• 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]
1207191 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
% W- f* O0 |8 G* z9 i; iNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
* H8 b* N4 |9 h# l7 _+ Author Affiliations/ o$ \% E6 L" E* z- F8 z+ x4 N
' e: W- s6 @$ ]
1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
4 O9 q5 k- x+ B5 s2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan - N# q1 ~- q& K' u
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
5 @+ X0 M. A8 C5 p, v4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan # g& p2 K# z( Z1 h
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan 4 |0 A+ N9 P/ H2 U8 a6 `" B: m
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
, Y$ g9 _' @! N. S7Kinki University School of Medicine, Osaka 589-8511, Japan ; k# |9 _7 W7 V3 n! u) b
8Izumi Municipal Hospital, Osaka 594-0071, Japan / z+ w& @" X. `
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
2 M& l/ p9 [, ^% BCorrespondence 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. n  K- Q1 k! Q" J
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! k1 {: S( J2 c$ F, w

: j0 p1 @. F% G- w
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 . A9 l  Z  e( ^; C& o4 ?

7 O3 F6 t% N" e: B% N3 cAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
* X& N. C9 K/ J9 C( g
: i, x. u  o: x; w6 eAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  4 x$ c, X! D* |; C
$ O7 `7 _1 L; J+ Q9 O$ S
Published online on: Thursday, December 1, 2011
2 Z- U- K" g$ |! a/ R/ r, G' D3 f% V- s3 b- e  ?
Doi: 10.3892/ol.2011.507 / v6 t1 W$ H) w' N. [% d

; f* q5 [/ C% I5 q) @Pages: 405-410 ' g7 y& T$ _2 x1 \; @0 S1 D. w

, y, ]9 H" B- a0 k0 _1 \% vAbstract:
' B2 j4 `, Y- a# l# o7 h1 L1 ^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.5 z2 }( ^* r7 g+ ^' {% y( ?

8 a* \, J( b9 \4 _3 x
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 population3 `; B2 [, X) s
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 ) d+ z0 v- l) R, d  U9 p
+ Author Affiliations, s! Q8 p- e6 F2 |9 R6 d
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
( @1 X. I8 U- \- o2 b2Department of Thoracic Surgery, Kyoto University, Kyoto : Z) T  m: {  ~! q  ?
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
2 x+ \! V5 ?' V% E7 I&#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 ! n) X+ u8 {6 [) F6 y/ O
Received September 3, 2010.
% X2 l: e0 ^# @Revision received November 11, 2010.
4 b1 E( m# d7 I* G: [: eAccepted November 17, 2010.
+ P3 t+ t+ P# RAbstract
% u4 z/ T4 {1 Y$ aBackground: 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.
0 j5 N7 z0 \- cPatients 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. ! @& j0 b& R  D* _
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.
6 G2 i' G; b, Q" U7 B, JConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study.
6 q5 P) [0 H( d+ n
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。& o' R2 a* h0 X% 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?0 f' u  o% m6 F# T5 J5 l$ t
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. Z6 P( w% {! c
http://clinicaltrials.gov/ct2/show/NCT01523587
4 V" S5 w( _, \0 D" c$ c' _3 s; {/ y' l& V; k
BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
6 J5 I2 _! l+ ^3 Z% _5 \- }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 0 `8 L! g/ A6 G2 D" o6 w+ Z

# \1 l  E$ R8 r2 \+ N0 a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。
5 o& J+ ^$ T$ T# K! N, X# r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, N9 m2 j" O1 n  B/ p
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。
3 n& u) `4 a# X  y  n至今为止,未出 ...
2 L, `* @( N& y/ ]9 ?0 V, y( X
没有副作用是第一追求,效果显著是第二追求。
5 ]; t3 {; \: X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