• 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]
1147693 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
4 f. e; |) {6 _NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 ; x) c  {+ E$ B2 y
+ Author Affiliations  G; z6 @0 p1 h" Y! C0 |6 l

& A0 }5 X7 v1 H( W' }1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan 4 ^4 K0 U7 k* Q1 z2 X# V1 L1 c
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
+ x: T, a, f0 N8 L/ g5 P' W; b3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
8 c: Q1 U% S% c6 ~' ]/ f4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan 5 X  I4 k0 L! e5 v. V, v$ y: g
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
- ]& \9 f) O: C6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
7 K% j5 e3 R, V' \4 C7Kinki University School of Medicine, Osaka 589-8511, Japan 8 }. o( a/ @6 a  N* H: I
8Izumi Municipal Hospital, Osaka 594-0071, Japan 8 l0 w) K. ^2 }; A" I3 T
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan 0 \3 Y  N) n* I* 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
0 P, Q- _2 X% v$ s' oAbstractBackground: 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. # P2 U; V+ W- [4 k
( m6 J/ M8 K9 L% A; K6 q
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 ! b( M, q9 o% S% D- L2 {% f+ N& e/ \7 U

% c  e6 _1 a2 aAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
8 Q6 `' F/ Z7 O( L8 U
  A6 \/ R/ e, e. H& H9 S) rAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
& j0 y5 ?3 P! c9 _: K; Z
3 r( T& T, \% M7 jPublished online on: Thursday, December 1, 2011
3 l3 I8 H4 [- A% X
& U$ R& n$ a- ?Doi: 10.3892/ol.2011.507 6 U/ @/ @5 C" G  c
) z6 a) b  Q! J* H  I& `& d  S) _" c2 ?
Pages: 405-410 " V9 J* R  d4 {0 |( f

* A( m4 {/ U; w" [. E& PAbstract:
, {1 g- }) \/ O: z/ X+ bS-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.
5 g& d7 D4 K: l, U( [8 \( e
8 H$ d) H4 r; I( B. Z
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
& f* \' ]' U! i* u0 T$ PF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
" l7 Y/ b5 n: ?+ Author Affiliations
; W& a; n$ F. Z$ o# |- A1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
# M9 ?. {8 b3 c3 U2Department of Thoracic Surgery, Kyoto University, Kyoto
% h  G$ Y, I8 `* ^6 T3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan 6 W/ \  Z0 p) t+ d6 J# D" R
&#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
8 U. c: E" y1 d, B' w& X8 sReceived September 3, 2010. ; G6 E- W5 r2 x* Z  Z1 U& F
Revision received November 11, 2010.
9 X& V9 m0 f, p. N$ K2 P% BAccepted November 17, 2010.
$ s! M8 e& m& \; lAbstract
+ }( J# D8 D' Z: [; e& d5 TBackground: 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. & Z; w. m0 V: 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. " M7 C7 y# {8 `5 ?0 c, g/ 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. - Q: O0 s$ h3 q4 P+ p' s' q, w
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. 5 Q4 `  o8 w9 W- ?: 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。
+ b. X1 A' k) K% w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?# ]9 }, ^' @( I. 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
: N% [6 ?% d9 F' f1 [http://clinicaltrials.gov/ct2/show/NCT015235872 J& f6 T6 w. ]" ~* A# _5 Z! I+ t

# q4 L0 \& t+ y: i6 E  ~6 h8 LBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
8 i5 b! ]" V) ~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
$ Q# `/ b3 x, s; X- y
8 t% [& {4 c3 N) E5 C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。! Z; F; S( c5 X+ J; N/ o9 P
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
: k5 W0 x% O* u4 c) y$ F& `( S& O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。8 j5 q: E/ F& t$ m( U0 J
至今为止,未出 ...

, }$ h/ v7 V0 ?没有副作用是第一追求,效果显著是第二追求。% s/ R! T) {& \' I
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