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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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1089071 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! k* N' v$ O, I: B
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 " K" [0 B( Z' V5 t4 u
+ Author Affiliations
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1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
$ c4 Y$ s  w* V8 p+ Y# s. C* G2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
: @' `0 A6 K7 B4 F7 V, n' c& v3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
6 w1 u7 b7 O0 R# g# i4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan ' q* \1 C2 d/ x6 v) @' v' R/ a8 {
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
, ~+ ?9 U  Y/ C9 S( O( `! u5 J: b6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan   U2 _. ]3 E8 R2 o2 J: h# Q
7Kinki University School of Medicine, Osaka 589-8511, Japan
  v( c/ w! r5 e6 S$ ~1 x8Izumi Municipal Hospital, Osaka 594-0071, Japan
# F7 t5 J- z: \2 Q9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan / K3 ]. v, ^$ H. ]) z. C/ W
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 $ T  I  c; z9 `% ]
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 # i7 M9 Z% C" C) Q
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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 . c5 W2 g1 a3 E8 K

& V2 N1 Z3 g* _- F3 n0 \Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
# G/ o! n7 H( I2 E8 e% X7 W( d9 }8 w, n) w- F
Published online on: Thursday, December 1, 2011 : }# b, a; X& }
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Doi: 10.3892/ol.2011.507 ; n2 u7 m* P0 M5 A* P" m4 Y' x3 a  Z
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Pages: 405-410 ! x* v  ]. o9 G7 q- ^. M* B

. Z+ T- W1 B& k( `7 j, q7 M5 b& jAbstract:
4 x1 `; Y) y" e& [) rS-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 R0 o( a6 a5 Q# p, d# B( ?6 J' T
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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
) b8 O! ~0 v$ M. U4 n- B! J0 eF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
* a0 m, {( X8 l: W. V' z+ Author Affiliations
5 l, W3 U+ C) B2 m, i/ F1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
8 G3 N8 B0 n! M2Department of Thoracic Surgery, Kyoto University, Kyoto . w2 k8 `5 d+ d; n3 c
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan / Y- Q* f5 A1 a, C
&#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
4 S2 `; k+ m0 x: T3 X. NReceived September 3, 2010.
$ ?) D( D+ K1 N9 [+ NRevision received November 11, 2010.
9 U+ C" q0 Y6 {- C' B. H0 v" V6 N; iAccepted November 17, 2010. 8 m$ x% H" G% l7 U8 Q. L
Abstract- U/ J5 u+ f3 l! F6 y) m
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.
1 Y) B  Z  u3 ]5 j1 ~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 {& h( L/ T3 j6 l- W2 W9 q- o
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. # f2 R* ?3 _6 z) i; ]% P! _# d
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. $ I' v+ ?' x' |% ~( ?$ T
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。9 ?  K* |6 l+ ^5 Q
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?9 J. a. ]1 y* C
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# l9 `6 {; V/ w! \7 y
http://clinicaltrials.gov/ct2/show/NCT01523587
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+ [5 S  U4 c# _. QBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC4 q  Z* w) p5 @2 Y0 U3 x
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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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。4 _, K, d5 d3 ?! Q# A( j! \+ Z/ y
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

" ]! r1 ?- w3 j9 m4 n没有副作用是第一追求,效果显著是第二追求。: A) x+ S5 c% I6 D
不错。

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