• 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]
1232738 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
+ C: j! ~0 d5 R8 a" X' o( ZNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 ; P! E1 W$ ]/ M, z* S6 M. X
+ Author Affiliations
/ t' \8 F/ Y! f
, c6 }" ]" }( _0 E1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
8 b1 `0 T% I! i* l  v: R2 Z( V9 u2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan " W% B9 v6 Z( {4 j
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan ' B) E$ I- d! z- m8 a0 Y
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
9 v! C) z  \$ `4 ^+ Z: l5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan # c5 F$ x& S% I  {4 p
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan : ]7 V2 X- ]9 U8 E* ^+ P  ^
7Kinki University School of Medicine, Osaka 589-8511, Japan
5 i: Q4 ]/ p% ?, X9 j0 j" g0 q. H8Izumi Municipal Hospital, Osaka 594-0071, Japan
9 R4 N, y) J: x) ]; `9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan ' N" x: Z6 u3 a, s9 ^2 `! c
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 8 x5 h( O; |) l& x
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. 3 t' x6 j/ y6 }

6 X6 W$ o. B; s' e9 F: I# n
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 ]" l9 ^: w0 F  P% s) Q% c
9 a0 r  {3 U1 M6 ~2 TAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato   m3 \$ ?& y# F* @& m4 L

5 V2 s, ?% W5 B$ K# EAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  3 R& a6 [5 E) o! E5 W$ @

  N+ j, p; [7 `- j3 L, [* m$ SPublished online on: Thursday, December 1, 2011 $ g$ h1 v5 ?* X. l. x% e
- a. R6 ]. P  G$ h& }: B/ `6 u
Doi: 10.3892/ol.2011.507 ) X9 n7 d! ^# B8 o
4 g0 M& z6 ~% F, @. _8 O. d
Pages: 405-410 . \' H: d  n9 b, m3 |* q

, l7 y* \: i" T" L0 f) @5 V, @! cAbstract:! v7 R: T. u% v8 x1 m- R
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.
3 |5 c4 A2 ]& `) D7 G2 m . D; i" m/ I6 }8 n- c+ j
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
# S' V% r- a! S. R% D; Y" oF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 3 ~9 {& `5 P7 o0 q* O! H
+ Author Affiliations
  N* P; _. t7 J/ {9 ]/ w1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu 6 T' P7 {. H( ]  D
2Department of Thoracic Surgery, Kyoto University, Kyoto 1 `* t7 V; O0 r& @9 j0 ~
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
# S+ N! }: Z$ r/ |% N&#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 ; C3 S" J" k! G( d2 \; E9 w
Received September 3, 2010. # @& y' P' ^' ~+ ~% z( `/ o! v
Revision received November 11, 2010.
  b& C9 P9 ]) d# `. rAccepted November 17, 2010.
' L' [- F7 E7 v9 l! _& g3 f/ |$ @Abstract
4 d8 W' \, N$ E* p9 E5 sBackground: 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. 9 b* @/ ~- s2 X- S1 A3 s, M3 s
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. 7 y; k5 R; ^. Z6 S# y
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.   W5 a" k& h2 R; x
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study.
4 l3 B7 N- N5 {" v* 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。
7 D& I! p/ J! I( O1 L! d  u- k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# J3 N0 {2 V! Y6 b! R% u9 l
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
' y# G1 B1 g  j* |% g) s$ m  ?http://clinicaltrials.gov/ct2/show/NCT01523587
  c! e) Y4 F+ b& A% L4 o" R7 A( [4 _' ~  w, Z
BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
. _3 c) _/ z% ~7 ^9 I  c' 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 2 }5 M/ U' Y- h2 D7 d# i
" h6 a. }4 M2 A8 \3 v6 y
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。
: q- M- U, T% i* n4 n, _1 c1 W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
6 q& c7 M- g( T$ U1 R; y
没有副作用是第一追求,效果显著是第二追求。' m7 s3 t, Y' Z4 c2 `; C
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