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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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1460762 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# F) K* {* }9 M" ?% S
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
3 o- _5 Y9 Y. s' C/ c3 H+ Author Affiliations9 }7 B, K$ r$ p
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1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan ' z% K4 l: x; p/ M
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan " h4 H& h/ c6 {8 y; z) I7 }; w8 V
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
4 w: F  Z2 o6 b1 i! r4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
" a/ v: M5 I7 x/ ~5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
' A5 r) `1 u6 q6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan   Q# x& Z. T- S) I6 q0 j/ n0 }/ ^2 H
7Kinki University School of Medicine, Osaka 589-8511, Japan , |; k( T1 a7 V, m4 d, W' l
8Izumi Municipal Hospital, Osaka 594-0071, Japan
; y0 ?+ K. f, p9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
8 Y3 x9 X, D$ z" @! G. DCorrespondence 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 : w! \$ b! ?5 y/ n$ s1 T+ c
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.
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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
. ]7 {9 ~+ Z3 e5 F6 c5 [
: q2 v& N# D$ W: w: l! {0 ^7 ~" x, xAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato / b+ n8 F5 \6 D# J/ X% H  D2 o2 P
& Q# E+ j; ~2 n7 i; i
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
( N) _. V1 E) J3 e
* o; \1 U# s  \8 CPublished online on: Thursday, December 1, 2011
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- s" a% G  Q: K+ u: A7 ]Doi: 10.3892/ol.2011.507 6 E8 }8 G% w" A1 j; ^7 Y3 J# F
* Y3 `" Q5 T9 j; }5 D& D8 r
Pages: 405-410
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; D  N- U$ B; ^. _5 `& rAbstract:' d7 ?1 T# B% s, s  P3 V/ j* d* K
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.9 x+ p+ m& p: S9 ~7 R

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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
+ @5 Y) T1 g, jF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
% [  ]3 |. [5 |/ P0 ]$ a& s+ Author Affiliations6 F! h  L* W1 E) @. z
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu : k, s6 T5 `) s& a( b
2Department of Thoracic Surgery, Kyoto University, Kyoto ' e+ w# b  h. a2 o+ \( o! @0 H1 j
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan 1 O, s% k0 z; X# S% c
&#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 1 L7 J- t; s% z% i& n6 Z# z
Received September 3, 2010. ; |! }! h  |/ G* `
Revision received November 11, 2010.
/ z* }  g! M- ~: VAccepted November 17, 2010.
6 e# i1 F: I, v5 ?. N4 w: BAbstract
: n2 d; a; ?, g: d  ]% ^5 rBackground: 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. + L+ C  g6 k  H! C8 I8 H9 U0 B
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. 4 r$ @; |- y. _; R8 F# ]
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 ?+ H" T, j! k! V6 X' M9 h' ]0 k3 _
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. : F4 y( r! Z; T" ]6 B
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。
% d4 ?& ^; k5 C) [: @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 Chemotherapy1 X0 k8 z7 }# l! `$ B
http://clinicaltrials.gov/ct2/show/NCT01523587
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
+ @! V- J6 j1 Z3 uhttp://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
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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。
: @) ~8 B+ `, ^. i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
  d, h  y' q( M4 O& @$ |( K- ^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。! u2 O: l- I; a2 Y/ {1 z
至今为止,未出 ...

4 {% B2 o, b$ M" R/ n7 v没有副作用是第一追求,效果显著是第二追求。( _7 }* I8 i0 m; U7 `1 N
不错。

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