• 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]
1252960 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+ X+ l8 r5 s1 f  O+ T( Q2 y6 J
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
4 r, b% j: S2 {+ Author Affiliations
$ ^6 F9 i0 P( L& H5 C/ s) x+ {9 u# a: o7 O& j. x& i. e; b3 i
1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
. G6 k" B. T: @) C& L2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 5 E% S/ L& d! Y; E. ^4 o& d: M# B
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan % m. d$ F5 j6 M* D- U
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
& n* s* u9 R( T% A8 L- a2 x/ ^5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
7 T, X* G6 o  M4 z3 H! d/ z6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan 8 K! y1 h) x: ]  v3 M- {$ Y
7Kinki University School of Medicine, Osaka 589-8511, Japan $ p! ?% e; |* |( m; \& o
8Izumi Municipal Hospital, Osaka 594-0071, Japan
* I$ V+ b' }' U2 q' W9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
! Z4 u' A/ l2 J4 i! bCorrespondence 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 ) _. l: y5 ^( g  r( k1 ?! y% T
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. 9 k& I1 L5 h+ N4 F# Z: D1 ~0 f9 E" t* N

6 Y* I' D# z6 r  q7 P8 D% u2 ?
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
1 N( N" M2 H6 B2 k  H5 R
# D. _. y0 ^9 ~+ Z1 q5 J! A5 g$ x4 S8 iAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
5 |. T- h8 k! ~' e# e* I* X% x8 u  _# H7 k/ M$ ]: X* @8 m
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
  l6 ~) P& f* A& P( s$ a
3 S' g3 c9 R8 h$ @6 F0 S# bPublished online on: Thursday, December 1, 2011 / O, _5 v1 T9 S+ C  I

2 k' F* D) m" i7 {9 B) aDoi: 10.3892/ol.2011.507
& W' p5 G, k& v( e( m9 ^+ U; }& Y1 g$ S+ j0 A0 f. H' }3 Y/ a# F3 g
Pages: 405-410
3 g: y: t1 u0 X3 O# }4 K7 A
: S8 o: o, q5 V7 l4 X- w/ QAbstract:5 n& O1 H/ f' n/ ^
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 k8 I8 B( S0 |8 D ( I+ N' Q2 ~4 }3 w: K( T* z- r
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. i, q- K7 W8 ?, D/ H2 j7 g
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 1 t. O' y& d7 ^
+ Author Affiliations
/ j9 m7 d4 F* R$ Z: T1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
) E3 l+ E- ~& L: `8 w7 C2 n3 q0 I6 w2Department of Thoracic Surgery, Kyoto University, Kyoto
# o) ]/ s/ v" K4 E0 v+ \2 N& C8 Z! s3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
: X9 }$ A0 i0 U9 B&#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 , q0 n/ i/ |8 d- y
Received September 3, 2010.
* u' I3 o9 S, U; p3 D- k* r) GRevision received November 11, 2010.
& \! K& }2 e- }1 mAccepted November 17, 2010.
# ~: ]# p( K$ j/ x; q5 ~Abstract
* B) e4 [0 T; t$ {! p# x8 I& IBackground: 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. : D! F+ X, f* @  b& V1 {
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.
, b4 [5 Q1 B- M5 P+ a4 b1 F/ _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. 4 |, O& C4 i( Q4 L8 j  p: ~
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. ; Z# B6 s0 F# J& W5 p% u1 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。
: M+ A+ \) x; \: A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?+ D2 F2 h! Z% m; v
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  i# j6 o3 q$ R
http://clinicaltrials.gov/ct2/show/NCT015235871 c' |; b5 {4 p0 `% l) n+ {

% a( K/ h9 U4 S! p1 D0 ]1 KBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
  Q' [. p. a3 `! t% J" K" N4 s- F* chttp://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
/ O* i* B, E8 e, S/ f) F. G" l) A6 V0 o7 s1 ?
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。
* x# m( o/ ]5 ?" H5 _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
7 T) {, i; U% f( u% w
没有副作用是第一追求,效果显著是第二追求。
0 `* J3 b; o# K) {1 G: l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