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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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1274589 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
4 x. K$ M: W; W! l+ c. uNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
' ?6 I5 B3 n. A9 Z7 P+ Author Affiliations
( p5 b. N. O) Q9 F1 L! n; g. z5 D" P0 F; O) M9 e) d& ?
1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
  h4 `  E0 k( J7 K8 d2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 1 q; }0 p/ Z/ h8 P% e
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan - a  i" @) h1 w& x7 D
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
  K. k8 A4 G& r! [0 l4 I& W6 L5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
5 H- O4 Z4 h9 ?! r7 _6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
& b6 R7 X& S' d& r9 O5 B7Kinki University School of Medicine, Osaka 589-8511, Japan
; `$ w/ S$ g7 q4 a8Izumi Municipal Hospital, Osaka 594-0071, Japan
2 m+ w- ]2 J% h6 k9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan & s6 ~7 [- q+ y" o2 z* \& P2 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
- ^4 A, O2 [- N. [1 n, S/ EAbstractBackground: 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 S% Q* i8 i- q, ^; s" Z
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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 * N- j$ x" f, c3 I) i2 Q
+ K! T0 d8 ^$ x& O
Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
+ b: W3 o8 @/ Q' [6 ]9 r6 [: b6 X, r8 `# r7 ?$ Q0 |) p9 C
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  + w* a$ P- V& g; k

6 a7 R4 G/ R& q# O0 z: _Published online on: Thursday, December 1, 2011 1 }& }0 |$ A* N

# E6 b, ~9 f# O8 iDoi: 10.3892/ol.2011.507
0 i+ E5 a- t. N# P% x& P# P% E5 Q( q% T: U4 c$ T
Pages: 405-410 ' a( J8 |; u# W
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Abstract:
! C, _2 ]( h& e8 E$ i3 AS-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./ @" k+ X1 i* e6 @; B
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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" e+ U" h9 l7 Z6 ^0 {; d
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 5 j! G( F) P6 U$ O. a# v
+ Author Affiliations
" `! `7 {3 o: d; a" q% N1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
+ Q& d& E% {' V+ K3 Z# w( e* T2 s2Department of Thoracic Surgery, Kyoto University, Kyoto ' V$ v. `$ L* m* K/ ~0 E
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
" R$ D9 l. ~* b3 K7 E1 d, C- a/ t&#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
4 A9 P2 ?! ~+ dReceived September 3, 2010.
9 h( Y0 V! s0 n. QRevision received November 11, 2010. % `& p' D' k, s4 C0 t( B/ `
Accepted November 17, 2010. & S+ `/ f" b5 U4 @+ Q& z' V
Abstract% i) ]9 w- O. a& k! E
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.
" b: e+ n$ K6 r$ v& }" i& w7 OPatients 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. 0 l4 N, r, ]/ ]; b; S3 H& Y
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. ; q) K8 m( u' ?5 u" j# R6 a3 x
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. + _6 V7 C3 C  g, F- A
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。
( z8 `# {% l& k% G1 p, v" z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, u/ x& ^, A# Z5 N2 _1 F
http://clinicaltrials.gov/ct2/show/NCT01523587' a! Z- j2 P: y( e- Q
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
: f: o; l$ R' s3 a/ Dhttp://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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$ M' c" n& T) W! ?% V  V1 v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 x( r; V+ ?" E* ]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
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没有副作用是第一追求,效果显著是第二追求。
" a* Q$ q6 I9 y6 d. C不错。

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