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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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1347056 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
: Q) n- O3 Q2 Z) |; f9 Q% Y- qNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
3 I) e& r$ r5 [6 B& w8 H+ Author Affiliations, V& b% ]9 k0 ~; C' Y! Y( i

5 G0 z9 M* Q' x8 k6 Y1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
- b: h5 s$ n+ t2 j" }  X7 i9 I. J2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 1 k, Z1 q/ v* r9 f
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan " I/ X$ _0 |! C
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan % B( y. ^# o2 e7 @3 k; }
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
! D  h2 B) K& H- L) Y6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan 6 Z1 `' J) Y. e6 ?) y7 [% |; c, I, x% ~
7Kinki University School of Medicine, Osaka 589-8511, Japan 4 h: w; u! |+ t0 @
8Izumi Municipal Hospital, Osaka 594-0071, Japan
1 h5 I: n! @5 q$ }5 J6 O5 h4 P6 h- K  f9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
3 H5 ^9 ?0 ^9 u6 QCorrespondence 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 E7 b( h/ m8 B. n
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. ' f( {1 ]( \7 X3 q' 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
( E/ z' `7 z/ I* J$ B$ e$ T4 y$ }! m1 e
Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato & c% A5 S) I, D" |
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Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  & N! ~3 @" e6 h+ A* ]7 N
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Published online on: Thursday, December 1, 2011 " O5 ^( n0 h; C
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Doi: 10.3892/ol.2011.507 ( f0 i$ w: A: g% i; J9 c3 Y9 N

9 A+ l! o- P+ U8 L1 VPages: 405-410 ! e$ A2 k% U. g1 x, c

2 e' }/ `  |. T3 n, E* f, o5 ^Abstract:. P! e2 W* t/ g% l5 Z$ H" X0 a
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.  L9 ]$ c9 q+ |9 a& J7 W0 f3 }

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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
7 V. p4 Z6 o+ D# J. OF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 / c3 Y1 x8 f3 U- t! r* q* c# s
+ Author Affiliations
/ i1 y/ y1 y( O1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu 5 _0 W0 _& @- d. o
2Department of Thoracic Surgery, Kyoto University, Kyoto 0 p( r. c' B2 _1 D" r# u
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
7 C7 e% `$ e& Z% r. u&#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
  {% u  x  T/ O; Z6 gReceived September 3, 2010.
' R8 ^6 ?; l6 t) Y7 C& hRevision received November 11, 2010.
2 ~. i5 C1 Y0 a, G8 P9 ~% j/ K/ DAccepted November 17, 2010. ; n5 @. R9 L9 i4 J
Abstract
# [/ Y: j0 g  D( i  W1 i, i& g- m5 A( ZBackground: 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.
: R9 B, ^0 g: A% Y  F1 S- \' S7 CPatients 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. ) _/ O2 W2 @' \( k4 ]$ x9 w
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" f/ g$ v2 d& j4 u
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 |' ?# [+ h; |- }1 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?! ]# s, ?( b- p( f# I" 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
! m7 O  E! c6 q7 ~1 Vhttp://clinicaltrials.gov/ct2/show/NCT01523587
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8 `; i9 {5 m. V- k" Q9 fBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC8 o: v# e+ E' d4 H# J8 `" f/ A
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 L5 ?/ ]% S) O6 r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。
  g2 Y3 F9 X2 Q3 ^* |% p$ ]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
* h) j& c3 P8 V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。
' r* K/ _* C4 [) Z" ^- ]" ]% o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。
- r1 J1 ?. e6 i" c不错。

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