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我父亲肺鳞癌的治疗贴(2014年3月1日驾鹤西去)

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1274424 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# S# @# N& U% c3 X: ~/ e6 W
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 " o3 c: }) z: Q8 r  k
+ Author Affiliations' H; l) V+ K. N) @+ L

  R6 r* y+ z7 Q  h4 }7 |7 F1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan 8 D4 y; G4 ?9 S3 v! G  h
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
" J6 y7 ~1 e# t" Y9 A& J; f# J3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 9 X# O: u+ d" _2 m
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
& Z9 k9 {/ t2 W0 K5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
) ?8 m+ }& ^+ _6 {5 M3 ?: c( C6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
5 ?% M1 N# K: i7Kinki University School of Medicine, Osaka 589-8511, Japan   p4 M5 Y9 B# {/ j- ^
8Izumi Municipal Hospital, Osaka 594-0071, Japan % R. F, r8 J2 h( G6 Q. ^
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan ; t' k! {3 B3 I; O: L. E# o
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 - F! y9 }5 A* T, \7 V4 ?$ A
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. / ~6 K& s( b1 X4 p& A
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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 2 C3 [; a/ F- U  U
' e* m- P) P, o$ }7 y. g+ w! c6 m
Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
" ?! U" H( [4 v
  L6 b0 z7 ?; I! g: N" iAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
  E* p- I% F+ Z( ]8 t3 i2 p7 _% f# G. S" x) o3 w6 V" N8 N! B; Z
Published online on: Thursday, December 1, 2011
) t2 l4 |7 w7 l7 K  x7 O0 y/ {4 I& M6 T: U  ~
Doi: 10.3892/ol.2011.507 : m3 v/ ~" c$ O

6 m# y  l& M7 [1 _Pages: 405-410
; m0 F% b& m' u# n, s$ J4 c+ e3 S
Abstract:
2 @- m% v4 A* v0 }, m! n: u7 [* sS-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.
( B# V7 ]  k. m; Y+ I$ V  y # W8 S5 M/ ?/ E$ ]% z3 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
6 L0 W: n$ L4 NF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
* \# c' Z' A% [5 l1 k3 ~+ Author Affiliations9 O9 @! Q3 ~" W! Q1 }/ b
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
- X& m$ b& `1 v& u6 {2Department of Thoracic Surgery, Kyoto University, Kyoto 2 l! a" W4 k( a4 p, H
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan ! W1 F0 F: H- J) V
&#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
/ `9 _; r% f" m% \- c- fReceived September 3, 2010. 1 R6 [6 s3 O& a  n( Q7 G. ^
Revision received November 11, 2010.
# S3 _6 r2 `) w/ p! x3 p# ?( [) NAccepted November 17, 2010. 9 K: d. z& u* u; v2 `
Abstract
" e6 _" q& P' m# x0 X2 YBackground: 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.
- b2 i: x) i  iPatients 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.
4 [, A2 T4 \7 b8 ~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.
4 j" ?4 Z8 v) g( y! ?. \/ IConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study.
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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。
$ r* |# h0 m$ K8 }9 u( x( s# ?# I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?
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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
1 }9 E5 F* Y$ j% j# D% nhttp://clinicaltrials.gov/ct2/show/NCT01523587
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6 W/ G( H* [+ |BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
0 {5 E$ I. I# Yhttp://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 * k! L4 V, y: M6 t! l' F' U" ^

7 N: q; `6 I& S. D3 a" U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。' }: W' \* R( `$ W$ v
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
6 A5 w* n/ q' U$ ?0 u* S2 m: d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。
  O% w* k4 j" m( ~! E1 ]. _至今为止,未出 ...

; S  N6 P: `( X- ?没有副作用是第一追求,效果显著是第二追求。6 _9 ]" c9 k! G. c& i" O1 R
不错。

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