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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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1126115 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 Type6 \) a# U4 T0 A& k2 c
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 ) {' p3 u' k$ I) G$ n
+ Author Affiliations& O1 T- B* V9 U
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1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan + @  P* l+ S* s1 [  o8 P9 l
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
, E1 R  O2 l2 c3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
5 D% v! r$ `- w$ y. l: n5 a4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
( i4 A4 v% F0 S- V+ z" F" b: D, p5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan 4 Z0 `3 Y7 h& g, ]9 U
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan   n/ o8 W0 `$ a' O
7Kinki University School of Medicine, Osaka 589-8511, Japan
) O) g3 L' A$ u9 _( X2 V% I8Izumi Municipal Hospital, Osaka 594-0071, Japan 3 f9 P+ H0 a7 C8 X$ y: o' }
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan # ]3 g2 K1 t( g) j& A+ ^& D
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 : B& P7 R+ d+ i. A0 i5 W
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. : U1 Y' S* B" {& [+ |& y2 w
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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 8 n2 v. ^5 X' @& v
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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 8 ^2 |2 K5 L& ?# ^1 d; `" k
* N" u- w6 W, ~& h2 d' Q4 [6 C& C) L. f
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
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0 \5 t  j3 L9 `+ q0 NPublished online on: Thursday, December 1, 2011 0 m  E$ |$ }" J2 P

& W, d  {) U0 D$ b; i$ WDoi: 10.3892/ol.2011.507 6 [# J8 r& `5 W0 }3 v, p% v6 z% o
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Pages: 405-410
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Abstract:* ]! P5 j3 ]( b4 t. p* o4 L
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
& \0 F. J# ?1 |( I( @. uF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
2 ]* |% G. K  s: l2 t2 x+ Author Affiliations
& Y% X# K% e, R6 p( n" ?  Z* T: [1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
: g4 w9 ?' o& z8 C- l. X2Department of Thoracic Surgery, Kyoto University, Kyoto
( P- i  F; [7 h3 k' U! \3 k0 |3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
8 b# C- ?1 `8 w3 H9 |+ L&#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
2 a6 P: e) W) QReceived September 3, 2010.
1 \& `4 }0 Q' n1 s0 h3 HRevision received November 11, 2010.   Z: Y0 L% w; ?; D  u# t
Accepted November 17, 2010.
& e% b# u. `& M" m& u1 Y5 I* ~Abstract1 p. z2 I' f) w1 a8 J# M. N
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. # u" C6 F4 L) i9 b- r" S' j" [
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. ' ]0 e' O  C5 q0 _
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.
2 F7 v" }* W. B9 S0 W! [; RConclusion: 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。8 @9 g8 |3 O( Z; G* ^9 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
; i5 v' o, B8 W( O$ Q& Rhttp://clinicaltrials.gov/ct2/show/NCT01523587
  h" `  `, d+ D4 Z9 ~3 D; u9 E4 s9 Y& ?8 x3 ^5 u/ P5 f& n  e: ]
BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC1 O3 K; U. p. c: p1 C3 p( o" ]5 e
http://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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" @0 O3 V+ ]  |* h$ O' g, Y( W' L7 w7 U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。/ J$ _* p5 F. D
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
: O( ~+ _& m& S/ b* p$ j, R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。. y5 P, ]" J! v: S" q* z9 [
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。
' C+ r/ Q& l! ]1 x不错。

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