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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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1271233 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
0 W6 [* \4 a  E3 b% I9 FNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
$ c6 o- X% x1 {/ E+ Author Affiliations
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1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
8 _  E) i# w/ u; ?8 B2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
9 ?( U6 c( ]5 J' q0 U& a( g$ S% T3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan , y2 G# r& ?( q6 w' y( p- {7 ^
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
# E9 ~8 \1 V7 p0 Z+ X5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan " j: w" U, g; @8 q. n
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
, O! d, S1 Y2 H3 P% G9 @7Kinki University School of Medicine, Osaka 589-8511, Japan ; i. R$ v) V+ V
8Izumi Municipal Hospital, Osaka 594-0071, Japan & s5 f4 ?- X: |) C
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
9 X# J0 Q0 g, h, b9 p$ C. K& \; P* pCorrespondence 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
* N0 L1 V( ^) H: V2 WAbstractBackground: 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. . r% O" U3 W$ ^" m2 A

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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
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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 & K0 m8 B9 k3 \# L# Q
$ K( }; q9 U8 c" ^: r
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  1 J2 O8 W4 f$ U
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Published online on: Thursday, December 1, 2011 % x( Z* D$ t( U9 a* |) I. `
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Doi: 10.3892/ol.2011.507 2 T1 i) v% d0 b) o8 p

* e3 U8 T, ~, f2 o2 P! V: {Pages: 405-410
+ I; [+ \% c% u7 q, o9 @( b- `0 H% Y& P) K( W
Abstract:8 z% p( I% }1 K. Q; M* E
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 population4 `; }1 p3 ^' A: H5 K
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 9 c6 v$ S5 }& E- E0 P& r
+ Author Affiliations, U- G( k1 S" h1 H% f& ?, h
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
$ p/ r3 u2 q, G! B3 y2Department of Thoracic Surgery, Kyoto University, Kyoto , V/ [. n0 j5 O7 E7 d0 |4 s! B
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan , S: r  U0 [4 P" [1 p. h1 x* f( Y
&#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 1 ^! Q7 m! o' e; m! l
Received September 3, 2010.
& z" q9 D5 c+ R+ g% {Revision received November 11, 2010.
8 P' Y, n2 u( u2 sAccepted November 17, 2010.
0 {$ h! {- \3 wAbstract' D$ Z1 F4 a2 V! r( `  p, ^
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.
. Y& D& V$ G# H9 D1 c, D2 y0 RPatients 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. 5 ]7 ~7 \" s9 c: I
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. ! f+ \" j5 J# q! c* X: f% J& s
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. & l+ F7 A% p5 G. f# I2 z, O' A7 R
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。( P9 {8 s8 S/ n9 ~# c' r
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
6 N' N* A' z6 W+ d" M' @' Ohttp://clinicaltrials.gov/ct2/show/NCT015235877 M6 S. M. T8 ?
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
  [; P% N/ Z4 y' A1 [: ^' d8 nhttp://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 p! f* q5 A' X! N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。
& t4 A$ }) C' `6 J9 Q5 `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 $ l4 n- ?3 z6 F
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) i4 G7 W: @; @, t2 @1 B
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。
( b  [$ z+ |9 F3 z不错。

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