• 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

手机动态码快速登录

手机号快速注册登录

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]
1466024 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+ u) b7 N7 H! n* |  G6 I+ I
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 / d0 a6 j$ c; C$ Y+ K( H7 x
+ Author Affiliations" V9 a! q1 S3 n

7 G0 x. S1 S, `0 C) t' Q6 L1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
& g9 V* H: W3 `7 f( N& }3 l+ L. u1 W2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 0 I9 y: }5 k1 D+ m! @
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
9 W( F/ J5 N& z/ Q4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan ' J' y7 A# |3 |( m3 f* v
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan & j4 D! i) H, W/ U8 H. }
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan / P, @2 h( h+ k7 h& Z  s7 q) |# L
7Kinki University School of Medicine, Osaka 589-8511, Japan ( w% p  [& }0 k- e5 |
8Izumi Municipal Hospital, Osaka 594-0071, Japan 7 h+ o! H0 x- p, Z
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan ; a2 N5 o+ g1 U- k0 |1 \
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
$ l% m; x: S1 K" L  EAbstractBackground: 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. " F! y; F2 x) X% W  d) s- `/ X* L
8 M5 _2 {% s3 D/ H
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
9 _# F/ T4 `: [6 B) f" P1 b
3 x1 I9 h- B  H  J$ iAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato / d) ~0 O/ ?8 ^4 `
6 K3 d- X9 t9 ?/ O  K
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
. U5 }9 J" A/ q& O2 R2 E+ q, m5 g9 j) L% A/ S& _! k: n
Published online on: Thursday, December 1, 2011 5 b. E( z1 n7 W" G0 H$ L

, G9 g1 B( S$ Z4 ZDoi: 10.3892/ol.2011.507 : _  z* ], p/ M! o5 U3 u& K) k0 ?+ m
% x) u" b& v# k0 v
Pages: 405-410
/ W0 j4 Z' N* i+ H+ `  C$ g# ^: F" E  |
Abstract:
5 J0 m: p7 N; ^- i$ a! nS-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.
2 M% C% X: _+ H ( s( M4 M5 r) W
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 population8 t- X- X2 d, h* Q9 _
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 # ~+ _8 K! O  H, m0 A
+ Author Affiliations
0 T$ j( a. ~6 H9 S. G1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
5 {6 d7 d0 e% Z' K& c) {2Department of Thoracic Surgery, Kyoto University, Kyoto 3 w2 `3 z% a# I8 O' ~- ^: Y  H9 M% z4 U
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan 1 ~9 p% k8 y% m! e1 ~* j+ [4 u, g9 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 : E* u* G! v: V
Received September 3, 2010. 9 _% @5 d/ J$ C. N7 h
Revision received November 11, 2010.
- }- z! J+ d; x: F# H7 gAccepted November 17, 2010.
# q6 f" ]7 s- C/ {Abstract6 b5 Z, t% n2 \) P( m7 L$ t+ 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. * i" I1 t9 W3 A8 |
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. 2 T* [3 g9 f; 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.
: b2 F$ B8 J3 IConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. 2 e9 p. N4 q; m* o
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。
8 Y& _& s% J' L" U8 Y1 A# 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?
/ U$ K6 X& K# E3 Z
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
7 K. Z4 L: I) v0 W! D/ k* I( y! [! Y1 `http://clinicaltrials.gov/ct2/show/NCT015235873 P6 ]# u0 l; P! ?" G3 A/ D
; a! Q  H& v1 Q2 M. T  S: i
BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
5 f7 L2 }; i# q0 X* \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 z/ T- c' v2 X$ {

. {5 ~% T. G& T4 I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。
9 K$ h5 W0 y% h9 ~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

1 I8 E3 K' _4 A& h: {4 I- k9 h/ i没有副作用是第一追求,效果显著是第二追求。
( {# |5 z) r+ u9 ?# q# u7 F/ q: l不错。

发表回复

您需要登录后才可以回帖 登录 | 立即注册 手机动态码快速登录

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