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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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1405182 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
/ x( J" b, G) Q. L) QNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 % G7 y6 I9 ]- t$ @9 e* X4 Z
+ Author Affiliations8 T5 g; T8 l* s  x

; A. q; V. `( j: p1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan + [& ]' d" J7 X( m/ R  U
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan ) l$ a. ~" u4 Q' V
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan % y5 s/ A7 x, G* o' `/ D( ^; n" h
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan + L6 R; L* {# Z4 r% W+ q3 `
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan 5 s1 n# k% i2 H% C
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
( U& S8 }$ `! M4 @7Kinki University School of Medicine, Osaka 589-8511, Japan
4 I. H7 ?4 f+ g! S( `8Izumi Municipal Hospital, Osaka 594-0071, Japan ! Y6 ]$ e- \% |/ h! j
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
" E) q; c" p, x/ V8 c1 h. I8 D1 YCorrespondence 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 ( ~5 c; q* j2 @2 X
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. ' m  t9 y& p, F. ^. b3 {. b
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:52:43 | 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 % D1 W5 c  \5 w1 Q2 C
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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
, [" P( X! p2 @' t# [3 X1 C$ O9 Y+ r( P$ E; o
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  . |; S! N/ n* P' G' G" z: Z0 [, s

4 m$ Z9 ^. h; UPublished online on: Thursday, December 1, 2011 9 V5 n* U9 C1 k- o

/ A! D7 ~: ]+ D6 L& P* n" v& e; [# MDoi: 10.3892/ol.2011.507
% y. f9 _& z( L/ d( E% p# \2 H+ q0 q& a
Pages: 405-410
* |5 y; A4 x! e$ k! g! `$ k, Z5 i! W1 W6 j. _# C; U% S9 F' }1 F
Abstract:
% k' m2 {  v& O5 m9 c" F; cS-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 population6 t0 }" k+ b- u( Q
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
$ n8 V; O4 J+ `3 k# n+ ?+ Author Affiliations2 X. N( R! {8 M. p: Q
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
6 B+ G. \( z& B/ R  C* O  J2Department of Thoracic Surgery, Kyoto University, Kyoto
& i3 ^4 T- {+ L" ~3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan ' J8 w, [2 E! Y( R
&#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 7 `" E4 }$ n: q, H
Received September 3, 2010.
8 U( n- Q" T' VRevision received November 11, 2010.
7 N' M1 D- h3 ?# kAccepted November 17, 2010.
0 Y: d- O8 o1 JAbstract
6 s9 U" P0 X  }3 J# d5 FBackground: 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.
; ?  K9 h( i2 IPatients 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.
! ~% y- W: q# ]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.
/ |) K" o9 o: {; l" m6 ^$ }# P% NConclusion: 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。
& z/ @  Y9 w, S" ~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
# k8 r! n* D! [9 ]# x- Y% a  d) Vhttp://clinicaltrials.gov/ct2/show/NCT015235878 W" z0 \' r) l% o3 e

7 m( C3 |. L  v# x' j( }BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
/ u1 H' R) w0 qhttp://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。% e) k; }5 h* O; `( u& c- \+ s
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。: r4 g( o$ Q$ T+ L
不错。

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