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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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1117395 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
& _+ m, d; l9 ^. INOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
. u0 G. C- z5 |4 L! J. u+ Author Affiliations9 D* @6 y$ s! S6 H& T' h& ~8 M
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1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan % N9 t! o8 G% u4 q
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan - O/ r# b0 w! z& n" K
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
7 S( W, b" x; j3 Z, i4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan / a' L+ w0 b) e8 t
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan * f& Q! Z% u% z; `2 Y
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
# i3 B+ e  e% n7Kinki University School of Medicine, Osaka 589-8511, Japan : H$ [3 g+ T5 p
8Izumi Municipal Hospital, Osaka 594-0071, Japan 0 M3 l# Y2 T; q6 K4 q
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan   _8 Y3 D; T* |
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
- R2 ]) X, @. z  yAbstractBackground: 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. 0 [3 V" c8 O4 w, q1 a8 L! e
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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 ; D$ [/ }$ s7 f$ Q. I2 k6 h# {1 p6 b. i

, d1 l# M2 A' R  M7 ?# I- ?Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato ) s( `0 Z0 B. _
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Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
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$ w% e- N' J& b* ^; m5 H) VPublished online on: Thursday, December 1, 2011
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; j3 J- O  f6 t" i2 W  V2 vDoi: 10.3892/ol.2011.507 1 ]$ U3 ^& i( ^, N7 D8 q

! Q4 z' V' n* Q5 S% ]/ b" JPages: 405-410 : w+ y6 w5 `4 q* x0 u% A- @$ g1 z% k

, Z2 R' W: ?4 H. ?0 R6 mAbstract:
2 h( [. m0 a: FS-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.
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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
8 Z8 j2 \( D, V' B8 b  R9 _F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 3 M" Z/ I) c( c) ^! k; l' Q
+ Author Affiliations
  K# d! k/ p# W" ~" u1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
! Z) D. Z, H" U1 ?2Department of Thoracic Surgery, Kyoto University, Kyoto # X- f$ J% o+ `9 q2 p6 j3 _3 `* Y2 z
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
2 o7 l$ Z9 ]4 k3 u&#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 y* ?3 u# j1 {' N
Received September 3, 2010. 1 D# I. m* S# D! U% e( q1 H; M
Revision received November 11, 2010. ( d0 l* L: K) B9 c
Accepted November 17, 2010.
  m* b3 ]: V3 C6 a& s- d) k% OAbstract- h- E) u" v; p/ c3 H( K( l+ L
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.
  p2 {4 J' [' v* d. d2 m  tPatients 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.
6 c% Z; H5 r$ F. \" H6 kResults: 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.
! }( {# x9 ^* m  pConclusion: 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。
: N/ {) w7 i5 R& V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: R( [9 W% Y( \# z
http://clinicaltrials.gov/ct2/show/NCT01523587" x- w$ E# w4 ^% v4 x/ X0 Y% M4 J
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC! v+ b- e/ i9 }4 l, \3 H/ G
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 ! K  e7 y! y  [% J1 `" G
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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。
$ N$ v. D: I; U' a, A0 x) p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
% b; ~5 p* ^* V/ |2 ?( r$ Z7 V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。
1 x6 Y7 [9 K2 E" J2 {8 ~至今为止,未出 ...

. d! }0 _2 d8 e2 E, h$ T没有副作用是第一追求,效果显著是第二追求。/ V# P0 K  a" K, V
不错。

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