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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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1226543 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
5 [/ q- k0 M% b) I: |+ o* vNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 ) f, G* q8 M& U/ H/ ]8 R; p* [
+ Author Affiliations# G2 z5 O% b7 ~# d, O4 a# H3 J

& ~7 d, b% Z- u2 Z  W' N8 x; c6 u1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
; f2 B! U% c4 ^# @0 q: G2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
9 C8 A) t' [0 I2 \; ^1 E3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
5 ^& n1 K2 {# `% _* l: s4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
" Z+ F0 W+ S$ K! q* u5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
* l  F! G5 o% z0 l& U6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan 9 {0 ?8 i/ t! D' y, ~' E
7Kinki University School of Medicine, Osaka 589-8511, Japan
% `8 a% A2 c) i8Izumi Municipal Hospital, Osaka 594-0071, Japan * J. p* |6 X/ {( y) K
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
+ X" n7 u! l1 l( \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 - q; D: k) Q/ y9 L7 F) R0 m: u
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 , o3 C& s2 A9 N# W8 K+ c

# x0 c2 @/ @6 f" O2 @Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
1 k' M  P- L3 [/ f
0 F& b! I, u* n- ]) G, pAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
: F2 M+ x$ L' M7 s5 e! B) t
, z! |; t' Y7 A4 rPublished online on: Thursday, December 1, 2011
$ Y" Z# j# y/ ~2 z1 Q
, z8 [+ ^" c$ ~$ i/ U1 c2 gDoi: 10.3892/ol.2011.507 ! n3 b0 i+ \2 k4 d( v: r! f/ y! Y
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Pages: 405-410 / X+ F0 d9 {5 R3 w/ {- y$ Z
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Abstract:
$ D' `# ?$ ?% C  IS-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." v5 f" j8 G- w8 V# y" J! R

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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
4 z3 t8 E3 t2 CF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 . d& g# B: C# f
+ Author Affiliations3 A; H  j! ?% \
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
6 c# T' g2 `+ Y) ?. b2Department of Thoracic Surgery, Kyoto University, Kyoto
0 j0 m6 |) {& ~8 i4 t9 R/ O1 t3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan 8 d9 |. ?9 W4 a& j9 J, M. _2 w  {
&#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 ' b7 F  ~( B8 g" q" Z! ~8 F; ]$ u- Y
Received September 3, 2010.
( U( A7 Z6 V# C& ?6 X/ s, k7 FRevision received November 11, 2010. 3 `" p2 v! A5 |% ^( ]  q# R
Accepted November 17, 2010.
: q. x* q3 E! {4 U9 A- cAbstract
3 x5 \1 I+ i# m/ x. F3 M& qBackground: 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' [: A  F; U! 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. " k) d& o3 t/ N& B6 r/ x
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.   u& O" ?  K3 _: i% ?0 }2 T
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. 4 O- d% i' I- P4 O. L$ O
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。
& ]3 c, ~" |2 `5 l- a7 c2 I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
& m; f( d" E2 k. f* Dhttp://clinicaltrials.gov/ct2/show/NCT01523587
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9 G4 X7 j6 v4 W1 I4 V* @2 fBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC$ y; h! c0 r& a( }$ C% }
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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4 h3 g" A% L0 |; ?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。; M8 k2 K. h6 \) K- v( v
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。
/ b9 J4 U  Y4 S' V* u+ F不错。

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