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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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1174257 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 Type4 _: S6 }2 r: e, F: Y8 m
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 ( a3 p! \; j, w. }! B
+ Author Affiliations# H$ p: \+ w5 _6 n' k

: S8 \+ S1 d, O* `1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan & m" o2 N- ^0 y7 f! e4 u. u2 D& L
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 3 O+ }0 t  R1 r
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan " K- o( p7 G" a2 D( ]
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
. l! y6 i! M  ~3 U5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
+ L# V' C+ j9 o6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan 8 h1 D! X1 r/ h
7Kinki University School of Medicine, Osaka 589-8511, Japan ! o2 I! b8 q7 R+ N3 {" r9 B5 D
8Izumi Municipal Hospital, Osaka 594-0071, Japan * ]$ d: i. T" [' w5 X: L# |& g) P
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
2 f% P. c/ O- S" h8 E3 fCorrespondence 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" S6 p3 _+ ]2 A9 s+ WAbstractBackground: 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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. a0 O+ T- t: t. ^" n7 J5 V9 n$ b" \Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato * S/ _0 h; K2 t+ B) T. x

% {5 o4 K+ r4 V; `, M* g7 {Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
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* F1 P( ]0 U3 M3 [& \& ]; yPublished online on: Thursday, December 1, 2011
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" ?1 T" g$ h: Q1 S3 rDoi: 10.3892/ol.2011.507 7 g* ~# S: C* A

, D  `# d: `1 \; c( ^+ xPages: 405-410 * S6 F2 w: E. Q6 C- }" p, G0 e6 S
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Abstract:3 z* u4 ^+ b/ N6 s* F& J
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.; K3 r7 J4 _2 b: p
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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 u, _. N3 o7 W5 BF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
+ |1 S/ \) q- z# C  m  q2 j$ X& i9 V+ Author Affiliations
9 Y5 B$ f' A9 Q3 x1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu 2 Q  C& `' O, p4 x. s
2Department of Thoracic Surgery, Kyoto University, Kyoto 1 u4 A; T0 i$ Y# C2 a3 ?! o  V' T5 z
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
$ t: ]1 `- p3 d6 n6 K&#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 F2 `" w0 X4 ^& i  m0 s" j
Received September 3, 2010.
3 U; L$ b+ D+ h0 ^0 a' u& aRevision received November 11, 2010. . r6 y2 T$ x/ o  m# [3 p
Accepted November 17, 2010. 7 X& w( c4 k. Y" x, }/ s
Abstract
' O$ F  v; F/ e. L2 ?% sBackground: 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. ! r" V) K& U, c% W1 ^7 e  I
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.
- k3 T; t6 k1 R4 ]( S; i2 C; RResults: 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.
2 Y0 N; t+ r; G2 B- Z4 JConclusion: 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。& o: S1 w4 t  ~+ g3 G
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 Chemotherapy6 ~( [/ d- J9 n- v3 B
http://clinicaltrials.gov/ct2/show/NCT01523587
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1 L7 n+ E7 v$ }- N8 p% tBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC; Z/ V1 e' R3 o( 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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: y- I8 n/ W- i" n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。
' G6 K! C: c' t  K, n8 r  K& ^' b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

2 a# i9 k4 q* s' [没有副作用是第一追求,效果显著是第二追求。$ e3 g" d! s! I
不错。

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