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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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1389160 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
0 {2 k; R7 R% ONOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 5 U# l) b& w- G+ L
+ Author Affiliations  t  x0 D8 [; ]3 ]+ b

5 Q& R# g& I4 X3 I; D1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
4 ?6 w! ?! w& p3 m& P2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan . M3 f+ b" x/ J; B& }& S
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan : u6 ?7 ^3 ^7 K' z6 D6 }( W
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan 2 s* c4 D/ J9 ~0 F
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan ; y" @. K, E( s% Q) w$ T
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan * s7 o9 n. w$ \$ g
7Kinki University School of Medicine, Osaka 589-8511, Japan 8 d( C: C; c* v, e; ~
8Izumi Municipal Hospital, Osaka 594-0071, Japan # ^8 ], G* j" R- `" x5 \! b
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
8 Z' \9 S, V4 w1 j& R/ U* b/ vCorrespondence 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 , R- E- B  }1 D9 e- T
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 , X3 U2 ^! }; b. ^3 V. i6 p
& [# `* i& G% p2 B; |% q
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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4 k9 w" c* g0 t4 i! S+ YAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  $ n5 V5 f( h* ^' ]- b3 W- l! U! M/ s

6 K9 n& T3 w  u8 [2 o, fPublished online on: Thursday, December 1, 2011
9 R( G: v) e9 W8 T4 I  S* I+ a7 T9 s/ I3 B% \0 @$ ^0 @
Doi: 10.3892/ol.2011.507
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Pages: 405-410 ; J4 |. S( j7 d0 A

5 n, Y7 W* W; ?' u. c# x: A, _6 pAbstract:
7 ^; r# z" v( I7 u& i. LS-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: d; _! x0 Z, E  R6 _7 G% M
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
# h8 u# x2 I& O0 v) C# ^! e( ?0 m+ Author Affiliations
3 A" }8 t9 X( d6 B; @1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
% T& h/ Q, O6 P# U/ N$ ]/ s2Department of Thoracic Surgery, Kyoto University, Kyoto * f3 d* [+ {4 f8 l/ Z) Q- [
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
- N' P4 I) O& 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 - X. {2 S6 @" `# Q/ v
Received September 3, 2010.
1 ?8 v7 L; p; V  URevision received November 11, 2010.
8 ?$ i+ N" s; [( [7 y* v0 Z- qAccepted November 17, 2010. 6 ]" K' J3 t& `* m2 x
Abstract
1 e4 E( S! X1 @! U; l1 jBackground: 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.
, p0 l( h8 }0 z' I" v8 s- c' A2 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. 6 N, f- j' V& }" H4 l
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.
" `, r( f, N5 gConclusion: 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。
. f8 w! \. B' M! v/ u- t& 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?# ]2 h% p8 y0 Q1 {7 E8 q4 L" Y
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 Chemotherapy1 ~6 F' F6 i/ ]( f  Z
http://clinicaltrials.gov/ct2/show/NCT015235876 S: f( {: F3 a! }1 }8 G* V
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
' Y# }, i4 Q4 j# o/ ^* Shttp://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 % A8 k5 ^$ E! s8 Q* V, W

8 }3 E. p6 F  e( e6 O8 B: h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。
- O5 R1 s1 z! ^) 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
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没有副作用是第一追求,效果显著是第二追求。
* h2 ?& G9 l# v, Q$ ?不错。

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