• 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]
1060330 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) m+ u' F2 |! q# ~
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 6 O/ B/ S8 m* N! K0 ?' u  S
+ Author Affiliations/ I3 t( Z; ?6 B) _

9 j# r) y3 ?3 M; a9 a1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan 9 {1 ~3 Q+ [7 }- S0 f& {! A
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
( ?. T4 x1 f/ Y1 T3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan : b( i& K2 R+ v4 }* [# a
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
, k. t" o; g0 o5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan : A3 W# Y  H: i7 |; F* T
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
) ^  h; s  C- n8 b7 k0 e1 t7Kinki University School of Medicine, Osaka 589-8511, Japan
6 Q5 y3 r0 e% Q8Izumi Municipal Hospital, Osaka 594-0071, Japan
+ A& g, y) S1 E3 n1 H9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
5 k' m( s/ @& c) K% p' o8 E& G: FCorrespondence 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
- `* E2 t: m7 TAbstractBackground: 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.
9 [% F4 V6 y- w3 T( W3 w
7 V1 y( K3 y& c* q2 H
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
% q- b5 T- g% H* e
# S1 g% m& s; |3 D1 U! QAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato 8 r4 k* v2 d0 U5 i
6 @. Z$ d. X: M! O! v2 g
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  $ X( s. ]+ u: k5 ~  X! L, G

! f7 i' p4 Q; z. }5 k: V+ Z0 IPublished online on: Thursday, December 1, 2011 . m, P+ H: ?7 x& i

! v3 q3 e- W  u  `$ T# p' o% h4 R# cDoi: 10.3892/ol.2011.507
: G( o0 C/ P1 P2 u6 i# |, i% d. T1 X( K* d% J
Pages: 405-410 7 a5 M4 l7 ]4 J" k0 T3 _
/ j+ M& A" F" r2 Z
Abstract:& h; h: u+ u7 J7 E' \) ~% Y
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.' n7 J8 |$ C- ^* s% Y, Q5 ]6 w, V
, r/ W2 Z6 d8 I
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% ?! M2 w: G, v! M1 R
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 ) r  [5 q8 @; b+ B* y! `
+ Author Affiliations1 g( @# ?6 l* f4 I+ P7 ^! X( a7 ~
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
4 u: x6 x# e+ P' W2 ^" x2Department of Thoracic Surgery, Kyoto University, Kyoto
- W+ q9 o& G: a& l  D8 W3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan . _: x9 i2 D. O% 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 : ?: t8 h3 X2 }0 m
Received September 3, 2010.
: |) |  N0 o1 J' b1 @( [Revision received November 11, 2010. $ n8 d! N3 i( |* E% c0 ?. o: ?, W
Accepted November 17, 2010. & O) _% H6 A# j& W; e/ F
Abstract
! l3 h, m. E5 h( i8 vBackground: 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. 3 w2 ]0 u% }) g
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. " k1 l9 w! F4 g) e$ N  ?/ 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. 1 e( Z+ w( i' I2 V2 B4 Z
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. ( F0 U0 I7 d2 V: `, L
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。/ F- p6 Y) O3 a5 o* f, z& Y
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?
' L* J% ~! k  ^1 h0 s* _# u
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( o* h8 w; _0 o7 k/ d
http://clinicaltrials.gov/ct2/show/NCT01523587% L9 Z9 Q0 A0 C, E/ S, Z
& d  c8 J  a; `  v
BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC% t& G" `3 M% z) Q; D  s
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 _" k% n# G9 _) ?
' o6 ]7 C  i, g* S; ?. [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。
) P2 l1 T. _4 Q. `1 U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

; y! o) t* V' W# z3 D+ q' f) @没有副作用是第一追求,效果显著是第二追求。9 ?( _( V+ v+ S  n* ]& A8 B9 @
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