• 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]
1203448 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( |( ^) Z3 ], @
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
' z0 k) t8 H  H7 j3 t+ o/ i+ Author Affiliations
4 [4 U0 q3 ]6 T7 J: v0 c# i6 U9 C, u4 I: X6 e4 D0 |# b! s6 T
1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan ; t$ T- ~- O+ @3 n( B# s
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan % X$ H, S# h+ z( z; W0 W8 W
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
# m4 {3 [' I$ {) B" T! d4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan ; A0 c2 o# I! Q: z: s- _& h5 L5 X
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan 3 p2 N. c! @1 f- D0 j& j+ x' H  G% e
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan 9 d" ~( ?! K2 f! E1 ^8 J! C# q
7Kinki University School of Medicine, Osaka 589-8511, Japan 9 \# m8 s% I( f- r
8Izumi Municipal Hospital, Osaka 594-0071, Japan
* i$ ^2 V/ Z/ Q& s: e9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan # O8 s( _& ~5 d3 A) g$ H
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 - `! D" n  {9 k$ p0 W
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. 1 o- H/ a$ C! c5 U+ x5 ~

6 G- _: C1 m: M  g, D
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
3 j+ Q# |8 _0 ~; b" F, F4 J! D6 S1 ^
Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
! g1 T) n, a% q+ c( t7 i( x+ s0 C2 b0 E9 v: X3 M# p  c  H& \, Z' c
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
$ B1 X1 T8 Z3 H; \9 R( Q$ ]0 S7 _+ y* K( ]
Published online on: Thursday, December 1, 2011 ) ]& }0 @+ i; J) C% x! J0 h1 l2 [

# _/ Q6 c! r- y, x: aDoi: 10.3892/ol.2011.507 1 @! t( [6 U9 I/ O

6 N2 x2 X* U) y, M( ~Pages: 405-410
4 w% h' j! F9 U% Q# l4 E! j2 R, W" ^1 f2 h* e9 t
Abstract:+ P3 G9 f$ c! [3 n
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.
1 D1 {8 z1 @; _8 i" n7 Y1 |6 ? ' g$ m! Z  V- \
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 population2 ]8 b' Q( `+ X) f  m) I
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 4 Y) H3 H* F% s  f6 M, p2 H
+ Author Affiliations0 V7 ^/ ~: c. R' C. e6 L$ ]6 v
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
+ v- I  F: g' P* Q2Department of Thoracic Surgery, Kyoto University, Kyoto . A! N' {/ A' l' K* s5 I% d
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan * P* V& K1 W: g3 e
&#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
" D; v  u" O! |' _2 ]) SReceived September 3, 2010. ; t$ S* r: F* t3 T0 K) u
Revision received November 11, 2010. * z4 a+ F8 S6 O2 Q% Z  i0 {
Accepted November 17, 2010.
' D9 P- G& y0 G% ?; }Abstract
% k# }# T. j- q6 k! X: ]" RBackground: 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.
8 z7 _' O* t) hPatients 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. " y: P0 U" T, V/ D5 X
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. 3 \' z/ h2 J& b4 \( I( C$ q" y
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study.
/ c5 f# w+ Y6 L/ d( ~2 q" b) {
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。  L& b/ Q/ c; u, _2 R5 ~
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 Q/ }" x; t4 {# m- _
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' c2 l% W! o8 D( ]" X/ }, V
http://clinicaltrials.gov/ct2/show/NCT01523587
0 ?& J3 p* u6 D( y& B8 V
$ g7 |' _# B, H3 T* @( JBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
' P+ Y. J% c- U; E! _) Nhttp://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 . `! C9 Y5 _" A, v/ R

% W) s, U2 O- `$ I7 \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 b/ ^2 j6 |1 d, T2 b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
- W6 w3 ]4 l$ g2 J9 Y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。
# w3 G" F5 d3 l" Q  o, b% d至今为止,未出 ...

" x. p- J% s3 `; h  K没有副作用是第一追求,效果显著是第二追求。8 k# ^1 y$ \" Q7 u; b
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