• 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]
1155513 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( [! h' x. @7 c7 s) {- n: J
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 ' t, \. k) e$ \6 v! B0 q" t
+ Author Affiliations8 L) S: C( Y! V+ [2 K
3 P! e) L% o8 i7 j- z
1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan : [' p" V2 P: n; I9 y( G8 J: Z1 O
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
; B6 V# Y; v0 L% P3 B3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
! ], H. n6 O9 X! k5 q. y: X4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan 3 v, h7 _3 z( l6 M5 \3 ?6 V) q
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan 8 U& [4 h9 ]. I2 T. r% R
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
1 W2 S3 S( ]$ Q. c/ O+ R7Kinki University School of Medicine, Osaka 589-8511, Japan & Q7 x9 H9 a; v' s
8Izumi Municipal Hospital, Osaka 594-0071, Japan
' }  Z* W- i7 ^! e7 A9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
8 y4 o+ H2 Y- 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 2 [3 e5 }4 U7 m! t2 E$ m
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. & M0 i2 i3 [8 V# A4 x: K6 U
/ n( n% R/ P6 f. z" E$ ]$ o0 F$ R
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 0 v3 {( H/ l4 S; Y  n! v, A$ {
- z& I3 }: \1 |5 O* B8 Q; Y* U
Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato . K$ Z5 ~. G6 b7 Y1 k  N
$ p6 c4 h8 G2 [! L1 c
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
4 s  F# T0 O" ~) ~% J3 p- d3 N; F
, Z/ j/ x5 K4 }$ L' H! N4 P0 UPublished online on: Thursday, December 1, 2011 & H3 E+ T' T9 v) V/ l

4 i1 n. C' s( c; gDoi: 10.3892/ol.2011.507
' {/ o9 w) H6 ]* M5 H5 Q
. v# K3 w7 U5 h) J# ZPages: 405-410
* [$ M: y6 u! Y; y. P2 y7 y, L% ~3 P2 Z, U8 `4 G
Abstract:) B7 w5 G. H' L& N, D5 t
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.8 |. i, [0 L& w2 @: ]

' i  N! E$ B# Y2 k3 h4 v
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
: R7 G2 @6 S# @F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
4 T! A  |! Q+ j+ Author Affiliations; g- B5 W3 Z' c( N
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu ; ^. n" o7 l2 l7 K# C( E
2Department of Thoracic Surgery, Kyoto University, Kyoto ) u% W: j" [& r4 ^
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
9 r  s; u3 M( Z! K&#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
# z1 Y6 d4 q6 R" ~2 aReceived September 3, 2010.
$ _+ c, U9 M- \+ m# qRevision received November 11, 2010.
8 E5 E8 i* P4 U1 k( XAccepted November 17, 2010. " f1 T  _0 Q. C. q7 s  F( V  R
Abstract
7 {( U) E% Y  F7 i" Z6 D# ]Background: 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.
8 _$ T% p) I1 y) N  w2 [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. 0 c8 {/ d7 M& Q6 S0 ^  b; ~
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.
0 l9 s% L# E' o2 Q+ N# p* @Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. , ~" M/ G' K( h% _. {% C+ E
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。
9 C# X& w  }5 A- L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?, G6 E0 v3 y" a. c; 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
+ ~: t3 @2 G0 Thttp://clinicaltrials.gov/ct2/show/NCT01523587
! J! R, e& {8 P# |3 W- @% y" r# d% U
: \- j4 b, Y* _1 h- _BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC3 \* Y7 \2 R1 H7 a5 k1 f
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 ' t* z0 i7 m# {" `# P4 v
" _0 G5 S' w+ J% r/ b; w
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。
6 F" x+ w* j; O+ L1 w$ K/ Y; f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

) Q  B% J- Z; J没有副作用是第一追求,效果显著是第二追求。
$ C1 a: |% n5 N( r  ^' |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