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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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1154711 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
+ i  [* A, e5 YNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 ( @* B# T& u- H7 a& d! G4 h
+ Author Affiliations3 V4 C" k$ A' n0 y; f
% G  b/ K: j1 z+ k$ w
1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
4 w& S* @  M- @; N5 Z9 ~: g" o2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
. E" @) y+ R" |# B- @+ u3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
0 N! n* q2 ^2 h0 u5 |7 z! \6 K: B- ]4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan * O8 d4 C3 q9 i4 h$ P( }* \* ]
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan ( p1 U* E$ q: ?* P( K- H
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan ' j* I$ g7 [* [6 R* Y. T
7Kinki University School of Medicine, Osaka 589-8511, Japan
' ^1 S' B3 M. {2 A" x8Izumi Municipal Hospital, Osaka 594-0071, Japan
4 u( K8 R/ V2 |0 ~# Z% K; N1 _9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan . ?& L4 o) [2 M6 |6 V7 y
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 8 j6 e! Q7 e+ K* W4 {* V$ k
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. 3 m  x  J( ?/ y. f" L- `- `8 F  Y
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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) p2 N. y5 y% P: l! t! O7 ^1 a3 {* D
Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato 8 e" H) _" o2 k0 w' y) G
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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  5 u* y: a: J6 N' a% u& a! c

/ v' U9 A' m& I% C; h5 @. RPublished online on: Thursday, December 1, 2011 $ ]/ q: N: d% p* U) s

9 x+ G1 v8 O* ]- D* BDoi: 10.3892/ol.2011.507 0 L" u# X$ ^( i: O/ Z

  `; }+ t6 Z4 P1 T# e7 t/ w" RPages: 405-410   H6 V3 |( c+ W+ }

7 m& Z. H" P6 n& \9 Y% kAbstract:
& ^0 p9 E0 t. ^& sS-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
" j2 Y' ^' D4 i; X) P# Q' W# gF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
0 o8 v( R3 m+ L) H, i6 U8 E) u+ Author Affiliations
# n+ d/ F6 L# C+ V+ i. i  C- K1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
8 v$ }+ y2 P( K2Department of Thoracic Surgery, Kyoto University, Kyoto
/ k: K2 ^% b" C8 l' Z0 V3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan 9 P; W4 r' |' i9 q* X% X
&#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+ K2 s# b- E/ X0 X' K* E3 h5 A
Received September 3, 2010.
6 }4 O3 z9 Q- D1 ARevision received November 11, 2010.
% v$ Z4 X- H  O$ DAccepted November 17, 2010.
# B3 W5 s' E& j9 R3 o, I8 `! SAbstract5 u" D$ l) x2 l, Q8 c
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.
3 |6 c0 g) s& D$ 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.
! u* C: J! p! ?+ D* pResults: 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. & D  O4 R  \. U( L! ~
Conclusion: 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。
( g4 Q  E+ I% y5 a9 V! z$ }( l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?  u# Z/ g9 K+ I* y6 X4 V/ k. C) H
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& X, w! @0 x- l8 V( C2 g8 F2 _9 s
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
2 l) d: ^% r- ]9 Xhttp://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 5 a7 u6 I( M. {6 m& K! d4 X- N& Z

5 `: j& I- X0 D, t& l- z4 A- B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。: H9 z. u4 p' s1 d9 W6 h9 ^& y  p; t' X( {
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
' ~3 e0 X# a5 W* n# 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。
$ U$ V8 E5 z" u; G$ ]" B- b至今为止,未出 ...

% q7 K7 m/ ^8 L( p$ c没有副作用是第一追求,效果显著是第二追求。
8 q; C" ]: b4 I# c不错。

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