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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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1151446 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 a% ~" F* x1 r4 n  M9 u% GNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
9 p, X& B5 z( Z1 q4 y+ Author Affiliations
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1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan $ ]  I: g# n# G0 U4 X/ e1 x& b9 |8 D
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
" C0 I+ l/ Z2 D% [- i3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
& c7 C% T0 S& G' A$ Z3 l" O  T4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
( e; W' E; W& k+ p9 n& |# M$ j0 O5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
- x5 {% Q# P+ A( r  A6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
- w6 _( Y& F3 z7Kinki University School of Medicine, Osaka 589-8511, Japan
+ U! G3 X% e4 n" _5 v: {8Izumi Municipal Hospital, Osaka 594-0071, Japan
/ V: Q0 ?" B5 d* i3 A9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan 9 W: c5 U0 Q) c3 Z, h. t8 Y/ o
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 0 Y& M4 [& U5 m! f
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. 5 u5 n: |8 ?0 |. h) w0 y: F* Y; ~6 W2 L
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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 ( v8 p& h' Z" y  g2 \
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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 ' X0 F- A1 i. C* ^$ G
$ _& S1 M7 l6 \6 v8 }9 X$ ?7 Q
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  8 [: D5 _- E  u

: i$ U( ^" W  V; t. u9 V0 YPublished online on: Thursday, December 1, 2011
. f5 X) d) a  _# V& _( e+ |
9 w; A# ^5 `7 ^! [Doi: 10.3892/ol.2011.507 & Z9 S) j2 ~, Q) `$ C

  O/ ~  {" t, J  K7 r7 ePages: 405-410
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/ ^- S) a& y0 F! N3 z' G- K1 H4 qAbstract:; O: l4 h- P1 g0 [
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.3 q( G* B4 f4 s7 i+ s

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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 r3 Z8 z' b$ o9 o3 N! S, p
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 " N7 d6 `# w0 Y+ P% v
+ Author Affiliations
# l9 @3 \- Y  |' B" }8 L) c* N1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu 9 B5 d$ ~& ^, d' \1 |1 O
2Department of Thoracic Surgery, Kyoto University, Kyoto
* @9 g' T1 a; c5 O; X* N7 I. d3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
) Y+ f# d$ C+ p) H- ?/ s$ @3 ~( 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
% J5 t& v9 y4 \9 R) rReceived September 3, 2010.
7 U* w: b* ]2 R3 z6 C( q" iRevision received November 11, 2010.
" F: s/ g7 m/ o4 ^5 AAccepted November 17, 2010. ) d$ R- J7 e8 d# E1 h$ }
Abstract
+ X7 }  N2 g+ l2 ^1 |- J4 oBackground: 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.
( z8 o$ ]5 l4 m8 c2 j1 r1 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. 0 t% H. z- w7 J3 g. i" f! t
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. 7 z; k' V: A9 |" \
Conclusion: 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。
1 g% p* J& }9 \8 p) Y+ R2 w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?# a, ?& E, k: S% q" B! m0 h% |7 B# _
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* I) w8 v# t( |! z1 g
http://clinicaltrials.gov/ct2/show/NCT01523587
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; X. ]. V& F- x" V  ]BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC! L* Y* }7 {6 D9 o$ K
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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3 C) A1 C. A- ]& l: ?1 y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。$ k$ f3 e9 P& W' A/ g5 u3 _
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

4 f: r& y3 H) ?. Z0 t没有副作用是第一追求,效果显著是第二追求。
& b6 ]( f- M, ]不错。

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