• 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]
1307157 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/ l+ f1 j% H6 j8 [# k
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
3 H" T' E9 k# n% f( r$ R% O+ Author Affiliations
; r3 u8 y1 k% N8 z" s0 f3 U
8 }7 x: a! g9 `- G. d1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan + {& [# w" d- h5 U4 u: c
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan / h2 E- j+ R$ |
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan . ~: t+ Y, a  |& w
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan 7 P& K; L- g5 y* @
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
% a" h' j5 z- A, Z6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
* ?# x, M" d2 |( S6 h& ~' @7Kinki University School of Medicine, Osaka 589-8511, Japan 2 Z7 ~* J3 x+ s0 ~2 O( G
8Izumi Municipal Hospital, Osaka 594-0071, Japan 2 J' ]' n+ W3 U  d; F2 M" B+ Q
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
) v/ {+ P7 S+ [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
& j, M9 g* ~7 JAbstractBackground: 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.
% p7 u2 s  |& [# L0 G0 C
# f4 `  h0 N. Z: _  q" r; `9 @
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
/ n2 q( }+ ?  r2 ]! Q6 I9 h  t* |9 M; D$ M( @1 q
Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato % v; @- M$ \1 `5 n2 P; N2 A
8 _: @, p! O5 G( Y" |
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
7 g6 }4 C8 K( N; z4 v( L! [/ D  a  S! |3 E% j: @9 l1 @2 L; L% K$ V
Published online on: Thursday, December 1, 2011
* }+ |& K8 o8 M. b" `& i7 A2 [& J  i4 ^, f! f6 \6 {
Doi: 10.3892/ol.2011.507
0 d) z9 r( s2 S& i. d1 z; C1 g# S9 D0 ]; }- r, }" l4 j
Pages: 405-410 8 ^1 p2 j% u1 m. T  z# [' f6 D7 r$ K

# Y% G" U, a( DAbstract:
. G" r3 x$ Q' v) JS-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.
+ h; k3 B. y7 t3 e4 }& O+ B- ? ( T4 n& z; ]& G9 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 population) O* e  r& H8 y2 P0 s4 ~
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 7 I7 l0 f; e; T: |' C& d. b
+ Author Affiliations5 o( X( s4 N# E+ S! _8 i
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
% u1 U1 {. Z& F: M2Department of Thoracic Surgery, Kyoto University, Kyoto . N0 X5 W5 [: f
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
! j4 G  y: n7 A& ?; |$ L9 Q# [) S&#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 6 _5 n* J$ j% G. n4 ], \
Received September 3, 2010.
3 A6 j/ g, |) J0 d$ ?Revision received November 11, 2010. : t% ]# [' B7 r
Accepted November 17, 2010.
( m! ~: v$ {$ G6 ?0 FAbstract& U' {4 i. p7 Z& E  A+ ]3 ?
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. - w0 p3 q( @8 Q
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.
7 x' y  N, ]6 r7 CResults: 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. & }% ~- Y9 r- y, Y( v( o
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study.
+ i" U8 q' x- q9 P" \
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。! h9 E) @2 c0 _% B8 l4 B  {
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?
1 f3 b4 y! _, `; h1 d
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- B- o+ ]. n
http://clinicaltrials.gov/ct2/show/NCT01523587! D: ~7 H. A% S  t  D

7 b6 H+ Y0 p- k* z" z3 BBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC$ Y* D: L: _3 B+ j; n
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
3 p; b8 \( i. G+ s/ |; c0 g  l. a( S1 k" o
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。
2 X5 J" O4 n- F- }( p2 j: G) u6 A- 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 e2 }# J6 W: {; |7 ~
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。2 q0 h2 s6 F- S6 k/ R$ `
至今为止,未出 ...

8 [* @9 J( b# a( A7 W没有副作用是第一追求,效果显著是第二追求。  S9 Y8 V, K( l" l! N7 J
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