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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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1464899 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
8 ]% F( F8 O4 m0 |& z' rNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 4 O2 M! @4 X# ]3 T6 [
+ Author Affiliations* \" Y) p  z4 I! e: E) T) i! K. v& J- B
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1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan * {, S. Y( l: G9 Q. P+ R1 ]
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan . ~4 y& n2 k' q1 P  Y1 n5 o- s
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan ( n: w, e) o3 G$ n
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
. Y' v% A4 ~. l; l; p- A5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
% {0 q. N( a5 q. N/ C. J8 E6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
! j  O1 L, i3 A# Y+ V# S4 {7Kinki University School of Medicine, Osaka 589-8511, Japan
8 i9 t% t0 V3 L9 g8Izumi Municipal Hospital, Osaka 594-0071, Japan # j  c# v2 A5 B& g5 ^- _+ s
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
, g  n3 O& b9 GCorrespondence 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 9 R" B4 \7 `, x
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. 2 R& D" k5 N) p. W% _2 d. x! e
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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 ! x5 p7 u4 |7 {6 }" I& L
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Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
3 G4 B" P6 ]; T( U; G7 c9 ^- ]( F6 c, A' _1 T" t4 s. ^9 S& o
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan    K% w' G: ?4 P: G* t7 w

' h! A! b2 m1 A2 E* iPublished online on: Thursday, December 1, 2011
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Doi: 10.3892/ol.2011.507
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Pages: 405-410
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Abstract:% g) n" K: n3 B% 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 population8 {# y; P* X; H
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 * D8 D7 R# J7 m6 @
+ Author Affiliations- f) q- ?) C' I
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
  R+ m0 a: B" z* x- {9 g/ g2Department of Thoracic Surgery, Kyoto University, Kyoto 3 b7 h# w5 V- b: \- ?5 l4 p
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan * U: Z# q9 O  k) h( e: y
&#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 7 y" `& z# H: P0 Z* U
Received September 3, 2010. 3 b& o" U  f% C  o" H% ~) H
Revision received November 11, 2010. & I0 ~' O' s8 k9 S  R
Accepted November 17, 2010.
) l- Z& I. l. [; vAbstract! Q0 d8 j9 z) L0 a! b! ]" M
Background: 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. . J, R! Z6 D& }$ \7 ]7 a" R
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.
; E+ f- H' X1 P8 z- IResults: 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. . Q' l7 u# G) }
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. 1 i  W9 Y# Q; V* C: C6 k
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。
$ Y: Y+ W8 b( C" G. ?5 n# X1 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?4 T8 e2 i: |( k
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 C5 v7 Q0 W) Q+ u' ]
http://clinicaltrials.gov/ct2/show/NCT015235877 m( d0 m) `1 y2 _* p

0 f6 _- o( y" z& n! V6 m  OBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC' s2 b6 m& i" p; u! S# R' K) A5 |
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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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。
7 i; K2 x& [2 q% `7 Z* V) x" O% M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 - C  {9 _% ]! D/ _! s$ l
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。' }6 l5 D3 s0 t& e
至今为止,未出 ...

9 K+ g, [2 j! X9 |没有副作用是第一追求,效果显著是第二追求。
$ W( T: c: h) @; s/ C0 h! f6 ^8 X不错。

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