• 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]
1399764 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  t5 r/ ^' i4 J
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 3 p4 C  J* e! J+ x0 e
+ Author Affiliations
# J2 j6 J) @+ N7 B" ]6 X8 N" A/ l7 S
1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
, S- E, F& p) z/ v' v2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
  t* }5 U3 X0 [5 R  a, i  p: q0 B3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 6 b9 {. q7 ~) \8 _- N- _3 h
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
9 Y0 L0 m! l! y# K0 Q  d, x7 }5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan + Z4 r' p! t- ~; A! `
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan 4 g5 h3 W$ V( l
7Kinki University School of Medicine, Osaka 589-8511, Japan - D* h8 Q2 Z( T$ r0 Y) k* Y
8Izumi Municipal Hospital, Osaka 594-0071, Japan ! u" j  G5 }" l: p( w0 b
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
% S6 [: Z0 ~+ U- {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 ) [; n! @' |# D$ Z% Q0 e4 d
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.
' c+ c  y+ c9 }
6 C- m- }; Y2 O2 s7 B5 i
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 : x. ?9 |. K" }7 h( Z0 L3 U# M( o

; r0 @% I/ ~" z8 e2 b7 q5 ~, pAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
" T$ Q3 q$ S: c# E
0 w& D) C0 d( N1 |3 CAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  7 D) h7 @/ Y& i; G0 {6 M  g

0 M; ]3 _3 |4 M5 LPublished online on: Thursday, December 1, 2011 ! X. w+ J- I1 I% k

. v" E  y9 h1 ZDoi: 10.3892/ol.2011.507 5 {* H+ _, q2 i( t

# t: `7 `' y4 p9 s, _% XPages: 405-410
' U7 b' ]. H( L! T6 [$ P8 R6 k# ]. y' L. n! `
Abstract:2 B& R6 q- F- Y" W2 i& K' R
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." z5 A3 t* p0 j/ v* h
9 S! v' n, g9 ^2 W% e8 Q$ A
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
3 Z7 B* W1 J* S( h+ S7 tF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 : Z; r% v, W3 x3 \8 E' m1 |
+ Author Affiliations
- E1 C- f/ }* Z, q1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
5 q1 U) @" S$ p5 c; F3 G* L2Department of Thoracic Surgery, Kyoto University, Kyoto
. f' |0 C: V. N0 s- X3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
/ Y- u% k- p6 E. G( f. ^' {0 [3 `&#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
  K5 o, p5 N5 x7 M- p' tReceived September 3, 2010.
7 p; e/ M* C0 K( r0 K  a3 G7 u2 ?# hRevision received November 11, 2010.
$ A6 M- V/ f- Q1 B0 ?( m/ WAccepted November 17, 2010. ) Q, D7 g/ r" D7 s! I3 b0 |' x5 M
Abstract
2 V% Q  l: h  \4 e' JBackground: 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 h% I, k- T# E, w& ~8 _. z
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. - K" f' c5 R3 j. h
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. ( o3 A+ }1 O- r1 s, r1 |
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study.
; |% o0 r9 B  y# Z# k7 l7 o5 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。
1 b. J3 ~; a. h6 O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?5 N. x0 G  D6 f/ f8 D) M3 I, \$ ?( F
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- q, H3 p4 V5 Z( {5 ~1 q* m
http://clinicaltrials.gov/ct2/show/NCT01523587
! H, q9 N: c9 Q. z0 g2 C  j5 j: ]$ F
BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC; |+ z/ F3 q0 `% D0 R8 k
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 5 V5 A! ^- ^3 N8 V# M* |, [

: p9 S* B2 @; w, o9 N( w; n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! R8 E) {" m, s8 ^4 p# r" t
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
+ F: [8 N7 h" ?. j$ f6 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。
: t+ |6 \0 |1 V' [4 }% ?" B. r至今为止,未出 ...
; x# ]  D. a0 q, A& Y
没有副作用是第一追求,效果显著是第二追求。
  \' Y/ S7 @/ x1 w# M& o5 J- q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