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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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1406254 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
& A! B9 |/ ?/ ]2 V! s( mNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 % F4 S5 ]) T7 E5 B4 Q0 r; N$ [9 z
+ Author Affiliations
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/ v0 V1 X+ H2 ~" p- ~) T1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
, i0 A0 B; x% F. X3 q2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 9 K$ N" ^% |: G1 K
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan : {( N; y0 O* q% u& x
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
9 E4 V' i5 A" i. n- Y- J- x5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan : `7 o0 `8 d7 y5 }* d
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
- C1 Q; V: t1 d, U5 _7Kinki University School of Medicine, Osaka 589-8511, Japan
5 i" s& N0 S- H) `8Izumi Municipal Hospital, Osaka 594-0071, Japan
/ D) W5 R9 G; o/ O9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
- t7 b0 D4 A  @2 e* wCorrespondence 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
! A/ o2 \  ]4 y( Y3 ~% }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 j- z8 p, s/ }* @4 I) d' kAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
3 K3 @/ ]7 w. r% z* H) H* Y' G* p: J7 v2 v/ {3 \1 m6 i
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
/ ?# S' ?: C  j9 S/ l$ [! j, ~) M7 q9 c4 W9 Y9 e( M' e
Published online on: Thursday, December 1, 2011 9 {* B3 ~( }! K" B. g/ J' H* b; c7 J2 d
6 t* r; y! R! a  l, @$ F# l, c
Doi: 10.3892/ol.2011.507 # o3 ~: }; h( S! X9 l5 u& s

6 i$ D6 E; p7 W' O8 xPages: 405-410
% A, s) u9 B# {/ S$ A. b
% ~% ], Y2 d9 W% DAbstract:0 f5 u& v. e: I
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.3 C  u/ U3 T5 S) r8 {" w" j, V
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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 population9 K: [; M# f& t2 ~) ~8 Y6 p
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
! Q. ~" j  o; d4 l$ g: `7 I6 o& ^+ Author Affiliations) Z; V' P6 ^, u
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
7 k# M# [- w& ?$ s2Department of Thoracic Surgery, Kyoto University, Kyoto 2 e/ Y- j' X4 c4 P! m" u
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
% N" N+ [; x4 Y5 O( z, B&#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 6 G9 |/ w2 ]8 R. D2 H- t
Received September 3, 2010. ( b' P9 ~* A% m5 G
Revision received November 11, 2010. $ \+ Q7 l7 A! [6 v4 z( n
Accepted November 17, 2010.
/ y3 F/ v' k/ Z& b/ @3 p7 o/ iAbstract
! C" k3 k$ M5 nBackground: 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.
0 S, n. B: @4 v$ C! oPatients 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.
$ z* E. ?) Q  E( L! @( @* b) t# T9 v- mResults: 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( d1 q# j6 ]0 G
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. ; l" z9 \1 e$ O) P+ ]1 X/ `
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。7 V; t( M! q2 L- Q7 f; ?2 j: ?
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?3 D1 C* q/ U8 \) ?$ t
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
2 l% r$ c  ^; z, ~  Q% ]% R6 t9 R0 Ahttp://clinicaltrials.gov/ct2/show/NCT01523587$ h9 g5 ^+ g- N
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC+ O! L' Z% w1 j/ H" m- I8 W
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 4 U. @- V# o: ^0 r
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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。
0 I( H/ @( m. _4 L& t1 Z( s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。
6 l5 P8 d& [* J  l0 w不错。

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