• 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]
1185788 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
: N, _( o# p* d6 v; W! P  @NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 & \% N$ b) X8 k2 d
+ Author Affiliations
6 T# k) p' U5 c8 c, i" ~7 `1 ?, f- v  J7 h' |
1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan 4 ^9 j/ @3 g9 B3 g- A$ B4 X
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 8 g7 A# n9 U; ^; W/ S; q
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
% _4 W# o& v+ x+ F4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
+ h% T7 q+ h9 W1 H. s# |- N$ \3 n5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
( ^1 m& E) m/ P% \, z3 }# |: w6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan 7 i: j9 Z; \3 W
7Kinki University School of Medicine, Osaka 589-8511, Japan
. n4 @4 g2 d- r7 m" p8Izumi Municipal Hospital, Osaka 594-0071, Japan
7 ~. ~, @7 M: h/ z) h9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan + b7 {$ z2 i# }. Q
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 " U6 O: D; _  o
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.
- l" E3 f% C3 ~9 [: n+ R  e; S% m' ?! P3 z
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& G6 T% J% L4 e5 Z# X
3 \  u0 y4 H$ i3 LAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato % w/ T* I+ d% U9 D9 }2 v
. y$ M4 k" q6 ]7 d1 N4 }2 U+ l
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
$ @+ I8 Y1 G, [; p: X9 Q
0 G# V  m1 @3 Z- E4 nPublished online on: Thursday, December 1, 2011 ' ^2 H" s' Y2 ?$ k9 @6 R8 J

. K1 q7 i2 _0 z& E, K7 C, xDoi: 10.3892/ol.2011.507
/ D( i7 G  N+ Y7 e2 N- I' B' v3 M! l; ?6 N) c: Q
Pages: 405-410
. n& f7 V7 O, t9 U0 p3 ?
' P/ I6 k5 t- t6 E5 l! b- [+ zAbstract:% K9 \0 q3 t1 J; L8 Q& `
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.% l8 }, z- }: Y

( f# Z* d) s* M/ h
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 population9 c) m+ l8 V) n2 m
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 0 G' N7 v* }+ C8 l6 I: B
+ Author Affiliations6 c6 R. ?) D4 p: J, Q: N
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu 1 q' [! k  e! S
2Department of Thoracic Surgery, Kyoto University, Kyoto
1 V- k/ [) x0 a( _3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
& N" M2 V% L/ C; }: }' U( a) z&#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 f* R1 J' ?! b% y5 c
Received September 3, 2010. / r3 ?! W0 k7 R4 ?3 K/ m
Revision received November 11, 2010.
* g" d7 k0 i9 OAccepted November 17, 2010.
5 F# O, ?3 Q' J9 S8 QAbstract
* J$ J  P. l& ?5 v# B, T4 qBackground: 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.
; U; v  c- P- ^; ^/ vPatients 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. 2 u% D/ `) C  t- w# p
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 v5 B+ Q) i9 O# ^* _
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study.
- X+ V/ Y' a" o7 ~8 [. W
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。
7 H5 k/ l1 A0 t& u0 Z1 J1 r3 k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 Z0 g' K) t1 O
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
9 ^5 Z' }, s; Y+ {! @http://clinicaltrials.gov/ct2/show/NCT01523587
/ U( n+ T5 i% C6 Q; L6 ^- b% t5 m1 G" x3 y- _8 I  J6 P
BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC- g$ B/ z' A0 ~. c. w; K: b. W* ~. _
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 - p! t4 e! d- G1 H$ J, S
# Z' G& A1 \! A. {5 b
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 m7 h9 W* I( o* y; _" 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
( c, d; C  P+ |4 O/ @. t. w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。$ M( \. O( o' A& Z; D' k
至今为止,未出 ...
) R. m/ n5 ^7 g1 u& U/ m
没有副作用是第一追求,效果显著是第二追求。8 ]% H( T  V6 i+ X5 z
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