• 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]
1306981 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
$ P4 H( Q4 O5 U5 I( u/ A. MNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
; E. z) z9 r# ?+ Author Affiliations. U& ?" E0 k- L- l) Z8 H5 j

* t- c4 `+ h2 g- V, f1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan 7 X! C& G8 G: S5 O" k6 o9 y' L# D1 T
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
. ^* `) D& h8 v) w4 L0 |3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 6 A$ ]4 v0 z, r
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
" o' m9 V9 ?7 ~- s% d/ B5 J+ o5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan # M9 U; R1 v% [
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan / M; j9 M" J0 Z& o( t7 v3 i+ h9 Q
7Kinki University School of Medicine, Osaka 589-8511, Japan ' A8 |( }8 z! `$ ]. ~6 G
8Izumi Municipal Hospital, Osaka 594-0071, Japan
# A% D7 {$ [: d5 l' H' d9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan . ^" b1 i- _4 v% u
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
  o& |: K7 t4 x6 N: `$ WAbstractBackground: 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.
8 K$ G& x- J& D' l7 F& q5 p9 p
- x% R9 b5 I2 U+ G9 F
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 : \7 m; B% M/ o7 Z

; U2 ~0 Z; _. ?3 U1 @: m7 XAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
0 Y3 J$ a/ V$ M- |- J3 _. [* h
$ W. ]* A& B9 X% r% Q1 aAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  $ |5 A4 _. H6 i) n
8 s; A1 ^2 o5 Q/ L# [2 s2 y8 _/ n
Published online on: Thursday, December 1, 2011
% a0 ?' p# g' i. ?3 W
9 l3 ^6 F: L: t& XDoi: 10.3892/ol.2011.507 - S) W, [+ a; f
& h  n6 s$ [  C; H) J4 `* f
Pages: 405-410 $ n! A# r& Z" t

; O' K" [& R# P! v8 a3 p( }Abstract:
7 g) X7 c/ k  `& @( BS-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.
9 s# G3 t. r$ k" T. F $ c- d5 @% J; T! @! b
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
; P  W% N  I& w# X3 {F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
( _. b2 K( |$ ?. q& ]9 ]+ _2 E+ Author Affiliations# l! V5 R! a- u% E. u: q* r
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu : T+ A5 W% Y1 F9 }
2Department of Thoracic Surgery, Kyoto University, Kyoto $ ]) z; ~6 r4 h: _
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan 1 ~1 \" Q9 M$ w, F
&#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
( {1 g* o" }8 p9 IReceived September 3, 2010.
9 S' ]1 w  y4 C5 a, k# \# mRevision received November 11, 2010.   `" s: A/ ]$ h: S8 N' v
Accepted November 17, 2010.
& }) z) A1 ?/ P: |2 f; _Abstract
7 s% x5 z8 `# KBackground: 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.
7 K6 a/ y3 B& m0 ?" cPatients 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.
  M9 j. G, q. a  d3 n# g) L$ uResults: 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. ! J/ J) V  ?6 |6 Y. O, V' X% e: s6 g1 @
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study.
( x, |# O  q) k
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。6 D/ T5 Y) E- f5 U) R6 m+ 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?2 t5 @* g* _- z& y
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- A5 A# W( U  P8 T, u$ X
http://clinicaltrials.gov/ct2/show/NCT01523587
1 |8 O* a2 ]3 g7 o7 f& M/ K2 G4 h9 R/ \. z2 C! k' S: e7 ]) F. L, K9 `
BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC) e! l1 W# x$ O* B& F. x4 m- z
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 2 s: u4 o' X6 n, t2 ?

7 z+ t' r7 l- b1 s& F+ ?$ i3 w+ w7 E7 q  }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。" Z1 M# C0 w* K% |& ^
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 @& n- t3 I! x& m# ?: e4 n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。
! o* s$ ]; X, K, T至今为止,未出 ...

4 m- p* Y4 j, a* ^' \2 t- a没有副作用是第一追求,效果显著是第二追求。( d( J7 R) p, F( Y; O
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