• 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]
1250284 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, u$ ~6 P7 j5 D5 s' Q
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
8 o' f/ K1 t; Z! Y- Y# r+ @& M+ Author Affiliations
: G+ z9 c/ C- b4 {3 [6 O3 k9 `0 ~) y$ G
1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan ( D" A8 N7 J  Y" g
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan % i/ v7 j: g0 G4 A
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan ! I: G4 i' q9 I8 H! X$ h
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan , M' n+ X2 @& E' E) `) G
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan / f8 R, n/ W  U1 D+ F$ S# f% K
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
" d* y* @; d+ T- F+ S) P7Kinki University School of Medicine, Osaka 589-8511, Japan ; p" ^8 o! n9 I: q! ]
8Izumi Municipal Hospital, Osaka 594-0071, Japan
" @$ b4 \0 Z  J! @9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
" e/ K5 T( n! {$ p0 iCorrespondence 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 `7 X$ U. m6 u" V# H
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.
/ H$ X$ O; M: g6 _  }
' `' V9 W- q$ N/ c
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 q; d7 X3 J1 Q( p  i! l" h. @# D% W! C
Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato ' `7 a5 l6 Z' i  u

. G5 u7 M/ Y6 C7 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  
) a8 q" C9 c9 d/ ?4 a( {/ N: c+ y6 i3 u  [4 a) G. t7 @6 G. f
Published online on: Thursday, December 1, 2011 + J: t0 b( v. h- i$ X- W
8 R5 W, _6 _1 \
Doi: 10.3892/ol.2011.507
; }- }" S+ y# n' N0 a. m  `: k% \: ^, F8 Z) N
Pages: 405-410 $ c# s: G0 }$ B

7 n* @1 F6 k  x3 lAbstract:4 k9 O! N6 S" q; L" I% L' {. f
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 v  P% {' L6 s  X- g+ M0 c5 R& ^

' L, M4 x. ~- k
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 population0 S: @% O, l' T8 p1 h- _1 C
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 : v1 d1 [2 D) w: b) l
+ Author Affiliations
: x* F$ M- ^3 n, i1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu ' N/ R- T4 P% z2 w8 T
2Department of Thoracic Surgery, Kyoto University, Kyoto
8 g  }* [9 Q" o1 g+ b# }) n3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
6 i0 G( ]+ w4 g3 T&#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 0 N; t+ B; v5 R. r
Received September 3, 2010.
4 j0 c- N+ x3 N. H& rRevision received November 11, 2010.
2 G& S. H$ D; d3 y# j! A* m" U/ gAccepted November 17, 2010.
% o. W6 b: y( l  CAbstract
9 O' L* E" ?; [3 q) ?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. " [' ^6 e& d7 s/ R
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. . X0 u0 E0 p3 R+ }7 `. `4 V
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.
% Q; x# ~: G) Y, j- R( _# X, YConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study.
, q9 i) N! m  K8 A- ?4 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。7 u2 L; {9 H5 _6 U/ x
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?
- ~, s, c7 E& b* Y! S
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) [4 p0 z* x9 m2 J1 J2 b3 }9 R+ G. e
http://clinicaltrials.gov/ct2/show/NCT01523587
7 f& e- R0 A8 X$ `7 z" r. d) h
4 F* S4 t( j& V) }1 ^# f+ u% fBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC" q/ [6 @( k1 F4 c; w
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 + c& V( z- Q8 ^, O: z4 d
4 u8 p. o4 z7 Q' k2 z1 y/ n" D
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* Q: a# ?# {. }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 9 y, q; P* ]0 }* {5 `* h
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。! c9 c/ n0 T' k4 Q3 g% |/ ^! U
至今为止,未出 ...

: S% f5 k5 o4 Z: ]4 ]1 {2 \% |没有副作用是第一追求,效果显著是第二追求。0 t2 |1 {2 e4 J7 g1 \
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