract
. n- O$ s# c  T% G2 m: mBackground: 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.
: c) M& H3 C  F8 aPatients 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. 4 H  i4 W4 S$ L2 D0 ?, k* \4 D
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.
8 r  n* q! k3 z) i6 i6 R/ @( @Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study.
9 y- w& `- J$ X4 y( D
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。4 _. L* ?8 X, O: e6 F0 H, h
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?
, G; s7 y. Z- Y  S7 ^& |
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
6 {8 t( c. w: {2 hhttp://clinicaltrials.gov/ct2/show/NCT015235872 A/ S+ r* S1 `* l5 S" L$ d

. `& a( Y/ Y* {9 y( a4 ^! o# RBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC  k4 s6 W" g/ _$ J: g
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 ; \, k5 C  ^5 b
1 `' o& E( R3 [" V
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。
5 C- Z8 X1 I! I1 G! 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
4 l& }; X+ \1 j( U+ {, 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。5 @  a& {& B) {; @2 j, t
至今为止,未出 ...
1 a" @" }+ K/ w" j, m
没有副作用是第一追求,效果显著是第二追求。
/ U+ o9 @- U5 ]4 e# R! p) s& N6 X不错。

发表回复

您需要登录后才可以回帖 登录 | 立即注册

本版积分规则

  • 回复
  • 转播
  • 评分
  • 分享
帮助中心
网友中心
购买须知
支付方式
服务支持
资源下载
售后服务
定制流程
关于我们
关于我们
友情链接
联系我们
关注我们
官方微博
官方空间
微信公号
快速回复 返回顶部 返回列表