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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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1206190 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
, {9 T) _8 P! P+ f% K, t( i" uNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
/ j2 a. o( m5 m$ u: |+ Author Affiliations( I, U4 n3 w% v# t" _/ q

% W  Q! S; a0 r& q$ u# \1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan - j$ x: }# D4 q
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan / [/ x' H8 e, I- U* V% S2 [" \+ K
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
: q$ Q- b% m+ x9 l+ ]4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan : k7 p" X6 N. ?0 K0 W: G" |% y
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan 4 p  }; M8 E: L' U# r1 U) h& k
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan 2 d( [6 s0 Y5 h1 ~
7Kinki University School of Medicine, Osaka 589-8511, Japan
, J2 I2 J! ^# i, L8Izumi Municipal Hospital, Osaka 594-0071, Japan
3 D2 q0 V+ [" y- u5 d9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
2 {+ K' B- Q: s$ XCorrespondence 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
. G* L; L  Y8 ]; k2 L- JAbstractBackground: 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. ; [5 U: M) s" T6 F% V+ S- J
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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   ^4 T; C0 Q" Z- Y7 t: ]
7 F2 G6 e$ b; U+ z
Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato ; b: |1 {. z1 m1 s5 Q- R1 @8 {0 L0 n

- W- s/ V$ d+ Q9 w3 EAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
0 a+ k4 q& J; W4 {" J5 q5 H
2 [; _& ^; Q! h' z  {, Y$ iPublished online on: Thursday, December 1, 2011
+ p, Y; s* L( E- Y  k6 {1 Q3 W0 n  U
Doi: 10.3892/ol.2011.507
! ^& r/ x. z0 L% G5 x5 h' s% }# V1 @' k7 w3 z1 ~
Pages: 405-410
  h( Y5 S* ~5 h. V8 @2 {: d5 ^' }0 p, M% r! Y/ q5 P/ o( p( b
Abstract:
+ u' i7 A% ?" f  bS-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
. v7 B3 c& c. N% _& DF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 ) \& H! l- H, J
+ Author Affiliations% ]* Y) u' x* J
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu : I, s4 m: S- ^: `2 ]: m3 u2 y1 O' T' }
2Department of Thoracic Surgery, Kyoto University, Kyoto
$ s4 g* V  `6 N9 K- D3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan 3 V9 j' v9 D% G( D. {! A) S2 R
&#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
0 R/ l. p! |/ C  z6 VReceived September 3, 2010. 8 L/ m: q8 G" k0 }7 W+ b
Revision received November 11, 2010. 8 B- c: a# @! p( D
Accepted November 17, 2010. 9 U& a3 Z$ L% ]0 v  q2 s
Abstract
/ l; P& e5 l6 u6 OBackground: 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. - d" M+ u# ?4 D0 e& ], 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.
; ^4 n! D1 l7 @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. ! E; O% g$ [+ C8 k; b( t4 _
Conclusion: 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。  X: e; A/ k8 L3 H8 c- b
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 Chemotherapy/ v3 Z% X  ~$ C
http://clinicaltrials.gov/ct2/show/NCT01523587; Y' b- p9 s# c% \

; P6 F' s8 v+ eBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
) G2 W! G; w" d8 z3 Xhttp://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 ) [  T) T( ?9 H& e0 e& R! i

% @9 u# E. i* O$ v  }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。
  j8 E% Y. z; b9 @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
% D8 S+ ?) a( t' h/ J. ?9 J' X. g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。
1 a" O: b7 d" y8 t) F: o8 @至今为止,未出 ...

  U. z: I6 b5 W0 P; V! p没有副作用是第一追求,效果显著是第二追求。
& L8 p6 r3 l$ z/ i不错。

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