• 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]
1127457 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 Type9 M1 ], p( F' E6 X9 Z8 B0 C
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
6 I% G6 U0 a' |2 k+ D+ Author Affiliations
& Z* [1 z1 c2 n9 B7 K
2 g  B: `* e& N/ q  ~8 G& F9 i. X1 [1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan   q0 Q, U% N5 v4 I7 c" ^& x, G' l/ z
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 1 F4 r5 M- K+ ~* s  l0 [
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
8 m$ R3 \  N( ~9 S- Q4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
: M4 f6 ?$ F/ g+ q5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan % Z' d$ ]! B! _5 s
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan 7 ~, f/ M, t# Z; I4 k4 h" U
7Kinki University School of Medicine, Osaka 589-8511, Japan 0 |: H& a6 G6 W' b# L
8Izumi Municipal Hospital, Osaka 594-0071, Japan 4 E- L& e) T" W' V6 w$ J
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
' k+ [5 ]) ?! E9 @" E+ PCorrespondence 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 * W4 P$ ]9 N) S6 }9 o
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.
8 ~' L7 l1 f" k/ y5 H- `3 l) h6 M: l; i! X0 i- i- u
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
% U# D% w% ^+ ^1 {
: h4 c4 D0 f! P0 z) L& w9 s5 ^Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
5 T% d/ |* c2 i7 b8 i3 T- Q( P) M% ~; i& x) _. ]: T; v
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
6 y3 e- k3 u# `* K- l7 ~( c* t0 D
- M* ~- x6 c& p* P7 y2 C% E# DPublished online on: Thursday, December 1, 2011
6 j7 d  N: M# A/ o8 A* i, Q
* ]3 u- a) a/ j0 {Doi: 10.3892/ol.2011.507
5 M$ S6 Q0 W1 V" h8 `- }9 n9 h7 O: A4 \1 a* M; M- Y9 f+ Q) B
Pages: 405-410 1 i; W, |& T: I: [
, B5 R6 p% J3 ^" r% D
Abstract:4 B. V! v/ A! K; L' E+ O3 a
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 W% u4 r7 c1 V( v
8 I# T5 o* X0 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
9 d* a5 ~4 q: }* l7 h' e4 rF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 ( `0 f- Q7 r) x9 S" u
+ Author Affiliations
& m, `+ K  P1 x1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
* \8 L& j* X5 Q* l2Department of Thoracic Surgery, Kyoto University, Kyoto
  `4 S( B* G4 U( X/ M3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
- K9 P5 u/ q% p$ R6 @  B6 [&#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 @) P5 A2 B( L% [3 |Received September 3, 2010.
3 p# a1 J4 b" |9 K) b% u% bRevision received November 11, 2010. 5 V9 X! G5 q/ A8 o
Accepted November 17, 2010. : k- w# Y( M, D* D, G0 ]. N/ s
Abstract
3 V5 H" U( ~7 D+ r/ T7 BBackground: 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.
% G0 O7 l' m9 A- W3 p. 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. " g$ G% R" r  I
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. 5 P7 T+ ^3 u" D/ x) ^, j: c
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study.   Z" m6 I) O. d( ~* H
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。
. x+ y+ `: a3 j; w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?; B8 q* D; N/ d# V& P, `5 B8 A
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
( v* G, i2 K# S  Fhttp://clinicaltrials.gov/ct2/show/NCT015235876 L6 R( Z" |: M8 [' w# p& H

2 H8 F7 |7 e5 u9 r' s& [* @BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC8 T( ~& p: A. 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 & ?4 W7 N$ _3 m
& q" c% \2 h0 l3 j
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。; W, B5 ]+ L6 K6 T6 o
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
' \4 D) }5 \) j$ ]
没有副作用是第一追求,效果显著是第二追求。
/ [4 G  X# D8 U" @$ ~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