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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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1271654 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, D2 B2 h2 u- P
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
( f3 Y3 A, t( F) L: `+ Author Affiliations2 o+ r+ }3 Z5 {- ]: e
9 k  H7 U8 Q; H0 S  X) I
1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
! \# L7 {* }* ^& N5 A6 w+ P* O% p2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan ; o: S7 b. |9 ~3 v) {' o+ c
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
2 X! ^  E! i( q3 y& M4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
9 Z& s; o1 q' e; }: d5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
' I' i+ _. O7 H/ i6 }6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
: E' E; o  N7 w" i7Kinki University School of Medicine, Osaka 589-8511, Japan 8 i" x- T7 [4 ?% ~
8Izumi Municipal Hospital, Osaka 594-0071, Japan
; S* a) c4 ^) l' B9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
$ ^3 w( z& S+ f* V2 UCorrespondence 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 % ?# \. t: d, {. j# L9 q6 L# v& E
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 + ]# V2 B' y7 u+ a# G2 M
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Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
2 E/ b7 Y- N5 ]8 J: u" x
% U' r6 t. D, HAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  , a2 c7 f' T4 t; q2 l

% ?' \5 _' l% p0 y7 P+ n) PPublished online on: Thursday, December 1, 2011 # x" @! u. s' u8 N- G( h1 n# ~
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Doi: 10.3892/ol.2011.507
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+ D5 R# P% q, Y! C) O; P' E2 m, IPages: 405-410 - H, F' B) O5 P4 F

8 v) A) M: Y( h4 m1 r' xAbstract:/ o: d! }1 X* @5 b2 }; t- z* m
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.4 n% d" X& {9 V9 v) y

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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:57:27 | 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 population8 q  L0 e' ^$ O. s: _' Y, S
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 ( Y+ j. ?  H8 \# H' P! \
+ Author Affiliations& J' X* f0 e* a5 E
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu , v5 x* P$ V1 f( q9 E  F6 w
2Department of Thoracic Surgery, Kyoto University, Kyoto
7 ^3 _; V- h8 R# `5 Z) j0 Z3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan ' B' D! L+ }! K/ X, 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 $ M! N/ k2 H, r5 I+ S1 j
Received September 3, 2010. ) C% Q. i# L) t. g
Revision received November 11, 2010. 5 ^( k1 l3 X0 c- a7 v7 Y) {/ Q: e
Accepted November 17, 2010. 1 Y0 g( C3 u+ H6 a6 s8 K
Abstract! X2 c4 b: L" N8 @8 x- x1 I: ?5 ~
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- {: ^6 }9 }" p3 h8 W+ 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.
& v2 U2 V4 r' g9 \/ G: @& oResults: 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. . |6 [: f7 S) K9 B  B# ], q
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. 3 r+ _7 H- W+ n2 r1 G$ 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。+ B6 s% i$ x. ]+ O
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?( t" r4 P$ ^% s5 V7 ]
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
4 Y; \/ [  P0 d% h2 G9 z, m' L. vhttp://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
" B7 b" S. R) G( f  Hhttp://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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1 J' b# A: y: l2 d7 l. M; I/ d9 ?5 \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。
# b. y( A) m" T# ^4 W$ [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 % F! L7 g$ y5 D7 K" R4 f0 L5 }
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。
6 M! f* t( Q, I$ ^1 K& w, S' t至今为止,未出 ...
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没有副作用是第一追求,效果显著是第二追求。/ z- s; V# t7 y7 U9 l& n& `
不错。

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