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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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1305827 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) n$ q! [0 v/ M/ G' h. k; G
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 1 e1 a. \, [. `* g  c9 k
+ Author Affiliations1 w+ M" r- f$ O7 L9 n, B6 V0 T

: _6 [- z/ H# ]1 d1 I1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan ( R$ c# l! l# j" o
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan : _: G2 l1 j% _, r
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan & @& @4 t0 }# w' |1 b" i/ s
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
! l& `4 c+ K9 e( n! {) p: |( Y/ N1 d6 W5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
- _. R) `6 J" `0 r9 O7 Q6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
6 F; x( n4 O1 E: c  i7Kinki University School of Medicine, Osaka 589-8511, Japan , _: [& Z6 k6 p6 ]2 c7 |$ X
8Izumi Municipal Hospital, Osaka 594-0071, Japan
/ z" f, Q$ b5 ~# g  o9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
% c% K; B+ ~8 Y2 h3 W5 cCorrespondence 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
' m+ {7 k' I7 S. |1 b6 s# B( 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.
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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 * E$ c8 k% A/ z  H. t6 G7 t: N

0 ^( @" T# M( ^0 |, W/ Q) Y  iAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
4 Y& f, y" Z8 H# z. z, u- Y  `
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  2 B2 r5 u" B& h7 Q, ~

$ y/ L, q2 b) e$ `  S# B! t4 j7 VPublished online on: Thursday, December 1, 2011
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Doi: 10.3892/ol.2011.507 ; _; H3 M4 Y" F2 w; |& K8 B

; Y  y  e1 K; e2 H- J& UPages: 405-410 , ?+ ^: r* n4 Q: f) I. ~, }* g
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Abstract:$ E0 T; H  P/ L! x. f, o! j! C
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.
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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
# _  \' [" G1 b- ]0 DF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 : N1 w9 \8 Z+ N( a* s0 C2 t) C
+ Author Affiliations; ~! |# F" h5 s& Y( N  j! R" X- r
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu   ]0 `) G- h9 I
2Department of Thoracic Surgery, Kyoto University, Kyoto 9 l; O& C0 @; D5 E
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
+ V. r; w1 B; k/ ?7 ?2 M9 a4 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
; b4 x) y0 m3 HReceived September 3, 2010.
* H7 u- A6 c2 b0 i' N. S9 b4 U/ @Revision received November 11, 2010.
& G- v) e1 X2 H% J0 z$ g  E! O1 TAccepted November 17, 2010.   W0 {1 |7 V4 a  C( C
Abstract
2 ~5 F: @; P; A" A( g9 _0 u2 TBackground: 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.
! Y/ |2 p  c+ V- L, bPatients 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.
( F* g" c5 X  f+ w' CResults: 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.
! H7 T8 w; d4 e4 B0 L+ E# v1 DConclusion: 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。5 B4 C; y' F% P5 F& Y
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?1 M  f' j+ z) t) M3 M' m
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 Chemotherapy3 D! m+ N6 w; P. f7 V
http://clinicaltrials.gov/ct2/show/NCT01523587) H* P  h" r, Z" {$ X
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
& m+ i. y/ D4 M7 U! v: bhttp://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。, X2 g5 l3 @# Z1 Z
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
1 O0 ^; R7 T1 ]2 W+ @0 X0 j! J! m2 x/ b+ 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。) \  D0 W9 X6 ?- i
至今为止,未出 ...

7 x, o0 L' b" `7 m7 P( [没有副作用是第一追求,效果显著是第二追求。
& _+ U2 b# G2 L不错。

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