• 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]
1227372 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 Type4 c  |- A" ^$ ^5 N- b1 o
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 2 @6 C) _* s* N( J& r/ f
+ Author Affiliations
" o5 h4 b- O, ~/ |# l! p4 N) g
+ m3 k  _! Z! l; y$ l- K0 A1 ~1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan   s$ T1 R+ k" V; d* l6 H
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan , h0 A( e. `$ b* \! D0 m- y
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 8 O4 ]9 D% l5 R' s$ P/ \
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
5 s8 D$ D, `" n$ X1 [3 U. b5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan 2 O. v! T! B2 M6 }2 P: y
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan " H& H& p0 M$ b; q8 r' _
7Kinki University School of Medicine, Osaka 589-8511, Japan & z# [" Z5 a- o1 e! S+ E# J
8Izumi Municipal Hospital, Osaka 594-0071, Japan , ?1 H/ S" [% Y0 n* I. S$ a
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan 0 X5 v5 ?" ~  G) L
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
$ x$ c& b, \& U2 N- ]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.
* W1 _+ Y5 J) ~0 d) P( {
  z; T8 S9 y; J0 o" Y) r# c& o9 y
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 ?7 M) s& t5 o1 L- s! [- @- F+ d' R# d
- E2 S% p' `1 F' K! o4 cAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
7 k, S+ n/ n6 q2 h! Q* p$ C7 u  ~* n5 q
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  ( i1 c8 |8 I( U7 n/ _
- W" W9 q4 O. u5 }3 {- D
Published online on: Thursday, December 1, 2011 ' o1 l1 y; z3 h  \/ e

3 e, |) {8 _/ W6 j- u- Y8 f3 XDoi: 10.3892/ol.2011.507
; ]; n5 W9 b  a# L. s
. {" m' D! C; e/ I1 RPages: 405-410
5 L3 Q' T0 d0 v5 s3 t
( n: F) `) F% V, E$ sAbstract:0 [9 N7 \# c1 \  X" m
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.
- \7 I# h8 o/ K9 z, Q
; f6 c8 b- j/ f
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
- f; {/ \# ]/ r  R) v% xF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 5 W/ n( q  E. x; M/ F: @
+ Author Affiliations7 [( I6 Y& h/ X; q" w  F/ I" X3 e
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu - c# Y3 k: m+ u1 a2 A
2Department of Thoracic Surgery, Kyoto University, Kyoto 8 l3 _1 d; Z- w" y" W2 v
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan " t+ q9 F' r2 Y) ^5 L) b# I
&#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 + r, V4 p5 n; x
Received September 3, 2010. ( T) p6 y0 V1 p8 o$ ~
Revision received November 11, 2010.
& _( M  k' Q1 K; d% sAccepted November 17, 2010.   e/ m6 h, V6 s4 h5 ^9 Z
Abstract2 ^, e+ V  o  B# ?1 U( Q7 x1 h* X- 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.
( x, U, t5 I# }; L- j! k  k6 XPatients 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.   {1 W. z4 k: d  w- u* A
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.
6 Q! Z7 _9 _* A0 EConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. + ~' R5 B4 V6 j9 S
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。: R( L5 n/ Z: H1 I" m; P
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?4 K7 b0 ?7 y* [& G
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  ]6 s$ B* \& }9 M. p$ }
http://clinicaltrials.gov/ct2/show/NCT01523587, L8 o# |6 E) N
% R0 g& l8 ]7 J" S0 a( [/ ~
BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC8 ]/ q/ @- n1 ]4 t! k! U$ E+ 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 ( h9 F& m# |) n% x9 n

' u# Y' M, P1 `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" n( x/ y+ E5 V) ~+ C
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
3 C; n# \7 d; g7 Z* h& l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。+ p4 |1 J1 X4 N& }' a% I* Q
至今为止,未出 ...
, y8 a8 P7 b* h! A6 b% M6 T! ]9 ?
没有副作用是第一追求,效果显著是第二追求。
. G/ V8 F* e. Z( u( {) j/ I* h  o5 Y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