• 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]
1248645 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
+ ?  R. `" o4 eNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 ; u2 O/ M5 y! v1 V3 m
+ Author Affiliations9 e7 [: z! f9 a
7 j, L0 f6 @# ?. V
1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan 8 g) ~! T. \6 l" m4 |. W4 U8 N
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
: x2 O+ C" e! Q  T  \& D+ A3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan ; `; H1 D% i. f8 X2 b  d3 v  F8 j
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
. f( w  T3 Q, ]" T- \5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan - l. l0 M) i8 |+ P" p# G; f
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
8 Q  r; g. V; S, F7Kinki University School of Medicine, Osaka 589-8511, Japan
5 {7 O" U+ ^: l" t6 s) V8Izumi Municipal Hospital, Osaka 594-0071, Japan
' J* x1 W3 D, M9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan ! m  F0 f* K( u" E' m
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
/ i( `, x3 v6 v, I) _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. ! J3 @" G" ]+ f4 e6 C

- _& X8 V1 d% n( H4 w: @& f; N1 P
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 & r( ~7 @) A7 Y
; R- P! b, p% u- V5 |: {
Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
$ k1 Z$ j' ]% D( u: t0 q' T& Y, t. V/ z) [8 W" 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  
8 `! \% H5 o9 t7 o* s7 t6 O, Y" @+ P, `1 m- _, B
Published online on: Thursday, December 1, 2011 4 C* o2 U; K4 J, v! [# D" Z

5 x9 e8 Y. w* {1 [; U/ {" }; xDoi: 10.3892/ol.2011.507 ( {* L: z2 F/ E  {
7 C" s& ?/ n  }  h
Pages: 405-410 3 l0 F% x: L. K/ n9 v5 m

9 x7 z3 Z0 u2 }# |Abstract:% |) A& `0 b' O2 m4 C3 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.; Q- s4 m, O& O1 v; Q
0 O& N  x0 I" B8 H
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
' i# x+ o) y2 I0 O& FF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 + u2 ?7 [# t9 l. [+ z# E8 j
+ Author Affiliations
* m' j, U2 H* A: J6 F1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
- o5 K, z1 K% d6 n9 b6 v4 Z" b2Department of Thoracic Surgery, Kyoto University, Kyoto
; {7 c8 D, z4 S$ y4 u, K; O& D) ]3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan 8 i. Z0 m" t- {6 C0 k5 a
&#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 6 {: L5 r4 ]1 I1 f% s
Received September 3, 2010. 8 o6 A5 d5 B2 k  r: r  t
Revision received November 11, 2010. ! ~# r0 i3 K) k* h6 f
Accepted November 17, 2010.
8 V0 I8 z3 D  W  ?& a1 ZAbstract: Y8 h9 ]+ A" t0 F3 p
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. 2 g$ @% |: E. L) r. P; ?
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. : L6 r  d% `1 ^
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.
7 q3 d- p+ |% Z/ Y! b, mConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. ! F; U; ~  s" i% A+ N
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。
- o- r$ Q  A9 y4 @0 ?1 E( S- 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?+ A, M0 n, Y; O/ `1 h
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
$ N8 v7 d0 l9 F% ~5 yhttp://clinicaltrials.gov/ct2/show/NCT01523587- D0 k9 B% T5 S( z5 t$ g$ ?
* d, ]% h# m' C* o& B
BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC% B1 n3 p  x6 u$ e: ?6 q! r5 r0 O
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 v; L, W' `# r  y' ^; }# _! Z
/ w$ D  G0 B, V6 a5 G+ _) U
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。3 ~  L; e1 O1 T2 p6 Y
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 5 ?0 z9 C4 N1 Q; X$ ~3 u4 m
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。
- J) P8 ^) D2 O" E* n* m$ k" m, n4 U( E2 ?至今为止,未出 ...
  [* @- q, V, g& ?! X5 G2 J$ ^1 n) v
没有副作用是第一追求,效果显著是第二追求。0 ~* z3 b5 T* V# G: ~/ e0 P4 @
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