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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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1388626 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. ~, o* A. v. b* `
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
5 S5 r* B9 a- i+ Author Affiliations4 m( \4 d4 K8 W) J

3 D4 c5 v/ C9 a# G3 L( A  Y& c1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
) p. o3 U& o4 C5 \2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
) j3 W' ~. w+ p( Y/ g& G3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 3 D. w. Y  D8 z' e
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan 4 Z2 @6 M+ P2 L! ]" D1 O7 p# f
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
& r0 }. ]1 _! ]1 y: a6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan 9 n0 Z0 ^2 D) g5 J9 [; h
7Kinki University School of Medicine, Osaka 589-8511, Japan
0 {* J; a2 Z; Z. }5 i8Izumi Municipal Hospital, Osaka 594-0071, Japan
" V2 K6 q9 L9 v7 U, t* \9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan . l& e4 f" c# f: K% K1 q
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 * m! \5 z$ {3 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.
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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
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4 s6 _' K6 R. U% V+ k  @Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
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# U7 I2 m+ w  H' l7 |( yAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  ( u2 d  o2 r+ X

0 o2 k8 G& `  Q- UPublished online on: Thursday, December 1, 2011
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- U8 c% @- n; }! c7 c6 |. wDoi: 10.3892/ol.2011.507 $ ^: w4 o+ F5 m
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Pages: 405-410
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Abstract:7 M, n2 N' ^: @. R5 I2 X$ W
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# G# a% D5 Q2 I  A8 P4 v' F: ?
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
. J+ m% C; O$ D3 F2 |- c* M+ Author Affiliations' ~+ t0 P: S- J9 u% L' b  X) [  I
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu / e1 b8 @9 Y, f# X
2Department of Thoracic Surgery, Kyoto University, Kyoto ( V$ b2 O, @* q/ ~8 t# O- a# a
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan + G, U0 u7 I7 P( p
&#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 . E7 [! k( g7 t1 x& I
Received September 3, 2010.
: Z) a7 w, K/ q6 p* IRevision received November 11, 2010.
( H8 ]2 n1 f; G  ^$ L2 S' SAccepted November 17, 2010.
7 ~2 F* Z$ h5 L) l' q! U: e6 IAbstract
2 [0 B: n( t" kBackground: 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.
8 ?, T" E4 r, h6 u7 w' m; @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. 4 n9 s3 H, F5 P' \4 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. * }1 Y# q2 W8 h* O
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. # {+ M1 I- M6 n# d" v7 u
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 O5 ~7 G8 R& c3 d8 `7 V1 p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 Chemotherapy4 V5 T* g) N9 @/ T8 W
http://clinicaltrials.gov/ct2/show/NCT01523587
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- I0 K8 B$ }$ X# NBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC3 }7 N# \7 W/ J+ m" k9 G+ ^
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 $ O) Q! d+ t8 F! [% o
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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。: n* Y, {' {7 W- J/ z2 a
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
/ j7 R5 J( F8 m$ M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。9 ]5 A. a* H: s  A+ Q' E* ?
至今为止,未出 ...
# ^2 ~' b) E$ i. Z2 c, c4 S
没有副作用是第一追求,效果显著是第二追求。
) `! v6 W: D+ x9 |' i3 l, t不错。

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